Item | Value |
---|---|
geneid | 55530 |
ensemblid | ENSG00000166111.10 |
hgncid | 25417 |
symbol | SVOP |
name | SV2 related protein |
refseq_nuc | NM_018711.5 |
refseq_prot | NP_061181.1 |
ensembl_nuc | ENST00000610966.5 |
ensembl_prot | ENSP00000479104.1 |
mane_status | MANE Select |
chr | chr12 |
start | 108907741 |
end | 109021068 |
strand | - |
ver | v1.2 |
region | chr12:108907741-109021068 |
region5000 | chr12:108902741-109026068 |
regionname0 | SVOP_chr12_108907741_109021068 |
regionname5000 | SVOP_chr12_108902741_109026068 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1644 | 180 | 44 | 37 | 66 | 5 | 26 | SVOP_chr12_108902741_109026068 | SVOP | ATGGA others(1639): Show |
chr12 | 108902741 | 109026068 | ||
a0001c0002 | 0/0 | 1644 | 90 | 39 | 18 | 22 | 3 | 8 | SVOP_chr12_108902741_109026068 | SVOP | ATGGA others(1639): Show |
chr12 | 108902741 | 109026068 | ||
a0001c0003 | 0/0 | 1644 | 9 | 4 | 1 | 4 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ATGGA others(1639): Show |
chr12 | 108902741 | 109026068 | ||
a0001c0004 | 0/0 | 1644 | 6 | 1 | 2 | 3 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ATGGA others(1639): Show |
chr12 | 108902741 | 109026068 | ||
a0001c0005 | 0/0 | 1644 | 2 | 0 | 0 | 2 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ATGGA others(1639): Show |
chr12 | 108902741 | 109026068 | ||
a0001c0006 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ATGGA others(1639): Show |
chr12 | 108902741 | 109026068 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6641 | 37 | 3 | 9 | 16 | 2 | 7 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0002 | 0/0 | 6641 | 17 | 0 | 1 | 13 | 1 | 2 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0003 | 0/0 | 6641 | 25 | 1 | 7 | 17 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0004 | 0/0 | 6641 | 9 | 2 | 5 | 0 | 0 | 2 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0005 | 0/0 | 6641 | 8 | 0 | 4 | 1 | 0 | 3 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0006 | 0/0 | 6641 | 5 | 4 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0007 | 0/0 | 6641 | 5 | 0 | 1 | 4 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0008 | 0/0 | 6642 | 7 | 4 | 3 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0009 | 0/0 | 6643 | 7 | 6 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6638): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0012 | 0/0 | 6641 | 4 | 4 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0013 | 0/0 | 6642 | 2 | 2 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0014 | 0/0 | 6639 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6634): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0015 | 0/0 | 6641 | 3 | 0 | 1 | 0 | 1 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0017 | 0/0 | 6641 | 4 | 0 | 0 | 4 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0019 | 0/0 | 6641 | 3 | 0 | 1 | 0 | 0 | 2 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0020 | 0/0 | 6641 | 2 | 2 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0022 | 0/0 | 6641 | 3 | 0 | 0 | 1 | 0 | 2 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0024 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0027 | 0/0 | 6642 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0029 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0030 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0031 | 0/0 | 6641 | 2 | 2 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0037 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0038 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0041 | 1/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0042 | 0/0 | 6642 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0043 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0044 | 0/0 | 6640 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0047 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0048 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0049 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0050 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0051 | 0/0 | 6643 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6638): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0052 | 0/0 | 6642 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0054 | 0/1 | 6641 | 1 | 0 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0056 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0058 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0059 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0060 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0062 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0063 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0065 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0066 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0067 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0068 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0069 | 0/0 | 6643 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6638): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0070 | 0/0 | 6642 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0075 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0076 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0077 | 0/0 | 6642 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0080 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0081 | 0/0 | 6640 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0083 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0001t0085 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0001 | 0/0 | 6641 | 14 | 2 | 2 | 8 | 0 | 2 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0002 | 0/0 | 6641 | 9 | 1 | 0 | 6 | 0 | 2 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0004 | 0/0 | 6641 | 2 | 0 | 2 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0005 | 0/0 | 6641 | 3 | 0 | 1 | 2 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0006 | 0/0 | 6641 | 3 | 3 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0010 | 0/0 | 6641 | 7 | 1 | 6 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0012 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0013 | 0/0 | 6642 | 3 | 3 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0014 | 0/0 | 6639 | 4 | 4 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6634): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0015 | 0/0 | 6641 | 2 | 0 | 1 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0020 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0021 | 0/0 | 6641 | 3 | 0 | 0 | 0 | 1 | 2 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0023 | 0/0 | 6641 | 3 | 3 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0024 | 0/0 | 6641 | 2 | 2 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0025 | 0/0 | 6641 | 3 | 2 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0026 | 0/0 | 6641 | 2 | 2 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0027 | 0/0 | 6642 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0028 | 0/0 | 6641 | 2 | 0 | 0 | 0 | 2 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0029 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0030 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0032 | 0/0 | 6641 | 2 | 2 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0033 | 0/0 | 6642 | 2 | 2 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0034 | 0/0 | 6642 | 2 | 0 | 0 | 2 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0036 | 0/0 | 6640 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0039 | 0/0 | 6642 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0040 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0045 | 0/0 | 6640 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0046 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0055 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0057 | 0/0 | 6642 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0061 | 0/0 | 6642 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0064 | 0/0 | 6642 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0071 | 0/0 | 6643 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6638): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0072 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0073 | 0/0 | 6640 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0074 | 0/0 | 6641 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0078 | 0/0 | 6640 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0079 | 0/0 | 6640 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0082 | 0/0 | 6642 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0002t0084 | 0/0 | 6641 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0003t0011 | 0/0 | 6641 | 3 | 0 | 0 | 3 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0003t0016 | 0/0 | 6643 | 3 | 3 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6638): Show |
chr12 | 108902741 | 109026068 |
a0001c0003t0018 | 0/0 | 6640 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0003t0035 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0003t0053 | 0/0 | 6642 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6637): Show |
chr12 | 108902741 | 109026068 |
a0001c0004t0011 | 0/0 | 6641 | 3 | 0 | 0 | 3 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0004t0016 | 0/0 | 6643 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6638): Show |
chr12 | 108902741 | 109026068 |
a0001c0004t0018 | 0/0 | 6640 | 2 | 0 | 2 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6635): Show |
chr12 | 108902741 | 109026068 |
a0001c0005t0007 | 0/0 | 6641 | 2 | 0 | 0 | 2 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
a0001c0006t0001 | 0/0 | 6641 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | ACTCT others(6636): Show |
chr12 | 108902741 | 109026068 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0007g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0008g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0008g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0009g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0012g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0012g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0013g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0015g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0015g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0015g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0017g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0017g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0017g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0017g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0019g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0019g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0019g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0020g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0020g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0022g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0022g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0022g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0024g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0027g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0029g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0030g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0031g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0031g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0037g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0038g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0041g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0042g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0043g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0044g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0047g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0048g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0049g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0050g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0051g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0052g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0054g0192 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0056g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0058g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0059g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0060g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0062g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0063g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0065g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0066g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0067g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0068g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0069g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0070g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0075g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0076g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0077g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0080g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0081g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0083g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0001t0085g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0010g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0010g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0010g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0010g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0010g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0013g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0013g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0014g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0014g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0014g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0015g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0015g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0020g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0021g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0021g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0021g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0023g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0023g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0023g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0024g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0024g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0025g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0025g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0025g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0026g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0026g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0027g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0028g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0028g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0029g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0030g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0032g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0032g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0033g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0033g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0034g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0034g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0036g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0039g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0040g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0045g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0046g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0055g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0057g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0061g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0064g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0071g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0072g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0073g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0074g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0078g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0079g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0082g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0002t0084g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0011g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0016g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0016g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0016g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0018g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0035g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0003t0053g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0004t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0004t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0004t0011g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0004t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0004t0018g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0004t0018g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0005t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0005t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
a0001c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0028 | g0262 | EUR | GBR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00280 | hp1 | a0001 | c0002 | t0028 | g0263 | EUR | FIN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00280 | hp2 | a0001 | c0002 | t0021 | g0149 | EUR | FIN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00408 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | CHS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0087 | EAS | CHS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00544 | hp2 | a0001 | c0002 | t0061 | g0159 | EAS | CHS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | CHS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0273 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00642 | hp2 | a0001 | c0004 | t0018 | g0228 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00733 | hp1 | a0001 | c0003 | t0018 | g0152 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00733 | hp2 | a0001 | c0002 | t0010 | g0054 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00738 | hp2 | a0001 | c0002 | t0030 | g0100 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00741 | hp1 | a0001 | c0002 | t0064 | g0267 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG00741 | hp2 | a0001 | c0001 | t0077 | g0074 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01071 | hp1 | a0001 | c0002 | t0078 | g0101 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01074 | hp2 | a0001 | c0002 | t0004 | g0268 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01081 | hp2 | a0001 | c0002 | t0010 | g0174 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01106 | hp1 | a0001 | c0002 | t0010 | g0067 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01109 | hp1 | a0001 | c0002 | t0025 | g0186 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01168 | hp1 | a0001 | c0001 | t0008 | g0239 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01168 | hp2 | a0001 | c0001 | t0019 | g0096 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0238 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01175 | hp2 | a0001 | c0002 | t0015 | g0150 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01192 | hp2 | a0001 | c0004 | t0018 | g0070 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0259 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01243 | hp2 | a0001 | c0002 | t0074 | g0264 | AMR | PUR | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01255 | hp1 | a0001 | c0001 | t0044 | g0043 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01256 | hp2 | a0001 | c0002 | t0010 | g0002 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0114 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01258 | hp1 | a0001 | c0002 | t0010 | g0002 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01261 | hp2 | a0001 | c0002 | t0027 | g0066 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01346 | hp2 | a0001 | c0002 | t0010 | g0068 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01361 | hp1 | a0001 | c0002 | t0005 | g0190 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01361 | hp2 | a0001 | c0001 | t0015 | g0117 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0220 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0143 | EUR | IBS | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01884 | hp1 | a0001 | c0001 | t0070 | g0250 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01884 | hp2 | a0001 | c0001 | t0037 | g0010 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01891 | hp1 | a0001 | c0002 | t0040 | g0012 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01943 | hp2 | a0001 | c0001 | t0007 | g0048 | AMR | PEL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01978 | hp2 | a0001 | c0001 | t0038 | g0045 | AMR | PEL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02040 | hp1 | a0001 | c0005 | t0007 | g0024 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02055 | hp1 | a0001 | c0002 | t0012 | g0251 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02055 | hp2 | a0001 | c0003 | t0016 | g0232 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02080 | hp2 | a0001 | c0003 | t0035 | g0011 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02083 | hp1 | a0001 | c0005 | t0007 | g0023 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02135 | hp2 | a0001 | c0001 | t0056 | g0077 | EAS | KHV | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0257 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02155 | hp1 | a0001 | c0004 | t0011 | g0203 | EAS | CDX | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CDX | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02258 | hp1 | a0001 | c0001 | t0020 | g0112 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02280 | hp1 | a0001 | c0003 | t0016 | g0170 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02280 | hp2 | a0001 | c0001 | t0013 | g0277 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02451 | hp1 | a0001 | c0001 | t0051 | g0052 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02451 | hp2 | a0001 | c0001 | t0062 | g0211 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02572 | hp1 | a0001 | c0001 | t0031 | g0168 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02572 | hp2 | a0001 | c0002 | t0026 | g0094 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02615 | hp1 | a0001 | c0002 | t0033 | g0198 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02615 | hp2 | a0001 | c0002 | t0025 | g0184 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02622 | hp1 | a0001 | c0001 | t0014 | g0240 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02630 | hp1 | a0001 | c0002 | t0010 | g0191 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0260 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02683 | hp1 | a0001 | c0001 | t0022 | g0092 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02683 | hp2 | a0001 | c0001 | t0075 | g0111 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0248 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02723 | hp1 | a0001 | c0004 | t0016 | g0165 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02723 | hp2 | a0001 | c0003 | t0053 | g0230 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02738 | hp1 | a0001 | c0002 | t0021 | g0272 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0156 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02818 | hp1 | a0001 | c0002 | t0055 | g0275 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02818 | hp2 | a0001 | c0002 | t0045 | g0004 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0246 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02886 | hp2 | a0001 | c0002 | t0071 | g0274 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02896 | hp1 | a0001 | c0002 | t0026 | g0144 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02896 | hp2 | a0001 | c0002 | t0014 | g0175 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02897 | hp1 | a0001 | c0002 | t0014 | g0180 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02897 | hp2 | a0001 | c0002 | t0023 | g0279 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0253 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02922 | hp2 | a0001 | c0001 | t0069 | g0166 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02965 | hp1 | a0001 | c0002 | t0006 | g0164 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02965 | hp2 | a0001 | c0001 | t0058 | g0221 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02970 | hp1 | a0001 | c0003 | t0016 | g0236 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0252 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02976 | hp1 | a0001 | c0002 | t0014 | g0280 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02976 | hp2 | a0001 | c0002 | t0032 | g0177 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03041 | hp1 | a0001 | c0001 | t0042 | g0014 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03098 | hp1 | a0001 | c0001 | t0083 | g0172 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03098 | hp2 | a0001 | c0002 | t0033 | g0199 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03130 | hp1 | a0001 | c0002 | t0006 | g0235 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03130 | hp2 | a0001 | c0002 | t0023 | g0183 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03139 | hp1 | a0001 | c0002 | t0020 | g0179 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03139 | hp2 | a0001 | c0001 | t0029 | g0244 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03195 | hp1 | a0001 | c0002 | t0073 | g0176 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03195 | hp2 | a0001 | c0002 | t0024 | g0237 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03209 | hp2 | a0001 | c0002 | t0039 | g0013 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03239 | hp1 | a0001 | c0001 | t0059 | g0123 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03239 | hp2 | a0001 | c0001 | t0081 | g0141 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03453 | hp1 | a0001 | c0001 | t0031 | g0254 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03453 | hp2 | a0001 | c0002 | t0013 | g0266 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03486 | hp1 | a0001 | c0001 | t0052 | g0255 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03486 | hp2 | a0001 | c0002 | t0014 | g0178 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0139 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03516 | hp1 | a0001 | c0002 | t0013 | g0276 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03516 | hp2 | a0001 | c0001 | t0067 | g0182 | AFR | ESN | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03540 | hp1 | a0001 | c0002 | t0036 | g0049 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03540 | hp2 | a0001 | c0002 | t0025 | g0185 | AFR | GWD | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03579 | hp1 | a0001 | c0002 | t0006 | g0270 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0162 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03688 | hp1 | a0001 | c0002 | t0084 | g0208 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0207 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03704 | hp1 | a0001 | c0001 | t0019 | g0109 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03704 | hp2 | a0001 | c0001 | t0076 | g0125 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03831 | hp1 | a0001 | c0001 | t0030 | g0065 | SAS | BEB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0147 | SAS | BEB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03834 | hp2 | a0001 | c0001 | t0048 | g0041 | SAS | BEB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0069 | SAS | BEB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG04115 | hp1 | a0001 | c0001 | t0022 | g0084 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG04115 | hp2 | a0001 | c0001 | t0085 | g0085 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG04199 | hp1 | a0001 | c0001 | t0019 | g0056 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG04199 | hp2 | a0001 | c0002 | t0021 | g0151 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0102 | SAS | STU | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18522 | hp1 | a0001 | c0002 | t0032 | g0095 | AFR | YRI | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0258 | AFR | YRI | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | CHB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | CHB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18747 | hp2 | a0001 | c0001 | t0017 | g0104 | EAS | CHB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18939 | hp1 | a0001 | c0006 | t0001 | g0205 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18944 | hp2 | a0001 | c0001 | t0022 | g0122 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18947 | hp1 | a0001 | c0002 | t0034 | g0284 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18947 | hp2 | a0001 | c0001 | t0080 | g0078 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18954 | hp2 | a0001 | c0002 | t0015 | g0160 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18960 | hp2 | a0001 | c0004 | t0011 | g0187 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18967 | hp1 | a0001 | c0003 | t0011 | g0146 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18973 | hp2 | a0001 | c0001 | t0050 | g0051 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18981 | hp1 | a0001 | c0002 | t0005 | g0217 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18981 | hp2 | a0001 | c0001 | t0007 | g0030 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18982 | hp1 | a0001 | c0004 | t0011 | g0064 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18982 | hp2 | a0001 | c0001 | t0065 | g0081 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18983 | hp2 | a0001 | c0003 | t0011 | g0132 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18984 | hp1 | a0001 | c0002 | t0082 | g0216 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18993 | hp1 | a0001 | c0001 | t0007 | g0034 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18993 | hp2 | a0001 | c0001 | t0027 | g0063 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19000 | hp1 | a0001 | c0001 | t0049 | g0017 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19002 | hp2 | a0001 | c0001 | t0063 | g0080 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19011 | hp2 | a0001 | c0001 | t0017 | g0072 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19030 | hp1 | a0001 | c0002 | t0024 | g0155 | AFR | LWK | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19030 | hp2 | a0001 | c0001 | t0012 | g0242 | AFR | LWK | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19043 | hp1 | a0001 | c0001 | t0066 | g0154 | AFR | LWK | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | LWK | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19064 | hp1 | a0001 | c0002 | t0034 | g0285 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19065 | hp2 | a0001 | c0003 | t0011 | g0133 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19066 | hp1 | a0001 | c0001 | t0017 | g0103 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19067 | hp2 | a0001 | c0001 | t0043 | g0020 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19074 | hp1 | a0001 | c0002 | t0005 | g0218 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19081 | hp2 | a0001 | c0001 | t0047 | g0021 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19082 | hp2 | a0001 | c0002 | t0046 | g0029 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19084 | hp2 | a0001 | c0001 | t0017 | g0061 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19085 | hp2 | a0001 | c0001 | t0060 | g0116 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19240 | hp1 | a0001 | c0002 | t0029 | g0231 | AFR | YRI | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA19240 | hp2 | a0001 | c0001 | t0012 | g0243 | AFR | YRI | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ASW | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20129 | hp2 | a0001 | c0002 | t0072 | g0233 | AFR | ASW | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20805 | hp1 | a0001 | c0001 | t0068 | g0082 | EUR | TSI | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20805 | hp2 | a0001 | c0001 | t0015 | g0075 | EUR | TSI | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20905 | hp1 | a0001 | c0002 | t0079 | g0269 | SAS | GIH | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20905 | hp2 | a0001 | c0001 | t0015 | g0148 | SAS | GIH | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0283 | AMR | CLM | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0171 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02109 | hp2 | a0001 | c0001 | t0024 | g0247 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0278 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0261 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0245 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG02559 | hp2 | a0001 | c0001 | t0020 | g0181 | AFR | ACB | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03471 | hp1 | a0001 | c0002 | t0023 | g0234 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0053 | AFR | MSL | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | USA | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
HG06807 | hp2 | a0001 | c0002 | t0013 | g0167 | AFR | USA | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20300 | hp1 | a0001 | c0002 | t0057 | g0153 | AFR | USA | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | USA | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0241 | AFR | LWK | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
homoSapiens | chm13v2 | a0001 | c0001 | t0054 | g0192 | REF | REF | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
homoSapiens | grch38p0 | a0001 | c0001 | t0041 | g0015 | REF | REF | SVOP_chr12_108902741_109026068 | SVOP | chr12 | 108902741 | 109026068 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108912577 | G | A | 1 | a0001c0006 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.1605C>T | p.His535His | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1805/6641 | 1605/1647 | 535/548 | chr12 | 108912577 | |||
chr12:108915795 | C | T | 2 | a0001c0003 a0001c0004 |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
synonymous_variant | LOW | c.1428G>A | p.Pro476Pro | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/16 | 1628/6641 | 1428/1647 | 476/548 | chr12 | 108915795 | |||
chr12:108977440 | G | A | 1 | a0001c0006 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.339C>T | p.Cys113Cys | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/16 | 539/6641 | 339/1647 | 113/548 | chr12 | 108977440 | |||
chr12:108983605 | A | G | 3 | a0001c0002 a0001c0004 a0001c0006 |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
synonymous_variant | LOW | c.192T>C | p.Thr64Thr | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/16 | 392/6641 | 192/1647 | 64/548 | chr12 | 108983605 | |||
chr12:108983758 | A | C | 1 | a0001c0005 | 2 | HG02040.hp1 HG02083.hp1 |
synonymous_variant | LOW | c.39T>G | p.Val13Val | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/16 | 239/6641 | 39/1647 | 13/548 | chr12 | 108983758 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108908057 | A | AT | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(45): Show |
132 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*4477dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4477 | chr12 | 108908057 | ||||||
chr12:108908085 | G | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0015 others(22): Show |
84 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*4450C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4450 | chr12 | 108908085 | ||||||
chr12:108908118 | G | A | 1 | a0001c0001t0068 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4417C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4417 | chr12 | 108908118 | ||||||
chr12:108908248 | C | T | 1 | a0001c0001t0052 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4287G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4287 | chr12 | 108908248 | ||||||
chr12:108908319 | T | C | 2 | a0001c0001t0020 a0001c0002t0020 |
3 | HG02258.hp1 HG02559.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4216A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4216 | chr12 | 108908319 | ||||||
chr12:108908330 | T | G | 7 | a0001c0001t0031 a0001c0001t0063 a0001c0003t0011 others(4): Show |
14 | HG02055.hp2 HG02080.hp2 HG02155.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4205A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4205 | chr12 | 108908330 | ||||||
chr12:108908481 | C | T | 1 | a0001c0001t0067 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4054G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4054 | chr12 | 108908481 | ||||||
chr12:108908534 | C | T | 3 | a0001c0001t0006 a0001c0001t0067 a0001c0002t0006 |
9 | HG01167.hp1 HG02622.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4001G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4001 | chr12 | 108908534 | ||||||
chr12:108908535 | C | A | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(45): Show |
132 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*4000G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 4000 | chr12 | 108908535 | ||||||
chr12:108908631 | C | G | 2 | a0001c0001t0029 a0001c0002t0029 |
2 | HG03139.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3904G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3904 | chr12 | 108908631 | ||||||
chr12:108908632 | C | T | 1 | a0001c0002t0057 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3903G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3903 | chr12 | 108908632 | ||||||
chr12:108908648 | A | C | 1 | a0001c0002t0072 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3887T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3887 | chr12 | 108908648 | ||||||
chr12:108908845 | C | T | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0015 others(22): Show |
84 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*3690G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3690 | chr12 | 108908845 | ||||||
chr12:108908905 | G | A | 1 | a0001c0001t0043 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3630C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3630 | chr12 | 108908905 | ||||||
chr12:108908982 | C | T | 2 | a0001c0002t0064 a0001c0003t0053 |
2 | HG00741.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3553G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3553 | chr12 | 108908982 | ||||||
chr12:108909019 | A | G | 10 | a0001c0001t0015 a0001c0001t0031 a0001c0001t0063 others(7): Show |
20 | HG00280.hp2 HG00741.hp2 HG01175.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3516T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3516 | chr12 | 108909019 | ||||||
chr12:108909102 | A | G | 30 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 others(27): Show |
66 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3433T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3433 | chr12 | 108909102 | ||||||
chr12:108909165 | T | A | 1 | a0001c0001t0080 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3370A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3370 | chr12 | 108909165 | ||||||
chr12:108909282 | A | G | 34 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 others(31): Show |
75 | HG00733.hp2 HG00741.hp1 HG01071.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3253T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3253 | chr12 | 108909282 | ||||||
chr12:108909385 | G | A | 21 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0031 others(18): Show |
34 | HG00741.hp1 HG01884.hp1 HG01884.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3150C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3150 | chr12 | 108909385 | ||||||
chr12:108909431 | G | A | 2 | a0001c0003t0018 a0001c0004t0018 |
3 | HG00642.hp2 HG00733.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3104C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3104 | chr12 | 108909431 | ||||||
chr12:108909446 | A | G | 53 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(50): Show |
138 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*3089T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3089 | chr12 | 108909446 | ||||||
chr12:108909464 | G | A | 1 | a0001c0001t0060 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3071C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3071 | chr12 | 108909464 | ||||||
chr12:108909466 | G | T | 1 | a0001c0001t0060 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3069 | chr12 | 108909466 | ||||||
chr12:108909476 | C | CA | 22 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0013 others(19): Show |
37 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3058dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3058 | chr12 | 108909476 | ||||||
chr12:108909476 | C | CAA | 4 | a0001c0001t0009 a0001c0001t0051 a0001c0001t0069 others(1): Show |
10 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3057_*3058dupTT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3058 | chr12 | 108909476 | ||||||
chr12:108909476 | CA | C | 5 | a0001c0001t0014 a0001c0001t0044 a0001c0002t0014 others(2): Show |
8 | HG01071.hp1 HG01255.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3058delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 3058 | chr12 | 108909476 | ||||||
chr12:108909742 | T | A | 2 | a0001c0001t0030 a0001c0002t0030 |
2 | HG00738.hp2 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2793A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2793 | chr12 | 108909742 | ||||||
chr12:108909755 | G | A | 8 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0066 others(5): Show |
21 | HG00733.hp2 HG01071.hp1 HG01081.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2780C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2780 | chr12 | 108909755 | ||||||
chr12:108909783 | A | G | 1 | a0001c0002t0039 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2752T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2752 | chr12 | 108909783 | ||||||
chr12:108909789 | G | A | 3 | a0001c0001t0009 a0001c0001t0051 a0001c0001t0069 |
9 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2746C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2746 | chr12 | 108909789 | ||||||
chr12:108909927 | G | A | 1 | a0001c0001t0062 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2608C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2608 | chr12 | 108909927 | ||||||
chr12:108909982 | T | C | 1 | a0001c0002t0046 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2553A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2553 | chr12 | 108909982 | ||||||
chr12:108909990 | T | C | 1 | a0001c0002t0046 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2545A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2545 | chr12 | 108909990 | ||||||
chr12:108909994 | C | T | 1 | a0001c0002t0039 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2541G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2541 | chr12 | 108909994 | ||||||
chr12:108909999 | G | A | 8 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0066 others(5): Show |
21 | HG00733.hp2 HG01071.hp1 HG01081.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2536C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2536 | chr12 | 108909999 | ||||||
chr12:108910000 | C | T | 1 | a0001c0002t0028 | 2 | HG00099.hp1 HG00280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2535G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2535 | chr12 | 108910000 | ||||||
chr12:108910003 | A | T | 8 | a0001c0001t0006 a0001c0001t0024 a0001c0001t0066 others(5): Show |
21 | HG00733.hp2 HG01071.hp1 HG01081.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2532T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2532 | chr12 | 108910003 | ||||||
chr12:108910020 | C | T | 3 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0069 |
8 | HG01168.hp2 HG02922.hp2 HG03704.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2515G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2515 | chr12 | 108910020 | ||||||
chr12:108910105 | A | G | 3 | a0001c0001t0059 a0001c0002t0039 a0001c0002t0040 |
3 | HG01891.hp1 HG03209.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2430T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2430 | chr12 | 108910105 | ||||||
chr12:108910117 | A | G | 59 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(56): Show |
147 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*2418T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2418 | chr12 | 108910117 | ||||||
chr12:108910126 | AT | A | 57 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(54): Show |
145 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2408delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2408 | chr12 | 108910126 | ||||||
chr12:108910175 | G | C | 1 | a0001c0001t0047 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2360C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2360 | chr12 | 108910175 | ||||||
chr12:108910213 | C | T | 2 | a0001c0002t0036 a0001c0002t0055 |
2 | HG02818.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2322G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2322 | chr12 | 108910213 | ||||||
chr12:108910253 | T | C | 1 | a0001c0001t0065 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2282A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2282 | chr12 | 108910253 | ||||||
chr12:108910363 | C | T | 7 | a0001c0001t0013 a0001c0001t0042 a0001c0001t0052 others(4): Show |
12 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2172G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2172 | chr12 | 108910363 | ||||||
chr12:108910366 | C | T | 1 | a0001c0001t0066 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2169G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2169 | chr12 | 108910366 | ||||||
chr12:108910386 | G | A | 1 | a0001c0002t0025 | 3 | HG01109.hp1 HG02615.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2149C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2149 | chr12 | 108910386 | ||||||
chr12:108910411 | C | T | 2 | a0001c0001t0031 a0001c0002t0073 |
3 | HG02572.hp1 HG03195.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2124G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2124 | chr12 | 108910411 | ||||||
chr12:108910428 | G | A | 1 | a0001c0001t0048 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2107C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 2107 | chr12 | 108910428 | ||||||
chr12:108910838 | A | T | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(41): Show |
129 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1697T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1697 | chr12 | 108910838 | ||||||
chr12:108910914 | T | A | 83 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(80): Show |
244 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1621A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1621 | chr12 | 108910914 | ||||||
chr12:108911031 | C | G | 2 | a0001c0002t0039 a0001c0002t0040 |
2 | HG01891.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1504G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1504 | chr12 | 108911031 | ||||||
chr12:108911159 | A | G | 9 | a0001c0002t0023 a0001c0003t0011 a0001c0003t0016 others(6): Show |
18 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1376T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1376 | chr12 | 108911159 | ||||||
chr12:108911200 | A | G | 1 | a0001c0002t0025 | 3 | HG01109.hp1 HG02615.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1335T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1335 | chr12 | 108911200 | ||||||
chr12:108911252 | C | T | 1 | a0001c0002t0074 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1283G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1283 | chr12 | 108911252 | ||||||
chr12:108911423 | T | C | 1 | a0001c0002t0073 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1112A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1112 | chr12 | 108911423 | ||||||
chr12:108911430 | C | T | 3 | a0001c0001t0075 a0001c0001t0076 a0001c0002t0074 |
3 | HG01243.hp2 HG02683.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1105G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 1105 | chr12 | 108911430 | ||||||
chr12:108911583 | C | T | 29 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(26): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*952G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 952 | chr12 | 108911583 | ||||||
chr12:108911745 | T | C | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(33): Show |
118 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*790A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 790 | chr12 | 108911745 | ||||||
chr12:108912152 | T | C | 1 | a0001c0001t0049 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 383 | chr12 | 108912152 | ||||||
chr12:108912284 | T | C | 1 | a0001c0002t0084 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*251A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 251 | chr12 | 108912284 | ||||||
chr12:108912338 | A | G | 8 | a0001c0003t0011 a0001c0003t0016 a0001c0003t0018 others(5): Show |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*197T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 197 | chr12 | 108912338 | ||||||
chr12:108912429 | T | G | 1 | a0001c0001t0085 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 106 | chr12 | 108912429 | ||||||
chr12:108912459 | A | G | 2 | a0001c0001t0008 a0001c0001t0052 |
8 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*76T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 16/16 | 76 | chr12 | 108912459 | ||||||
chr12:109020936 | C | T | 1 | a0001c0001t0051 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/16 | 68 | chr12 | 109020936 | ||||||
chr12:109020964 | C | T | 1 | a0001c0001t0050 | 1 | NA18973.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/16 | 96 | chr12 | 109020964 | ||||||
chr12:109021001 | G | C | 1 | a0001c0002t0034 | 2 | NA18947.hp1 NA19064.hp1 |
5_prime_UTR_variant | MODIFIER | c.-133C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/16 | 133 | chr12 | 109021001 | ||||||
chr12:109021051 | G | A | 85 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(82): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-183C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/16 | chr12 | 109021051 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:108912851 | A | G | 52 | a0001c0001t0002g0057 a0001c0001t0002g0073 a0001c0001t0002g0079 others(49): Show |
52 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1441-110T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108912851 | |||||||
chr12:108912967 | C | T | 1 | a0001c0002t0064g0267 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1441-226G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108912967 | |||||||
chr12:108913032 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1441-291A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913032 | |||||||
chr12:108913066 | GT | G | 14 | a0001c0001t0008g0162 a0001c0001t0008g0171 a0001c0001t0008g0220 others(11): Show |
14 | HG01081.hp2 HG01109.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.1441-326delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913066 | |||||||
chr12:108913073 | G | GT | 5 | a0001c0001t0001g0059 a0001c0001t0043g0020 a0001c0002t0001g0202 others(2): Show |
5 | HG01175.hp1 NA18939.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-333dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913073 | |||||||
chr12:108913133 | G | A | 11 | a0001c0001t0008g0162 a0001c0001t0008g0171 a0001c0001t0008g0220 others(8): Show |
11 | HG01081.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1441-392C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913133 | |||||||
chr12:108913148 | C | T | 2 | a0001c0002t0023g0234 a0001c0002t0023g0279 |
2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1441-407G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913148 | |||||||
chr12:108913202 | C | T | 1 | a0001c0002t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1441-461G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913202 | |||||||
chr12:108913352 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1441-611G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913352 | |||||||
chr12:108913462 | G | C | 5 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-721C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913462 | |||||||
chr12:108913796 | A | G | 254 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(251): Show |
256 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.1441-1055T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913796 | |||||||
chr12:108913930 | T | A | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1441-1189A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108913930 | |||||||
chr12:108914077 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(239): Show |
244 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.1441-1336G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914077 | |||||||
chr12:108914117 | C | T | 1 | a0001c0002t0010g0191 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1441-1376G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914117 | |||||||
chr12:108914120 | C | A | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1441-1379G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914120 | |||||||
chr12:108914132 | T | A | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1441-1391A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914132 | |||||||
chr12:108914172 | A | T | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1441-1431T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914172 | |||||||
chr12:108914260 | A | T | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1441-1519T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914260 | |||||||
chr12:108914317 | C | T | 10 | a0001c0001t0008g0162 a0001c0001t0008g0171 a0001c0001t0008g0220 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1440+1466G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914317 | |||||||
chr12:108914329 | C | T | 10 | a0001c0001t0008g0162 a0001c0001t0008g0171 a0001c0001t0008g0220 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.1440+1454G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914329 | |||||||
chr12:108914359 | C | T | 1 | a0001c0001t0015g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1440+1424G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914359 | |||||||
chr12:108914362 | T | G | 1 | a0001c0004t0011g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1440+1421A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914362 | |||||||
chr12:108914457 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1440+1326G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914457 | |||||||
chr12:108914487 | C | T | 1 | a0001c0002t0027g0066 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1440+1296G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914487 | |||||||
chr12:108914673 | A | G | 122 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(119): Show |
123 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.1440+1110T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914673 | |||||||
chr12:108914688 | C | A | 13 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(10): Show |
13 | HG00741.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1440+1095G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914688 | |||||||
chr12:108914837 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1440+946G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914837 | |||||||
chr12:108914849 | C | A | 1 | a0001c0001t0051g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1440+934G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914849 | |||||||
chr12:108914860 | T | C | 103 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(100): Show |
104 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1440+923A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914860 | |||||||
chr12:108914878 | A | T | 1 | a0001c0002t0074g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1440+905T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914878 | |||||||
chr12:108914885 | A | T | 13 | a0001c0001t0013g0277 a0001c0001t0013g0278 a0001c0001t0019g0056 others(10): Show |
13 | HG01168.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1440+898T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914885 | |||||||
chr12:108914886 | A | AT | 6 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(3): Show |
6 | HG01978.hp2 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+896dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914886 | |||||||
chr12:108914886 | A | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(105): Show |
109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1440+897T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914886 | |||||||
chr12:108914887 | T | A | 5 | a0001c0002t0045g0004 a0001c0003t0016g0170 a0001c0003t0016g0232 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1440+896A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914887 | |||||||
chr12:108914959 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(98): Show |
102 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1440+824C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914959 | |||||||
chr12:108914989 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1440+794C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108914989 | |||||||
chr12:108915045 | C | T | 7 | a0001c0001t0008g0171 a0001c0001t0008g0220 a0001c0001t0008g0238 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1440+738G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915045 | |||||||
chr12:108915066 | G | A | 2 | a0001c0001t0005g0069 a0001c0001t0005g0102 |
2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1440+717C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915066 | |||||||
chr12:108915090 | T | C | 2 | a0001c0002t0033g0198 a0001c0002t0033g0199 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1440+693A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915090 | |||||||
chr12:108915172 | C | CA | 8 | a0001c0001t0003g0028 a0001c0001t0003g0039 a0001c0001t0005g0102 others(5): Show |
8 | HG01070.hp2 HG01243.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1440+610dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915172 | |||||||
chr12:108915172 | C | CAAA | 10 | a0001c0001t0008g0162 a0001c0001t0008g0171 a0001c0001t0008g0220 others(7): Show |
10 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1440+608_1440+610d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915172 | |||||||
chr12:108915172 | CA | C | 7 | a0001c0001t0001g0059 a0001c0001t0003g0037 a0001c0001t0003g0038 others(4): Show |
7 | HG00741.hp2 HG01175.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+610delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915172 | |||||||
chr12:108915172 | CAA | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0062 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1440+609_1440+610d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915172 | |||||||
chr12:108915173 | A | C | 1 | a0001c0002t0057g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1440+610T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915173 | |||||||
chr12:108915175 | A | C | 2 | a0001c0001t0001g0118 a0001c0002t0027g0066 |
2 | HG01261.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1440+608T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915175 | |||||||
chr12:108915266 | G | T | 103 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(100): Show |
104 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1440+517C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915266 | |||||||
chr12:108915290 | T | A | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1440+493A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915290 | |||||||
chr12:108915326 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1440+457G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915326 | |||||||
chr12:108915648 | T | C | 104 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(101): Show |
105 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1440+135A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 15/15 | chr12 | 108915648 | |||||||
chr12:108915986 | T | C | 21 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(18): Show |
21 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1351-114A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108915986 | |||||||
chr12:108916049 | C | T | 1 | a0001c0002t0010g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1351-177G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916049 | |||||||
chr12:108916115 | G | T | 1 | a0001c0002t0072g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1351-243C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916115 | |||||||
chr12:108916121 | C | G | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1351-249G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916121 | |||||||
chr12:108916122 | T | C | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1351-250A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916122 | |||||||
chr12:108916123 | C | T | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1351-251G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916123 | |||||||
chr12:108916155 | A | G | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1351-283T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916155 | |||||||
chr12:108916178 | T | C | 3 | a0001c0002t0025g0184 a0001c0002t0025g0185 a0001c0002t0025g0186 |
3 | HG01109.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1351-306A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916178 | |||||||
chr12:108916195 | C | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1351-323G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916195 | |||||||
chr12:108916209 | C | T | 8 | a0001c0001t0003g0018 a0001c0001t0003g0031 a0001c0001t0003g0040 others(5): Show |
8 | HG00738.hp1 HG01255.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1351-337G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916209 | |||||||
chr12:108916233 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1351-361G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916233 | |||||||
chr12:108916264 | G | A | 1 | a0001c0002t0023g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1351-392C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916264 | |||||||
chr12:108916391 | T | A | 1 | a0001c0001t0003g0005 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1351-519A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916391 | |||||||
chr12:108916468 | A | G | 1 | a0001c0001t0003g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1351-596T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916468 | |||||||
chr12:108916490 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1351-618C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916490 | |||||||
chr12:108916516 | C | T | 3 | a0001c0002t0025g0184 a0001c0002t0025g0185 a0001c0002t0025g0186 |
3 | HG01109.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1351-644G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916516 | |||||||
chr12:108916524 | C | T | 3 | a0001c0002t0032g0095 a0001c0002t0032g0177 a0001c0002t0072g0233 |
3 | HG02976.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1351-652G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916524 | |||||||
chr12:108916549 | C | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(88): Show |
93 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1351-677G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916549 | |||||||
chr12:108916568 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(91): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1351-696A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916568 | |||||||
chr12:108916630 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1351-758G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916630 | |||||||
chr12:108916835 | C | T | 15 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 others(12): Show |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1351-963G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916835 | |||||||
chr12:108916839 | G | T | 24 | a0001c0001t0013g0277 a0001c0001t0013g0278 a0001c0001t0031g0168 others(21): Show |
24 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1351-967C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108916839 | |||||||
chr12:108917007 | G | A | 96 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(93): Show |
97 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1350+1036C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917007 | |||||||
chr12:108917035 | C | T | 1 | a0001c0001t0006g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1350+1008G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917035 | |||||||
chr12:108917078 | G | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(96): Show |
101 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1350+965C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917078 | |||||||
chr12:108917211 | A | C | 1 | a0001c0001t0003g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1350+832T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917211 | |||||||
chr12:108917279 | T | A | 3 | a0001c0002t0004g0273 a0001c0002t0028g0262 a0001c0002t0028g0263 |
3 | HG00099.hp1 HG00280.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1350+764A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917279 | |||||||
chr12:108917281 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(91): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1350+762A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917281 | |||||||
chr12:108917355 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(91): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1350+688A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917355 | |||||||
chr12:108917358 | T | TTCAGTCC others(40): Show |
1 | a0001c0001t0003g0018 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1350+684_1350+685i others(49): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917358 | |||||||
chr12:108917359 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1350+684G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917359 | |||||||
chr12:108917518 | A | G | 1 | a0001c0001t0004g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1350+525T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917518 | |||||||
chr12:108917566 | A | ATAT | 244 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(241): Show |
247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1350+474_1350+476d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917566 | |||||||
chr12:108917646 | C | CT | 89 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(86): Show |
91 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1350+396dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917646 | |||||||
chr12:108917730 | A | G | 3 | a0001c0002t0023g0183 a0001c0002t0023g0234 a0001c0002t0023g0279 |
3 | HG02897.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1350+313T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917730 | |||||||
chr12:108917792 | G | A | 1 | a0001c0001t0005g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1350+251C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108917792 | |||||||
chr12:108918011 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0038g0045 |
2 | HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1350+32C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 14/15 | chr12 | 108918011 | |||||||
chr12:108918399 | G | A | 3 | a0001c0003t0016g0170 a0001c0003t0016g0232 a0001c0003t0016g0236 |
3 | HG02055.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1269-275C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108918399 | |||||||
chr12:108918430 | G | A | 1 | a0001c0001t0006g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1269-306C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108918430 | |||||||
chr12:108918436 | C | T | 11 | a0001c0001t0001g0118 a0001c0001t0001g0196 a0001c0001t0001g0209 others(8): Show |
11 | HG00099.hp2 HG01123.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1269-312G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108918436 | |||||||
chr12:108918447 | C | G | 3 | a0001c0002t0023g0183 a0001c0002t0023g0234 a0001c0002t0023g0279 |
3 | HG02897.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1269-323G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108918447 | |||||||
chr12:108918509 | C | T | 5 | a0001c0001t0001g0131 a0001c0001t0007g0025 a0001c0002t0001g0189 others(2): Show |
5 | HG02040.hp1 HG02083.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.1269-385G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108918509 | |||||||
chr12:108918730 | A | C | 3 | a0001c0002t0025g0184 a0001c0002t0025g0185 a0001c0002t0025g0186 |
3 | HG01109.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1269-606T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108918730 | |||||||
chr12:108918755 | T | C | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1269-631A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108918755 | |||||||
chr12:108919017 | T | C | 3 | a0001c0001t0037g0010 a0001c0002t0036g0049 a0001c0002t0055g0275 |
3 | HG01884.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1268+658A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919017 | |||||||
chr12:108919040 | G | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(61): Show |
65 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1268+635C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919040 | |||||||
chr12:108919041 | CA | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(239): Show |
245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1268+633delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919041 | |||||||
chr12:108919106 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(91): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1268+569G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919106 | |||||||
chr12:108919149 | C | A | 1 | a0001c0004t0011g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1268+526G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919149 | |||||||
chr12:108919242 | C | T | 1 | a0001c0002t0057g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1268+433G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919242 | |||||||
chr12:108919244 | A | G | 15 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 others(12): Show |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1268+431T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919244 | |||||||
chr12:108919274 | C | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(189): Show |
195 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1268+401G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919274 | |||||||
chr12:108919304 | TACCCACA others(11): Show |
T | 3 | a0001c0001t0005g0110 a0001c0001t0005g0271 a0001c0001t0077g0074 |
3 | HG00741.hp2 HG01106.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1268+353_1268+370d others(20): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919304 | |||||||
chr12:108919376 | C | T | 2 | a0001c0002t0032g0095 a0001c0002t0032g0177 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1268+299G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919376 | |||||||
chr12:108919384 | C | T | 15 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 others(12): Show |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1268+291G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 13/15 | chr12 | 108919384 | |||||||
chr12:108920038 | G | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(252): Show |
258 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1157-252C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920038 | |||||||
chr12:108920165 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(92): Show |
97 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1157-379G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920165 | |||||||
chr12:108920277 | T | C | 15 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 others(12): Show |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1157-491A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920277 | |||||||
chr12:108920364 | G | T | 15 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 others(12): Show |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1157-578C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920364 | |||||||
chr12:108920550 | A | C | 3 | a0001c0002t0023g0183 a0001c0002t0023g0234 a0001c0002t0023g0279 |
3 | HG02897.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1157-764T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920550 | |||||||
chr12:108920594 | C | CT | 52 | a0001c0001t0002g0079 a0001c0001t0004g0001 a0001c0001t0004g0099 others(49): Show |
53 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1157-809dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920594 | |||||||
chr12:108920594 | C | CTT | 94 | a0001c0001t0001g0173 a0001c0001t0002g0057 a0001c0001t0002g0058 others(91): Show |
95 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1157-810_1157-809d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920594 | |||||||
chr12:108920594 | C | CTTT | 8 | a0001c0001t0002g0145 a0001c0001t0005g0069 a0001c0001t0005g0156 others(5): Show |
8 | HG00741.hp2 HG01106.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157-811_1157-809d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920594 | |||||||
chr12:108920683 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1157-897G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920683 | |||||||
chr12:108920690 | T | C | 1 | a0001c0002t0057g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1157-904A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920690 | |||||||
chr12:108920747 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(91): Show |
96 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1157-961C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920747 | |||||||
chr12:108920851 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1157-1065G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108920851 | |||||||
chr12:108921079 | T | C | 3 | a0001c0002t0014g0175 a0001c0002t0014g0178 a0001c0002t0014g0180 |
3 | HG02896.hp2 HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1157-1293A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921079 | |||||||
chr12:108921080 | AAATAAAG | A | 51 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(48): Show |
51 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1157-1301_1157-129 others(11): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921080 | |||||||
chr12:108921212 | C | A | 21 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(18): Show |
21 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1157-1426G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921212 | |||||||
chr12:108921326 | C | T | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1156+1364G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921326 | |||||||
chr12:108921437 | C | A | 11 | a0001c0001t0004g0256 a0001c0001t0009g0053 a0001c0001t0009g0252 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1156+1253G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921437 | |||||||
chr12:108921473 | A | G | 1 | a0001c0002t0010g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1156+1217T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921473 | |||||||
chr12:108921483 | A | G | 2 | a0001c0002t0033g0198 a0001c0002t0033g0199 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1156+1207T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921483 | |||||||
chr12:108921752 | A | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(78): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1156+938T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921752 | |||||||
chr12:108921996 | C | T | 3 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 |
3 | NA18967.hp1 NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1156+694G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108921996 | |||||||
chr12:108922034 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(78): Show |
83 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1156+656G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108922034 | |||||||
chr12:108922123 | A | T | 13 | a0001c0001t0008g0162 a0001c0001t0008g0171 a0001c0001t0008g0220 others(10): Show |
13 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1156+567T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108922123 | |||||||
chr12:108922535 | T | C | 1 | a0001c0002t0002g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1156+155A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108922535 | |||||||
chr12:108922608 | A | G | 5 | a0001c0001t0004g0099 a0001c0001t0004g0139 a0001c0001t0004g0140 others(2): Show |
5 | HG00639.hp1 HG01081.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1156+82T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 12/15 | chr12 | 108922608 | |||||||
chr12:108922822 | G | A | 3 | a0001c0002t0023g0183 a0001c0002t0023g0234 a0001c0002t0023g0279 |
3 | HG02897.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1049-25C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108922822 | |||||||
chr12:108922860 | G | T | 2 | a0001c0002t0033g0198 a0001c0002t0033g0199 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1049-63C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108922860 | |||||||
chr12:108923028 | A | G | 15 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 others(12): Show |
15 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1049-231T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923028 | |||||||
chr12:108923075 | A | C | 99 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(96): Show |
100 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1049-278T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923075 | |||||||
chr12:108923200 | T | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(67): Show |
71 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.1049-403A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923200 | |||||||
chr12:108923201 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1049-404C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923201 | |||||||
chr12:108923259 | A | C | 99 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(96): Show |
100 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1049-462T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923259 | |||||||
chr12:108923312 | G | A | 3 | a0001c0002t0025g0184 a0001c0002t0025g0185 a0001c0002t0025g0186 |
3 | HG01109.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1049-515C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923312 | |||||||
chr12:108923321 | G | A | 2 | a0001c0002t0033g0198 a0001c0002t0033g0199 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1049-524C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923321 | |||||||
chr12:108923343 | GC | G | 15 | a0001c0001t0013g0277 a0001c0001t0013g0278 a0001c0001t0014g0240 others(12): Show |
15 | HG02280.hp2 HG02486.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1049-547delG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923343 | |||||||
chr12:108923654 | A | G | 2 | a0001c0002t0033g0198 a0001c0002t0033g0199 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1049-857T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108923654 | |||||||
chr12:108924133 | G | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0206 |
2 | NA18971.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1049-1336C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108924133 | |||||||
chr12:108924392 | C | T | 3 | a0001c0002t0025g0184 a0001c0002t0025g0185 a0001c0002t0025g0186 |
3 | HG01109.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1049-1595G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108924392 | |||||||
chr12:108924610 | C | A | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1049-1813G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108924610 | |||||||
chr12:108924774 | T | C | 2 | a0001c0002t0033g0198 a0001c0002t0033g0199 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1049-1977A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108924774 | |||||||
chr12:108925057 | C | G | 95 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(92): Show |
96 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1049-2260G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925057 | |||||||
chr12:108925058 | C | T | 95 | a0001c0001t0002g0057 a0001c0001t0002g0058 a0001c0001t0002g0073 others(92): Show |
96 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1049-2261G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925058 | |||||||
chr12:108925216 | C | T | 14 | a0001c0001t0013g0277 a0001c0001t0013g0278 a0001c0001t0014g0240 others(11): Show |
14 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1049-2419G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925216 | |||||||
chr12:108925324 | C | CG | 7 | a0001c0002t0001g0097 a0001c0002t0001g0227 a0001c0002t0004g0268 others(4): Show |
7 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1049-2528dupC | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925324 | |||||||
chr12:108925427 | C | T | 9 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1049-2630G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925427 | |||||||
chr12:108925619 | T | C | 1 | a0001c0002t0002g0200 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1049-2822A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925619 | |||||||
chr12:108925727 | G | C | 8 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0222 others(5): Show |
8 | HG01167.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1049-2930C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925727 | |||||||
chr12:108925766 | A | G | 16 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(13): Show |
16 | HG01109.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1049-2969T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925766 | |||||||
chr12:108925866 | T | A | 65 | a0001c0001t0002g0058 a0001c0001t0002g0073 a0001c0001t0002g0105 others(62): Show |
66 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1049-3069A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925866 | |||||||
chr12:108925922 | C | CT | 37 | a0001c0001t0004g0113 a0001c0001t0004g0256 a0001c0001t0006g0249 others(34): Show |
37 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1049-3126dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925922 | |||||||
chr12:108925987 | C | T | 4 | a0001c0001t0014g0240 a0001c0002t0010g0191 a0001c0002t0072g0233 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-3190G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108925987 | |||||||
chr12:108926039 | C | G | 1 | a0001c0001t0005g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1049-3242G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926039 | |||||||
chr12:108926060 | A | G | 9 | a0001c0001t0007g0048 a0001c0001t0008g0220 a0001c0001t0008g0238 others(6): Show |
9 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1049-3263T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926060 | |||||||
chr12:108926160 | A | G | 2 | a0001c0001t0008g0162 a0001c0002t0032g0177 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1049-3363T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926160 | |||||||
chr12:108926268 | A | G | 2 | a0001c0002t0023g0234 a0001c0002t0023g0279 |
2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1049-3471T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926268 | |||||||
chr12:108926442 | T | C | 1 | a0001c0002t0005g0190 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1049-3645A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926442 | |||||||
chr12:108926515 | T | C | 2 | a0001c0002t0023g0234 a0001c0002t0023g0279 |
2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1049-3718A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926515 | |||||||
chr12:108926564 | C | G | 2 | a0001c0001t0042g0014 a0001c0002t0013g0276 |
2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1049-3767G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926564 | |||||||
chr12:108926570 | T | G | 2 | a0001c0001t0042g0014 a0001c0002t0013g0276 |
2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1049-3773A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926570 | |||||||
chr12:108926571 | G | A | 4 | a0001c0001t0014g0240 a0001c0002t0010g0191 a0001c0002t0033g0198 others(1): Show |
4 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-3774C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926571 | |||||||
chr12:108926882 | T | C | 2 | a0001c0002t0023g0234 a0001c0002t0023g0279 |
2 | HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1049-4085A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926882 | |||||||
chr12:108926885 | G | A | 2 | a0001c0001t0008g0162 a0001c0002t0032g0177 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1049-4088C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926885 | |||||||
chr12:108926944 | G | A | 1 | a0001c0001t0002g0145 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1049-4147C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108926944 | |||||||
chr12:108927004 | A | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(188): Show |
193 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.1049-4207T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927004 | |||||||
chr12:108927439 | A | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(94): Show |
99 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1049-4642T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927439 | |||||||
chr12:108927464 | T | C | 1 | a0001c0001t0030g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1049-4667A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927464 | |||||||
chr12:108927471 | T | C | 2 | a0001c0001t0007g0048 a0001c0002t0073g0176 |
2 | HG01943.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1049-4674A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927471 | |||||||
chr12:108927552 | C | T | 1 | a0001c0001t0015g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1049-4755G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927552 | |||||||
chr12:108927589 | C | CT | 11 | a0001c0001t0001g0173 a0001c0001t0002g0158 a0001c0001t0049g0017 others(8): Show |
11 | HG01109.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1049-4793dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927589 | |||||||
chr12:108927589 | C | CTT | 64 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(61): Show |
64 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1049-4794_1049-479 others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927589 | |||||||
chr12:108927589 | CT | C | 18 | a0001c0001t0002g0105 a0001c0001t0004g0113 a0001c0001t0006g0193 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1049-4793delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927589 | |||||||
chr12:108927589 | CTTT | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0213 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1049-4795_1049-479 others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927589 | |||||||
chr12:108927589 | CTTTT | C | 86 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(83): Show |
87 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1049-4796_1049-479 others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927589 | |||||||
chr12:108927594 | T | C | 1 | a0001c0001t0005g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1049-4797A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927594 | |||||||
chr12:108927645 | GGATTGTG others(39): Show |
G | 1 | a0001c0001t0003g0018 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1049-4894_1049-484 others(50): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927645 | |||||||
chr12:108927679 | A | C | 1 | a0001c0001t0005g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1049-4882T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927679 | |||||||
chr12:108927907 | C | CT | 36 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1049-5111dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927907 | |||||||
chr12:108927912 | T | A | 4 | a0001c0001t0008g0162 a0001c0002t0023g0234 a0001c0002t0023g0279 others(1): Show |
4 | HG02897.hp2 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1049-5115A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927912 | |||||||
chr12:108927992 | G | A | 1 | a0001c0002t0082g0216 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1049-5195C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108927992 | |||||||
chr12:108928095 | A | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(161): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1049-5298T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928095 | |||||||
chr12:108928275 | T | A | 58 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(55): Show |
59 | HG00597.hp1 HG00639.hp2 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.1049-5478A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928275 | |||||||
chr12:108928317 | C | T | 1 | a0001c0002t0072g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1049-5520G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928317 | |||||||
chr12:108928434 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(195): Show |
201 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.1049-5637A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928434 | |||||||
chr12:108928442 | G | A | 36 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1049-5645C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928442 | |||||||
chr12:108928460 | A | C | 38 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(35): Show |
38 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1049-5663T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928460 | |||||||
chr12:108928557 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(118): Show |
124 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1048+5638G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928557 | |||||||
chr12:108928568 | A | AT | 114 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(111): Show |
117 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1048+5626dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928568 | |||||||
chr12:108928568 | A | ATT | 9 | a0001c0001t0060g0116 a0001c0002t0001g0201 a0001c0002t0001g0202 others(6): Show |
9 | HG00544.hp2 NA18747.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+5625_1048+562 others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928568 | |||||||
chr12:108928568 | AT | A | 34 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(31): Show |
34 | HG00597.hp1 HG00639.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.1048+5626delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928568 | |||||||
chr12:108928635 | C | T | 11 | a0001c0001t0008g0171 a0001c0001t0012g0241 a0001c0001t0012g0242 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+5560G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928635 | |||||||
chr12:108928668 | G | A | 1 | a0001c0002t0006g0164 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1048+5527C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928668 | |||||||
chr12:108928670 | G | A | 2 | a0001c0001t0008g0162 a0001c0002t0032g0177 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1048+5525C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928670 | |||||||
chr12:108928715 | C | T | 1 | a0001c0002t0023g0234 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1048+5480G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928715 | |||||||
chr12:108928728 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0007g0048 a0001c0001t0008g0162 others(23): Show |
27 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1048+5467C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928728 | |||||||
chr12:108928788 | G | A | 2 | a0001c0001t0005g0110 a0001c0001t0077g0074 |
2 | HG00741.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1048+5407C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928788 | |||||||
chr12:108928815 | G | A | 2 | a0001c0002t0028g0262 a0001c0002t0028g0263 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.1048+5380C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928815 | |||||||
chr12:108928816 | C | T | 1 | a0001c0001t0075g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1048+5379G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928816 | |||||||
chr12:108928892 | A | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(112): Show |
117 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1048+5303T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928892 | |||||||
chr12:108928901 | A | T | 3 | a0001c0001t0083g0172 a0001c0002t0002g0248 a0001c0002t0010g0174 |
3 | HG01081.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1048+5294T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928901 | |||||||
chr12:108928968 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(112): Show |
117 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1048+5227C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928968 | |||||||
chr12:108928996 | C | A | 7 | a0001c0001t0004g0001 a0001c0001t0007g0048 a0001c0001t0019g0056 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+5199G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108928996 | |||||||
chr12:108929091 | T | C | 1 | a0001c0001t0065g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1048+5104A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929091 | |||||||
chr12:108929276 | T | C | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1048+4919A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929276 | |||||||
chr12:108929287 | A | C | 8 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+4908T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929287 | |||||||
chr12:108929304 | G | T | 88 | a0001c0001t0001g0121 a0001c0001t0001g0212 a0001c0001t0002g0057 others(85): Show |
89 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1048+4891C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929304 | |||||||
chr12:108929308 | G | T | 42 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(39): Show |
43 | HG00597.hp1 HG00639.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1048+4887C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929308 | |||||||
chr12:108929442 | C | T | 26 | a0001c0001t0004g0001 a0001c0001t0007g0048 a0001c0001t0008g0171 others(23): Show |
27 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1048+4753G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929442 | |||||||
chr12:108929557 | C | T | 1 | a0001c0001t0014g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1048+4638G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929557 | |||||||
chr12:108929560 | T | C | 4 | a0001c0002t0045g0004 a0001c0003t0018g0152 a0001c0004t0018g0070 others(1): Show |
4 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+4635A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929560 | |||||||
chr12:108929622 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(108): Show |
113 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1048+4573C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929622 | |||||||
chr12:108929688 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(111): Show |
116 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1048+4507G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929688 | |||||||
chr12:108929730 | G | C | 2 | a0001c0005t0007g0023 a0001c0005t0007g0024 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1048+4465C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929730 | |||||||
chr12:108929794 | T | G | 8 | a0001c0001t0006g0249 a0001c0001t0067g0182 a0001c0001t0083g0172 others(5): Show |
8 | HG01081.hp2 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048+4401A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929794 | |||||||
chr12:108929858 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(100): Show |
105 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1048+4337T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929858 | |||||||
chr12:108929871 | G | A | 36 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1048+4324C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929871 | |||||||
chr12:108929951 | C | G | 36 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(33): Show |
36 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1048+4244G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929951 | |||||||
chr12:108929990 | AG | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(100): Show |
105 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1048+4204delC | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108929990 | |||||||
chr12:108930063 | T | C | 3 | a0001c0001t0020g0112 a0001c0001t0020g0181 a0001c0001t0024g0247 |
3 | HG02109.hp2 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1048+4132A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930063 | |||||||
chr12:108930091 | G | A | 1 | a0001c0003t0011g0146 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1048+4104C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930091 | |||||||
chr12:108930435 | CT | C | 128 | a0001c0001t0001g0173 a0001c0001t0002g0058 a0001c0001t0002g0073 others(125): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1048+3759delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930435 | |||||||
chr12:108930435 | CTT | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0071 others(12): Show |
16 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1048+3758_1048+375 others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930435 | |||||||
chr12:108930435 | CTTT | C | 135 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0076 others(132): Show |
136 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1048+3757_1048+375 others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930435 | |||||||
chr12:108930442 | T | C | 4 | a0001c0002t0045g0004 a0001c0003t0018g0152 a0001c0004t0018g0070 others(1): Show |
4 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+3753A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930442 | |||||||
chr12:108930507 | G | A | 1 | a0001c0001t0003g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1048+3688C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930507 | |||||||
chr12:108930635 | G | A | 4 | a0001c0002t0045g0004 a0001c0003t0018g0152 a0001c0004t0018g0070 others(1): Show |
4 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048+3560C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930635 | |||||||
chr12:108930716 | G | T | 11 | a0001c0001t0008g0171 a0001c0001t0012g0241 a0001c0001t0012g0242 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+3479C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930716 | |||||||
chr12:108930833 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(109): Show |
114 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1048+3362A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930833 | |||||||
chr12:108930928 | A | G | 38 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(35): Show |
38 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1048+3267T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108930928 | |||||||
chr12:108931079 | G | A | 2 | a0001c0002t0026g0094 a0001c0002t0026g0144 |
2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1048+3116C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931079 | |||||||
chr12:108931186 | G | A | 11 | a0001c0001t0008g0171 a0001c0001t0012g0241 a0001c0001t0012g0242 others(8): Show |
11 | HG02055.hp1 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1048+3009C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931186 | |||||||
chr12:108931201 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1048+2994T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931201 | |||||||
chr12:108931244 | T | C | 38 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0002g0079 others(35): Show |
38 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.1048+2951A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931244 | |||||||
chr12:108931289 | C | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(114): Show |
119 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.1048+2906G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931289 | |||||||
chr12:108931377 | G | C | 3 | a0001c0001t0020g0112 a0001c0001t0020g0181 a0001c0001t0024g0247 |
3 | HG02109.hp2 HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1048+2818C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931377 | |||||||
chr12:108931464 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(158): Show |
163 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1048+2731T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931464 | |||||||
chr12:108931497 | A | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(109): Show |
114 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1048+2698T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931497 | |||||||
chr12:108931557 | T | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(175): Show |
181 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.1048+2638A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931557 | |||||||
chr12:108931615 | C | T | 5 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(2): Show |
5 | HG02055.hp1 HG02630.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+2580G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931615 | |||||||
chr12:108931698 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
199 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(196): Show |
intron_variant | MODIFIER | c.1048+2497T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931698 | |||||||
chr12:108931702 | C | T | 20 | a0001c0001t0004g0001 a0001c0001t0007g0048 a0001c0001t0012g0241 others(17): Show |
21 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1048+2493G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931702 | |||||||
chr12:108931707 | G | A | 2 | a0001c0001t0008g0162 a0001c0002t0032g0177 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1048+2488C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931707 | |||||||
chr12:108931741 | G | C | 2 | a0001c0001t0008g0162 a0001c0002t0032g0177 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1048+2454C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931741 | |||||||
chr12:108931761 | G | A | 1 | a0001c0001t0008g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1048+2434C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931761 | |||||||
chr12:108931791 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1048+2404C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931791 | |||||||
chr12:108931832 | CAA | C | 157 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0071 others(154): Show |
159 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1048+2361_1048+236 others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931832 | |||||||
chr12:108931832 | CAAA | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0088 a0001c0001t0001g0119 others(3): Show |
7 | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048+2360_1048+236 others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931832 | |||||||
chr12:108931985 | G | C | 3 | a0001c0003t0018g0152 a0001c0004t0018g0070 a0001c0004t0018g0228 |
3 | HG00642.hp2 HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1048+2210C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108931985 | |||||||
chr12:108932069 | G | A | 1 | a0001c0002t0064g0267 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1048+2126C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932069 | |||||||
chr12:108932255 | G | C | 3 | a0001c0001t0014g0240 a0001c0002t0023g0234 a0001c0002t0023g0279 |
3 | HG02622.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1048+1940C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932255 | |||||||
chr12:108932356 | A | G | 2 | a0001c0001t0008g0162 a0001c0002t0032g0177 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1048+1839T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932356 | |||||||
chr12:108932455 | T | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(129): Show |
135 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1048+1740A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932455 | |||||||
chr12:108932458 | T | G | 1 | a0001c0001t0077g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1048+1737A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932458 | |||||||
chr12:108932525 | C | T | 47 | a0001c0001t0001g0121 a0001c0001t0002g0057 a0001c0001t0003g0005 others(44): Show |
47 | HG00597.hp1 HG00642.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.1048+1670G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932525 | |||||||
chr12:108932652 | C | T | 2 | a0001c0001t0031g0168 a0001c0002t0013g0167 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1048+1543G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932652 | |||||||
chr12:108932671 | G | A | 2 | a0001c0002t0010g0054 a0001c0002t0010g0067 |
2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1048+1524C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932671 | |||||||
chr12:108932785 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(97): Show |
102 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1048+1410A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932785 | |||||||
chr12:108932891 | G | A | 2 | a0001c0001t0031g0168 a0001c0002t0013g0167 |
2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1048+1304C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932891 | |||||||
chr12:108932941 | C | T | 65 | a0001c0001t0001g0121 a0001c0001t0002g0058 a0001c0001t0002g0073 others(62): Show |
65 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1048+1254G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108932941 | |||||||
chr12:108933166 | C | T | 2 | a0001c0001t0015g0075 a0001c0002t0036g0049 |
2 | HG03540.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1048+1029G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933166 | |||||||
chr12:108933379 | A | AAAT | 147 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(144): Show |
147 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1048+813_1048+815d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933379 | |||||||
chr12:108933397 | G | A | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1048+798C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933397 | |||||||
chr12:108933515 | TA | T | 162 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(159): Show |
162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1048+679delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933515 | |||||||
chr12:108933605 | A | T | 8 | a0001c0002t0004g0268 a0001c0002t0004g0273 a0001c0002t0006g0164 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048+590T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933605 | |||||||
chr12:108933675 | G | A | 1 | a0001c0002t0002g0163 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1048+520C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933675 | |||||||
chr12:108933698 | T | A | 9 | a0001c0001t0003g0033 a0001c0001t0003g0035 a0001c0001t0003g0036 others(6): Show |
9 | HG03490.hp1 HG03492.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.1048+497A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933698 | |||||||
chr12:108933865 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1048+330C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933865 | |||||||
chr12:108933976 | G | A | 5 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048+219C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 11/15 | chr12 | 108933976 | |||||||
chr12:108934337 | C | G | 4 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(1): Show |
4 | NA18952.hp2 NA18994.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-66G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108934337 | |||||||
chr12:108934479 | T | A | 187 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(184): Show |
188 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.972-208A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108934479 | |||||||
chr12:108934585 | A | G | 187 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(184): Show |
188 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.972-314T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108934585 | |||||||
chr12:108934649 | C | T | 1 | a0001c0002t0036g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.972-378G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108934649 | |||||||
chr12:108934759 | C | T | 5 | a0001c0001t0008g0162 a0001c0002t0014g0175 a0001c0002t0014g0178 others(2): Show |
5 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.972-488G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108934759 | |||||||
chr12:108934823 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.972-552C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108934823 | |||||||
chr12:108934995 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.972-724C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108934995 | |||||||
chr12:108935128 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0015g0075 |
2 | HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.972-857G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935128 | |||||||
chr12:108935235 | T | C | 1 | a0001c0001t0059g0123 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.972-964A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935235 | |||||||
chr12:108935307 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0126 |
2 | NA18939.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.972-1036A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935307 | |||||||
chr12:108935342 | C | T | 59 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(56): Show |
59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.972-1071G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935342 | |||||||
chr12:108935522 | C | T | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.972-1251G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935522 | |||||||
chr12:108935523 | A | G | 186 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(183): Show |
187 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.972-1252T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935523 | |||||||
chr12:108935542 | T | C | 188 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(185): Show |
189 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.972-1271A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935542 | |||||||
chr12:108935607 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.972-1336C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935607 | |||||||
chr12:108935979 | A | C | 1 | a0001c0001t0008g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.971+1285T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108935979 | |||||||
chr12:108936023 | T | TAC | 46 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(43): Show |
46 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.971+1239_971+1240d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACAC | 9 | a0001c0001t0003g0035 a0001c0001t0008g0171 a0001c0002t0001g0201 others(6): Show |
9 | HG02109.hp1 HG02897.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.971+1237_971+1240d others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACAC | 9 | a0001c0001t0020g0181 a0001c0002t0006g0235 a0001c0002t0010g0174 others(6): Show |
9 | HG01081.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+1235_971+1240d others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(1): Show |
11 | a0001c0001t0003g0033 a0001c0001t0003g0037 a0001c0001t0003g0038 others(8): Show |
11 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+1233_971+1240d others(10): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(3): Show |
11 | a0001c0001t0003g0018 a0001c0001t0003g0039 a0001c0001t0012g0241 others(8): Show |
11 | HG01070.hp2 HG01496.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+1231_971+1240d others(12): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(5): Show |
46 | a0001c0001t0001g0173 a0001c0001t0002g0129 a0001c0001t0003g0005 others(43): Show |
46 | HG00280.hp2 HG00597.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.971+1229_971+1240d others(14): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(7): Show |
16 | a0001c0001t0003g0019 a0001c0001t0003g0031 a0001c0001t0003g0044 others(13): Show |
16 | HG01106.hp1 HG01123.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+1227_971+1240d others(16): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(9): Show |
19 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0224 others(16): Show |
20 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.971+1225_971+1240d others(18): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(11): Show |
8 | a0001c0001t0083g0172 a0001c0002t0006g0164 a0001c0002t0021g0272 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.971+1223_971+1240d others(20): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(13): Show |
2 | a0001c0002t0002g0248 a0001c0002t0036g0049 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.971+1221_971+1240d others(22): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | T | TACACACA others(15): Show |
1 | a0001c0002t0004g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.971+1219_971+1240d others(24): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936023 | TAC | T | 6 | a0001c0001t0008g0162 a0001c0001t0066g0154 a0001c0002t0014g0175 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.971+1239_971+1240d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936023 | |||||||
chr12:108936055 | T | C | 2 | a0001c0005t0007g0023 a0001c0005t0007g0024 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.971+1209A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936055 | |||||||
chr12:108936114 | C | T | 1 | a0001c0002t0036g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.971+1150G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936114 | |||||||
chr12:108936138 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.971+1126G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936138 | |||||||
chr12:108936167 | T | C | 1 | a0001c0002t0001g0281 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.971+1097A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936167 | |||||||
chr12:108936183 | C | A | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.971+1081G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936183 | |||||||
chr12:108936420 | T | G | 62 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(59): Show |
62 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.971+844A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936420 | |||||||
chr12:108936650 | A | AT | 5 | a0001c0001t0013g0277 a0001c0001t0013g0278 a0001c0001t0037g0010 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.971+613dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936650 | |||||||
chr12:108936668 | G | A | 1 | a0001c0002t0004g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.971+596C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936668 | |||||||
chr12:108936822 | C | CA | 166 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(163): Show |
167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.971+441_971+442ins others(1): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936822 | |||||||
chr12:108936975 | T | C | 1 | a0001c0001t0009g0261 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.971+289A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108936975 | |||||||
chr12:108937139 | G | A | 135 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(132): Show |
136 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.971+125C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108937139 | |||||||
chr12:108937140 | A | T | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.971+124T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108937140 | |||||||
chr12:108937146 | T | C | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.971+118A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 10/15 | chr12 | 108937146 | |||||||
chr12:108937357 | T | A | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-20A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937357 | |||||||
chr12:108937386 | C | T | 169 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(166): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.898-49G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937386 | |||||||
chr12:108937387 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.898-50C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937387 | |||||||
chr12:108937394 | G | A | 1 | a0001c0003t0016g0236 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.898-57C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937394 | |||||||
chr12:108937552 | G | T | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-215C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937552 | |||||||
chr12:108937618 | C | T | 3 | a0001c0001t0024g0247 a0001c0001t0042g0014 a0001c0002t0024g0237 |
3 | HG02109.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.898-281G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937618 | |||||||
chr12:108937685 | T | TCA | 5 | a0001c0001t0002g0073 a0001c0001t0002g0105 a0001c0001t0002g0106 others(2): Show |
5 | HG02083.hp2 NA18612.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-350_898-349dup others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937685 | |||||||
chr12:108937846 | C | T | 29 | a0001c0001t0001g0173 a0001c0001t0002g0129 a0001c0001t0007g0048 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.898-509G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937846 | |||||||
chr12:108937987 | G | T | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-650C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108937987 | |||||||
chr12:108938283 | G | A | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.897+544C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108938283 | |||||||
chr12:108938348 | C | T | 1 | a0001c0001t0027g0063 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.897+479G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108938348 | |||||||
chr12:108938350 | T | C | 5 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0089 others(2): Show |
5 | NA18953.hp2 NA18956.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+477A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108938350 | |||||||
chr12:108938676 | G | C | 1 | a0001c0001t0038g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.897+151C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108938676 | |||||||
chr12:108938792 | C | T | 1 | a0001c0002t0024g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.897+35G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 9/15 | chr12 | 108938792 | |||||||
chr12:108938985 | G | A | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.769-30C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108938985 | |||||||
chr12:108939123 | C | T | 1 | a0001c0002t0023g0234 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769-168G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108939123 | |||||||
chr12:108939247 | T | A | 2 | a0001c0001t0001g0121 a0001c0001t0002g0058 |
2 | HG00597.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.769-292A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108939247 | |||||||
chr12:108939526 | C | A | 26 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0222 others(23): Show |
27 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.769-571G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108939526 | |||||||
chr12:108939545 | G | A | 62 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(59): Show |
62 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.769-590C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108939545 | |||||||
chr12:108940227 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(111): Show |
116 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.768+557G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108940227 | |||||||
chr12:108940302 | G | T | 1 | a0001c0002t0002g0204 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.768+482C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108940302 | |||||||
chr12:108940643 | C | A | 2 | a0001c0002t0026g0094 a0001c0002t0026g0144 |
2 | HG02572.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.768+141G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108940643 | |||||||
chr12:108940652 | C | T | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.768+132G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108940652 | |||||||
chr12:108940658 | T | G | 2 | a0001c0001t0020g0181 a0001c0002t0055g0275 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.768+126A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108940658 | |||||||
chr12:108940750 | C | T | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.768+34G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 8/15 | chr12 | 108940750 | |||||||
chr12:108940928 | G | T | 1 | a0001c0002t0033g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.643-19C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108940928 | |||||||
chr12:108940942 | G | A | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.643-33C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108940942 | |||||||
chr12:108941087 | C | T | 4 | a0001c0001t0020g0181 a0001c0001t0042g0014 a0001c0002t0024g0237 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-178G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941087 | |||||||
chr12:108941103 | C | A | 4 | a0001c0001t0020g0181 a0001c0001t0042g0014 a0001c0002t0024g0237 others(1): Show |
4 | HG02559.hp2 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-194G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941103 | |||||||
chr12:108941152 | G | A | 2 | a0001c0001t0004g0055 a0001c0001t0007g0048 |
2 | HG01261.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.643-243C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941152 | |||||||
chr12:108941193 | G | A | 1 | a0001c0001t0049g0017 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.643-284C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941193 | |||||||
chr12:108941233 | G | A | 1 | a0001c0002t0021g0149 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.643-324C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941233 | |||||||
chr12:108941363 | C | G | 4 | a0001c0003t0011g0132 a0001c0003t0011g0133 a0001c0003t0011g0146 others(1): Show |
4 | NA18967.hp1 NA18982.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-454G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941363 | |||||||
chr12:108941409 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(112): Show |
117 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.643-500T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941409 | |||||||
chr12:108941466 | G | A | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.643-557C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941466 | |||||||
chr12:108941536 | A | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0120 a0001c0001t0056g0077 |
3 | HG02056.hp1 HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.643-627T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941536 | |||||||
chr12:108941614 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.643-705G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941614 | |||||||
chr12:108941660 | AT | A | 9 | a0001c0001t0001g0098 a0001c0001t0001g0135 a0001c0001t0002g0129 others(6): Show |
9 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.643-752delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941660 | |||||||
chr12:108941700 | C | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(246): Show |
252 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.643-791G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941700 | |||||||
chr12:108941767 | T | G | 1 | a0001c0002t0036g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.643-858A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941767 | |||||||
chr12:108941786 | C | G | 129 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(126): Show |
130 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.643-877G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941786 | |||||||
chr12:108941797 | G | A | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.643-888C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941797 | |||||||
chr12:108941854 | G | A | 2 | a0001c0002t0010g0174 a0001c0002t0072g0233 |
2 | HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.643-945C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941854 | |||||||
chr12:108941871 | G | A | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-962C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941871 | |||||||
chr12:108941896 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.643-987G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941896 | |||||||
chr12:108941955 | A | G | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.643-1046T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941955 | |||||||
chr12:108941956 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.643-1047G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941956 | |||||||
chr12:108941984 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(122): Show |
127 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.643-1075C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941984 | |||||||
chr12:108941987 | A | C | 5 | a0001c0001t0066g0154 a0001c0002t0001g0281 a0001c0002t0045g0004 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1078T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108941987 | |||||||
chr12:108942124 | C | T | 62 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(59): Show |
62 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.643-1215G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942124 | |||||||
chr12:108942167 | G | A | 5 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(2): Show |
5 | HG03139.hp2 HG03516.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1258C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942167 | |||||||
chr12:108942270 | A | G | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.643-1361T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942270 | |||||||
chr12:108942401 | C | T | 1 | a0001c0001t0009g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-1492G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942401 | |||||||
chr12:108942477 | A | G | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.643-1568T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942477 | |||||||
chr12:108942496 | G | A | 1 | a0001c0001t0004g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.643-1587C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942496 | |||||||
chr12:108942583 | C | T | 2 | a0001c0002t0001g0283 a0001c0002t0074g0264 |
2 | HG01123.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.643-1674G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942583 | |||||||
chr12:108942607 | G | T | 1 | a0001c0001t0081g0141 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.643-1698C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942607 | |||||||
chr12:108942877 | G | T | 58 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(55): Show |
58 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.643-1968C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942877 | |||||||
chr12:108942924 | C | G | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.643-2015G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942924 | |||||||
chr12:108942942 | T | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(249): Show |
255 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.643-2033A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942942 | |||||||
chr12:108942969 | C | G | 5 | a0001c0001t0066g0154 a0001c0002t0001g0281 a0001c0002t0045g0004 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-2060G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108942969 | |||||||
chr12:108943043 | G | A | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.642+2060C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943043 | |||||||
chr12:108943045 | C | G | 4 | a0001c0001t0020g0112 a0001c0002t0020g0179 a0001c0002t0033g0198 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+2058G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943045 | |||||||
chr12:108943192 | A | G | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.642+1911T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943192 | |||||||
chr12:108943207 | C | A | 1 | a0001c0002t0023g0234 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.642+1896G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943207 | |||||||
chr12:108943244 | G | A | 30 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
30 | HG00597.hp1 HG01070.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.642+1859C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943244 | |||||||
chr12:108943414 | G | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(115): Show |
120 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.642+1689C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943414 | |||||||
chr12:108943440 | CA | C | 5 | a0001c0001t0066g0154 a0001c0002t0001g0281 a0001c0002t0045g0004 others(2): Show |
5 | HG00642.hp2 HG01192.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+1662delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943440 | |||||||
chr12:108943441 | A | C | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+1662T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943441 | |||||||
chr12:108943500 | G | A | 1 | a0001c0001t0009g0257 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.642+1603C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943500 | |||||||
chr12:108943513 | G | A | 1 | a0001c0002t0061g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.642+1590C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943513 | |||||||
chr12:108943552 | C | A | 29 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(26): Show |
29 | HG00597.hp1 HG01070.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.642+1551G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943552 | |||||||
chr12:108943553 | G | A | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.642+1550C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943553 | |||||||
chr12:108943598 | AC | A | 3 | a0001c0001t0066g0154 a0001c0002t0001g0281 a0001c0002t0045g0004 |
3 | HG01891.hp2 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.642+1504delG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943598 | |||||||
chr12:108943599 | C | A | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.642+1504G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943599 | |||||||
chr12:108943599 | CA | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(237): Show |
243 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.642+1503delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943599 | |||||||
chr12:108943637 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(115): Show |
120 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.642+1466G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943637 | |||||||
chr12:108943821 | GCTC | G | 10 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.642+1279_642+1281d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943821 | |||||||
chr12:108943821 | GCTCCTC | G | 5 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(2): Show |
5 | HG03139.hp2 HG03516.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+1276_642+1281d others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943821 | |||||||
chr12:108943842 | C | CCTT | 3 | a0001c0001t0066g0154 a0001c0004t0018g0070 a0001c0004t0018g0228 |
3 | HG00642.hp2 HG01192.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.642+1258_642+1260d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943842 | |||||||
chr12:108943842 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(123): Show |
128 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.642+1261G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943842 | |||||||
chr12:108943872 | CTCT | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(118): Show |
123 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.642+1228_642+1230d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108943872 | |||||||
chr12:108944001 | C | T | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+1102G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944001 | |||||||
chr12:108944052 | G | T | 1 | a0001c0001t0005g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.642+1051C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944052 | |||||||
chr12:108944147 | C | T | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+956G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944147 | |||||||
chr12:108944223 | G | A | 3 | a0001c0001t0066g0154 a0001c0004t0018g0070 a0001c0004t0018g0228 |
3 | HG00642.hp2 HG01192.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.642+880C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944223 | |||||||
chr12:108944229 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.642+874C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944229 | |||||||
chr12:108944335 | T | C | 254 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(251): Show |
257 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.642+768A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944335 | |||||||
chr12:108944390 | C | A | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.642+713G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944390 | |||||||
chr12:108944426 | C | T | 1 | a0001c0001t0008g0171 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.642+677G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944426 | |||||||
chr12:108944469 | A | C | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+634T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944469 | |||||||
chr12:108944569 | G | A | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.642+534C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944569 | |||||||
chr12:108944806 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(87): Show |
92 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.642+297G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944806 | |||||||
chr12:108944895 | T | C | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.642+208A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944895 | |||||||
chr12:108944914 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0038g0045 |
3 | HG01074.hp1 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.642+189C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944914 | |||||||
chr12:108944938 | C | T | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.642+165G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944938 | |||||||
chr12:108944974 | G | A | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.642+129C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108944974 | |||||||
chr12:108945059 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(87): Show |
92 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.642+44G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 7/15 | chr12 | 108945059 | |||||||
chr12:108945247 | C | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(121): Show |
126 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.579-81G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108945247 | |||||||
chr12:108945584 | T | C | 7 | a0001c0001t0013g0277 a0001c0001t0013g0278 a0001c0001t0037g0010 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.579-418A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108945584 | |||||||
chr12:108945591 | G | T | 136 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(133): Show |
137 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.579-425C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108945591 | |||||||
chr12:108945762 | T | C | 4 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(1): Show |
4 | HG03139.hp2 NA19030.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-596A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108945762 | |||||||
chr12:108945843 | A | C | 1 | a0001c0001t0062g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.579-677T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108945843 | |||||||
chr12:108945867 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.579-701G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108945867 | |||||||
chr12:108945966 | C | G | 4 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(1): Show |
4 | HG03139.hp2 NA19030.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-800G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108945966 | |||||||
chr12:108946084 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.579-918T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946084 | |||||||
chr12:108946152 | G | A | 1 | a0001c0002t0036g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.579-986C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946152 | |||||||
chr12:108946228 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.579-1062G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946228 | |||||||
chr12:108946263 | A | AT | 47 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(44): Show |
47 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.579-1098dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946263 | |||||||
chr12:108946263 | AT | A | 6 | a0001c0001t0001g0062 a0001c0001t0004g0226 a0001c0001t0066g0154 others(3): Show |
6 | HG00639.hp1 HG00642.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-1098delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946263 | |||||||
chr12:108946407 | T | C | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.579-1241A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946407 | |||||||
chr12:108946421 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.579-1255A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946421 | |||||||
chr12:108946491 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.579-1325G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946491 | |||||||
chr12:108946623 | T | A | 7 | a0001c0001t0002g0129 a0001c0002t0001g0169 a0001c0002t0001g0189 others(4): Show |
7 | HG02572.hp2 HG02896.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.579-1457A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946623 | |||||||
chr12:108946690 | T | TTTA | 107 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0071 others(104): Show |
108 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.579-1527_579-1525d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946690 | T | TTTATTA | 20 | a0001c0001t0001g0076 a0001c0001t0001g0127 a0001c0001t0001g0131 others(17): Show |
21 | HG00408.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.579-1530_579-1525d others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946690 | TTTA | T | 14 | a0001c0001t0001g0209 a0001c0001t0002g0129 a0001c0001t0006g0224 others(11): Show |
14 | HG00280.hp2 HG01175.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.579-1527_579-1525d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946690 | TTTATTA | T | 10 | a0001c0001t0001g0003 a0001c0001t0002g0105 a0001c0001t0008g0162 others(7): Show |
11 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.579-1530_579-1525d others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946690 | TTTATTAT others(2): Show |
T | 5 | a0001c0001t0002g0057 a0001c0001t0081g0141 a0001c0001t0083g0172 others(2): Show |
5 | HG02717.hp2 HG03098.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.579-1533_579-1525d others(11): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946690 | TTTATTAT others(5): Show |
T | 52 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(49): Show |
52 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.579-1536_579-1525d others(14): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946690 | TTTATTAT others(8): Show |
T | 4 | a0001c0001t0002g0158 a0001c0001t0044g0043 a0001c0002t0001g0281 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-1539_579-1525d others(17): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946690 | TTTATTAT others(11): Show |
T | 29 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(26): Show |
29 | HG00597.hp1 HG01070.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-1542_579-1525d others(20): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946690 | |||||||
chr12:108946826 | C | T | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.579-1660G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946826 | |||||||
chr12:108946912 | G | C | 1 | a0001c0002t0021g0272 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.579-1746C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946912 | |||||||
chr12:108946922 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.579-1756C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108946922 | |||||||
chr12:108947242 | G | A | 2 | a0001c0001t0020g0181 a0001c0002t0055g0275 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.579-2076C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947242 | |||||||
chr12:108947347 | A | G | 1 | a0001c0002t0010g0191 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.579-2181T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947347 | |||||||
chr12:108947436 | T | A | 3 | a0001c0001t0066g0154 a0001c0004t0018g0070 a0001c0004t0018g0228 |
3 | HG00642.hp2 HG01192.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.579-2270A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947436 | |||||||
chr12:108947624 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.579-2458C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947624 | |||||||
chr12:108947771 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.579-2605T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947771 | |||||||
chr12:108947810 | G | A | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-2644C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947810 | |||||||
chr12:108947884 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(115): Show |
120 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.579-2718G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947884 | |||||||
chr12:108947901 | G | T | 2 | a0001c0002t0001g0281 a0001c0002t0045g0004 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.579-2735C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947901 | |||||||
chr12:108947905 | G | A | 30 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
30 | HG00597.hp1 HG01070.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.579-2739C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108947905 | |||||||
chr12:108948088 | C | T | 6 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-2922G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948088 | |||||||
chr12:108948105 | T | A | 1 | a0001c0002t0084g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-2939A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948105 | |||||||
chr12:108948116 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.579-2950A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948116 | |||||||
chr12:108948210 | G | T | 21 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0008g0162 others(18): Show |
21 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.579-3044C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948210 | |||||||
chr12:108948253 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.579-3087G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948253 | |||||||
chr12:108948285 | A | G | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.579-3119T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948285 | |||||||
chr12:108948304 | C | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0038g0045 |
3 | HG01074.hp1 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.579-3138G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948304 | |||||||
chr12:108948325 | A | T | 1 | a0001c0003t0053g0230 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.579-3159T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948325 | |||||||
chr12:108948784 | C | G | 1 | a0001c0002t0002g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.579-3618G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948784 | |||||||
chr12:108948953 | C | T | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.579-3787G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108948953 | |||||||
chr12:108949061 | T | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(126): Show |
131 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.579-3895A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108949061 | |||||||
chr12:108949220 | T | C | 1 | a0001c0002t0015g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.579-4054A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108949220 | |||||||
chr12:108949275 | C | CT | 128 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(125): Show |
130 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.579-4110dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108949275 | |||||||
chr12:108949396 | T | C | 4 | a0001c0001t0020g0181 a0001c0002t0001g0281 a0001c0002t0045g0004 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-4230A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108949396 | |||||||
chr12:108949969 | C | G | 1 | a0001c0001t0004g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.579-4803G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108949969 | |||||||
chr12:108950014 | G | A | 1 | a0001c0001t0051g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.579-4848C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950014 | |||||||
chr12:108950087 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.579-4921T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950087 | |||||||
chr12:108950245 | C | CT | 16 | a0001c0001t0004g0256 a0001c0001t0009g0252 a0001c0001t0009g0253 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.579-5080dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950245 | |||||||
chr12:108950326 | G | T | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579-5160C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950326 | |||||||
chr12:108950357 | G | A | 29 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(26): Show |
29 | HG00597.hp1 HG01070.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-5191C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950357 | |||||||
chr12:108950410 | G | A | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579-5244C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950410 | |||||||
chr12:108950464 | G | C | 4 | a0001c0001t0001g0173 a0001c0002t0025g0184 a0001c0002t0025g0185 others(1): Show |
4 | HG01109.hp1 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.579-5298C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950464 | |||||||
chr12:108950645 | G | A | 7 | a0001c0001t0020g0181 a0001c0001t0066g0154 a0001c0002t0001g0281 others(4): Show |
7 | HG00642.hp2 HG01192.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.579-5479C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950645 | |||||||
chr12:108950667 | G | A | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-5501C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950667 | |||||||
chr12:108950813 | A | G | 4 | a0001c0001t0020g0181 a0001c0002t0001g0281 a0001c0002t0045g0004 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-5647T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108950813 | |||||||
chr12:108951055 | G | A | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.579-5889C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108951055 | |||||||
chr12:108951181 | T | C | 3 | a0001c0001t0020g0181 a0001c0002t0001g0281 a0001c0002t0045g0004 |
3 | HG01891.hp2 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.579-6015A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108951181 | |||||||
chr12:108951729 | C | T | 1 | a0001c0002t0002g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.579-6563G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108951729 | |||||||
chr12:108951845 | C | T | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579-6679G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108951845 | |||||||
chr12:108951849 | T | C | 3 | a0001c0001t0020g0181 a0001c0002t0001g0281 a0001c0002t0045g0004 |
3 | HG01891.hp2 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.579-6683A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108951849 | |||||||
chr12:108951866 | G | T | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-6700C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108951866 | |||||||
chr12:108951879 | A | G | 1 | a0001c0002t0004g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579-6713T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108951879 | |||||||
chr12:108952230 | C | CT | 121 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(118): Show |
123 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.579-7065dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952230 | |||||||
chr12:108952233 | T | C | 1 | a0001c0002t0072g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.579-7067A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952233 | |||||||
chr12:108952292 | T | C | 60 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(57): Show |
60 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.579-7126A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952292 | |||||||
chr12:108952662 | C | A | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.579-7496G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952662 | |||||||
chr12:108952682 | A | C | 1 | a0001c0002t0082g0216 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.579-7516T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952682 | |||||||
chr12:108952739 | C | T | 5 | a0001c0002t0001g0207 a0001c0002t0001g0283 a0001c0002t0005g0190 others(2): Show |
5 | HG01123.hp2 HG01243.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-7573G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952739 | |||||||
chr12:108952772 | T | A | 1 | a0001c0002t0084g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-7606A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952772 | |||||||
chr12:108952845 | C | T | 3 | a0001c0001t0020g0181 a0001c0002t0001g0281 a0001c0002t0045g0004 |
3 | HG01891.hp2 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.579-7679G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952845 | |||||||
chr12:108952900 | T | A | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.579-7734A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952900 | |||||||
chr12:108952936 | C | T | 6 | a0001c0001t0020g0181 a0001c0001t0066g0154 a0001c0002t0001g0281 others(3): Show |
6 | HG00642.hp2 HG01192.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-7770G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108952936 | |||||||
chr12:108953038 | G | A | 1 | a0001c0002t0036g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.579-7872C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953038 | |||||||
chr12:108953136 | C | CT | 31 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(28): Show |
31 | HG00544.hp1 HG01106.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.578+7786dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953136 | |||||||
chr12:108953136 | C | CTT | 19 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0027 others(16): Show |
19 | HG01070.hp2 HG01255.hp1 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.578+7785_578+7786d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953136 | |||||||
chr12:108953136 | C | CTTT | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0008 others(7): Show |
10 | HG00597.hp1 HG01123.hp1 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.578+7784_578+7786d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953136 | |||||||
chr12:108953151 | TTC | T | 50 | a0001c0001t0001g0098 a0001c0001t0001g0120 a0001c0001t0001g0121 others(47): Show |
50 | HG00408.hp1 HG00544.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.578+7770_578+7771d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953151 | |||||||
chr12:108953152 | TC | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0071 a0001c0001t0001g0091 others(17): Show |
20 | HG00597.hp2 HG01167.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.578+7770delG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953152 | |||||||
chr12:108953153 | C | T | 165 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(162): Show |
167 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.578+7770G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953153 | |||||||
chr12:108953210 | A | G | 66 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(63): Show |
66 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.578+7713T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953210 | |||||||
chr12:108953382 | G | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(235): Show |
241 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.578+7541C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953382 | |||||||
chr12:108953389 | C | T | 2 | a0001c0002t0013g0266 a0001c0002t0013g0276 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.578+7534G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953389 | |||||||
chr12:108953398 | TC | T | 58 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(55): Show |
58 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.578+7524delG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953398 | |||||||
chr12:108953407 | C | T | 1 | a0001c0001t0038g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.578+7516G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953407 | |||||||
chr12:108953451 | T | C | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.578+7472A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953451 | |||||||
chr12:108953570 | C | T | 1 | a0001c0001t0067g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.578+7353G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953570 | |||||||
chr12:108953838 | G | A | 1 | a0001c0002t0001g0202 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.578+7085C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108953838 | |||||||
chr12:108954000 | T | C | 1 | a0001c0001t0020g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.578+6923A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954000 | |||||||
chr12:108954005 | G | A | 4 | a0001c0001t0001g0173 a0001c0002t0025g0184 a0001c0002t0025g0185 others(1): Show |
4 | HG01109.hp1 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+6918C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954005 | |||||||
chr12:108954086 | C | T | 1 | a0001c0001t0022g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.578+6837G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954086 | |||||||
chr12:108954113 | C | CA | 107 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0098 others(104): Show |
108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.578+6809dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954113 | |||||||
chr12:108954113 | C | CAA | 16 | a0001c0001t0008g0162 a0001c0001t0009g0258 a0001c0001t0009g0261 others(13): Show |
16 | HG00738.hp1 HG02040.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.578+6808_578+6809d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954113 | |||||||
chr12:108954113 | CA | C | 17 | a0001c0001t0001g0135 a0001c0001t0001g0265 a0001c0001t0002g0129 others(14): Show |
17 | HG00642.hp2 HG01123.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.578+6809delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954113 | |||||||
chr12:108954269 | T | C | 1 | a0001c0001t0067g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.578+6654A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954269 | |||||||
chr12:108954456 | C | T | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.578+6467G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954456 | |||||||
chr12:108954529 | T | C | 1 | a0001c0001t0009g0261 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.578+6394A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954529 | |||||||
chr12:108954549 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(116): Show |
121 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.578+6374C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954549 | |||||||
chr12:108954608 | G | A | 2 | a0001c0001t0042g0014 a0001c0002t0024g0237 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.578+6315C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108954608 | |||||||
chr12:108955308 | C | T | 1 | a0001c0001t0009g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.578+5615G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108955308 | |||||||
chr12:108955347 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.578+5576C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108955347 | |||||||
chr12:108955700 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(119): Show |
124 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.578+5223C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108955700 | |||||||
chr12:108955795 | A | G | 1 | a0001c0001t0038g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.578+5128T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108955795 | |||||||
chr12:108955808 | T | A | 19 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.578+5115A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108955808 | |||||||
chr12:108955972 | C | T | 32 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0222 others(29): Show |
33 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.578+4951G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108955972 | |||||||
chr12:108956029 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(140): Show |
145 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.578+4894T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956029 | |||||||
chr12:108956074 | G | C | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.578+4849C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956074 | |||||||
chr12:108956122 | AACCCCGT others(4): Show |
A | 2 | a0001c0001t0042g0014 a0001c0002t0024g0237 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.578+4790_578+4800d others(13): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956122 | |||||||
chr12:108956144 | C | CA | 124 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(121): Show |
126 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.578+4778dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956144 | |||||||
chr12:108956194 | C | T | 19 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.578+4729G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956194 | |||||||
chr12:108956208 | A | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(119): Show |
124 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.578+4715T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956208 | |||||||
chr12:108956301 | C | CA | 231 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(228): Show |
234 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.578+4621dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956301 | |||||||
chr12:108956301 | C | CAA | 7 | a0001c0001t0001g0209 a0001c0001t0004g0113 a0001c0001t0005g0087 others(4): Show |
7 | HG00544.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.578+4620_578+4621d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956301 | |||||||
chr12:108956496 | G | T | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.578+4427C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956496 | |||||||
chr12:108956513 | A | G | 2 | a0001c0004t0018g0070 a0001c0004t0018g0228 |
2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.578+4410T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956513 | |||||||
chr12:108956608 | T | C | 5 | a0001c0002t0001g0215 a0001c0002t0001g0282 a0001c0002t0002g0194 others(2): Show |
5 | HG00544.hp2 NA18747.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+4315A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956608 | |||||||
chr12:108956646 | T | C | 19 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.578+4277A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956646 | |||||||
chr12:108956660 | A | G | 15 | a0001c0001t0008g0162 a0001c0002t0010g0002 a0001c0002t0010g0054 others(12): Show |
16 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.578+4263T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956660 | |||||||
chr12:108956706 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.578+4217G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956706 | |||||||
chr12:108956780 | C | T | 2 | a0001c0001t0062g0211 a0001c0002t0013g0167 |
2 | HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.578+4143G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956780 | |||||||
chr12:108956800 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(76): Show |
81 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.578+4123G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956800 | |||||||
chr12:108956844 | A | G | 235 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(232): Show |
238 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.578+4079T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108956844 | |||||||
chr12:108957128 | G | A | 60 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(57): Show |
60 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.578+3795C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957128 | |||||||
chr12:108957163 | T | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(237): Show |
243 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.578+3760A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957163 | |||||||
chr12:108957203 | G | A | 3 | a0001c0001t0020g0181 a0001c0002t0001g0281 a0001c0002t0045g0004 |
3 | HG01891.hp2 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.578+3720C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957203 | |||||||
chr12:108957249 | C | T | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.578+3674G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957249 | |||||||
chr12:108957368 | C | A | 1 | a0001c0001t0019g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.578+3555G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957368 | |||||||
chr12:108957399 | C | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(237): Show |
243 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.578+3524G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957399 | |||||||
chr12:108957443 | C | T | 1 | a0001c0004t0011g0064 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.578+3480G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957443 | |||||||
chr12:108957567 | A | C | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.578+3356T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957567 | |||||||
chr12:108957630 | C | T | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.578+3293G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957630 | |||||||
chr12:108957708 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(119): Show |
124 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.578+3215G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957708 | |||||||
chr12:108957780 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.578+3143G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957780 | |||||||
chr12:108957814 | G | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.578+3109C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957814 | |||||||
chr12:108957919 | G | A | 1 | a0001c0002t0010g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.578+3004C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108957919 | |||||||
chr12:108958120 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(138): Show |
143 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.578+2803A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958120 | |||||||
chr12:108958202 | C | T | 1 | a0001c0001t0020g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.578+2721G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958202 | |||||||
chr12:108958258 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.578+2665G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958258 | |||||||
chr12:108958303 | C | CTT | 17 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.578+2618_578+2619d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958303 | |||||||
chr12:108958316 | T | A | 30 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
30 | HG00597.hp1 HG01070.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.578+2607A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958316 | |||||||
chr12:108958316 | T | TA | 88 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
90 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.578+2606dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958316 | |||||||
chr12:108958459 | C | T | 19 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(16): Show |
19 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.578+2464G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958459 | |||||||
chr12:108958528 | G | T | 2 | a0001c0001t0083g0172 a0001c0002t0002g0248 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.578+2395C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958528 | |||||||
chr12:108958982 | C | T | 7 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0212 others(4): Show |
7 | HG00099.hp2 HG01255.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.578+1941G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108958982 | |||||||
chr12:108959351 | CT | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(147): Show |
153 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.578+1571delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108959351 | |||||||
chr12:108959351 | CTT | C | 12 | a0001c0001t0001g0093 a0001c0001t0003g0036 a0001c0001t0004g0226 others(9): Show |
12 | HG00639.hp1 HG01891.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.578+1570_578+1571d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108959351 | |||||||
chr12:108959351 | CTTTTT | C | 46 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0124 others(43): Show |
46 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.578+1567_578+1571d others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108959351 | |||||||
chr12:108959502 | C | T | 17 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0222 others(14): Show |
17 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.578+1421G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108959502 | |||||||
chr12:108959795 | T | G | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.578+1128A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108959795 | |||||||
chr12:108960022 | C | A | 1 | a0001c0001t0069g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.578+901G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960022 | |||||||
chr12:108960240 | G | A | 1 | a0001c0002t0032g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.578+683C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960240 | |||||||
chr12:108960373 | C | A | 4 | a0001c0001t0012g0260 a0001c0002t0014g0280 a0001c0002t0029g0231 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+550G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960373 | |||||||
chr12:108960411 | C | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.578+512G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960411 | |||||||
chr12:108960432 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(138): Show |
143 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.578+491C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960432 | |||||||
chr12:108960471 | G | C | 1 | a0001c0001t0009g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.578+452C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960471 | |||||||
chr12:108960601 | G | T | 2 | a0001c0002t0028g0262 a0001c0002t0028g0263 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.578+322C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960601 | |||||||
chr12:108960616 | A | G | 60 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(57): Show |
60 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.578+307T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960616 | |||||||
chr12:108960685 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(135): Show |
140 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.578+238G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960685 | |||||||
chr12:108960765 | T | G | 1 | a0001c0001t0020g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.578+158A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960765 | |||||||
chr12:108960856 | T | C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(234): Show |
240 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.578+67A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 6/15 | chr12 | 108960856 | |||||||
chr12:108961053 | G | A | 2 | a0001c0001t0008g0238 a0001c0001t0008g0239 |
2 | HG01168.hp1 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.454-6C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961053 | |||||||
chr12:108961067 | G | A | 59 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0120 others(56): Show |
59 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.454-20C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961067 | |||||||
chr12:108961173 | G | C | 1 | a0001c0001t0006g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.454-126C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961173 | |||||||
chr12:108961385 | G | T | 7 | a0001c0001t0002g0142 a0001c0001t0065g0081 a0001c0003t0011g0132 others(4): Show |
7 | HG02040.hp2 HG02080.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.454-338C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961385 | |||||||
chr12:108961427 | CT | C | 11 | a0001c0001t0001g0196 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
11 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.454-381delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961427 | |||||||
chr12:108961427 | CTT | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(219): Show |
225 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(222): Show |
intron_variant | MODIFIER | c.454-382_454-381del others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961427 | |||||||
chr12:108961545 | C | A | 18 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.454-498G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961545 | |||||||
chr12:108961702 | T | C | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.454-655A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961702 | |||||||
chr12:108961860 | A | G | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.454-813T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108961860 | |||||||
chr12:108962014 | G | A | 15 | a0001c0001t0008g0162 a0001c0002t0010g0002 a0001c0002t0010g0054 others(12): Show |
16 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.454-967C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962014 | |||||||
chr12:108962132 | T | C | 30 | a0001c0001t0001g0060 a0001c0001t0001g0076 a0001c0001t0001g0118 others(27): Show |
30 | HG00544.hp1 HG01074.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.454-1085A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962132 | |||||||
chr12:108962339 | T | C | 2 | a0001c0001t0042g0014 a0001c0002t0024g0237 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.454-1292A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962339 | |||||||
chr12:108962344 | C | T | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.454-1297G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962344 | |||||||
chr12:108962524 | C | T | 8 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0089 others(5): Show |
8 | HG00408.hp1 NA18939.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.454-1477G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962524 | |||||||
chr12:108962526 | C | T | 1 | a0001c0001t0085g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.454-1479G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962526 | |||||||
chr12:108962907 | G | A | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.454-1860C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962907 | |||||||
chr12:108962910 | A | G | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.454-1863T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108962910 | |||||||
chr12:108963095 | T | C | 1 | a0001c0002t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.454-2048A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108963095 | |||||||
chr12:108963245 | T | C | 29 | a0001c0001t0001g0173 a0001c0001t0006g0161 a0001c0001t0006g0193 others(26): Show |
29 | HG01167.hp1 HG01943.hp2 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.454-2198A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108963245 | |||||||
chr12:108963317 | T | A | 1 | a0001c0002t0001g0215 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.454-2270A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108963317 | |||||||
chr12:108963457 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(130): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.454-2410A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108963457 | |||||||
chr12:108963495 | A | AT | 15 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(12): Show |
15 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.454-2449dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108963495 | |||||||
chr12:108963746 | A | G | 1 | a0001c0002t0024g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.454-2699T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108963746 | |||||||
chr12:108964008 | T | A | 2 | a0001c0005t0007g0023 a0001c0005t0007g0024 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.454-2961A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964008 | |||||||
chr12:108964054 | T | C | 16 | a0001c0001t0001g0173 a0001c0001t0006g0161 a0001c0001t0006g0193 others(13): Show |
16 | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.454-3007A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964054 | |||||||
chr12:108964094 | C | T | 1 | a0001c0001t0004g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.454-3047G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964094 | |||||||
chr12:108964121 | G | A | 2 | a0001c0001t0009g0261 a0001c0001t0024g0247 |
2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.454-3074C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964121 | |||||||
chr12:108964312 | T | C | 1 | a0001c0001t0070g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.454-3265A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964312 | |||||||
chr12:108964365 | T | G | 32 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(29): Show |
32 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-3318A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964365 | |||||||
chr12:108964471 | C | T | 1 | a0001c0001t0031g0168 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.454-3424G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964471 | |||||||
chr12:108964755 | G | A | 3 | a0001c0001t0020g0181 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.454-3708C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964755 | |||||||
chr12:108964946 | A | G | 3 | a0001c0001t0076g0125 a0001c0005t0007g0023 a0001c0005t0007g0024 |
3 | HG02040.hp1 HG02083.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.454-3899T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964946 | |||||||
chr12:108964988 | AAACACAT others(4): Show |
A | 1 | a0001c0001t0004g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.454-3952_454-3942d others(13): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108964988 | |||||||
chr12:108965002 | C | A | 5 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0019 others(2): Show |
5 | HG01123.hp1 HG01496.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.454-3955G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965002 | |||||||
chr12:108965109 | C | T | 1 | a0001c0001t0003g0035 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.454-4062G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965109 | |||||||
chr12:108965118 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.454-4071G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965118 | |||||||
chr12:108965235 | T | C | 1 | a0001c0002t0020g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.454-4188A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965235 | |||||||
chr12:108965329 | C | T | 1 | a0001c0001t0003g0009 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.454-4282G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965329 | |||||||
chr12:108965544 | C | A | 1 | a0001c0001t0001g0003 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.454-4497G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965544 | |||||||
chr12:108965646 | C | CA | 226 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(223): Show |
229 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.454-4600_454-4599i others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965646 | |||||||
chr12:108965761 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(271): Show |
277 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.454-4714C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965761 | |||||||
chr12:108965880 | G | A | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.454-4833C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965880 | |||||||
chr12:108965901 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0005g0114 a0001c0001t0005g0115 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-4854C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965901 | |||||||
chr12:108965902 | T | C | 1 | a0001c0001t0020g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.454-4855A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108965902 | |||||||
chr12:108966097 | G | A | 1 | a0001c0001t0068g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.454-5050C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966097 | |||||||
chr12:108966104 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.454-5057G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966104 | |||||||
chr12:108966474 | C | G | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.454-5427G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966474 | |||||||
chr12:108966517 | G | A | 16 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0007g0026 others(13): Show |
16 | HG00408.hp2 HG01243.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.454-5470C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966517 | |||||||
chr12:108966521 | GT | G | 4 | a0001c0002t0036g0049 a0001c0002t0039g0013 a0001c0002t0040g0012 others(1): Show |
4 | HG01891.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.454-5475delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966521 | |||||||
chr12:108966572 | T | C | 8 | a0001c0001t0008g0162 a0001c0002t0001g0207 a0001c0002t0001g0283 others(5): Show |
8 | HG01123.hp2 HG01243.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.454-5525A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966572 | |||||||
chr12:108966919 | G | A | 2 | a0001c0005t0007g0023 a0001c0005t0007g0024 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.453+5486C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966919 | |||||||
chr12:108966936 | C | CAAATG | 73 | a0001c0001t0001g0173 a0001c0001t0005g0069 a0001c0001t0005g0102 others(70): Show |
74 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.453+5468_453+5469i others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966936 | |||||||
chr12:108966938 | G | T | 73 | a0001c0001t0001g0173 a0001c0001t0005g0069 a0001c0001t0005g0102 others(70): Show |
74 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.453+5467C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966938 | |||||||
chr12:108966939 | T | A | 73 | a0001c0001t0001g0173 a0001c0001t0005g0069 a0001c0001t0005g0102 others(70): Show |
74 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.453+5466A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966939 | |||||||
chr12:108966951 | A | G | 67 | a0001c0001t0005g0069 a0001c0001t0005g0102 a0001c0002t0001g0097 others(64): Show |
68 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.453+5454T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108966951 | |||||||
chr12:108967026 | G | A | 2 | a0001c0001t0002g0086 a0001c0001t0007g0030 |
2 | NA18981.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.453+5379C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967026 | |||||||
chr12:108967048 | T | G | 1 | a0001c0001t0005g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.453+5357A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967048 | |||||||
chr12:108967055 | G | A | 12 | a0001c0001t0004g0256 a0001c0001t0009g0252 a0001c0001t0009g0253 others(9): Show |
12 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.453+5350C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967055 | |||||||
chr12:108967118 | C | T | 1 | a0001c0001t0005g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.453+5287G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967118 | |||||||
chr12:108967174 | C | T | 6 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 others(3): Show |
6 | HG01891.hp1 HG02559.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+5231G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967174 | |||||||
chr12:108967285 | G | A | 3 | a0001c0002t0036g0049 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.453+5120C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967285 | |||||||
chr12:108967293 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.453+5112C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967293 | |||||||
chr12:108967296 | C | T | 2 | a0001c0002t0012g0251 a0001c0004t0016g0165 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.453+5109G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967296 | |||||||
chr12:108967297 | G | A | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.453+5108C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967297 | |||||||
chr12:108967464 | A | C | 3 | a0001c0002t0036g0049 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.453+4941T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967464 | |||||||
chr12:108967537 | T | C | 67 | a0001c0001t0005g0069 a0001c0001t0005g0102 a0001c0002t0001g0097 others(64): Show |
68 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.453+4868A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967537 | |||||||
chr12:108967607 | G | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(31): Show |
34 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.453+4798C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967607 | |||||||
chr12:108967774 | C | T | 1 | a0001c0001t0014g0240 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.453+4631G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967774 | |||||||
chr12:108967775 | G | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.453+4630C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967775 | |||||||
chr12:108967805 | G | T | 2 | a0001c0002t0012g0251 a0001c0004t0016g0165 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.453+4600C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967805 | |||||||
chr12:108967869 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(255): Show |
261 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.453+4536G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108967869 | |||||||
chr12:108968055 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+4350A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968055 | |||||||
chr12:108968252 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.453+4153C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968252 | |||||||
chr12:108968296 | G | A | 3 | a0001c0002t0036g0049 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.453+4109C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968296 | |||||||
chr12:108968709 | A | C | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+3696T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968709 | |||||||
chr12:108968710 | AGT | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(166): Show |
171 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.453+3693_453+3694d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968710 | |||||||
chr12:108968710 | AGTGTGTG others(1): Show |
A | 16 | a0001c0002t0002g0248 a0001c0002t0010g0002 a0001c0002t0010g0054 others(13): Show |
17 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.453+3687_453+3694d others(10): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968710 | |||||||
chr12:108968736 | T | C | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.453+3669A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968736 | |||||||
chr12:108968744 | T | TTG | 3 | a0001c0001t0002g0129 a0001c0001t0004g0055 a0001c0001t0022g0084 |
3 | HG01261.hp1 HG04115.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.453+3659_453+3660d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968744 | |||||||
chr12:108968744 | T | TTGTG | 9 | a0001c0001t0002g0057 a0001c0001t0008g0171 a0001c0001t0013g0277 others(6): Show |
9 | HG01123.hp2 HG01243.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+3657_453+3660d others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968744 | |||||||
chr12:108968744 | T | TTGTGTG | 151 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(148): Show |
153 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.453+3655_453+3660d others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968744 | |||||||
chr12:108968744 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0003g0032 a0001c0001t0024g0247 a0001c0003t0018g0152 |
3 | HG00597.hp1 HG00733.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.453+3653_453+3660d others(10): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968744 | |||||||
chr12:108968744 | T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001g0265 a0001c0001t0004g0099 a0001c0001t0004g0226 others(1): Show |
4 | HG00639.hp1 HG01081.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+3649_453+3660d others(14): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968744 | |||||||
chr12:108968744 | TTGTGTG | T | 73 | a0001c0001t0001g0173 a0001c0001t0005g0069 a0001c0001t0005g0102 others(70): Show |
74 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.453+3655_453+3660d others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968744 | |||||||
chr12:108968937 | G | A | 2 | a0001c0005t0007g0023 a0001c0005t0007g0024 |
2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.453+3468C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108968937 | |||||||
chr12:108969081 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.453+3324C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969081 | |||||||
chr12:108969083 | C | A | 73 | a0001c0001t0001g0173 a0001c0001t0005g0069 a0001c0001t0005g0102 others(70): Show |
74 | HG00544.hp2 HG00642.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.453+3322G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969083 | |||||||
chr12:108969313 | C | T | 6 | a0001c0002t0010g0174 a0001c0002t0014g0175 a0001c0002t0014g0178 others(3): Show |
6 | HG01081.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+3092G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969313 | |||||||
chr12:108969384 | CT | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(253): Show |
259 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.453+3020delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969384 | |||||||
chr12:108969474 | T | C | 1 | a0001c0001t0009g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.453+2931A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969474 | |||||||
chr12:108969476 | C | A | 3 | a0001c0002t0012g0251 a0001c0002t0024g0237 a0001c0004t0016g0165 |
3 | HG02055.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.453+2929G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969476 | |||||||
chr12:108969515 | T | C | 1 | a0001c0004t0011g0064 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.453+2890A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969515 | |||||||
chr12:108969554 | T | A | 1 | a0001c0002t0002g0147 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.453+2851A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969554 | |||||||
chr12:108969620 | T | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(255): Show |
261 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.453+2785A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969620 | |||||||
chr12:108969716 | T | TTCCTTCC others(8): Show |
153 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(150): Show |
155 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.453+2674_453+2688d others(17): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969716 | |||||||
chr12:108969717 | T | TCCTTCCT others(9): Show |
43 | a0001c0001t0001g0173 a0001c0001t0003g0005 a0001c0001t0003g0006 others(40): Show |
43 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.453+2687_453+2688i others(18): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969717 | |||||||
chr12:108969758 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.453+2647C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969758 | |||||||
chr12:108969813 | G | A | 1 | a0001c0001t0005g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.453+2592C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969813 | |||||||
chr12:108969909 | GC | G | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+2495delG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969909 | |||||||
chr12:108969950 | T | G | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.453+2455A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969950 | |||||||
chr12:108969984 | G | A | 5 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 others(2): Show |
5 | HG01891.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+2421C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108969984 | |||||||
chr12:108970019 | C | A | 1 | a0001c0002t0002g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.453+2386G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970019 | |||||||
chr12:108970217 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.453+2188T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970217 | |||||||
chr12:108970236 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
198 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.453+2169T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970236 | |||||||
chr12:108970244 | T | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
198 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.453+2161A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970244 | |||||||
chr12:108970286 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+2119A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970286 | |||||||
chr12:108970296 | A | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(255): Show |
261 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.453+2109T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970296 | |||||||
chr12:108970297 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+2108C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970297 | |||||||
chr12:108970396 | A | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
198 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.453+2009T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970396 | |||||||
chr12:108970399 | G | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
198 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.453+2006C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970399 | |||||||
chr12:108970404 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+2001C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970404 | |||||||
chr12:108970455 | G | A | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+1950C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970455 | |||||||
chr12:108970601 | TA | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+1803delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970601 | |||||||
chr12:108970630 | G | T | 1 | a0001c0002t0005g0217 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.453+1775C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970630 | |||||||
chr12:108970757 | G | T | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+1648C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970757 | |||||||
chr12:108970898 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+1507C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108970898 | |||||||
chr12:108971102 | C | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+1303G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971102 | |||||||
chr12:108971136 | G | A | 3 | a0001c0001t0066g0154 a0001c0005t0007g0023 a0001c0005t0007g0024 |
3 | HG02040.hp1 HG02083.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.453+1269C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971136 | |||||||
chr12:108971172 | T | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(188): Show |
193 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.453+1233A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971172 | |||||||
chr12:108971200 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0003g0050 |
2 | NA18983.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.453+1205G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971200 | |||||||
chr12:108971257 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+1148A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971257 | |||||||
chr12:108971302 | G | A | 1 | a0001c0002t0084g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.453+1103C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971302 | |||||||
chr12:108971383 | C | T | 25 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0222 others(22): Show |
25 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.453+1022G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971383 | |||||||
chr12:108971428 | C | CA | 18 | a0001c0002t0001g0215 a0001c0002t0002g0248 a0001c0002t0010g0002 others(15): Show |
19 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.453+976dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971428 | |||||||
chr12:108971428 | C | CAA | 43 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(40): Show |
43 | HG00544.hp2 HG00642.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.453+975_453+976dup others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971428 | |||||||
chr12:108971428 | CAAA | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+974_453+976del others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971428 | |||||||
chr12:108971440 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+965T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971440 | |||||||
chr12:108971579 | C | T | 33 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
33 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.453+826G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971579 | |||||||
chr12:108971580 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+825T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971580 | |||||||
chr12:108971587 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
196 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.453+818T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971587 | |||||||
chr12:108971793 | C | G | 1 | a0001c0001t0005g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.453+612G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971793 | |||||||
chr12:108971926 | T | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(202): Show |
208 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.453+479A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971926 | |||||||
chr12:108971930 | T | A | 3 | a0001c0001t0066g0154 a0001c0005t0007g0023 a0001c0005t0007g0024 |
3 | HG02040.hp1 HG02083.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.453+475A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971930 | |||||||
chr12:108971965 | G | A | 1 | a0001c0001t0006g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.453+440C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108971965 | |||||||
chr12:108972157 | G | A | 1 | a0001c0002t0001g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.453+248C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 5/15 | chr12 | 108972157 | |||||||
chr12:108972558 | G | A | 1 | a0001c0001t0020g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.382-82C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108972558 | |||||||
chr12:108972631 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-155G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108972631 | |||||||
chr12:108972667 | T | C | 1 | a0001c0001t0047g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.382-191A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108972667 | |||||||
chr12:108972762 | G | A | 189 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(186): Show |
191 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.382-286C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108972762 | |||||||
chr12:108972862 | A | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(181): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.382-386T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108972862 | |||||||
chr12:108973031 | C | T | 1 | a0001c0001t0022g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382-555G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973031 | |||||||
chr12:108973038 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-562T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973038 | |||||||
chr12:108973179 | C | T | 4 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(1): Show |
4 | HG03139.hp2 NA19030.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-703G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973179 | |||||||
chr12:108973198 | C | G | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.382-722G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973198 | |||||||
chr12:108973239 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-763C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973239 | |||||||
chr12:108973364 | G | GAC | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-890_382-889dup others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973364 | |||||||
chr12:108973383 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-907T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973383 | |||||||
chr12:108973461 | G | A | 1 | a0001c0002t0002g0195 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.382-985C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973461 | |||||||
chr12:108973589 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(127): Show |
132 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.382-1113C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973589 | |||||||
chr12:108973688 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(186): Show |
191 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.382-1212A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973688 | |||||||
chr12:108973752 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(186): Show |
191 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.382-1276A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973752 | |||||||
chr12:108973767 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-1291C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973767 | |||||||
chr12:108973775 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-1299T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973775 | |||||||
chr12:108973820 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(256): Show |
262 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(259): Show |
intron_variant | MODIFIER | c.382-1344T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973820 | |||||||
chr12:108973841 | C | A | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.382-1365G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973841 | |||||||
chr12:108973860 | G | A | 15 | a0001c0001t0008g0171 a0001c0001t0008g0220 a0001c0001t0008g0238 others(12): Show |
15 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.382-1384C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973860 | |||||||
chr12:108973870 | C | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-1394G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973870 | |||||||
chr12:108973907 | A | C | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.382-1431T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973907 | |||||||
chr12:108973990 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-1514T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108973990 | |||||||
chr12:108974047 | A | G | 1 | a0001c0001t0068g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.382-1571T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974047 | |||||||
chr12:108974106 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-1630T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974106 | |||||||
chr12:108974130 | T | A | 2 | a0001c0002t0013g0266 a0001c0002t0013g0276 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.382-1654A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974130 | |||||||
chr12:108974186 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-1710T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974186 | |||||||
chr12:108974202 | T | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(181): Show |
186 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.382-1726A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974202 | |||||||
chr12:108974343 | G | C | 7 | a0001c0002t0001g0169 a0001c0002t0001g0189 a0001c0002t0001g0227 others(4): Show |
7 | HG00642.hp2 HG03130.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-1867C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974343 | |||||||
chr12:108974348 | T | G | 1 | a0001c0002t0061g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.382-1872A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974348 | |||||||
chr12:108974509 | T | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-2033A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974509 | |||||||
chr12:108974688 | G | A | 1 | a0001c0001t0017g0061 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.382-2212C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974688 | |||||||
chr12:108974730 | C | CA | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
222 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.382-2255dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974730 | |||||||
chr12:108974801 | A | T | 16 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0008g0162 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.382-2325T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974801 | |||||||
chr12:108974861 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.382-2385G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108974861 | |||||||
chr12:108975239 | C | T | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.381+2159G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975239 | |||||||
chr12:108975382 | C | G | 1 | a0001c0002t0002g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.381+2016G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975382 | |||||||
chr12:108975421 | A | G | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.381+1977T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975421 | |||||||
chr12:108975477 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1921C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975477 | |||||||
chr12:108975546 | C | T | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.381+1852G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975546 | |||||||
chr12:108975588 | G | C | 33 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
33 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.381+1810C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975588 | |||||||
chr12:108975616 | G | T | 1 | a0001c0001t0020g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+1782C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975616 | |||||||
chr12:108975641 | C | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1757G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975641 | |||||||
chr12:108975660 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1738T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975660 | |||||||
chr12:108975666 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1732C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975666 | |||||||
chr12:108975730 | G | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1668C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975730 | |||||||
chr12:108975843 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1555T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975843 | |||||||
chr12:108975848 | G | A | 1 | a0001c0002t0010g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.381+1550C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975848 | |||||||
chr12:108975889 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(255): Show |
261 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.381+1509G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108975889 | |||||||
chr12:108976024 | T | C | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1374A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976024 | |||||||
chr12:108976048 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1350C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976048 | |||||||
chr12:108976108 | C | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1290G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976108 | |||||||
chr12:108976256 | C | T | 1 | a0001c0001t0003g0027 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.381+1142G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976256 | |||||||
chr12:108976280 | C | T | 2 | a0001c0002t0015g0150 a0001c0002t0021g0149 |
2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.381+1118G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976280 | |||||||
chr12:108976381 | C | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+1017G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976381 | |||||||
chr12:108976445 | C | T | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.381+953G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976445 | |||||||
chr12:108976513 | G | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.381+885C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976513 | |||||||
chr12:108976614 | CT | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(127): Show |
132 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.381+783delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976614 | |||||||
chr12:108976616 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+782A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976616 | |||||||
chr12:108976811 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+587G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976811 | |||||||
chr12:108976920 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.381+478G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108976920 | |||||||
chr12:108977133 | T | G | 1 | a0001c0001t0003g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.381+265A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108977133 | |||||||
chr12:108977312 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.381+86G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 4/15 | chr12 | 108977312 | |||||||
chr12:108977605 | C | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.283-109G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108977605 | |||||||
chr12:108977666 | G | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(127): Show |
132 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.283-170C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108977666 | |||||||
chr12:108977696 | C | A | 1 | a0001c0002t0023g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.283-200G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108977696 | |||||||
chr12:108977793 | GA | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.283-298delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108977793 | |||||||
chr12:108977956 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.283-460G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108977956 | |||||||
chr12:108977973 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.283-477G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108977973 | |||||||
chr12:108978064 | C | A | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.282+514G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108978064 | |||||||
chr12:108978187 | G | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.282+391C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108978187 | |||||||
chr12:108978280 | A | G | 16 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0008g0162 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+298T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108978280 | |||||||
chr12:108978418 | G | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.282+160C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108978418 | |||||||
chr12:108978435 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.282+143G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108978435 | |||||||
chr12:108978461 | T | C | 1 | a0001c0004t0018g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.282+117A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 3/15 | chr12 | 108978461 | |||||||
chr12:108978736 | G | T | 15 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.197-73C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108978736 | |||||||
chr12:108979025 | T | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(186): Show |
191 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.197-362A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979025 | |||||||
chr12:108979037 | G | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.197-374C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979037 | |||||||
chr12:108979087 | G | GTGCATAT others(3): Show |
1 | a0001c0001t0002g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.197-425_197-424ins others(10): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979087 | |||||||
chr12:108979090 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.197-427A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979090 | |||||||
chr12:108979090 | T | TATATATA others(3): Show |
186 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(183): Show |
188 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.197-428_197-427ins others(10): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979090 | |||||||
chr12:108979105 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.197-442C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979105 | |||||||
chr12:108979131 | A | G | 10 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-468T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979131 | |||||||
chr12:108979220 | GA | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.197-558delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979220 | |||||||
chr12:108979228 | A | G | 15 | a0001c0002t0002g0248 a0001c0002t0010g0002 a0001c0002t0010g0054 others(12): Show |
16 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.197-565T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979228 | |||||||
chr12:108979271 | G | A | 1 | a0001c0001t0004g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.197-608C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979271 | |||||||
chr12:108979276 | G | C | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.197-613C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979276 | |||||||
chr12:108979325 | T | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.197-662A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979325 | |||||||
chr12:108979384 | C | T | 1 | a0001c0001t0038g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.197-721G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979384 | |||||||
chr12:108979390 | T | C | 274 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(271): Show |
277 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.197-727A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979390 | |||||||
chr12:108979406 | T | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.197-743A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979406 | |||||||
chr12:108979440 | C | G | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.197-777G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979440 | |||||||
chr12:108979468 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(184): Show |
189 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.197-805G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979468 | |||||||
chr12:108979831 | GA | G | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1169delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979831 | |||||||
chr12:108979894 | G | A | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1231C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979894 | |||||||
chr12:108979907 | T | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1244A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979907 | |||||||
chr12:108979996 | T | A | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1333A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108979996 | |||||||
chr12:108980039 | T | G | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1376A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980039 | |||||||
chr12:108980049 | G | A | 94 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(91): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.197-1386C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980049 | |||||||
chr12:108980097 | G | A | 25 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0222 others(22): Show |
25 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.197-1434C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980097 | |||||||
chr12:108980097 | G | T | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.197-1434C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980097 | |||||||
chr12:108980182 | T | TA | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1520dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980182 | |||||||
chr12:108980263 | C | A | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.197-1600G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980263 | |||||||
chr12:108980344 | T | C | 94 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(91): Show |
95 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.197-1681A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980344 | |||||||
chr12:108980476 | T | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1813A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980476 | |||||||
chr12:108980527 | T | G | 1 | a0001c0002t0026g0144 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.197-1864A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980527 | |||||||
chr12:108980536 | G | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.197-1873C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980536 | |||||||
chr12:108980578 | G | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-1915C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980578 | |||||||
chr12:108980580 | C | T | 1 | a0001c0002t0024g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197-1917G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980580 | |||||||
chr12:108980586 | TGAAAATA others(169): Show |
T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-2099_197-1924d others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980586 | |||||||
chr12:108980587 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.197-1924C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980587 | |||||||
chr12:108980610 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.197-1947G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980610 | |||||||
chr12:108980612 | C | T | 2 | a0001c0001t0059g0123 a0001c0001t0081g0141 |
2 | HG03239.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.197-1949G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980612 | |||||||
chr12:108980622 | C | T | 3 | a0001c0001t0007g0048 a0001c0001t0042g0014 a0001c0001t0066g0154 |
3 | HG01943.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.197-1959G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980622 | |||||||
chr12:108980706 | C | T | 1 | a0001c0001t0012g0243 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.197-2043G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980706 | |||||||
chr12:108980751 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.197-2088G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980751 | |||||||
chr12:108980756 | C | CA | 46 | a0001c0001t0001g0209 a0001c0001t0002g0145 a0001c0001t0003g0005 others(43): Show |
46 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.197-2094dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980756 | |||||||
chr12:108980756 | C | CAA | 16 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0008g0162 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.197-2095_197-2094d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980756 | |||||||
chr12:108980764 | A | G | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-2101T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980764 | |||||||
chr12:108980768 | A | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-2105T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980768 | |||||||
chr12:108980770 | A | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-2107T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980770 | |||||||
chr12:108980797 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.197-2134A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980797 | |||||||
chr12:108980879 | C | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-2216G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980879 | |||||||
chr12:108980965 | G | A | 1 | a0001c0001t0008g0246 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197-2302C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108980965 | |||||||
chr12:108981006 | T | C | 3 | a0001c0001t0007g0048 a0001c0001t0042g0014 a0001c0001t0066g0154 |
3 | HG01943.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.197-2343A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108981006 | |||||||
chr12:108981078 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(102): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.197-2415C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108981078 | |||||||
chr12:108981256 | A | G | 1 | a0001c0002t0004g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.196+2345T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108981256 | |||||||
chr12:108981317 | G | A | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+2284C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108981317 | |||||||
chr12:108981446 | C | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+2155G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108981446 | |||||||
chr12:108981548 | T | TG | 98 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(95): Show |
100 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.196+2052dupC | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108981548 | |||||||
chr12:108981918 | C | A | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+1683G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108981918 | |||||||
chr12:108982053 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.196+1548G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982053 | |||||||
chr12:108982054 | G | A | 3 | a0001c0001t0007g0048 a0001c0001t0042g0014 a0001c0001t0066g0154 |
3 | HG01943.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196+1547C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982054 | |||||||
chr12:108982108 | G | A | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+1493C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982108 | |||||||
chr12:108982239 | A | G | 1 | a0001c0001t0038g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.196+1362T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982239 | |||||||
chr12:108982255 | C | T | 1 | a0001c0001t0003g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.196+1346G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982255 | |||||||
chr12:108982347 | T | C | 1 | a0001c0001t0003g0022 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.196+1254A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982347 | |||||||
chr12:108982348 | CATCATCA others(224): Show |
C | 1 | a0001c0001t0005g0271 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.196+1022_196+1252d others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982348 | |||||||
chr12:108982385 | A | G | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+1216T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982385 | |||||||
chr12:108982428 | T | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+1173A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982428 | |||||||
chr12:108982579 | TATC | T | 4 | a0001c0001t0017g0061 a0001c0001t0017g0072 a0001c0001t0017g0103 others(1): Show |
4 | NA18747.hp2 NA19011.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+1019_196+1021d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982579 | |||||||
chr12:108982661 | A | G | 15 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.196+940T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982661 | |||||||
chr12:108982672 | TATCATCA others(8): Show |
T | 55 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(52): Show |
55 | HG00544.hp2 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.196+914_196+928del others(15): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982672 | |||||||
chr12:108982680 | CCAT | C | 41 | a0001c0002t0001g0281 a0001c0002t0002g0147 a0001c0002t0002g0248 others(38): Show |
42 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.196+918_196+920del others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982680 | |||||||
chr12:108982759 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.196+842A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982759 | |||||||
chr12:108982836 | CCAT | C | 33 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
33 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.196+762_196+764del others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982836 | |||||||
chr12:108982839 | T | TCATCATC others(50): Show |
17 | a0001c0002t0002g0248 a0001c0002t0010g0002 a0001c0002t0010g0054 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.196+761_196+762ins others(57): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982839 | |||||||
chr12:108982839 | T | TCATCATC others(53): Show |
77 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(74): Show |
77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.196+761_196+762ins others(60): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982839 | |||||||
chr12:108982842 | T | TCATCATC others(50): Show |
2 | a0001c0002t0012g0251 a0001c0004t0016g0165 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.196+758_196+759ins others(57): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982842 | |||||||
chr12:108982846 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.196+755G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982846 | |||||||
chr12:108982879 | TATC | T | 33 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
33 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.196+719_196+721del others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982879 | |||||||
chr12:108982909 | T | TATC | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+689_196+691dup others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108982909 | |||||||
chr12:108983137 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.196+464G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108983137 | |||||||
chr12:108983286 | C | CCAT | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+312_196+314dup others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108983286 | |||||||
chr12:108983319 | T | C | 11 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0001c0002t0001g0206 others(8): Show |
11 | HG00544.hp2 NA18747.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+282A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108983319 | |||||||
chr12:108983355 | C | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+246G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108983355 | |||||||
chr12:108983417 | G | A | 1 | a0001c0001t0008g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.196+184C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108983417 | |||||||
chr12:108983454 | G | A | 25 | a0001c0002t0001g0281 a0001c0002t0002g0147 a0001c0002t0004g0268 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.196+147C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108983454 | |||||||
chr12:108983465 | T | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+136A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 2/15 | chr12 | 108983465 | |||||||
chr12:108983838 | G | A | 99 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 others(96): Show |
100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.36-77C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108983838 | |||||||
chr12:108983932 | C | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-171G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108983932 | |||||||
chr12:108984149 | G | T | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.36-388C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984149 | |||||||
chr12:108984213 | T | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-452A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984213 | |||||||
chr12:108984229 | T | A | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-468A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984229 | |||||||
chr12:108984267 | G | A | 1 | a0001c0002t0021g0272 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.36-506C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984267 | |||||||
chr12:108984316 | T | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-555A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984316 | |||||||
chr12:108984402 | G | T | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.36-641C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984402 | |||||||
chr12:108984428 | C | G | 95 | a0001c0002t0001g0097 a0001c0002t0001g0189 a0001c0002t0001g0197 others(92): Show |
96 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.36-667G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984428 | |||||||
chr12:108984637 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.36-876G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984637 | |||||||
chr12:108984721 | T | G | 1 | a0001c0002t0036g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.36-960A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984721 | |||||||
chr12:108984732 | G | A | 15 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.36-971C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984732 | |||||||
chr12:108984762 | T | C | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-1001A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984762 | |||||||
chr12:108984810 | G | T | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.36-1049C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984810 | |||||||
chr12:108984862 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0020g0181 a0001c0001t0067g0182 |
3 | HG02559.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.36-1101A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108984862 | |||||||
chr12:108985016 | A | C | 178 | a0001c0001t0001g0173 a0001c0001t0003g0005 a0001c0001t0003g0006 others(175): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.36-1255T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985016 | |||||||
chr12:108985020 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.36-1259T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985020 | |||||||
chr12:108985070 | G | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-1309C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985070 | |||||||
chr12:108985160 | G | C | 3 | a0001c0002t0015g0150 a0001c0002t0021g0149 a0001c0002t0021g0151 |
3 | HG00280.hp2 HG01175.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.36-1399C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985160 | |||||||
chr12:108985176 | G | A | 25 | a0001c0002t0001g0281 a0001c0002t0002g0147 a0001c0002t0004g0268 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.36-1415C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985176 | |||||||
chr12:108985266 | A | G | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-1505T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985266 | |||||||
chr12:108985274 | G | A | 97 | a0001c0001t0002g0158 a0001c0002t0001g0097 a0001c0002t0001g0169 others(94): Show |
98 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.36-1513C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985274 | |||||||
chr12:108985309 | GAAAT | G | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-1552_36-1549del others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985309 | |||||||
chr12:108985356 | TAAAAGG | T | 4 | a0001c0002t0001g0283 a0001c0002t0005g0190 a0001c0002t0010g0191 others(1): Show |
4 | HG01123.hp2 HG01243.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-1601_36-1596del others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985356 | |||||||
chr12:108985375 | A | G | 2 | a0001c0002t0012g0251 a0001c0004t0016g0165 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.36-1614T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985375 | |||||||
chr12:108985402 | T | A | 1 | a0001c0004t0018g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.36-1641A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985402 | |||||||
chr12:108985409 | C | T | 95 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(92): Show |
96 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.36-1648G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985409 | |||||||
chr12:108985594 | C | T | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-1833G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985594 | |||||||
chr12:108985732 | A | G | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.36-1971T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985732 | |||||||
chr12:108985759 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.36-1998A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985759 | |||||||
chr12:108985781 | A | C | 1 | a0001c0002t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.36-2020T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985781 | |||||||
chr12:108985966 | C | G | 96 | a0001c0002t0001g0097 a0001c0002t0001g0169 a0001c0002t0001g0189 others(93): Show |
97 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-2205G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108985966 | |||||||
chr12:108986043 | A | T | 1 | a0001c0001t0002g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.36-2282T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986043 | |||||||
chr12:108986065 | C | T | 267 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(264): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.36-2304G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986065 | |||||||
chr12:108986100 | C | T | 1 | a0001c0002t0010g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.36-2339G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986100 | |||||||
chr12:108986136 | T | C | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.36-2375A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986136 | |||||||
chr12:108986207 | A | C | 1 | a0001c0001t0007g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.36-2446T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986207 | |||||||
chr12:108986419 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(223): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.36-2658A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986419 | |||||||
chr12:108986690 | A | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(222): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.36-2929T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986690 | |||||||
chr12:108986730 | T | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.36-2969A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986730 | |||||||
chr12:108986758 | G | A | 197 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(194): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.36-2997C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986758 | |||||||
chr12:108986778 | AG | A | 124 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(121): Show |
125 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.36-3018delC | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986778 | |||||||
chr12:108986864 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.36-3103T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986864 | |||||||
chr12:108986957 | C | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.36-3196G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986957 | |||||||
chr12:108986998 | T | C | 1 | a0001c0001t0083g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.36-3237A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108986998 | |||||||
chr12:108987013 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.36-3252G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987013 | |||||||
chr12:108987409 | G | A | 1 | a0001c0002t0023g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.36-3648C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987409 | |||||||
chr12:108987519 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.36-3758C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987519 | |||||||
chr12:108987522 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-3761A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987522 | |||||||
chr12:108987706 | T | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0131 a0001c0001t0002g0128 others(1): Show |
4 | HG02056.hp2 HG02155.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-3945A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987706 | |||||||
chr12:108987771 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.36-4010G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987771 | |||||||
chr12:108987799 | C | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4038G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987799 | |||||||
chr12:108987814 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4053C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987814 | |||||||
chr12:108987875 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4114C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987875 | |||||||
chr12:108987904 | T | C | 1 | a0001c0001t0037g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36-4143A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987904 | |||||||
chr12:108987905 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4144G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987905 | |||||||
chr12:108987925 | GA | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4165delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108987925 | |||||||
chr12:108988088 | A | AT | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4328dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988088 | |||||||
chr12:108988250 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.36-4489G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988250 | |||||||
chr12:108988442 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.36-4681C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988442 | |||||||
chr12:108988451 | A | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(263): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.36-4690T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988451 | |||||||
chr12:108988715 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4954A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988715 | |||||||
chr12:108988745 | T | TCTTC | 195 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.36-4988_36-4985dup others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988745 | |||||||
chr12:108988753 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4992A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988753 | |||||||
chr12:108988757 | A | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-4996T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988757 | |||||||
chr12:108988761 | C | CCT | 24 | a0001c0001t0001g0157 a0001c0001t0001g0196 a0001c0001t0002g0079 others(21): Show |
24 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.36-5001_36-5000ins others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988761 | |||||||
chr12:108988763 | T | C | 24 | a0001c0001t0001g0157 a0001c0001t0001g0196 a0001c0001t0002g0079 others(21): Show |
24 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.36-5002A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988763 | |||||||
chr12:108988766 | C | T | 24 | a0001c0001t0001g0157 a0001c0001t0001g0196 a0001c0001t0002g0079 others(21): Show |
24 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.36-5005G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988766 | |||||||
chr12:108988770 | C | CT | 50 | a0001c0001t0004g0226 a0001c0001t0005g0069 a0001c0001t0005g0102 others(47): Show |
51 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.36-5010dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988770 | |||||||
chr12:108988770 | C | CTT | 23 | a0001c0001t0001g0265 a0001c0002t0001g0197 a0001c0002t0001g0207 others(20): Show |
23 | HG00280.hp1 HG01123.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.36-5011_36-5010dup others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988770 | |||||||
chr12:108988770 | C | CTTT | 17 | a0001c0001t0001g0003 a0001c0001t0005g0271 a0001c0002t0004g0268 others(14): Show |
18 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.36-5012_36-5010dup others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988770 | |||||||
chr12:108988770 | C | CTTTT | 15 | a0001c0001t0003g0039 a0001c0001t0007g0048 a0001c0001t0015g0148 others(12): Show |
15 | HG00280.hp2 HG00738.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.36-5013_36-5010dup others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988770 | |||||||
chr12:108988770 | C | CTTTTT | 30 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(27): Show |
30 | HG01123.hp1 HG01255.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.36-5014_36-5010dup others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988770 | |||||||
chr12:108988770 | C | CTTTTTT | 6 | a0001c0001t0003g0032 a0001c0001t0003g0046 a0001c0001t0007g0025 others(3): Show |
6 | HG00408.hp2 HG00597.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-5015_36-5010dup others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988770 | |||||||
chr12:108988770 | CT | C | 79 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(76): Show |
80 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.36-5010delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988770 | |||||||
chr12:108988772 | T | C | 24 | a0001c0001t0001g0157 a0001c0001t0001g0196 a0001c0001t0002g0079 others(21): Show |
24 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.36-5011A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988772 | |||||||
chr12:108988834 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-5073T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988834 | |||||||
chr12:108988965 | G | A | 1 | a0001c0001t0063g0080 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.36-5204C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988965 | |||||||
chr12:108988997 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0005g0271 a0001c0001t0015g0148 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.36-5236A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108988997 | |||||||
chr12:108989092 | C | T | 1 | a0001c0001t0022g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.36-5331G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989092 | |||||||
chr12:108989100 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0265 others(101): Show |
106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.36-5339G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989100 | |||||||
chr12:108989221 | C | A | 1 | a0001c0002t0001g0281 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.36-5460G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989221 | |||||||
chr12:108989268 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0265 others(101): Show |
106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.36-5507A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989268 | |||||||
chr12:108989347 | T | C | 1 | a0001c0001t0009g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.36-5586A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989347 | |||||||
chr12:108989360 | A | G | 2 | a0001c0002t0001g0201 a0001c0002t0001g0206 |
2 | NA18971.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.36-5599T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989360 | |||||||
chr12:108989382 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-5621G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989382 | |||||||
chr12:108989397 | C | T | 55 | a0001c0001t0001g0173 a0001c0001t0001g0265 a0001c0001t0004g0226 others(52): Show |
55 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.36-5636G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989397 | |||||||
chr12:108989434 | G | GGGAAGCA others(3): Show |
219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-5674_36-5673ins others(10): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989434 | |||||||
chr12:108989436 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.36-5675T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989436 | |||||||
chr12:108989472 | C | G | 1 | a0001c0001t0013g0277 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-5711G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989472 | |||||||
chr12:108989545 | G | A | 1 | a0001c0002t0023g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.36-5784C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989545 | |||||||
chr12:108989587 | T | A | 1 | a0001c0001t0065g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.36-5826A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989587 | |||||||
chr12:108989598 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-5837T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989598 | |||||||
chr12:108989617 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-5856T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989617 | |||||||
chr12:108989664 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-5903T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989664 | |||||||
chr12:108989820 | A | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6059T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989820 | |||||||
chr12:108989854 | G | A | 1 | a0001c0002t0001g0281 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.36-6093C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989854 | |||||||
chr12:108989861 | A | G | 1 | a0001c0002t0021g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.36-6100T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989861 | |||||||
chr12:108989983 | C | T | 1 | a0001c0001t0019g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.36-6222G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108989983 | |||||||
chr12:108990019 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6258T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990019 | |||||||
chr12:108990241 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6480G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990241 | |||||||
chr12:108990250 | A | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6489T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990250 | |||||||
chr12:108990317 | T | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6556A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990317 | |||||||
chr12:108990333 | C | T | 1 | a0001c0002t0036g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.36-6572G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990333 | |||||||
chr12:108990370 | A | G | 1 | a0001c0001t0068g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.36-6609T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990370 | |||||||
chr12:108990403 | G | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6642C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990403 | |||||||
chr12:108990417 | C | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6656G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990417 | |||||||
chr12:108990451 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6690G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990451 | |||||||
chr12:108990497 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6736G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990497 | |||||||
chr12:108990564 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-6803G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990564 | |||||||
chr12:108990678 | AATAAAAC others(5): Show |
A | 28 | a0001c0001t0001g0003 a0001c0001t0005g0271 a0001c0001t0015g0148 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.36-6929_36-6918del others(12): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990678 | |||||||
chr12:108990680 | T | C | 191 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(188): Show |
193 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.36-6919A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990680 | |||||||
chr12:108990685 | CAAAACAG | C | 190 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(187): Show |
192 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.36-6931_36-6925del others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990685 | |||||||
chr12:108990687 | AAACAGAA others(4): Show |
A | 1 | a0001c0002t0072g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.36-6937_36-6927del others(11): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990687 | |||||||
chr12:108990692 | G | C | 28 | a0001c0001t0001g0003 a0001c0001t0005g0271 a0001c0001t0015g0148 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.36-6931C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990692 | |||||||
chr12:108990696 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.36-6935T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990696 | |||||||
chr12:108990864 | G | A | 21 | a0001c0001t0006g0161 a0001c0001t0006g0193 a0001c0001t0006g0222 others(18): Show |
21 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.36-7103C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990864 | |||||||
chr12:108990870 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-7109G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990870 | |||||||
chr12:108990964 | G | A | 1 | a0001c0002t0015g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.36-7203C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990964 | |||||||
chr12:108990996 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-7235G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108990996 | |||||||
chr12:108991145 | C | T | 1 | a0001c0001t0067g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.36-7384G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991145 | |||||||
chr12:108991251 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-7490G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991251 | |||||||
chr12:108991343 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-7582A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991343 | |||||||
chr12:108991437 | TTTTGCTT others(5): Show |
T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.36-7688_36-7677del others(12): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991437 | |||||||
chr12:108991442 | C | CTTGT | 24 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(21): Show |
24 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.36-7685_36-7682dup others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991442 | |||||||
chr12:108991442 | C | CTTGTTTG others(1): Show |
11 | a0001c0001t0003g0031 a0001c0001t0003g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01109.hp2 HG01255.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.36-7689_36-7682dup others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991442 | |||||||
chr12:108991442 | C | CTTGTTTG others(5): Show |
3 | a0001c0001t0003g0033 a0001c0001t0003g0035 a0001c0001t0003g0038 |
3 | NA18612.hp1 NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.36-7693_36-7682dup others(12): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991442 | |||||||
chr12:108991534 | C | A | 1 | a0001c0001t0002g0158 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.36-7773G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991534 | |||||||
chr12:108991782 | A | AAAC | 5 | a0001c0001t0001g0135 a0001c0001t0038g0045 a0001c0002t0002g0223 others(2): Show |
5 | HG01978.hp2 HG02738.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.36-8022_36-8021ins others(3): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991782 | |||||||
chr12:108991784 | C | A | 6 | a0001c0001t0001g0135 a0001c0001t0038g0045 a0001c0001t0043g0020 others(3): Show |
6 | HG01978.hp2 HG02738.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-8023G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991784 | |||||||
chr12:108991784 | C | CAA | 212 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.36-8025_36-8024dup others(2): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991784 | |||||||
chr12:108991821 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.36-8060A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991821 | |||||||
chr12:108991827 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.36-8066A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991827 | |||||||
chr12:108991831 | G | A | 1 | a0001c0002t0023g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.36-8070C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991831 | |||||||
chr12:108991837 | T | G | 115 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(112): Show |
116 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.36-8076A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991837 | |||||||
chr12:108991839 | A | G | 1 | a0001c0002t0023g0183 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.36-8078T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991839 | |||||||
chr12:108991919 | T | C | 37 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(34): Show |
37 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.36-8158A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991919 | |||||||
chr12:108991926 | C | T | 7 | a0001c0001t0001g0091 a0001c0001t0003g0016 a0001c0001t0003g0018 others(4): Show |
7 | HG01123.hp1 HG01496.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.36-8165G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991926 | |||||||
chr12:108991946 | A | C | 2 | a0001c0001t0005g0069 a0001c0001t0005g0102 |
2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.36-8185T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108991946 | |||||||
chr12:108992025 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.36-8264G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992025 | |||||||
chr12:108992072 | C | T | 55 | a0001c0001t0001g0173 a0001c0001t0001g0265 a0001c0001t0004g0226 others(52): Show |
55 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.36-8311G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992072 | |||||||
chr12:108992241 | T | TA | 104 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0265 others(101): Show |
106 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.36-8481dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992241 | |||||||
chr12:108992241 | TA | T | 47 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(44): Show |
47 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.36-8481delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992241 | |||||||
chr12:108992283 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.36-8522C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992283 | |||||||
chr12:108992305 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.36-8544G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992305 | |||||||
chr12:108992306 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0265 others(81): Show |
85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.36-8545C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992306 | |||||||
chr12:108992325 | C | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.36-8564G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992325 | |||||||
chr12:108992411 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.36-8650A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992411 | |||||||
chr12:108992431 | C | T | 2 | a0001c0001t0013g0277 a0001c0001t0013g0278 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.36-8670G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992431 | |||||||
chr12:108992474 | G | A | 1 | a0001c0002t0021g0151 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.36-8713C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992474 | |||||||
chr12:108992513 | G | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.36-8752C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992513 | |||||||
chr12:108992594 | C | A | 1 | a0001c0002t0024g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.36-8833G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992594 | |||||||
chr12:108992824 | G | A | 2 | a0001c0002t0012g0251 a0001c0004t0016g0165 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.36-9063C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108992824 | |||||||
chr12:108993155 | G | A | 10 | a0001c0001t0008g0220 a0001c0001t0008g0238 a0001c0001t0008g0239 others(7): Show |
10 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.36-9394C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993155 | |||||||
chr12:108993315 | C | A | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.36-9554G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993315 | |||||||
chr12:108993358 | C | T | 267 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(264): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.36-9597G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993358 | |||||||
chr12:108993364 | G | A | 4 | a0001c0001t0003g0022 a0001c0001t0003g0032 a0001c0001t0043g0020 others(1): Show |
4 | HG00597.hp1 NA19067.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-9603C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993364 | |||||||
chr12:108993365 | T | C | 2 | a0001c0001t0004g0099 a0001c0003t0018g0152 |
2 | HG00733.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.36-9604A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993365 | |||||||
chr12:108993378 | C | CA | 253 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(250): Show |
256 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.36-9618dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993378 | |||||||
chr12:108993461 | G | A | 1 | a0001c0001t0076g0125 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.36-9700C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993461 | |||||||
chr12:108993766 | C | T | 1 | a0001c0001t0015g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.36-10005G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993766 | |||||||
chr12:108993802 | G | A | 93 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(90): Show |
94 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.36-10041C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108993802 | |||||||
chr12:108994006 | C | T | 4 | a0001c0002t0024g0237 a0001c0002t0071g0274 a0001c0005t0007g0023 others(1): Show |
4 | HG02040.hp1 HG02083.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-10245G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994006 | |||||||
chr12:108994024 | C | T | 1 | a0001c0002t0001g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.36-10263G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994024 | |||||||
chr12:108994259 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0089 others(2): Show |
5 | NA18953.hp2 NA18956.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-10498G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994259 | |||||||
chr12:108994260 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.36-10499T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994260 | |||||||
chr12:108994368 | C | T | 9 | a0001c0001t0015g0148 a0001c0002t0001g0097 a0001c0002t0002g0147 others(6): Show |
9 | HG00280.hp2 HG00738.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.36-10607G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994368 | |||||||
chr12:108994385 | T | A | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.36-10624A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994385 | |||||||
chr12:108994419 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.36-10658C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994419 | |||||||
chr12:108994479 | G | A | 1 | a0001c0001t0068g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.36-10718C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994479 | |||||||
chr12:108994555 | G | A | 4 | a0001c0002t0006g0235 a0001c0002t0023g0234 a0001c0003t0016g0170 others(1): Show |
4 | HG02280.hp1 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-10794C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994555 | |||||||
chr12:108994587 | C | T | 27 | a0001c0001t0001g0173 a0001c0001t0005g0069 a0001c0001t0005g0102 others(24): Show |
28 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.36-10826G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994587 | |||||||
chr12:108994648 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0265 a0001c0001t0004g0226 others(73): Show |
77 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.36-10887G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994648 | |||||||
chr12:108994652 | C | T | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.36-10891G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994652 | |||||||
chr12:108994757 | C | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.36-10996G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994757 | |||||||
chr12:108994811 | G | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0265 others(107): Show |
112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.36-11050C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994811 | |||||||
chr12:108994917 | G | A | 9 | a0001c0001t0001g0265 a0001c0002t0001g0207 a0001c0002t0001g0283 others(6): Show |
9 | HG01123.hp2 HG01243.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.36-11156C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994917 | |||||||
chr12:108994959 | A | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(170): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.36-11198T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994959 | |||||||
chr12:108994972 | T | C | 37 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(34): Show |
37 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.36-11211A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994972 | |||||||
chr12:108994981 | A | G | 2 | a0001c0002t0001g0201 a0001c0002t0001g0206 |
2 | NA18971.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.36-11220T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108994981 | |||||||
chr12:108995016 | G | A | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.36-11255C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995016 | |||||||
chr12:108995089 | G | A | 1 | a0001c0003t0016g0232 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.36-11328C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995089 | |||||||
chr12:108995428 | T | C | 93 | a0001c0001t0001g0173 a0001c0001t0001g0225 a0001c0001t0001g0265 others(90): Show |
94 | HG00280.hp2 HG00544.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.36-11667A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995428 | |||||||
chr12:108995816 | G | A | 2 | a0001c0001t0005g0069 a0001c0001t0005g0102 |
2 | HG03942.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.36-12055C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995816 | |||||||
chr12:108995830 | G | A | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.36-12069C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995830 | |||||||
chr12:108995832 | G | C | 2 | a0001c0002t0001g0207 a0001c0002t0084g0208 |
2 | HG03688.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.36-12071C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995832 | |||||||
chr12:108995896 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0225 others(110): Show |
115 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.36-12135A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995896 | |||||||
chr12:108995901 | C | CA | 58 | a0001c0001t0001g0091 a0001c0001t0002g0142 a0001c0001t0003g0006 others(55): Show |
58 | HG00408.hp2 HG01070.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.36-12141dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995901 | |||||||
chr12:108995942 | T | C | 27 | a0001c0002t0001g0197 a0001c0002t0001g0201 a0001c0002t0001g0202 others(24): Show |
27 | HG00544.hp2 HG02155.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.36-12181A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108995942 | |||||||
chr12:108996006 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.36-12245T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996006 | |||||||
chr12:108996157 | C | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0225 a0001c0001t0001g0265 others(80): Show |
84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.36-12396G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996157 | |||||||
chr12:108996203 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0089 others(2): Show |
5 | NA18953.hp2 NA18956.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-12442G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996203 | |||||||
chr12:108996265 | C | T | 1 | a0001c0001t0008g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.36-12504G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996265 | |||||||
chr12:108996512 | G | A | 1 | a0001c0002t0010g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.36-12751C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996512 | |||||||
chr12:108996711 | G | A | 6 | a0001c0001t0015g0148 a0001c0002t0001g0097 a0001c0002t0002g0147 others(3): Show |
6 | HG00280.hp2 HG00738.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-12950C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996711 | |||||||
chr12:108996727 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0005g0271 a0001c0001t0015g0148 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.36-12966A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996727 | |||||||
chr12:108996761 | G | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.36-13000C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996761 | |||||||
chr12:108996907 | G | A | 2 | a0001c0001t0001g0003 a0001c0002t0004g0273 |
3 | HG00642.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.36-13146C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996907 | |||||||
chr12:108996953 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0043g0020 a0001c0001t0047g0021 |
3 | NA19067.hp2 NA19080.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.36-13192T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108996953 | |||||||
chr12:108997161 | G | T | 19 | a0001c0001t0007g0048 a0001c0001t0008g0171 a0001c0001t0008g0220 others(16): Show |
19 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.36-13400C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997161 | |||||||
chr12:108997275 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.36-13514G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997275 | |||||||
chr12:108997312 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.36-13551C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997312 | |||||||
chr12:108997317 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.36-13556G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997317 | |||||||
chr12:108997321 | G | A | 1 | a0001c0002t0001g0169 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.36-13560C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997321 | |||||||
chr12:108997328 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.36-13567A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997328 | |||||||
chr12:108997410 | G | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(277): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.36-13649C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997410 | |||||||
chr12:108997431 | A | G | 5 | a0001c0001t0007g0048 a0001c0001t0012g0241 a0001c0001t0012g0242 others(2): Show |
5 | HG01943.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-13670T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997431 | |||||||
chr12:108997440 | G | A | 278 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.36-13679C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997440 | |||||||
chr12:108997448 | T | C | 1 | a0001c0003t0011g0133 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.36-13687A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997448 | |||||||
chr12:108997502 | C | G | 3 | a0001c0002t0006g0164 a0001c0002t0012g0251 a0001c0004t0016g0165 |
3 | HG02055.hp1 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.36-13741G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997502 | |||||||
chr12:108997619 | C | T | 4 | a0001c0002t0028g0262 a0001c0002t0028g0263 a0001c0002t0064g0267 others(1): Show |
4 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-13858G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997619 | |||||||
chr12:108997662 | C | T | 1 | a0001c0002t0002g0200 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.36-13901G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997662 | |||||||
chr12:108997669 | C | A | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.36-13908G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997669 | |||||||
chr12:108997708 | A | C | 16 | a0001c0001t0001g0265 a0001c0001t0060g0116 a0001c0002t0001g0207 others(13): Show |
16 | HG01123.hp2 HG01243.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.36-13947T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997708 | |||||||
chr12:108997709 | C | A | 3 | a0001c0002t0006g0164 a0001c0002t0012g0251 a0001c0004t0016g0165 |
3 | HG02055.hp1 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.36-13948G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997709 | |||||||
chr12:108997715 | A | C | 15 | a0001c0001t0001g0265 a0001c0002t0001g0207 a0001c0002t0001g0283 others(12): Show |
15 | HG01123.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.36-13954T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997715 | |||||||
chr12:108997736 | C | T | 3 | a0001c0001t0042g0014 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.36-13975G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997736 | |||||||
chr12:108997756 | T | C | 3 | a0001c0001t0042g0014 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.36-13995A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997756 | |||||||
chr12:108997758 | T | A | 1 | a0001c0001t0002g0128 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.36-13997A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997758 | |||||||
chr12:108997772 | A | G | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.36-14011T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997772 | |||||||
chr12:108997774 | C | A | 3 | a0001c0001t0042g0014 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.36-14013G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997774 | |||||||
chr12:108997790 | T | C | 3 | a0001c0001t0042g0014 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.36-14029A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997790 | |||||||
chr12:108997802 | C | T | 2 | a0001c0001t0007g0048 a0001c0002t0036g0049 |
2 | HG01943.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.36-14041G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108997802 | |||||||
chr12:108998009 | C | T | 2 | a0001c0001t0008g0238 a0001c0001t0008g0239 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.36-14248G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998009 | |||||||
chr12:108998041 | G | A | 1 | a0001c0001t0030g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.36-14280C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998041 | |||||||
chr12:108998079 | C | T | 6 | a0001c0001t0070g0250 a0001c0002t0013g0266 a0001c0002t0013g0276 others(3): Show |
6 | HG01884.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-14318G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998079 | |||||||
chr12:108998197 | A | G | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.36-14436T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998197 | |||||||
chr12:108998390 | G | A | 39 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(36): Show |
39 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.36-14629C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998390 | |||||||
chr12:108998411 | C | T | 2 | a0001c0002t0014g0178 a0001c0002t0020g0179 |
2 | HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.36-14650G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998411 | |||||||
chr12:108998620 | A | G | 21 | a0001c0001t0007g0048 a0001c0001t0008g0171 a0001c0001t0008g0220 others(18): Show |
21 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.36-14859T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998620 | |||||||
chr12:108998643 | T | C | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.36-14882A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998643 | |||||||
chr12:108998783 | G | T | 36 | a0001c0001t0001g0225 a0001c0001t0004g0226 a0001c0002t0001g0169 others(33): Show |
36 | HG00544.hp2 HG00639.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.36-15022C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998783 | |||||||
chr12:108998878 | C | T | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.36-15117G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998878 | |||||||
chr12:108998895 | T | A | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.36-15134A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998895 | |||||||
chr12:108998899 | T | C | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.36-15138A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108998899 | |||||||
chr12:108999062 | A | C | 1 | a0001c0001t0003g0016 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.36-15301T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999062 | |||||||
chr12:108999076 | G | A | 2 | a0001c0002t0033g0198 a0001c0002t0033g0199 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.36-15315C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999076 | |||||||
chr12:108999143 | A | G | 2 | a0001c0001t0005g0114 a0001c0001t0005g0115 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.36-15382T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999143 | |||||||
chr12:108999419 | C | A | 1 | a0001c0001t0003g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.36-15658G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999419 | |||||||
chr12:108999444 | G | C | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.36-15683C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999444 | |||||||
chr12:108999577 | G | C | 5 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0005g0190 others(2): Show |
5 | HG01123.hp2 HG01243.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-15816C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999577 | |||||||
chr12:108999616 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.36-15855A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999616 | |||||||
chr12:108999780 | A | G | 9 | a0001c0001t0001g0225 a0001c0001t0004g0226 a0001c0002t0001g0169 others(6): Show |
9 | HG00639.hp1 HG00642.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.36-16019T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999780 | |||||||
chr12:108999874 | T | C | 2 | a0001c0001t0020g0181 a0001c0002t0023g0183 |
2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.36-16113A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999874 | |||||||
chr12:108999892 | A | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0225 others(89): Show |
93 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.36-16131T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999892 | |||||||
chr12:108999918 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.36-16157G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 108999918 | |||||||
chr12:109000060 | C | T | 1 | a0001c0001t0037g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36-16299G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000060 | |||||||
chr12:109000138 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0005g0271 a0001c0002t0001g0281 others(13): Show |
17 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.36-16377C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000138 | |||||||
chr12:109000219 | G | GAT | 8 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0035 others(5): Show |
8 | HG00597.hp1 NA18612.hp1 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.36-16460_36-16459d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000219 | |||||||
chr12:109000238 | A | G | 11 | a0001c0001t0005g0069 a0001c0001t0005g0102 a0001c0002t0010g0002 others(8): Show |
12 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.36-16477T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000238 | |||||||
chr12:109000429 | GA | G | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.36-16669delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000429 | |||||||
chr12:109000578 | A | C | 1 | a0001c0001t0004g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.36-16817T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000578 | |||||||
chr12:109000579 | C | T | 59 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(56): Show |
59 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.36-16818G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000579 | |||||||
chr12:109000660 | C | T | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.36-16899G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000660 | |||||||
chr12:109000670 | T | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0225 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.36-16909A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000670 | |||||||
chr12:109000676 | T | C | 1 | a0001c0002t0002g0195 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.36-16915A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000676 | |||||||
chr12:109000758 | A | G | 1 | a0001c0001t0012g0241 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.36-16997T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000758 | |||||||
chr12:109000777 | A | G | 4 | a0001c0001t0005g0110 a0001c0001t0020g0112 a0001c0001t0075g0111 others(1): Show |
4 | HG00741.hp2 HG01256.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-17016T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000777 | |||||||
chr12:109000805 | C | T | 1 | a0001c0001t0083g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.36-17044G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109000805 | |||||||
chr12:109001171 | G | GACAA | 268 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(265): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.36-17411_36-17410i others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001171 | |||||||
chr12:109001357 | C | T | 1 | a0001c0002t0001g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.36-17596G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001357 | |||||||
chr12:109001478 | CA | C | 8 | a0001c0001t0001g0173 a0001c0002t0010g0174 a0001c0002t0014g0175 others(5): Show |
8 | HG01081.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.36-17718delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001478 | |||||||
chr12:109001491 | G | A | 1 | a0001c0002t0002g0248 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.36-17730C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001491 | |||||||
chr12:109001508 | C | T | 3 | a0001c0001t0042g0014 a0001c0002t0039g0013 a0001c0002t0040g0012 |
3 | HG01891.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.36-17747G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001508 | |||||||
chr12:109001654 | G | A | 62 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(59): Show |
62 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.36-17893C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001654 | |||||||
chr12:109001944 | A | C | 1 | a0001c0002t0025g0186 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.36-18183T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001944 | |||||||
chr12:109001954 | C | A | 1 | a0001c0002t0025g0186 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.36-18193G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001954 | |||||||
chr12:109001991 | G | T | 7 | a0001c0001t0001g0091 a0001c0001t0003g0016 a0001c0001t0003g0018 others(4): Show |
7 | HG01123.hp1 HG01496.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.36-18230C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109001991 | |||||||
chr12:109002030 | A | G | 1 | a0001c0001t0051g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.36-18269T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109002030 | |||||||
chr12:109002150 | T | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.36-18389A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109002150 | |||||||
chr12:109002255 | G | A | 39 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(36): Show |
39 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.36-18494C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109002255 | |||||||
chr12:109002291 | TAAA | T | 5 | a0001c0001t0001g0265 a0001c0002t0001g0283 a0001c0002t0005g0190 others(2): Show |
5 | HG01123.hp2 HG01243.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-18533_36-18531d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109002291 | |||||||
chr12:109002620 | A | G | 39 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(36): Show |
39 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.35+18214T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109002620 | |||||||
chr12:109002702 | G | A | 2 | a0001c0001t0001g0059 a0001c0002t0029g0231 |
2 | HG01175.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.35+18132C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109002702 | |||||||
chr12:109002978 | A | AAAAT | 82 | a0001c0001t0001g0003 a0001c0001t0001g0225 a0001c0001t0001g0265 others(79): Show |
83 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.35+17852_35+17855d others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109002978 | |||||||
chr12:109003006 | A | T | 1 | a0001c0001t0085g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.35+17828T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109003006 | |||||||
chr12:109003008 | T | A | 1 | a0001c0001t0085g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.35+17826A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109003008 | |||||||
chr12:109003014 | T | TA | 262 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(259): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.35+17819dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109003014 | |||||||
chr12:109003444 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0225 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.35+17390C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109003444 | |||||||
chr12:109003814 | C | T | 4 | a0001c0002t0001g0197 a0001c0002t0013g0167 a0001c0002t0033g0198 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+17020G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109003814 | |||||||
chr12:109003936 | C | T | 2 | a0001c0001t0015g0148 a0001c0002t0021g0149 |
2 | HG00280.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.35+16898G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109003936 | |||||||
chr12:109004406 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.35+16428C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004406 | |||||||
chr12:109004407 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.35+16427G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004407 | |||||||
chr12:109004409 | A | G | 6 | a0001c0002t0002g0219 a0001c0002t0005g0217 a0001c0002t0005g0218 others(3): Show |
6 | NA18947.hp1 NA18954.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+16425T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004409 | |||||||
chr12:109004409 | A | T | 1 | a0001c0001t0004g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.35+16425T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004409 | |||||||
chr12:109004410 | C | CTTT | 21 | a0001c0001t0001g0059 a0001c0001t0001g0127 a0001c0001t0001g0137 others(18): Show |
22 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.35+16421_35+16423d others(5): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004410 | |||||||
chr12:109004410 | C | CTTTT | 88 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0071 others(85): Show |
89 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.35+16420_35+16423d others(6): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004410 | |||||||
chr12:109004410 | CT | C | 12 | a0001c0001t0001g0091 a0001c0001t0007g0030 a0001c0001t0007g0048 others(9): Show |
12 | HG01243.hp1 HG01943.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.35+16423delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004410 | |||||||
chr12:109004479 | C | T | 1 | a0001c0002t0072g0233 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.35+16355G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004479 | |||||||
chr12:109004490 | C | T | 4 | a0001c0001t0002g0145 a0001c0003t0011g0132 a0001c0003t0011g0133 others(1): Show |
4 | NA18967.hp1 NA18967.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+16344G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004490 | |||||||
chr12:109004559 | G | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.35+16275C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004559 | |||||||
chr12:109004702 | TATTTC | T | 111 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(108): Show |
113 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.35+16127_35+16131d others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004702 | |||||||
chr12:109004702 | TATTTCAT others(3): Show |
T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0173 others(141): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.35+16122_35+16131d others(12): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004702 | |||||||
chr12:109004702 | TATTTCAT others(8): Show |
T | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+16117_35+16131d others(17): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004702 | |||||||
chr12:109004702 | TATTTCAT others(13): Show |
T | 3 | a0001c0002t0001g0281 a0001c0002t0002g0147 a0001c0002t0024g0237 |
3 | HG01891.hp2 HG03195.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.35+16112_35+16131d others(22): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004702 | |||||||
chr12:109004766 | C | T | 1 | a0001c0001t0024g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.35+16068G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004766 | |||||||
chr12:109004831 | G | A | 1 | a0001c0002t0001g0281 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.35+16003C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004831 | |||||||
chr12:109004957 | C | G | 1 | a0001c0002t0030g0100 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.35+15877G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109004957 | |||||||
chr12:109005194 | T | C | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.35+15640A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109005194 | |||||||
chr12:109005195 | C | T | 1 | a0001c0002t0074g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.35+15639G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109005195 | |||||||
chr12:109005419 | A | G | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.35+15415T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109005419 | |||||||
chr12:109005592 | A | G | 2 | a0001c0001t0006g0224 a0001c0001t0069g0166 |
2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.35+15242T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109005592 | |||||||
chr12:109005716 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.35+15118T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109005716 | |||||||
chr12:109006014 | C | T | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.35+14820G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006014 | |||||||
chr12:109006043 | GTTGTT | G | 39 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(36): Show |
39 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.35+14786_35+14790d others(7): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006043 | |||||||
chr12:109006061 | G | A | 1 | a0001c0004t0011g0064 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.35+14773C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006061 | |||||||
chr12:109006099 | C | A | 4 | a0001c0002t0006g0235 a0001c0002t0023g0234 a0001c0003t0016g0170 others(1): Show |
4 | HG02280.hp1 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+14735G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006099 | |||||||
chr12:109006158 | T | C | 9 | a0001c0001t0001g0173 a0001c0002t0010g0174 a0001c0002t0014g0175 others(6): Show |
9 | HG01081.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.35+14676A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006158 | |||||||
chr12:109006185 | T | C | 114 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(111): Show |
116 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.35+14649A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006185 | |||||||
chr12:109006283 | C | T | 2 | a0001c0001t0051g0052 a0001c0001t0070g0250 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.35+14551G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006283 | |||||||
chr12:109006325 | T | C | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.35+14509A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006325 | |||||||
chr12:109006451 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.35+14383G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006451 | |||||||
chr12:109006633 | T | A | 1 | a0001c0002t0001g0215 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.35+14201A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006633 | |||||||
chr12:109006704 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0085g0085 |
2 | HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.35+14130A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006704 | |||||||
chr12:109006952 | G | C | 4 | a0001c0001t0012g0241 a0001c0001t0012g0242 a0001c0001t0012g0243 others(1): Show |
4 | HG03139.hp2 NA19030.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+13882C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109006952 | |||||||
chr12:109007124 | G | T | 8 | a0001c0001t0001g0091 a0001c0001t0003g0016 a0001c0001t0003g0018 others(5): Show |
8 | HG01123.hp1 HG01496.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.35+13710C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007124 | |||||||
chr12:109007308 | T | C | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.35+13526A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007308 | |||||||
chr12:109007406 | A | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0196 a0001c0001t0001g0209 others(100): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.35+13428T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007406 | |||||||
chr12:109007415 | T | C | 4 | a0001c0002t0014g0175 a0001c0002t0014g0178 a0001c0002t0014g0180 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+13419A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007415 | |||||||
chr12:109007469 | A | G | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+13365T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007469 | |||||||
chr12:109007497 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.35+13337C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007497 | |||||||
chr12:109007665 | A | G | 1 | a0001c0001t0003g0009 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.35+13169T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007665 | |||||||
chr12:109007820 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.35+13014G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007820 | |||||||
chr12:109007836 | G | A | 1 | a0001c0001t0008g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35+12998C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007836 | |||||||
chr12:109007840 | C | A | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.35+12994G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007840 | |||||||
chr12:109007899 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.35+12935C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109007899 | |||||||
chr12:109008037 | CA | C | 106 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(103): Show |
108 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.35+12796delT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109008037 | |||||||
chr12:109008248 | T | C | 1 | a0001c0003t0018g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.35+12586A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109008248 | |||||||
chr12:109008381 | A | T | 1 | a0001c0002t0073g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.35+12453T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109008381 | |||||||
chr12:109008511 | G | T | 106 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(103): Show |
108 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.35+12323C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109008511 | |||||||
chr12:109008611 | A | G | 5 | a0001c0001t0002g0073 a0001c0001t0002g0105 a0001c0001t0002g0106 others(2): Show |
5 | HG02083.hp2 NA18612.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+12223T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109008611 | |||||||
chr12:109008960 | C | CT | 92 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0209 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.35+11873dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109008960 | |||||||
chr12:109008960 | C | CTT | 19 | a0001c0001t0001g0196 a0001c0001t0004g0256 a0001c0001t0006g0249 others(16): Show |
19 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.35+11872_35+11873d others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109008960 | |||||||
chr12:109009032 | G | A | 6 | a0001c0002t0002g0219 a0001c0002t0005g0217 a0001c0002t0005g0218 others(3): Show |
6 | NA18947.hp1 NA18954.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+11802C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009032 | |||||||
chr12:109009054 | C | T | 1 | a0001c0001t0042g0014 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.35+11780G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009054 | |||||||
chr12:109009322 | C | T | 3 | a0001c0001t0008g0220 a0001c0002t0006g0164 a0001c0004t0016g0165 |
3 | HG01433.hp2 HG02723.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.35+11512G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009322 | |||||||
chr12:109009404 | G | A | 106 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(103): Show |
108 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.35+11430C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009404 | |||||||
chr12:109009505 | T | C | 92 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(89): Show |
93 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.35+11329A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009505 | |||||||
chr12:109009548 | G | A | 1 | a0001c0002t0034g0285 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.35+11286C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009548 | |||||||
chr12:109009562 | G | A | 1 | a0001c0004t0018g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.35+11272C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009562 | |||||||
chr12:109009616 | T | C | 40 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0006 others(37): Show |
40 | HG00408.hp2 HG00597.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.35+11218A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009616 | |||||||
chr12:109009706 | C | T | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+11128G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009706 | |||||||
chr12:109009737 | G | C | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.35+11097C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109009737 | |||||||
chr12:109010127 | C | CA | 112 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0088 others(109): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.35+10706dupT | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109010127 | |||||||
chr12:109010152 | T | A | 3 | a0001c0001t0007g0030 a0001c0002t0046g0029 a0001c0003t0035g0011 |
3 | HG02080.hp2 NA18981.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.35+10682A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109010152 | |||||||
chr12:109010192 | A | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.35+10642T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109010192 | |||||||
chr12:109010243 | T | A | 1 | a0001c0001t0002g0138 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.35+10591A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109010243 | |||||||
chr12:109010361 | T | C | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+10473A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109010361 | |||||||
chr12:109010607 | A | G | 1 | a0001c0001t0004g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.35+10227T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109010607 | |||||||
chr12:109011002 | C | A | 14 | a0001c0001t0005g0069 a0001c0001t0005g0102 a0001c0002t0010g0002 others(11): Show |
15 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.35+9832G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011002 | |||||||
chr12:109011064 | G | A | 1 | a0001c0002t0024g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.35+9770C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011064 | |||||||
chr12:109011113 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.35+9721G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011113 | |||||||
chr12:109011121 | T | G | 221 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.35+9713A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011121 | |||||||
chr12:109011145 | C | A | 6 | a0001c0001t0013g0277 a0001c0001t0013g0278 a0001c0002t0013g0276 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+9689G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011145 | |||||||
chr12:109011428 | A | C | 1 | a0001c0001t0006g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.35+9406T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011428 | |||||||
chr12:109011547 | C | A | 5 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0089 others(2): Show |
5 | NA18953.hp2 NA18956.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.35+9287G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011547 | |||||||
chr12:109011616 | A | C | 17 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0008g0162 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.35+9218T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011616 | |||||||
chr12:109011818 | G | A | 1 | a0001c0002t0023g0279 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.35+9016C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011818 | |||||||
chr12:109011910 | T | C | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+8924A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109011910 | |||||||
chr12:109012332 | C | T | 106 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(103): Show |
108 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.35+8502G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109012332 | |||||||
chr12:109012397 | A | G | 3 | a0001c0001t0017g0072 a0001c0001t0017g0103 a0001c0001t0017g0104 |
3 | NA18747.hp2 NA19011.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.35+8437T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109012397 | |||||||
chr12:109012428 | G | A | 2 | a0001c0001t0004g0139 a0001c0001t0004g0140 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.35+8406C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109012428 | |||||||
chr12:109012567 | A | T | 116 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(113): Show |
118 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.35+8267T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109012567 | |||||||
chr12:109012568 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.35+8266T>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109012568 | |||||||
chr12:109012666 | G | A | 13 | a0001c0001t0008g0171 a0001c0001t0008g0238 a0001c0001t0008g0239 others(10): Show |
13 | HG01168.hp1 HG01169.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.35+8168C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109012666 | |||||||
chr12:109012774 | A | G | 1 | a0001c0001t0008g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.35+8060T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109012774 | |||||||
chr12:109013022 | C | G | 1 | a0001c0001t0066g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.35+7812G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013022 | |||||||
chr12:109013277 | C | T | 2 | a0001c0002t0039g0013 a0001c0002t0040g0012 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.35+7557G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013277 | |||||||
chr12:109013392 | C | CT | 35 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0210 others(32): Show |
35 | HG00099.hp2 HG00544.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.35+7441dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013392 | |||||||
chr12:109013453 | C | T | 234 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(231): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.35+7381G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013453 | |||||||
chr12:109013472 | C | A | 1 | a0001c0001t0081g0141 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.35+7362G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013472 | |||||||
chr12:109013580 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.35+7254C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013580 | |||||||
chr12:109013857 | G | A | 12 | a0001c0001t0008g0238 a0001c0001t0008g0239 a0001c0001t0008g0245 others(9): Show |
12 | HG01168.hp1 HG01169.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.35+6977C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013857 | |||||||
chr12:109013959 | T | C | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+6875A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109013959 | |||||||
chr12:109014018 | C | CT | 230 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(227): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.35+6815dupA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109014018 | |||||||
chr12:109014126 | G | A | 90 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(87): Show |
91 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.35+6708C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109014126 | |||||||
chr12:109014156 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0265 a0001c0001t0005g0271 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.35+6678G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109014156 | |||||||
chr12:109014206 | G | A | 17 | a0001c0001t0005g0069 a0001c0001t0005g0102 a0001c0002t0010g0002 others(14): Show |
18 | HG00733.hp2 HG00738.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.35+6628C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109014206 | |||||||
chr12:109014441 | C | A | 1 | a0001c0002t0013g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.35+6393G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109014441 | |||||||
chr12:109014713 | G | T | 2 | a0001c0002t0025g0184 a0001c0002t0025g0185 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.35+6121C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109014713 | |||||||
chr12:109015017 | G | T | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+5817C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015017 | |||||||
chr12:109015094 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(231): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.35+5740A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015094 | |||||||
chr12:109015269 | G | C | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+5565C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015269 | |||||||
chr12:109015477 | G | A | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.35+5357C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015477 | |||||||
chr12:109015531 | G | A | 86 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(83): Show |
87 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.35+5303C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015531 | |||||||
chr12:109015611 | G | C | 1 | a0001c0001t0022g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.35+5223C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015611 | |||||||
chr12:109015643 | A | AAAAAAAT others(2): Show |
234 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(231): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.35+5190_35+5191ins others(9): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015643 | |||||||
chr12:109015699 | A | C | 1 | a0001c0001t0037g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.35+5135T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015699 | |||||||
chr12:109015699 | A | G | 3 | a0001c0001t0020g0181 a0001c0001t0067g0182 a0001c0002t0023g0183 |
3 | HG02559.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.35+5135T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015699 | |||||||
chr12:109015862 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0196 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.35+4972G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109015862 | |||||||
chr12:109016015 | C | T | 9 | a0001c0001t0001g0173 a0001c0002t0010g0174 a0001c0002t0014g0175 others(6): Show |
9 | HG01081.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.35+4819G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016015 | |||||||
chr12:109016085 | A | G | 1 | a0001c0001t0009g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.35+4749T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016085 | |||||||
chr12:109016142 | G | T | 1 | a0001c0004t0011g0064 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.35+4692C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016142 | |||||||
chr12:109016260 | G | A | 1 | a0001c0001t0008g0162 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35+4574C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016260 | |||||||
chr12:109016295 | G | T | 2 | a0001c0002t0028g0262 a0001c0002t0028g0263 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.35+4539C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016295 | |||||||
chr12:109016473 | G | T | 9 | a0001c0001t0001g0173 a0001c0002t0010g0174 a0001c0002t0014g0175 others(6): Show |
9 | HG01081.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.35+4361C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016473 | |||||||
chr12:109016716 | G | A | 1 | a0001c0001t0003g0009 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.35+4118C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016716 | |||||||
chr12:109016744 | CT | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0001g0173 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.35+4089delA | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016744 | |||||||
chr12:109016934 | T | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.35+3900A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109016934 | |||||||
chr12:109017216 | G | A | 3 | a0001c0002t0026g0094 a0001c0002t0026g0144 a0001c0002t0032g0095 |
3 | HG02572.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.35+3618C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017216 | |||||||
chr12:109017238 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0265 a0001c0001t0005g0271 others(28): Show |
32 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.35+3596C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017238 | |||||||
chr12:109017292 | AG | A | 17 | a0001c0001t0004g0256 a0001c0001t0006g0249 a0001c0001t0009g0252 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.35+3541delC | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017292 | |||||||
chr12:109017481 | T | A | 1 | a0001c0001t0003g0047 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.35+3353A>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017481 | |||||||
chr12:109017763 | C | T | 88 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0210 others(85): Show |
88 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.35+3071G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017763 | |||||||
chr12:109017785 | C | T | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.35+3049G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017785 | |||||||
chr12:109017860 | A | C | 1 | a0001c0001t0027g0063 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.35+2974T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017860 | |||||||
chr12:109017921 | C | A | 1 | a0001c0001t0003g0047 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.35+2913G>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109017921 | |||||||
chr12:109018010 | G | A | 2 | a0001c0001t0002g0145 a0001c0003t0011g0146 |
2 | NA18967.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.35+2824C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018010 | |||||||
chr12:109018023 | G | A | 17 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 others(14): Show |
17 | HG00597.hp1 HG01070.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.35+2811C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018023 | |||||||
chr12:109018097 | AATGG | A | 5 | a0001c0001t0001g0098 a0001c0001t0020g0181 a0001c0001t0067g0182 others(2): Show |
5 | HG02559.hp2 HG03130.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.35+2733_35+2736del others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018097 | |||||||
chr12:109018101 | G | GATGA | 15 | a0001c0001t0001g0136 a0001c0001t0002g0058 a0001c0001t0002g0073 others(12): Show |
15 | HG00597.hp2 HG01168.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.35+2732_35+2733ins others(4): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018101 | |||||||
chr12:109018101 | G | GATGAATG others(1): Show |
56 | a0001c0001t0001g0062 a0001c0001t0001g0071 a0001c0001t0001g0076 others(53): Show |
58 | HG00639.hp2 HG00733.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.35+2732_35+2733ins others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018101 | |||||||
chr12:109018101 | G | GATGAATG others(5): Show |
27 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0120 others(24): Show |
27 | HG00408.hp1 HG00544.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.35+2732_35+2733ins others(12): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018101 | |||||||
chr12:109018101 | G | GATGAATG others(9): Show |
6 | a0001c0001t0001g0093 a0001c0001t0001g0124 a0001c0001t0001g0157 others(3): Show |
6 | HG03710.hp1 HG04204.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+2732_35+2733ins others(16): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018101 | |||||||
chr12:109018101 | GATGGATG others(1): Show |
G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0173 a0001c0001t0001g0196 others(122): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.35+2725_35+2732del others(8): Show |
SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018101 | |||||||
chr12:109018105 | G | A | 108 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(105): Show |
110 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.35+2729C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018105 | |||||||
chr12:109018263 | C | T | 2 | a0001c0002t0005g0190 a0001c0002t0010g0191 |
2 | HG01361.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.35+2571G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018263 | |||||||
chr12:109018268 | C | G | 2 | a0001c0001t0001g0173 a0001c0002t0010g0174 |
2 | HG01081.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.35+2566G>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018268 | |||||||
chr12:109018551 | G | A | 1 | a0001c0001t0083g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.35+2283C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018551 | |||||||
chr12:109018725 | T | C | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.35+2109A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018725 | |||||||
chr12:109018756 | G | C | 1 | a0001c0002t0001g0281 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.35+2078C>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018756 | |||||||
chr12:109018822 | G | A | 1 | a0001c0003t0016g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.35+2012C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018822 | |||||||
chr12:109018854 | G | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0060 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.35+1980C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018854 | |||||||
chr12:109018903 | T | C | 1 | a0001c0002t0045g0004 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.35+1931A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018903 | |||||||
chr12:109018995 | G | A | 2 | a0001c0001t0007g0048 a0001c0002t0036g0049 |
2 | HG01943.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.35+1839C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109018995 | |||||||
chr12:109019016 | A | C | 1 | a0001c0002t0057g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.35+1818T>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109019016 | |||||||
chr12:109019456 | T | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0196 a0001c0001t0001g0209 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.35+1378A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109019456 | |||||||
chr12:109019461 | T | C | 1 | a0001c0002t0001g0282 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.35+1373A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109019461 | |||||||
chr12:109019615 | T | C | 1 | a0001c0002t0001g0283 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.35+1219A>G | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109019615 | |||||||
chr12:109019644 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.35+1190T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109019644 | |||||||
chr12:109020110 | A | G | 1 | a0001c0003t0016g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.35+724T>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020110 | |||||||
chr12:109020203 | T | G | 1 | a0001c0002t0001g0169 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.35+631A>C | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020203 | |||||||
chr12:109020286 | C | T | 1 | a0001c0001t0019g0096 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.35+548G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020286 | |||||||
chr12:109020287 | G | A | 1 | a0001c0003t0018g0152 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.35+547C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020287 | |||||||
chr12:109020291 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.35+543C>T | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020291 | |||||||
chr12:109020381 | C | T | 2 | a0001c0001t0008g0171 a0001c0001t0083g0172 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.35+453G>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020381 | |||||||
chr12:109020666 | G | T | 1 | a0001c0003t0016g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.35+168C>A | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020666 | |||||||
chr12:109020754 | A | AC | 22 | a0001c0001t0001g0157 a0001c0001t0002g0158 a0001c0001t0003g0005 others(19): Show |
22 | HG00544.hp2 HG01167.hp1 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.35+79dupG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020754 | |||||||
chr12:109020754 | A | ACC | 58 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0119 others(55): Show |
59 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.35+78_35+79dupGG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020754 | |||||||
chr12:109020754 | A | ACCC | 34 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0083 others(31): Show |
34 | HG00544.hp1 HG00639.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.35+77_35+79dupGGG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020754 | |||||||
chr12:109020754 | A | ACCCC | 12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0062 others(9): Show |
13 | HG00597.hp2 HG00733.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.35+76_35+79dupGGGG | SVOP | ENSG00000166111.10 | transcript | ENST00000610966.5 | protein_coding | 1/15 | chr12 | 109020754 |