Item | Value |
---|---|
geneid | 388795 |
ensemblid | ENSG00000215529.13 |
hgncid | 34532 |
symbol | EFCAB8 |
name | EF-hand calcium binding domain 8 |
refseq_nuc | NM_001143967.2 |
refseq_prot | NP_001137439.1 |
ensembl_nuc | ENST00000400522.9 |
ensembl_prot | ENSP00000383366.5 |
mane_status | MANE Select |
chr | chr20 |
start | 32858923 |
end | 32961845 |
strand | + |
ver | v1.2 |
region | chr20:32858923-32961845 |
region5000 | chr20:32853923-32966845 |
regionname0 | EFCAB8_chr20_32858923_32961845 |
regionname5000 | EFCAB8_chr20_32853923_32966845 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1288 | 75 | 11 | 20 | 30 | 2 | 11 | 23 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0002 | 0/0 | 1288 | 58 | 30 | 2 | 17 | 1 | 8 | 16 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0003 | 0/0 | 1288 | 15 | 5 | 1 | 9 | 0 | 0 | 7 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0004 | 0/0 | 964 | 14 | 1 | 4 | 1 | 4 | 4 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(959): Show |
chr20 | 32853923 | 32966845 |
a0005 | 0/0 | 148 | 13 | 5 | 1 | 6 | 0 | 1 | 5 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(143): Show |
chr20 | 32853923 | 32966845 |
a0006 | 0/0 | 1288 | 12 | 0 | 10 | 0 | 0 | 2 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0007 | 0/0 | 1288 | 9 | 6 | 0 | 3 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0008 | 0/0 | 964 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(959): Show |
chr20 | 32853923 | 32966845 |
a0009 | 0/0 | 1288 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0010 | 0/0 | 964 | 5 | 0 | 4 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(959): Show |
chr20 | 32853923 | 32966845 |
a0011 | 0/0 | 1288 | 5 | 2 | 0 | 2 | 0 | 1 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0012 | 0/0 | 1288 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0013 | 0/1 | 1288 | 3 | 0 | 0 | 0 | 1 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0014 | 0/0 | 1288 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0015 | 0/0 | 1288 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0016 | 0/0 | 1288 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0017 | 0/0 | 1288 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0018 | 0/0 | 1288 | 3 | 0 | 0 | 2 | 1 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0019 | 0/0 | 1288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0020 | 0/0 | 1288 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0021 | 0/0 | 1288 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0022 | 0/0 | 1288 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0023 | 0/0 | 1288 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0024 | 0/0 | 1288 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0025 | 0/0 | 1288 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0026 | 0/0 | 1288 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0027 | 0/0 | 964 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(959): Show |
chr20 | 32853923 | 32966845 |
a0028 | 0/0 | 1288 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0029 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0030 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0031 | 0/0 | 964 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(959): Show |
chr20 | 32853923 | 32966845 |
a0032 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0033 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0034 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0035 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0036 | 0/0 | 148 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(143): Show |
chr20 | 32853923 | 32966845 |
a0037 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0038 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0039 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0040 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0041 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0042 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0043 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0044 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0045 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0046 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0047 | 0/0 | 964 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(959): Show |
chr20 | 32853923 | 32966845 |
a0048 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0049 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0050 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
a0051 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | MSSED others(1283): Show |
chr20 | 32853923 | 32966845 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3864 | 73 | 11 | 19 | 29 | 2 | 11 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0001c0052 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0001c0056 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0002c0002 | 0/0 | 3864 | 50 | 24 | 2 | 17 | 1 | 6 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0002c0011 | 0/0 | 3864 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0002c0022 | 0/0 | 3864 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0002c0042 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0002c0046 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0003c0003 | 0/0 | 3864 | 15 | 5 | 1 | 9 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0004c0004 | 0/0 | 3864 | 14 | 1 | 4 | 1 | 4 | 4 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0005c0008 | 0/0 | 3865 | 5 | 1 | 0 | 3 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0005c0013 | 0/0 | 3865 | 3 | 2 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0005c0033 | 0/0 | 3865 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0005c0034 | 0/0 | 3865 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0005c0035 | 0/0 | 3865 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0005c0036 | 0/0 | 3865 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0005c0037 | 0/0 | 3865 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0006c0005 | 0/0 | 3864 | 12 | 0 | 10 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0007c0006 | 0/0 | 3864 | 7 | 4 | 0 | 3 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0007c0030 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0008c0007 | 0/0 | 3864 | 6 | 0 | 2 | 0 | 1 | 3 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0009c0015 | 0/0 | 3864 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0009c0023 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0009c0041 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0010c0010 | 0/0 | 3864 | 5 | 0 | 4 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0011c0009 | 0/0 | 3864 | 5 | 2 | 0 | 2 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0012c0012 | 0/0 | 3864 | 4 | 0 | 3 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0013c0016 | 0/1 | 3864 | 3 | 0 | 0 | 0 | 1 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0014c0019 | 0/0 | 3864 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0015c0020 | 0/0 | 3864 | 3 | 0 | 2 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0016c0026 | 0/0 | 3864 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0016c0051 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0017c0018 | 0/0 | 3864 | 3 | 1 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0018c0014 | 0/0 | 3864 | 3 | 0 | 0 | 2 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0019c0017 | 0/0 | 3864 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0020c0025 | 0/0 | 3864 | 2 | 1 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0021c0061 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0021c0062 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0022c0031 | 0/0 | 3864 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0023c0024 | 0/0 | 3864 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0024c0032 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0025c0027 | 0/0 | 3864 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0026c0028 | 0/0 | 3864 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0027c0029 | 0/0 | 3864 | 2 | 0 | 0 | 1 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0028c0021 | 0/0 | 3864 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0029c0053 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0030c0043 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0031c0064 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0032c0060 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0033c0065 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0034c0063 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0035c0058 | 0/0 | 3864 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0036c0059 | 0/0 | 3865 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3860): Show |
chr20 | 32853923 | 32966845 | ||
a0037c0047 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0038c0044 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0039c0066 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0040c0048 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0041c0049 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0042c0067 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0043c0050 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0044c0045 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0045c0055 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0046c0054 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0047c0057 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0048c0039 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0049c0040 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0050c0038 | 0/0 | 3864 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 | ||
a0051c0068 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | ATGTC others(3859): Show |
chr20 | 32853923 | 32966845 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4197 | 64 | 8 | 18 | 25 | 2 | 10 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0001c0001t0002 | 0/0 | 4197 | 4 | 0 | 0 | 3 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0001c0001t0004 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0001c0001t0005 | 0/0 | 4197 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0001c0001t0009 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0001c0052t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0001c0056t0001 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0002t0001 | 0/0 | 4197 | 18 | 15 | 2 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0002t0002 | 0/0 | 4197 | 24 | 1 | 0 | 16 | 1 | 6 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0002t0003 | 0/0 | 4197 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0002t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0011t0001 | 0/0 | 4197 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0022t0002 | 0/0 | 4197 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0042t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0002c0046t0003 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0003c0003t0001 | 0/0 | 4197 | 11 | 3 | 1 | 7 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0003c0003t0002 | 0/0 | 4197 | 4 | 2 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0004c0004t0001 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0004c0004t0003 | 0/0 | 4197 | 13 | 1 | 4 | 1 | 3 | 4 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0005c0008t0001 | 0/0 | 4198 | 3 | 1 | 0 | 1 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0008t0002 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0008t0004 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0013t0001 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0013t0002 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0013t0004 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0033t0008 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0034t0002 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0035t0001 | 0/0 | 4198 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0036t0004 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0005c0037t0004 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0006c0005t0003 | 0/0 | 4197 | 11 | 0 | 9 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0006c0005t0006 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0007c0006t0001 | 0/0 | 4197 | 4 | 2 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0007c0006t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0007c0006t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0007c0030t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0008c0007t0003 | 0/0 | 4197 | 3 | 0 | 0 | 0 | 0 | 3 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0008c0007t0006 | 0/0 | 4197 | 3 | 0 | 2 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0009c0015t0001 | 0/0 | 4197 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0009c0023t0001 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0009c0041t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0010c0010t0003 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0010c0010t0006 | 0/0 | 4197 | 4 | 0 | 3 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0011c0009t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0011c0009t0004 | 0/0 | 4197 | 3 | 1 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0011c0009t0005 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0012c0012t0004 | 0/0 | 4197 | 4 | 0 | 3 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0013c0016t0001 | 0/1 | 4197 | 3 | 0 | 0 | 0 | 1 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0014c0019t0005 | 0/0 | 4197 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0015c0020t0003 | 0/0 | 4197 | 3 | 0 | 2 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0016c0026t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0016c0026t0003 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0016c0051t0003 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0017c0018t0004 | 0/0 | 4197 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0017c0018t0005 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0018c0014t0002 | 0/0 | 4197 | 3 | 0 | 0 | 2 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0019c0017t0007 | 0/0 | 4197 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0020c0025t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0020c0025t0002 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0021c0061t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0021c0062t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0022c0031t0002 | 0/0 | 4197 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0023c0024t0005 | 0/0 | 4197 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0024c0032t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0025c0027t0003 | 0/0 | 4197 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0026c0028t0002 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0026c0028t0005 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0027c0029t0003 | 0/0 | 4197 | 2 | 0 | 0 | 1 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0028c0021t0002 | 0/0 | 4197 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0029c0053t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0030c0043t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0031c0064t0003 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0032c0060t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0033c0065t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0034c0063t0004 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0035c0058t0002 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0036c0059t0003 | 0/0 | 4198 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4193): Show |
chr20 | 32853923 | 32966845 |
a0037c0047t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0038c0044t0002 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0039c0066t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0040c0048t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0041c0049t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0042c0067t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0043c0050t0002 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0044c0045t0007 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0045c0055t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0046c0054t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0047c0057t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0048c0039t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0049c0040t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0050c0038t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
a0051c0068t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | TTTGT others(4192): Show |
chr20 | 32853923 | 32966845 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0151 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0052t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0056t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0022t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0022t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0042t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0046t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0013t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0013t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0013t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0033t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0034t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0035t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0036t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0037t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0030t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0030t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0015t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0015t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0015t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0023t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0023t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0041t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0010t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0010t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0010t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0010t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0010t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0009t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0009t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0009t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0009t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0009t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0013c0016t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0013c0016t0001g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0013c0016t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0014c0019t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0014c0019t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0014c0019t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0015c0020t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0015c0020t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0015c0020t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0016c0026t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0016c0026t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0016c0051t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0017c0018t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0017c0018t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0017c0018t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0018c0014t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0018c0014t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0018c0014t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0019c0017t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0019c0017t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0019c0017t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0020c0025t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0020c0025t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0021c0061t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0021c0062t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0022c0031t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0022c0031t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0023c0024t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0023c0024t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0024c0032t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0024c0032t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0025c0027t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0025c0027t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0026c0028t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0026c0028t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0027c0029t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0027c0029t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0028c0021t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0028c0021t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0029c0053t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0030c0043t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0031c0064t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0032c0060t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0033c0065t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0034c0063t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0035c0058t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0036c0059t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0037c0047t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0038c0044t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0039c0066t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0040c0048t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0041c0049t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0042c0067t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0043c0050t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0044c0045t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0045c0055t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0046c0054t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0047c0057t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0048c0039t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0049c0040t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0050c0038t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0051c0068t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0013 | c0016 | t0001 | g0181 | EUR | GBR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00280 | hp1 | a0004 | c0004 | t0001 | g0091 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00280 | hp2 | a0004 | c0004 | t0003 | g0078 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00323 | hp1 | a0020 | c0025 | t0002 | g0021 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00621 | hp2 | a0029 | c0053 | t0002 | g0031 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00639 | hp1 | a0030 | c0043 | t0001 | g0186 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00639 | hp2 | a0006 | c0005 | t0003 | g0071 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00642 | hp1 | a0031 | c0064 | t0003 | g0085 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00733 | hp1 | a0008 | c0007 | t0006 | g0015 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00733 | hp2 | a0032 | c0060 | t0001 | g0080 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00741 | hp1 | a0014 | c0019 | t0005 | g0234 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00741 | hp2 | a0004 | c0004 | t0003 | g0086 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01070 | hp1 | a0006 | c0005 | t0003 | g0079 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01070 | hp2 | a0001 | c0001 | t0009 | g0116 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01071 | hp1 | a0006 | c0005 | t0003 | g0077 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01071 | hp2 | a0001 | c0052 | t0001 | g0187 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01081 | hp1 | a0033 | c0065 | t0001 | g0062 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01081 | hp2 | a0006 | c0005 | t0003 | g0239 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01099 | hp1 | a0015 | c0020 | t0003 | g0081 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01099 | hp2 | a0021 | c0062 | t0001 | g0073 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01109 | hp2 | a0016 | c0026 | t0001 | g0281 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01167 | hp1 | a0017 | c0018 | t0004 | g0194 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01167 | hp2 | a0022 | c0031 | t0002 | g0198 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01168 | hp1 | a0008 | c0007 | t0006 | g0018 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01169 | hp2 | a0017 | c0018 | t0004 | g0149 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01175 | hp1 | a0006 | c0005 | t0003 | g0066 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01192 | hp1 | a0015 | c0020 | t0003 | g0092 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01243 | hp1 | a0034 | c0063 | t0004 | g0083 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01243 | hp2 | a0022 | c0031 | t0002 | g0232 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01255 | hp2 | a0004 | c0004 | t0003 | g0082 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01257 | hp1 | a0006 | c0005 | t0006 | g0022 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01261 | hp1 | a0010 | c0010 | t0006 | g0012 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01261 | hp2 | a0035 | c0058 | t0002 | g0259 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01346 | hp1 | a0023 | c0024 | t0005 | g0043 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0277 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01361 | hp1 | a0006 | c0005 | t0003 | g0084 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01433 | hp1 | a0012 | c0012 | t0004 | g0110 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01496 | hp1 | a0004 | c0004 | t0003 | g0061 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01515 | hp1 | a0018 | c0014 | t0002 | g0016 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01515 | hp2 | a0008 | c0007 | t0006 | g0046 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01516 | hp1 | a0004 | c0004 | t0003 | g0069 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01516 | hp2 | a0004 | c0004 | t0003 | g0255 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01884 | hp2 | a0014 | c0019 | t0005 | g0221 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01891 | hp1 | a0019 | c0017 | t0007 | g0229 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01891 | hp2 | a0024 | c0032 | t0004 | g0275 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01943 | hp2 | a0010 | c0010 | t0006 | g0011 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01975 | hp2 | a0036 | c0059 | t0003 | g0072 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01981 | hp2 | a0012 | c0012 | t0004 | g0096 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01993 | hp2 | a0006 | c0005 | t0003 | g0070 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02027 | hp1 | a0005 | c0008 | t0002 | g0052 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02027 | hp2 | a0007 | c0006 | t0001 | g0182 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02040 | hp2 | a0037 | c0047 | t0002 | g0037 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02055 | hp1 | a0038 | c0044 | t0002 | g0204 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02055 | hp2 | a0005 | c0008 | t0001 | g0004 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0212 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02083 | hp2 | a0007 | c0006 | t0001 | g0184 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02129 | hp2 | a0040 | c0048 | t0002 | g0034 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02145 | hp1 | a0019 | c0017 | t0007 | g0230 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02145 | hp2 | a0002 | c0002 | t0003 | g0265 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02148 | hp1 | a0006 | c0005 | t0003 | g0075 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02148 | hp2 | a0012 | c0012 | t0004 | g0111 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02257 | hp2 | a0020 | c0025 | t0001 | g0195 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02280 | hp1 | a0002 | c0002 | t0003 | g0267 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0280 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02293 | hp1 | a0010 | c0010 | t0003 | g0143 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02300 | hp1 | a0006 | c0005 | t0003 | g0067 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02300 | hp2 | a0010 | c0010 | t0006 | g0051 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0273 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0223 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02572 | hp1 | a0009 | c0015 | t0001 | g0114 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02572 | hp2 | a0014 | c0019 | t0005 | g0233 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02602 | hp2 | a0025 | c0027 | t0003 | g0128 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02615 | hp1 | a0002 | c0011 | t0001 | g0246 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02622 | hp1 | a0003 | c0003 | t0002 | g0138 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02630 | hp1 | a0002 | c0002 | t0004 | g0104 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02630 | hp2 | a0011 | c0009 | t0004 | g0252 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02683 | hp1 | a0011 | c0009 | t0005 | g0009 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02683 | hp2 | a0004 | c0004 | t0003 | g0089 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02717 | hp1 | a0009 | c0015 | t0001 | g0100 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0264 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02738 | hp2 | a0008 | c0007 | t0003 | g0196 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02818 | hp1 | a0011 | c0009 | t0001 | g0250 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02818 | hp2 | a0041 | c0049 | t0001 | g0199 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02886 | hp1 | a0002 | c0002 | t0004 | g0103 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02886 | hp2 | a0009 | c0023 | t0001 | g0127 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0272 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02922 | hp1 | a0007 | c0006 | t0004 | g0144 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02922 | hp2 | a0042 | c0067 | t0004 | g0193 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02965 | hp2 | a0002 | c0011 | t0001 | g0247 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02970 | hp1 | a0024 | c0032 | t0004 | g0064 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02970 | hp2 | a0005 | c0013 | t0001 | g0202 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02976 | hp1 | a0002 | c0046 | t0003 | g0235 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02976 | hp2 | a0021 | c0061 | t0001 | g0240 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03017 | hp2 | a0008 | c0007 | t0003 | g0278 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03041 | hp2 | a0007 | c0006 | t0004 | g0201 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03098 | hp1 | a0007 | c0030 | t0004 | g0129 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03098 | hp2 | a0043 | c0050 | t0002 | g0220 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03130 | hp1 | a0026 | c0028 | t0005 | g0260 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03130 | hp2 | a0016 | c0026 | t0003 | g0228 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03139 | hp2 | a0002 | c0011 | t0001 | g0102 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03209 | hp2 | a0017 | c0018 | t0005 | g0231 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0274 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03225 | hp2 | a0007 | c0006 | t0001 | g0238 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03239 | hp1 | a0006 | c0005 | t0003 | g0076 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03453 | hp1 | a0019 | c0017 | t0007 | g0219 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0132 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03491 | hp2 | a0004 | c0004 | t0003 | g0060 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03492 | hp1 | a0015 | c0020 | t0003 | g0256 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03516 | hp1 | a0045 | c0055 | t0001 | g0276 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03516 | hp2 | a0046 | c0054 | t0004 | g0101 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0225 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03579 | hp2 | a0002 | c0042 | t0001 | g0200 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03654 | hp1 | a0026 | c0028 | t0002 | g0020 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03654 | hp2 | a0002 | c0022 | t0002 | g0017 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03669 | hp1 | a0002 | c0022 | t0002 | g0010 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03688 | hp1 | a0027 | c0029 | t0003 | g0241 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0049 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03831 | hp2 | a0004 | c0004 | t0003 | g0088 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03834 | hp1 | a0023 | c0024 | t0005 | g0113 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0112 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03927 | hp2 | a0008 | c0007 | t0003 | g0279 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04115 | hp1 | a0005 | c0008 | t0001 | g0065 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0136 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04184 | hp1 | a0013 | c0016 | t0001 | g0145 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04184 | hp2 | a0006 | c0005 | t0003 | g0093 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04199 | hp2 | a0004 | c0004 | t0003 | g0191 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18522 | hp1 | a0007 | c0006 | t0001 | g0249 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18522 | hp2 | a0047 | c0057 | t0004 | g0251 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18906 | hp1 | a0007 | c0030 | t0004 | g0268 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18906 | hp2 | a0009 | c0041 | t0001 | g0253 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0175 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18950 | hp2 | a0048 | c0039 | t0002 | g0045 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18951 | hp2 | a0004 | c0004 | t0003 | g0068 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18952 | hp1 | a0027 | c0029 | t0003 | g0119 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18952 | hp2 | a0001 | c0056 | t0001 | g0123 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18953 | hp1 | a0005 | c0013 | t0002 | g0026 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18959 | hp1 | a0005 | c0034 | t0002 | g0033 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18961 | hp1 | a0005 | c0008 | t0001 | g0216 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18966 | hp1 | a0011 | c0009 | t0004 | g0122 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18968 | hp2 | a0003 | c0003 | t0002 | g0023 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18979 | hp2 | a0018 | c0014 | t0002 | g0042 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18986 | hp1 | a0028 | c0021 | t0002 | g0013 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18992 | hp1 | a0049 | c0040 | t0002 | g0261 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18998 | hp1 | a0005 | c0037 | t0004 | g0185 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18998 | hp2 | a0007 | c0006 | t0002 | g0028 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19007 | hp2 | a0011 | c0009 | t0004 | g0124 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19011 | hp2 | a0050 | c0038 | t0002 | g0262 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19030 | hp1 | a0025 | c0027 | t0003 | g0094 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19030 | hp2 | a0005 | c0033 | t0008 | g0115 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19043 | hp1 | a0009 | c0023 | t0001 | g0224 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0130 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0176 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19060 | hp2 | a0028 | c0021 | t0002 | g0040 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19064 | hp1 | a0003 | c0003 | t0001 | g0203 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19068 | hp2 | a0005 | c0008 | t0004 | g0207 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19081 | hp1 | a0018 | c0014 | t0002 | g0044 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19081 | hp2 | a0010 | c0010 | t0006 | g0032 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19085 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20129 | hp1 | a0051 | c0068 | t0004 | g0218 | AFR | ASW | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20129 | hp2 | a0004 | c0004 | t0003 | g0074 | AFR | ASW | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0019 | EUR | TSI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20805 | hp2 | a0012 | c0012 | t0004 | g0197 | EUR | TSI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01123 | hp1 | a0004 | c0004 | t0003 | g0087 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01123 | hp2 | a0005 | c0035 | t0001 | g0097 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02109 | hp1 | a0005 | c0013 | t0004 | g0099 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02109 | hp2 | a0039 | c0066 | t0004 | g0109 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02486 | hp1 | a0003 | c0003 | t0002 | g0137 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02486 | hp2 | a0002 | c0011 | t0001 | g0248 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03471 | hp1 | a0005 | c0036 | t0004 | g0183 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03471 | hp2 | a0044 | c0045 | t0007 | g0135 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA21309 | hp1 | a0016 | c0051 | t0003 | g0226 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA21309 | hp2 | a0009 | c0015 | t0001 | g0098 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
homoSapiens | chm13v2 | a0013 | c0016 | t0001 | g0180 | REF | REF | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0151 | REF | REF | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32867732 | A | G | 2 | a0042 a0051 |
2 | HG02922.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.193A>G | p.Ile65Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/27 | 287/4197 | 193/3867 | 65/1288 | chr20 | 32867732 | |||
chr20:32875928 | C | G | 1 | a0039 | 1 | HG02109.hp2 | missense_variant&splice_region_variant | MODERATE | c.211C>G | p.Leu71Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/27 | 305/4197 | 211/3867 | 71/1288 | chr20 | 32875928 | |||
chr20:32878728 | C | T | 10 | a0004 a0006 a0015 others(7): Show |
38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
missense_variant | MODERATE | c.352C>T | p.Arg118Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/27 | 446/4197 | 352/3867 | 118/1288 | chr20 | 32878728 | |||
chr20:32878768 | A | AC | 2 | a0005 a0036 |
14 | HG01123.hp2 HG01975.hp2 HG02027.hp1 others(11): Show |
frameshift_variant | HIGH | c.394dupC | p.Arg132fs | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/27 | 489/4197 | 395/3867 | 132/1288 | INFO_REALIGN_3_PRIME | chr20 | 32878768 | ||
chr20:32892246 | G | C | 4 | a0018 a0048 a0049 others(1): Show |
6 | HG01515.hp1 NA18950.hp2 NA18979.hp2 others(3): Show |
missense_variant | MODERATE | c.707G>C | p.Arg236Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/27 | 801/4197 | 707/3867 | 236/1288 | chr20 | 32892246 | |||
chr20:32893184 | C | T | 1 | a0035 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.769C>T | p.His257Tyr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/27 | 863/4197 | 769/3867 | 257/1288 | chr20 | 32893184 | |||
chr20:32893271 | C | T | 6 | a0014 a0017 a0019 others(3): Show |
13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
missense_variant | MODERATE | c.856C>T | p.Arg286Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/27 | 950/4197 | 856/3867 | 286/1288 | chr20 | 32893271 | |||
chr20:32898568 | G | A | 1 | a0028 | 2 | NA18986.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.1033G>A | p.Glu345Lys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/27 | 1127/4197 | 1033/3867 | 345/1288 | chr20 | 32898568 | |||
chr20:32906576 | G | A | 42 | a0002 a0003 a0004 others(39): Show |
179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
missense_variant | MODERATE | c.1103G>A | p.Arg368His | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 12/27 | 1197/4197 | 1103/3867 | 368/1288 | chr20 | 32906576 | |||
chr20:32908386 | A | G | 1 | a0012 | 4 | HG01433.hp1 HG01981.hp2 HG02148.hp2 others(1): Show |
missense_variant | MODERATE | c.1420A>G | p.Asn474Asp | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/27 | 1514/4197 | 1420/3867 | 474/1288 | chr20 | 32908386 | |||
chr20:32909876 | G | T | 7 | a0011 a0014 a0024 others(4): Show |
15 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
missense_variant | MODERATE | c.1502G>T | p.Arg501Met | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/27 | 1596/4197 | 1502/3867 | 501/1288 | chr20 | 32909876 | |||
chr20:32911501 | G | A | 1 | a0009 | 6 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
missense_variant | MODERATE | c.1579G>A | p.Gly527Ser | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/27 | 1673/4197 | 1579/3867 | 527/1288 | chr20 | 32911501 | |||
chr20:32917383 | C | T | 3 | a0006 a0025 a0031 |
15 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(12): Show |
missense_variant | MODERATE | c.1939C>T | p.Arg647Trp | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 2033/4197 | 1939/3867 | 647/1288 | chr20 | 32917383 | |||
chr20:32917483 | C | A | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2039C>A | p.Pro680His | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 2133/4197 | 2039/3867 | 680/1288 | chr20 | 32917483 | |||
chr20:32917486 | C | T | 32 | a0002 a0004 a0005 others(29): Show |
158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
missense_variant | MODERATE | c.2042C>T | p.Ser681Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 2136/4197 | 2042/3867 | 681/1288 | chr20 | 32917486 | |||
chr20:32918434 | A | G | 1 | a0047 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.2134A>G | p.Thr712Ala | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/27 | 2228/4197 | 2134/3867 | 712/1288 | chr20 | 32918434 | |||
chr20:32920085 | C | G | 1 | a0022 | 2 | HG01167.hp2 HG01243.hp2 |
missense_variant | MODERATE | c.2282C>G | p.Ser761Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/27 | 2376/4197 | 2282/3867 | 761/1288 | chr20 | 32920085 | |||
chr20:32930423 | G | A | 1 | a0013 | 2 | HG00099.hp1 HG04184.hp1 |
missense_variant | MODERATE | c.2438G>A | p.Arg813His | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/27 | 2532/4197 | 2438/3867 | 813/1288 | chr20 | 32930423 | |||
chr20:32930492 | A | G | 12 | a0005 a0006 a0015 others(9): Show |
30 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
missense_variant | MODERATE | c.2507A>G | p.Glu836Gly | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/27 | 2601/4197 | 2507/3867 | 836/1288 | chr20 | 32930492 | |||
chr20:32930534 | A | G | 2 | a0040 a0048 |
2 | HG02129.hp2 NA18950.hp2 |
missense_variant | MODERATE | c.2549A>G | p.Asn850Ser | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/27 | 2643/4197 | 2549/3867 | 850/1288 | chr20 | 32930534 | |||
chr20:32943738 | C | T | 8 | a0004 a0005 a0008 others(5): Show |
31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
stop_gained | HIGH | c.2893C>T | p.Gln965* | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/27 | 2987/4197 | 2893/3867 | 965/1288 | chr20 | 32943738 | |||
chr20:32958472 | C | T | 1 | a0051 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.3011C>T | p.Pro1004Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/27 | 3105/4197 | 3011/3867 | 1004/1288 | chr20 | 32958472 | |||
chr20:32959800 | G | A | 1 | a0037 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.3112G>A | p.Ala1038Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 25/27 | 3206/4197 | 3112/3867 | 1038/1288 | chr20 | 32959800 | |||
chr20:32959816 | G | A | 1 | a0041 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.3128G>A | p.Arg1043Gln | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 25/27 | 3222/4197 | 3128/3867 | 1043/1288 | chr20 | 32959816 | |||
chr20:32961238 | A | G | 3 | a0005 a0020 a0043 |
4 | HG00323.hp1 HG01123.hp2 HG02257.hp2 others(1): Show |
missense_variant | MODERATE | c.3496A>G | p.Ile1166Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3590/4197 | 3496/3867 | 1166/1288 | chr20 | 32961238 | |||
chr20:32961241 | C | T | 3 | a0005 a0019 a0044 |
5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
missense_variant | MODERATE | c.3499C>T | p.Arg1167Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3593/4197 | 3499/3867 | 1167/1288 | chr20 | 32961241 | |||
chr20:32961299 | T | C | 1 | a0030 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.3557T>C | p.Leu1186Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3651/4197 | 3557/3867 | 1186/1288 | chr20 | 32961299 | |||
chr20:32961301 | G | A | 1 | a0029 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.3559G>A | p.Asp1187Asn | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3653/4197 | 3559/3867 | 1187/1288 | chr20 | 32961301 | |||
chr20:32961317 | C | T | 4 | a0012 a0023 a0034 others(1): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
missense_variant | MODERATE | c.3575C>T | p.Thr1192Met | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3669/4197 | 3575/3867 | 1192/1288 | chr20 | 32961317 | |||
chr20:32961466 | T | C | 2 | a0005 a0046 |
2 | HG03471.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.3724T>C | p.Ser1242Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3818/4197 | 3724/3867 | 1242/1288 | chr20 | 32961466 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32896486 | T | C | 3 | a0002c0042 a0009c0015 a0009c0041 |
5 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(2): Show |
synonymous_variant | LOW | c.916T>C | p.Leu306Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/27 | 1010/4197 | 916/3867 | 306/1288 | chr20 | 32896486 | |||
chr20:32898549 | A | T | 1 | a0047c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1014A>T | p.Val338Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/27 | 1108/4197 | 1014/3867 | 338/1288 | chr20 | 32898549 | |||
chr20:32906868 | C | T | 1 | a0047c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1182C>T | p.Ile394Ile | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/27 | 1276/4197 | 1182/3867 | 394/1288 | chr20 | 32906868 | |||
chr20:32906872 | C | T | 1 | a0035c0058 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1186C>T | p.Leu396Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/27 | 1280/4197 | 1186/3867 | 396/1288 | chr20 | 32906872 | |||
chr20:32911500 | C | A | 1 | a0002c0022 | 2 | HG03654.hp2 HG03669.hp1 |
synonymous_variant | LOW | c.1578C>A | p.Arg526Arg | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/27 | 1672/4197 | 1578/3867 | 526/1288 | chr20 | 32911500 | |||
chr20:32911584 | C | T | 1 | a0002c0042 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1662C>T | p.Thr554Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/27 | 1756/4197 | 1662/3867 | 554/1288 | chr20 | 32911584 | |||
chr20:32917319 | A | G | 1 | a0047c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1875A>G | p.Pro625Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 1969/4197 | 1875/3867 | 625/1288 | chr20 | 32917319 | |||
chr20:32917346 | C | G | 1 | a0047c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1902C>G | p.Thr634Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 1996/4197 | 1902/3867 | 634/1288 | chr20 | 32917346 | |||
chr20:32918415 | T | C | 1 | a0002c0046 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.2115T>C | p.Tyr705Tyr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/27 | 2209/4197 | 2115/3867 | 705/1288 | chr20 | 32918415 | |||
chr20:32918445 | C | G | 1 | a0001c0056 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.2145C>G | p.Thr715Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/27 | 2239/4197 | 2145/3867 | 715/1288 | chr20 | 32918445 | |||
chr20:32920209 | G | A | 1 | a0001c0052 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.2406G>A | p.Val802Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/27 | 2500/4197 | 2406/3867 | 802/1288 | chr20 | 32920209 | |||
chr20:32931204 | A | G | 1 | a0009c0041 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2658A>G | p.Ala886Ala | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/27 | 2752/4197 | 2658/3867 | 886/1288 | chr20 | 32931204 | |||
chr20:32959874 | C | T | 1 | a0016c0051 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.3186C>T | p.Asp1062Asp | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 25/27 | 3280/4197 | 3186/3867 | 1062/1288 | chr20 | 32959874 | |||
chr20:32960092 | G | A | 3 | a0002c0011 a0007c0030 a0021c0061 |
7 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.3324G>A | p.Lys1108Lys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/27 | 3418/4197 | 3324/3867 | 1108/1288 | chr20 | 32960092 | |||
chr20:32961141 | G | A | 2 | a0009c0015 a0009c0023 |
5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.3399G>A | p.Ser1133Ser | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3493/4197 | 3399/3867 | 1133/1288 | chr20 | 32961141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32858936 | G | C | 33 | a0001c0001t0002 a0001c0001t0005 a0002c0002t0002 others(30): Show |
79 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/27 | 4857 | chr20 | 32858936 | ||||||
chr20:32961618 | G | A | 16 | a0002c0002t0003 a0002c0046t0003 a0004c0004t0003 others(13): Show |
54 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 9 | chr20 | 32961618 | ||||||
chr20:32961759 | C | T | 1 | a0001c0001t0009 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 150 | chr20 | 32961759 | ||||||
chr20:32961778 | T | G | 40 | a0001c0001t0004 a0001c0001t0005 a0002c0002t0003 others(37): Show |
93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 169 | chr20 | 32961778 | ||||||
chr20:32961827 | G | A | 3 | a0005c0033t0008 a0019c0017t0007 a0044c0045t0007 |
5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*218G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 218 | chr20 | 32961827 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32859052 | A | G | 20 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0263 others(17): Show |
22 | HG01358.hp2 HG01361.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11+46A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859052 | |||||||
chr20:32859052 | A | T | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+46A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859052 | |||||||
chr20:32859085 | G | T | 2 | a0049c0040t0002g0261 a0050c0038t0002g0262 |
2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-11+79G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859085 | |||||||
chr20:32859099 | C | T | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+93C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859099 | |||||||
chr20:32859518 | CTG | C | 4 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0026c0028t0005g0260 others(1): Show |
4 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+514_-11+515del others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32859518 | ||||||
chr20:32859562 | A | G | 5 | a0003c0003t0001g0277 a0003c0003t0001g0280 a0008c0007t0003g0278 others(2): Show |
5 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+556A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859562 | |||||||
chr20:32859763 | A | G | 1 | a0015c0020t0003g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-11+757A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859763 | |||||||
chr20:32859774 | C | T | 1 | a0004c0004t0003g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-11+768C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859774 | |||||||
chr20:32859796 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-11+790A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859796 | |||||||
chr20:32859797 | TAC | T | 8 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+793_-11+794del others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32859797 | ||||||
chr20:32859836 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-11+830A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859836 | |||||||
chr20:32859887 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-11+881C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859887 | |||||||
chr20:32859891 | C | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-11+885C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859891 | |||||||
chr20:32859942 | T | C | 1 | a0005c0008t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11+936T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859942 | |||||||
chr20:32860033 | G | A | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-11+1027G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860033 | |||||||
chr20:32860153 | C | T | 1 | a0027c0029t0003g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-11+1147C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860153 | |||||||
chr20:32860313 | C | CA | 57 | a0001c0001t0002g0030 a0001c0001t0002g0054 a0001c0001t0002g0059 others(54): Show |
57 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-11+1316dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860313 | ||||||
chr20:32860322 | A | C | 1 | a0021c0061t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+1316A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860322 | |||||||
chr20:32860339 | A | C | 1 | a0006c0005t0003g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-11+1333A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860339 | |||||||
chr20:32860469 | T | A | 8 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+1463T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860469 | |||||||
chr20:32860479 | G | A | 4 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1473G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860479 | |||||||
chr20:32860493 | C | CAT | 3 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0003c0003t0002g0007 |
3 | NA18946.hp2 NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-11+1487_-11+1488i others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860493 | |||||||
chr20:32860493 | C | CT | 33 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(30): Show |
33 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11+1518dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | C | CTTTT | 10 | a0001c0001t0005g0222 a0002c0002t0001g0223 a0002c0002t0001g0227 others(7): Show |
10 | HG01884.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+1515_-11+1518d others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | C | CTTTTT | 10 | a0002c0002t0001g0236 a0002c0002t0001g0237 a0002c0046t0003g0235 others(7): Show |
10 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+1514_-11+1518d others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CT | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0118 others(38): Show |
44 | HG00099.hp2 HG00642.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-11+1518delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTT | C | 16 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(13): Show |
16 | HG01433.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+1517_-11+1518d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTTT | C | 10 | a0002c0002t0001g0095 a0002c0011t0001g0246 a0002c0011t0001g0247 others(7): Show |
10 | HG01123.hp2 HG01981.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+1516_-11+1518d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTTTTTTT others(4): Show |
C | 2 | a0002c0022t0002g0010 a0025c0027t0003g0094 |
2 | HG03669.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+1508_-11+1518d others(13): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTTTTTTT others(5): Show |
C | 2 | a0002c0002t0002g0008 a0011c0009t0005g0009 |
2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-11+1507_-11+1518d others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTTTTTTT others(6): Show |
C | 1 | a0006c0005t0003g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-11+1506_-11+1518d others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTTTTTTT others(7): Show |
C | 36 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0244 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-11+1505_-11+1518d others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTTTTTTT others(8): Show |
C | 1 | a0004c0004t0003g0060 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-11+1504_-11+1518d others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860493 | CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11+1501_-11+1518d others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | ||||||
chr20:32860718 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-11+1712T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860718 | |||||||
chr20:32860735 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-11+1729T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860735 | |||||||
chr20:32860842 | A | G | 42 | a0001c0001t0002g0030 a0001c0001t0002g0054 a0001c0001t0002g0059 others(39): Show |
42 | HG00423.hp1 HG00621.hp2 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.-11+1836A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860842 | |||||||
chr20:32860890 | C | T | 38 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0244 others(35): Show |
38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-11+1884C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860890 | |||||||
chr20:32860966 | C | G | 1 | a0015c0020t0003g0092 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-11+1960C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860966 | |||||||
chr20:32861043 | G | A | 68 | a0001c0001t0002g0030 a0001c0001t0002g0054 a0001c0001t0002g0059 others(65): Show |
68 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.-11+2037G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861043 | |||||||
chr20:32861101 | T | G | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+2095T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861101 | |||||||
chr20:32861102 | C | T | 7 | a0008c0007t0006g0046 a0018c0014t0002g0042 a0018c0014t0002g0044 others(4): Show |
7 | HG01346.hp1 HG01515.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+2096C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861102 | |||||||
chr20:32861105 | T | A | 2 | a0009c0041t0001g0253 a0011c0009t0001g0250 |
2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11+2099T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861105 | |||||||
chr20:32861189 | C | G | 1 | a0006c0005t0006g0022 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-11+2183C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861189 | |||||||
chr20:32861313 | A | G | 1 | a0003c0003t0001g0203 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-11+2307A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861313 | |||||||
chr20:32861319 | G | A | 13 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0003g0264 others(10): Show |
13 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+2313G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861319 | |||||||
chr20:32861384 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0090 others(192): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-11+2378A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861384 | |||||||
chr20:32861491 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(13): Show |
17 | HG00099.hp2 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-2292G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861491 | |||||||
chr20:32861579 | G | A | 6 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(3): Show |
6 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-2204G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861579 | |||||||
chr20:32861580 | C | T | 37 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0244 others(34): Show |
37 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10-2203C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861580 | |||||||
chr20:32861702 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(13): Show |
17 | HG00099.hp2 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-2081C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861702 | |||||||
chr20:32861726 | C | G | 3 | a0012c0012t0004g0110 a0012c0012t0004g0111 a0012c0012t0004g0197 |
3 | HG01433.hp1 HG02148.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-10-2057C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861726 | |||||||
chr20:32861897 | A | G | 5 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0004g0103 others(2): Show |
5 | HG02630.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1886A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861897 | |||||||
chr20:32861919 | CTT | C | 79 | a0001c0001t0002g0030 a0001c0001t0002g0054 a0001c0001t0002g0059 others(76): Show |
79 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10-1863_-10-1862d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861919 | |||||||
chr20:32861933 | T | G | 5 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0004g0103 others(2): Show |
5 | HG02630.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1850T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861933 | |||||||
chr20:32862040 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01346.hp2 HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-10-1743T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862040 | |||||||
chr20:32862065 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-10-1718C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862065 | |||||||
chr20:32862066 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-10-1717T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862066 | |||||||
chr20:32862134 | C | CT | 15 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0003g0264 others(12): Show |
15 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-1635dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32862134 | ||||||
chr20:32862134 | CT | C | 10 | a0001c0001t0001g0205 a0002c0002t0001g0121 a0002c0002t0001g0130 others(7): Show |
10 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-1635delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32862134 | ||||||
chr20:32862139 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-10-1644T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862139 | |||||||
chr20:32862230 | A | G | 4 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0003c0003t0001g0132 others(1): Show |
4 | HG03098.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-1553A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862230 | |||||||
chr20:32862240 | C | G | 1 | a0004c0004t0001g0091 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-10-1543C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862240 | |||||||
chr20:32862245 | C | T | 10 | a0002c0002t0001g0223 a0002c0002t0001g0227 a0002c0002t0001g0236 others(7): Show |
10 | HG02451.hp2 HG02809.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1538C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862245 | |||||||
chr20:32862487 | CT | C | 6 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(3): Show |
6 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1294delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32862487 | ||||||
chr20:32862723 | G | C | 1 | a0002c0002t0003g0267 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-1060G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862723 | |||||||
chr20:32862732 | A | G | 13 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0003g0264 others(10): Show |
13 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10-1051A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862732 | |||||||
chr20:32862840 | G | A | 1 | a0011c0009t0004g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-10-943G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862840 | |||||||
chr20:32862858 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0090 others(194): Show |
200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-10-925G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862858 | |||||||
chr20:32862919 | C | T | 1 | a0011c0009t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-864C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862919 | |||||||
chr20:32863011 | AT | A | 153 | a0001c0001t0001g0063 a0001c0001t0001g0245 a0001c0001t0002g0030 others(150): Show |
155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-10-759delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32863011 | ||||||
chr20:32863011 | ATT | A | 13 | a0002c0002t0001g0223 a0002c0002t0001g0227 a0002c0002t0001g0236 others(10): Show |
13 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-760_-10-759del others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32863011 | ||||||
chr20:32863111 | C | G | 1 | a0050c0038t0002g0262 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-10-672C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863111 | |||||||
chr20:32863216 | A | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(190): Show |
196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.-10-567A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863216 | |||||||
chr20:32863231 | G | A | 1 | a0017c0018t0005g0231 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-552G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863231 | |||||||
chr20:32863233 | T | G | 1 | a0002c0002t0001g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-10-550T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863233 | |||||||
chr20:32863290 | C | T | 1 | a0039c0066t0004g0109 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-493C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863290 | |||||||
chr20:32863437 | C | G | 4 | a0002c0002t0003g0264 a0002c0002t0003g0265 a0002c0011t0001g0102 others(1): Show |
4 | HG02145.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-346C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863437 | |||||||
chr20:32863544 | T | A | 96 | a0001c0001t0001g0245 a0001c0001t0002g0030 a0001c0001t0002g0054 others(93): Show |
96 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.-10-239T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863544 | |||||||
chr20:32863545 | C | A | 96 | a0001c0001t0001g0245 a0001c0001t0002g0030 a0001c0001t0002g0054 others(93): Show |
96 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.-10-238C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863545 | |||||||
chr20:32863567 | G | A | 2 | a0024c0032t0004g0064 a0024c0032t0004g0275 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-10-216G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863567 | |||||||
chr20:32863758 | A | T | 1 | a0004c0004t0003g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-10-25A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863758 | |||||||
chr20:32863874 | A | G | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42+40A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32863874 | |||||||
chr20:32863982 | AT | A | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+160delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32863982 | ||||||
chr20:32864322 | A | G | 1 | a0002c0022t0002g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.42+488A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864322 | |||||||
chr20:32864336 | C | G | 2 | a0008c0007t0003g0196 a0025c0027t0003g0128 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.42+502C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864336 | |||||||
chr20:32864487 | T | G | 2 | a0003c0003t0001g0132 a0007c0030t0004g0129 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.42+653T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864487 | |||||||
chr20:32864488 | G | A | 1 | a0005c0033t0008g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42+654G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864488 | |||||||
chr20:32864641 | T | C | 4 | a0002c0002t0001g0223 a0002c0002t0001g0236 a0002c0002t0001g0237 others(1): Show |
4 | HG02451.hp2 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+807T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864641 | |||||||
chr20:32864756 | T | C | 2 | a0011c0009t0004g0252 a0047c0057t0004g0251 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.42+922T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864756 | |||||||
chr20:32864893 | T | G | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42+1059T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864893 | |||||||
chr20:32864942 | C | G | 2 | a0003c0003t0002g0137 a0003c0003t0002g0138 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.42+1108C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864942 | |||||||
chr20:32864997 | C | T | 1 | a0002c0002t0001g0192 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.42+1163C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864997 | |||||||
chr20:32865119 | A | G | 11 | a0001c0001t0005g0222 a0014c0019t0005g0221 a0014c0019t0005g0233 others(8): Show |
11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.42+1285A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865119 | |||||||
chr20:32865150 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(56): Show |
60 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.42+1316C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865150 | |||||||
chr20:32865220 | T | C | 7 | a0002c0002t0001g0263 a0002c0011t0001g0102 a0003c0003t0001g0277 others(4): Show |
7 | HG01358.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.42+1386T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865220 | |||||||
chr20:32865319 | AC | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(188): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.42+1486delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865319 | |||||||
chr20:32865390 | G | C | 1 | a0007c0006t0004g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42+1556G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865390 | |||||||
chr20:32865669 | C | T | 1 | a0051c0068t0004g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.42+1835C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865669 | |||||||
chr20:32865719 | A | G | 13 | a0001c0001t0005g0222 a0009c0041t0001g0253 a0011c0009t0001g0250 others(10): Show |
13 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.43-1863A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865719 | |||||||
chr20:32865761 | G | A | 1 | a0002c0022t0002g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43-1821G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865761 | |||||||
chr20:32865794 | C | CA | 45 | a0001c0001t0001g0108 a0001c0001t0001g0133 a0001c0001t0001g0206 others(42): Show |
45 | HG00423.hp1 HG00621.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.43-1771dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32865794 | ||||||
chr20:32865827 | G | A | 2 | a0005c0035t0001g0097 a0039c0066t0004g0109 |
2 | HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.43-1755G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865827 | |||||||
chr20:32866102 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.43-1480G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866102 | |||||||
chr20:32866256 | G | A | 1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.43-1326G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866256 | |||||||
chr20:32866303 | A | G | 11 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(8): Show |
13 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.43-1279A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866303 | |||||||
chr20:32866357 | G | A | 1 | a0044c0045t0007g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-1225G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866357 | |||||||
chr20:32866724 | TCTTC | T | 6 | a0002c0002t0002g0014 a0002c0002t0002g0047 a0002c0002t0002g0048 others(3): Show |
6 | HG01358.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-836_43-833delTT others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32866724 | ||||||
chr20:32866778 | TTCTTCCT others(26): Show |
T | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-781_43-749delCT others(31): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32866778 | ||||||
chr20:32866851 | T | TTCTCTCT others(36): Show |
1 | a0011c0009t0004g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.43-708_43-666dupCT others(41): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32866851 | ||||||
chr20:32866934 | T | G | 1 | a0002c0002t0003g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.43-648T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866934 | |||||||
chr20:32866946 | C | G | 2 | a0004c0004t0003g0088 a0004c0004t0003g0089 |
2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.43-636C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866946 | |||||||
chr20:32867160 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.43-422T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32867160 | |||||||
chr20:32867195 | T | C | 1 | a0006c0005t0003g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43-387T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32867195 | |||||||
chr20:32867275 | T | C | 3 | a0002c0002t0001g0263 a0011c0009t0004g0252 a0047c0057t0004g0251 |
3 | HG01884.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.43-307T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32867275 | |||||||
chr20:32867761 | G | A | 1 | a0007c0006t0004g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208+14G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32867761 | |||||||
chr20:32867821 | G | A | 1 | a0021c0061t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+74G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32867821 | |||||||
chr20:32867964 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(53): Show |
57 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.208+217G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32867964 | |||||||
chr20:32868015 | C | CT | 10 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0141 others(7): Show |
10 | HG00639.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+278dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32868015 | ||||||
chr20:32868169 | C | T | 1 | a0009c0041t0001g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208+422C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868169 | |||||||
chr20:32868299 | C | T | 1 | a0003c0003t0002g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208+552C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868299 | |||||||
chr20:32868362 | C | G | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208+615C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868362 | |||||||
chr20:32868691 | A | C | 1 | a0029c0053t0002g0031 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.208+944A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868691 | |||||||
chr20:32868921 | G | A | 5 | a0002c0002t0002g0008 a0002c0022t0002g0017 a0008c0007t0006g0015 others(2): Show |
5 | HG00733.hp1 HG01515.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+1174G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868921 | |||||||
chr20:32868953 | C | T | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+1206C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868953 | |||||||
chr20:32869046 | C | A | 1 | a0005c0008t0004g0207 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.208+1299C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869046 | |||||||
chr20:32869196 | A | G | 1 | a0023c0024t0005g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.208+1449A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869196 | |||||||
chr20:32869239 | A | AT | 7 | a0001c0001t0002g0054 a0002c0002t0002g0053 a0005c0033t0008g0115 others(4): Show |
7 | HG00423.hp1 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+1507dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32869239 | ||||||
chr20:32869344 | T | C | 1 | a0002c0002t0002g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208+1597T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869344 | |||||||
chr20:32869424 | C | A | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+1677C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869424 | |||||||
chr20:32869461 | C | G | 4 | a0002c0002t0002g0014 a0002c0002t0002g0047 a0002c0002t0002g0048 others(1): Show |
4 | HG02257.hp1 HG03688.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+1714C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869461 | |||||||
chr20:32869487 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(164): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.208+1740T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869487 | |||||||
chr20:32869531 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(70): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.208+1784T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869531 | |||||||
chr20:32869570 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01346.hp2 HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.208+1823C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869570 | |||||||
chr20:32869732 | C | CT | 12 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0001g0130 others(9): Show |
12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1986dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32869732 | ||||||
chr20:32869734 | G | A | 12 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0001g0130 others(9): Show |
12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1987G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869734 | |||||||
chr20:32869735 | T | A | 12 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0001g0130 others(9): Show |
12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1988T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869735 | |||||||
chr20:32869902 | C | T | 1 | a0007c0006t0001g0184 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.208+2155C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869902 | |||||||
chr20:32870081 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.208+2334T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870081 | |||||||
chr20:32870159 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.208+2412T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870159 | |||||||
chr20:32870230 | A | G | 7 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+2483A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870230 | |||||||
chr20:32870289 | T | C | 1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208+2542T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870289 | |||||||
chr20:32870343 | C | T | 5 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(2): Show |
5 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+2596C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870343 | |||||||
chr20:32870405 | T | G | 2 | a0002c0011t0001g0246 a0007c0006t0001g0249 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.208+2658T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870405 | |||||||
chr20:32870487 | T | C | 2 | a0002c0002t0001g0192 a0030c0043t0001g0186 |
2 | HG00639.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.208+2740T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870487 | |||||||
chr20:32870710 | C | T | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+2963C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870710 | |||||||
chr20:32870781 | C | T | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.208+3034C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870781 | |||||||
chr20:32870859 | CTT | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(63): Show |
67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.208+3125_208+3126d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32870859 | ||||||
chr20:32870886 | T | G | 2 | a0003c0003t0001g0277 a0003c0003t0001g0280 |
2 | HG01358.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.208+3139T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870886 | |||||||
chr20:32870910 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.208+3163G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870910 | |||||||
chr20:32870927 | C | T | 2 | a0014c0019t0005g0233 a0014c0019t0005g0234 |
2 | HG00741.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.208+3180C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870927 | |||||||
chr20:32870933 | A | C | 4 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3186A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870933 | |||||||
chr20:32870967 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+3220G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870967 | |||||||
chr20:32871097 | C | T | 14 | a0002c0002t0002g0008 a0002c0002t0002g0014 a0002c0002t0002g0019 others(11): Show |
14 | HG00323.hp1 HG00733.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+3350C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871097 | |||||||
chr20:32871105 | G | A | 1 | a0015c0020t0003g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.208+3358G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871105 | |||||||
chr20:32871117 | TCTGGGAT others(3062): Show |
T | 1 | a0009c0015t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208+3379_209-1732d others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32871117 | ||||||
chr20:32871226 | A | G | 11 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0001g0130 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+3479A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871226 | |||||||
chr20:32871234 | C | T | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+3487C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871234 | |||||||
chr20:32871317 | A | G | 38 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(35): Show |
38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.208+3570A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871317 | |||||||
chr20:32871320 | G | A | 3 | a0002c0002t0002g0014 a0002c0002t0002g0048 a0002c0002t0002g0049 |
3 | HG03688.hp2 HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.208+3573G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871320 | |||||||
chr20:32871496 | T | A | 1 | a0001c0052t0001g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.208+3749T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871496 | |||||||
chr20:32871517 | A | G | 1 | a0008c0007t0003g0278 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.208+3770A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871517 | |||||||
chr20:32871554 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.208+3807C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871554 | |||||||
chr20:32871729 | G | A | 76 | a0001c0001t0002g0030 a0001c0001t0002g0054 a0001c0001t0002g0059 others(73): Show |
76 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.208+3982G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871729 | |||||||
chr20:32871747 | C | T | 4 | a0002c0042t0001g0200 a0002c0046t0003g0235 a0005c0013t0001g0202 others(1): Show |
4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+4000C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871747 | |||||||
chr20:32871756 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+4009C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871756 | |||||||
chr20:32871915 | G | A | 6 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(3): Show |
6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-4011G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871915 | |||||||
chr20:32871940 | G | A | 1 | a0005c0008t0004g0207 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.209-3986G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871940 | |||||||
chr20:32871960 | G | A | 1 | a0008c0007t0003g0279 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.209-3966G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871960 | |||||||
chr20:32872116 | A | G | 1 | a0001c0001t0002g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.209-3810A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872116 | |||||||
chr20:32872240 | C | T | 1 | a0007c0030t0004g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.209-3686C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872240 | |||||||
chr20:32872270 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-3656G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872270 | |||||||
chr20:32872357 | C | T | 1 | a0002c0002t0002g0036 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.209-3569C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872357 | |||||||
chr20:32872398 | G | A | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-3528G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872398 | |||||||
chr20:32872438 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-3488A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872438 | |||||||
chr20:32872495 | G | A | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-3431G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872495 | |||||||
chr20:32872496 | A | G | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-3430A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872496 | |||||||
chr20:32872515 | C | T | 11 | a0001c0001t0005g0222 a0014c0019t0005g0221 a0014c0019t0005g0233 others(8): Show |
11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-3411C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872515 | |||||||
chr20:32872781 | G | A | 38 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(35): Show |
38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.209-3145G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872781 | |||||||
chr20:32872792 | T | TCAAAAA | 16 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0223 others(13): Show |
16 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-3122_209-3117d others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32872792 | ||||||
chr20:32872866 | C | T | 1 | a0005c0033t0008g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-3060C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872866 | |||||||
chr20:32872912 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-3014C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872912 | |||||||
chr20:32872964 | C | T | 2 | a0002c0042t0001g0200 a0002c0046t0003g0235 |
2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.209-2962C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872964 | |||||||
chr20:32872965 | G | T | 3 | a0005c0013t0004g0099 a0009c0015t0001g0100 a0009c0015t0001g0114 |
3 | HG02109.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.209-2961G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872965 | |||||||
chr20:32873276 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-2650T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873276 | |||||||
chr20:32873462 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.209-2464A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873462 | |||||||
chr20:32873478 | C | A | 1 | a0002c0002t0002g0029 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.209-2448C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873478 | |||||||
chr20:32873809 | C | CA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(48): Show |
52 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.209-2117_209-2116i others(3): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873809 | |||||||
chr20:32873809 | C | CAA | 7 | a0002c0002t0001g0121 a0002c0002t0001g0263 a0004c0004t0003g0082 others(4): Show |
7 | HG00639.hp2 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2117_209-2116i others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873809 | |||||||
chr20:32873810 | C | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(71): Show |
75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.209-2116C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873810 | |||||||
chr20:32873982 | G | T | 1 | a0038c0044t0002g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209-1944G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873982 | |||||||
chr20:32874111 | C | T | 1 | a0009c0023t0001g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.209-1815C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874111 | |||||||
chr20:32874379 | C | T | 11 | a0001c0001t0005g0222 a0014c0019t0005g0221 a0014c0019t0005g0233 others(8): Show |
11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-1547C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874379 | |||||||
chr20:32874392 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.209-1534T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874392 | |||||||
chr20:32874398 | A | G | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-1528A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874398 | |||||||
chr20:32874556 | T | G | 1 | a0002c0002t0001g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.209-1370T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874556 | |||||||
chr20:32874976 | T | G | 16 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0223 others(13): Show |
16 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-950T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874976 | |||||||
chr20:32875120 | G | A | 6 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0007c0006t0001g0238 others(3): Show |
6 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-806G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875120 | |||||||
chr20:32875208 | G | C | 1 | a0002c0002t0003g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.209-718G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875208 | |||||||
chr20:32875263 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.209-663G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875263 | |||||||
chr20:32875265 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(63): Show |
67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.209-661G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875265 | |||||||
chr20:32875350 | G | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA18962.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.209-576G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875350 | |||||||
chr20:32875418 | G | A | 1 | a0022c0031t0002g0198 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.209-508G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875418 | |||||||
chr20:32875446 | G | T | 11 | a0001c0001t0005g0222 a0014c0019t0005g0221 a0014c0019t0005g0233 others(8): Show |
11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-480G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875446 | |||||||
chr20:32875478 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-448T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875478 | |||||||
chr20:32875502 | G | GT | 14 | a0001c0001t0001g0105 a0002c0022t0002g0017 a0005c0008t0001g0004 others(11): Show |
14 | HG00741.hp1 HG02027.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.209-406dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(3): Show |
4 | a0012c0012t0004g0096 a0012c0012t0004g0197 a0023c0024t0005g0043 others(1): Show |
4 | HG01346.hp1 HG01981.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-415_209-406dup others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(4): Show |
1 | a0012c0012t0004g0111 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.209-416_209-406dup others(11): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(5): Show |
1 | a0006c0005t0003g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.209-417_209-406dup others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(10): Show |
1 | a0002c0011t0001g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.209-422_209-406dup others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(12): Show |
12 | a0004c0004t0001g0091 a0004c0004t0003g0068 a0004c0004t0003g0069 others(9): Show |
12 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(13): Show |
18 | a0001c0001t0001g0242 a0003c0003t0001g0277 a0003c0003t0001g0280 others(15): Show |
18 | HG00099.hp2 HG00280.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(14): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0243 a0004c0004t0003g0082 others(9): Show |
13 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(15): Show |
11 | a0002c0002t0001g0121 a0003c0003t0001g0203 a0004c0004t0003g0060 others(8): Show |
11 | HG00741.hp2 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(22): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(16): Show |
2 | a0004c0004t0003g0087 a0020c0025t0001g0195 |
2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.209-406_209-405ins others(23): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(18): Show |
1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209-406_209-405ins others(25): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(20): Show |
1 | a0003c0003t0001g0125 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.209-406_209-405ins others(27): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | G | GTTTTTTT others(21): Show |
1 | a0001c0001t0001g0126 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.209-406_209-405ins others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875502 | GT | G | 10 | a0001c0001t0001g0108 a0002c0002t0001g0002 a0002c0002t0001g0003 others(7): Show |
12 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-406delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | ||||||
chr20:32875585 | A | G | 16 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0223 others(13): Show |
16 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-341A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875585 | |||||||
chr20:32875590 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-336T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875590 | |||||||
chr20:32875640 | G | T | 1 | a0014c0019t0005g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209-286G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875640 | |||||||
chr20:32875654 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-272A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875654 | |||||||
chr20:32875760 | C | A | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-166C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875760 | |||||||
chr20:32876245 | C | T | 1 | a0026c0028t0005g0260 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.327+201C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876245 | |||||||
chr20:32876261 | G | A | 4 | a0002c0042t0001g0200 a0002c0046t0003g0235 a0005c0013t0001g0202 others(1): Show |
4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+217G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876261 | |||||||
chr20:32876295 | C | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.327+251C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876295 | |||||||
chr20:32876422 | GTTACA | G | 4 | a0002c0042t0001g0200 a0002c0046t0003g0235 a0005c0013t0001g0202 others(1): Show |
4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+380_327+384del others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32876422 | ||||||
chr20:32876571 | A | G | 2 | a0001c0001t0002g0059 a0005c0008t0002g0052 |
2 | HG02027.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.327+527A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876571 | |||||||
chr20:32876642 | A | G | 1 | a0025c0027t0003g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327+598A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876642 | |||||||
chr20:32876661 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.327+617G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876661 | |||||||
chr20:32876688 | C | T | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0013c0016t0001g0145 others(1): Show |
4 | HG00099.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+644C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876688 | |||||||
chr20:32876702 | C | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(10): Show |
14 | HG00099.hp2 HG00642.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+658C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876702 | |||||||
chr20:32876914 | GCTGAGAT others(3): Show |
G | 1 | a0003c0003t0002g0023 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.327+871_327+880del others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876914 | |||||||
chr20:32877079 | C | T | 2 | a0024c0032t0004g0064 a0024c0032t0004g0275 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+1035C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877079 | |||||||
chr20:32877114 | C | T | 3 | a0002c0002t0001g0263 a0011c0009t0004g0252 a0047c0057t0004g0251 |
3 | HG01884.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.327+1070C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877114 | |||||||
chr20:32877199 | A | C | 11 | a0001c0001t0001g0108 a0001c0001t0001g0142 a0002c0002t0001g0095 others(8): Show |
11 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+1155A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877199 | |||||||
chr20:32877203 | C | A | 43 | a0001c0001t0001g0148 a0001c0001t0005g0257 a0001c0001t0005g0258 others(40): Show |
45 | HG00621.hp1 HG01109.hp2 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.327+1159C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877203 | |||||||
chr20:32877207 | C | CT | 18 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0002g0030 others(15): Show |
18 | HG01109.hp2 HG01261.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.327+1182dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | ||||||
chr20:32877207 | C | CTTTT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(10): Show |
14 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+1179_327+1182d others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | ||||||
chr20:32877207 | C | CTTTTT | 32 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0068 others(29): Show |
32 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.327+1178_327+1182d others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | ||||||
chr20:32877207 | CT | C | 8 | a0001c0001t0001g0150 a0001c0001t0001g0178 a0001c0001t0001g0217 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+1182delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | ||||||
chr20:32877211 | T | C | 12 | a0001c0001t0001g0245 a0002c0002t0001g0095 a0002c0002t0001g0130 others(9): Show |
12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.327+1167T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877211 | |||||||
chr20:32877247 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0244 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.327+1203C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877247 | |||||||
chr20:32877532 | A | G | 3 | a0002c0002t0001g0263 a0011c0009t0004g0252 a0047c0057t0004g0251 |
3 | HG01884.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.328-1172A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877532 | |||||||
chr20:32877568 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-1136G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877568 | |||||||
chr20:32877644 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-1060T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877644 | |||||||
chr20:32877888 | C | G | 2 | a0018c0014t0002g0044 a0048c0039t0002g0045 |
2 | NA18950.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.328-816C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877888 | |||||||
chr20:32877914 | C | T | 18 | a0004c0004t0003g0069 a0004c0004t0003g0078 a0006c0005t0003g0066 others(15): Show |
18 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.328-790C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877914 | |||||||
chr20:32878098 | T | G | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-606T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878098 | |||||||
chr20:32878126 | A | G | 86 | a0001c0001t0002g0030 a0001c0001t0002g0054 a0001c0001t0002g0059 others(83): Show |
88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.328-578A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878126 | |||||||
chr20:32878389 | C | T | 11 | a0001c0001t0005g0222 a0014c0019t0005g0221 a0014c0019t0005g0233 others(8): Show |
11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.328-315C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878389 | |||||||
chr20:32878407 | AC | A | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-295delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32878407 | ||||||
chr20:32878476 | G | C | 1 | a0011c0009t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.328-228G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878476 | |||||||
chr20:32878508 | C | CT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0148 others(74): Show |
78 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.328-176dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32878508 | ||||||
chr20:32878541 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-163C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878541 | |||||||
chr20:32878556 | G | A | 1 | a0004c0004t0003g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.328-148G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878556 | |||||||
chr20:32878558 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-146C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878558 | |||||||
chr20:32878579 | G | A | 1 | a0004c0004t0003g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.328-125G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878579 | |||||||
chr20:32878581 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-123A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878581 | |||||||
chr20:32878619 | G | A | 1 | a0011c0009t0004g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.328-85G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878619 | |||||||
chr20:32878846 | C | A | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+39C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32878846 | |||||||
chr20:32878995 | G | A | 1 | a0040c0048t0002g0034 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.431+188G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32878995 | |||||||
chr20:32879013 | A | T | 1 | a0003c0003t0002g0023 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.431+206A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879013 | |||||||
chr20:32879194 | G | C | 4 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+387G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879194 | |||||||
chr20:32879308 | G | A | 14 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0223 others(11): Show |
14 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.431+501G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879308 | |||||||
chr20:32879409 | C | T | 1 | a0002c0002t0002g0029 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.431+602C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879409 | |||||||
chr20:32879569 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0208 others(160): Show |
166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.431+762T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879569 | |||||||
chr20:32879570 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+763G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879570 | |||||||
chr20:32879614 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.431+807A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879614 | |||||||
chr20:32879617 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+810C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879617 | |||||||
chr20:32879670 | C | T | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+863C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879670 | |||||||
chr20:32879745 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+938T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879745 | |||||||
chr20:32880005 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(54): Show |
58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.431+1198C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880005 | |||||||
chr20:32880186 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(157): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.431+1379T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880186 | |||||||
chr20:32880188 | A | C | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+1381A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880188 | |||||||
chr20:32880272 | C | CT | 73 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(70): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.431+1479dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32880272 | ||||||
chr20:32880272 | CT | C | 12 | a0001c0001t0005g0222 a0011c0009t0001g0250 a0014c0019t0005g0221 others(9): Show |
12 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.431+1479delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32880272 | ||||||
chr20:32880307 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+1500T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880307 | |||||||
chr20:32880413 | C | T | 2 | a0003c0003t0001g0132 a0007c0030t0004g0129 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.431+1606C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880413 | |||||||
chr20:32880636 | A | T | 1 | a0033c0065t0001g0062 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431+1829A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880636 | |||||||
chr20:32880720 | C | T | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+1913C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880720 | |||||||
chr20:32880898 | C | CAT | 56 | a0001c0001t0002g0030 a0001c0001t0002g0054 a0001c0001t0002g0059 others(53): Show |
56 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.431+2103_431+2104d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32880898 | ||||||
chr20:32881069 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.431+2262G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881069 | |||||||
chr20:32881126 | G | A | 3 | a0019c0017t0007g0219 a0019c0017t0007g0229 a0019c0017t0007g0230 |
3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.431+2319G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881126 | |||||||
chr20:32881446 | T | G | 1 | a0005c0037t0004g0185 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.431+2639T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881446 | |||||||
chr20:32881685 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0090 others(270): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.431+2878A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881685 | |||||||
chr20:32881740 | G | A | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(4): Show |
7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+2933G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881740 | |||||||
chr20:32881769 | G | A | 2 | a0015c0020t0003g0092 a0032c0060t0001g0080 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.431+2962G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881769 | |||||||
chr20:32881771 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(57): Show |
61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.431+2964G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881771 | |||||||
chr20:32881864 | C | T | 11 | a0001c0001t0005g0222 a0014c0019t0005g0221 a0014c0019t0005g0233 others(8): Show |
11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.431+3057C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881864 | |||||||
chr20:32881881 | A | G | 4 | a0001c0001t0001g0214 a0003c0003t0001g0147 a0003c0003t0001g0175 others(1): Show |
4 | HG00621.hp1 NA18947.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+3074A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881881 | |||||||
chr20:32882401 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.432-3104C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882401 | |||||||
chr20:32882596 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(148): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.432-2909C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882596 | |||||||
chr20:32882607 | A | G | 92 | a0001c0001t0001g0174 a0001c0001t0002g0030 a0001c0001t0002g0054 others(89): Show |
92 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.432-2898A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882607 | |||||||
chr20:32882669 | C | T | 1 | a0025c0027t0003g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-2836C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882669 | |||||||
chr20:32882678 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(48): Show |
52 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.432-2827G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882678 | |||||||
chr20:32882686 | G | A | 1 | a0011c0009t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.432-2819G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882686 | |||||||
chr20:32882901 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.432-2604T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882901 | |||||||
chr20:32882974 | C | G | 7 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(4): Show |
7 | HG01109.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-2531C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882974 | |||||||
chr20:32883031 | G | A | 1 | a0007c0006t0001g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.432-2474G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883031 | |||||||
chr20:32883200 | C | A | 6 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(3): Show |
6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.432-2305C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883200 | |||||||
chr20:32883206 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.432-2299C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883206 | |||||||
chr20:32883251 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(139): Show |
143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.432-2254G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883251 | |||||||
chr20:32883252 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432-2253T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883252 | |||||||
chr20:32883495 | A | G | 1 | a0004c0004t0003g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.432-2010A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883495 | |||||||
chr20:32883507 | T | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(159): Show |
165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.432-1998T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883507 | |||||||
chr20:32883751 | C | T | 49 | a0001c0001t0002g0059 a0002c0002t0002g0005 a0002c0002t0002g0006 others(46): Show |
49 | HG00323.hp1 HG00733.hp1 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.432-1754C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883751 | |||||||
chr20:32883752 | G | A | 4 | a0002c0042t0001g0200 a0002c0046t0003g0235 a0005c0013t0001g0202 others(1): Show |
4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-1753G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883752 | |||||||
chr20:32883899 | C | T | 6 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(3): Show |
6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.432-1606C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883899 | |||||||
chr20:32884058 | C | G | 68 | a0001c0001t0002g0059 a0001c0001t0005g0222 a0002c0002t0002g0005 others(65): Show |
68 | HG00323.hp1 HG00733.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.432-1447C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884058 | |||||||
chr20:32884376 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.432-1129C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884376 | |||||||
chr20:32884626 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(148): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.432-879T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884626 | |||||||
chr20:32884630 | G | A | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-875G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884630 | |||||||
chr20:32884657 | G | A | 1 | a0004c0004t0003g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.432-848G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884657 | |||||||
chr20:32884659 | C | T | 6 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-846C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884659 | |||||||
chr20:32884686 | C | G | 1 | a0009c0023t0001g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.432-819C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884686 | |||||||
chr20:32884949 | G | A | 1 | a0027c0029t0003g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.432-556G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884949 | |||||||
chr20:32885138 | TC | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(131): Show |
135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.432-365delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32885138 | ||||||
chr20:32885182 | C | T | 13 | a0002c0002t0002g0035 a0002c0002t0002g0036 a0002c0002t0002g0038 others(10): Show |
13 | HG02040.hp2 HG02129.hp2 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-323C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885182 | |||||||
chr20:32885207 | G | A | 10 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(7): Show |
12 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.432-298G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885207 | |||||||
chr20:32885374 | A | G | 141 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0105 others(138): Show |
143 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.432-131A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885374 | |||||||
chr20:32885376 | G | T | 125 | a0001c0001t0001g0063 a0001c0001t0001g0090 a0001c0001t0001g0105 others(122): Show |
127 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.432-129G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885376 | |||||||
chr20:32885379 | C | CGTGCGTG others(3): Show |
1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.432-117_432-116ins others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32885379 | ||||||
chr20:32885394 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.432-111C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885394 | |||||||
chr20:32885677 | G | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0156 a0001c0001t0001g0208 others(152): Show |
158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.567+37G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885677 | |||||||
chr20:32885750 | G | T | 17 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0223 others(14): Show |
17 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.567+110G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885750 | |||||||
chr20:32885852 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(144): Show |
150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.567+212C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885852 | |||||||
chr20:32885860 | G | A | 1 | a0011c0009t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.567+220G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885860 | |||||||
chr20:32885941 | T | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.567+301T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885941 | |||||||
chr20:32886061 | T | C | 2 | a0005c0013t0004g0099 a0016c0026t0001g0281 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.567+421T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886061 | |||||||
chr20:32886097 | C | A | 1 | a0007c0006t0001g0184 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.567+457C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886097 | |||||||
chr20:32886196 | T | G | 36 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.567+556T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886196 | |||||||
chr20:32886204 | G | A | 1 | a0002c0042t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.567+564G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886204 | |||||||
chr20:32886348 | T | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.567+708T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886348 | |||||||
chr20:32886378 | G | A | 20 | a0002c0002t0001g0095 a0002c0002t0001g0130 a0002c0002t0001g0131 others(17): Show |
20 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.567+738G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886378 | |||||||
chr20:32886387 | G | A | 1 | a0042c0067t0004g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.567+747G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886387 | |||||||
chr20:32886524 | C | T | 3 | a0019c0017t0007g0219 a0019c0017t0007g0229 a0019c0017t0007g0230 |
3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.567+884C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886524 | |||||||
chr20:32886581 | C | G | 2 | a0008c0007t0003g0196 a0025c0027t0003g0128 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.567+941C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886581 | |||||||
chr20:32886641 | A | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(138): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.567+1001A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886641 | |||||||
chr20:32886773 | G | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(191): Show |
197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.567+1133G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886773 | |||||||
chr20:32886803 | C | T | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.567+1163C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886803 | |||||||
chr20:32886860 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(138): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.567+1220C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886860 | |||||||
chr20:32886964 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(140): Show |
144 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.567+1324A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886964 | |||||||
chr20:32887065 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(138): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.567+1425A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887065 | |||||||
chr20:32887109 | G | C | 1 | a0011c0009t0004g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.567+1469G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887109 | |||||||
chr20:32887110 | T | C | 1 | a0008c0007t0006g0018 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.567+1470T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887110 | |||||||
chr20:32887294 | C | T | 1 | a0005c0008t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.567+1654C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887294 | |||||||
chr20:32887311 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567+1671C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887311 | |||||||
chr20:32887440 | G | A | 1 | a0001c0052t0001g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.567+1800G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887440 | |||||||
chr20:32887449 | C | A | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.567+1809C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887449 | |||||||
chr20:32887484 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.568-1817G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887484 | |||||||
chr20:32887500 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.568-1801C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887500 | |||||||
chr20:32887684 | A | G | 2 | a0002c0002t0001g0263 a0007c0006t0001g0249 |
2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.568-1617A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887684 | |||||||
chr20:32887768 | C | T | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1533C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887768 | |||||||
chr20:32887880 | C | T | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1421C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887880 | |||||||
chr20:32887894 | A | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1407A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887894 | |||||||
chr20:32888051 | A | G | 15 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(12): Show |
17 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.568-1250A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888051 | |||||||
chr20:32888070 | C | CT | 62 | a0001c0001t0001g0126 a0001c0001t0002g0030 a0001c0001t0002g0054 others(59): Show |
62 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.568-1220dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr20 | 32888070 | ||||||
chr20:32888118 | G | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1183G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888118 | |||||||
chr20:32888148 | C | T | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1153C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888148 | |||||||
chr20:32888155 | C | T | 1 | a0007c0030t0004g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.568-1146C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888155 | |||||||
chr20:32888173 | T | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1128T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888173 | |||||||
chr20:32888189 | A | G | 8 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0003c0003t0001g0132 others(5): Show |
8 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-1112A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888189 | |||||||
chr20:32888219 | G | A | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1082G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888219 | |||||||
chr20:32888223 | C | A | 1 | a0002c0002t0002g0024 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.568-1078C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888223 | |||||||
chr20:32888331 | T | A | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-970T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888331 | |||||||
chr20:32888836 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.568-465G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888836 | |||||||
chr20:32888858 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(139): Show |
143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.568-443T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888858 | |||||||
chr20:32888866 | T | C | 1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568-435T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888866 | |||||||
chr20:32888895 | T | C | 7 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0111 others(4): Show |
7 | HG01123.hp2 HG01243.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.568-406T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888895 | |||||||
chr20:32888958 | T | G | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-343T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888958 | |||||||
chr20:32888960 | T | G | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-341T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888960 | |||||||
chr20:32889022 | C | T | 8 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0003c0003t0001g0132 others(5): Show |
8 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-279C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32889022 | |||||||
chr20:32889035 | C | A | 8 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0003c0003t0001g0132 others(5): Show |
8 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-266C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32889035 | |||||||
chr20:32889436 | T | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+30T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889436 | |||||||
chr20:32889535 | A | C | 5 | a0003c0003t0001g0277 a0003c0003t0001g0280 a0008c0007t0003g0278 others(2): Show |
5 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+129A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889535 | |||||||
chr20:32889569 | G | A | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+163G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889569 | |||||||
chr20:32889580 | G | A | 1 | a0050c0038t0002g0262 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.673+174G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889580 | |||||||
chr20:32889591 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(128): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.673+185G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889591 | |||||||
chr20:32889696 | A | G | 2 | a0007c0006t0004g0144 a0007c0030t0004g0268 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.673+290A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889696 | |||||||
chr20:32889724 | G | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(124): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.673+318G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889724 | |||||||
chr20:32889727 | T | C | 8 | a0005c0035t0001g0097 a0012c0012t0004g0096 a0012c0012t0004g0110 others(5): Show |
8 | HG01123.hp2 HG01243.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.673+321T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889727 | |||||||
chr20:32889752 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0242 others(126): Show |
130 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.673+346A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889752 | |||||||
chr20:32889794 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(124): Show |
128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.673+388G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889794 | |||||||
chr20:32889915 | T | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+509T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889915 | |||||||
chr20:32889949 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(130): Show |
134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.673+543T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889949 | |||||||
chr20:32889955 | C | T | 2 | a0002c0002t0003g0273 a0002c0002t0003g0274 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.673+549C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889955 | |||||||
chr20:32889986 | G | A | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+580G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889986 | |||||||
chr20:32890000 | TA | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(111): Show |
115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.673+613delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32890000 | ||||||
chr20:32890002 | A | T | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.673+596A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890002 | |||||||
chr20:32890003 | A | T | 1 | a0011c0009t0004g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.673+597A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890003 | |||||||
chr20:32890167 | A | G | 2 | a0002c0002t0001g0263 a0007c0006t0001g0249 |
2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.673+761A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890167 | |||||||
chr20:32890175 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(71): Show |
75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.673+769C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890175 | |||||||
chr20:32890220 | C | T | 7 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(4): Show |
7 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+814C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890220 | |||||||
chr20:32890241 | GTGCTGTG others(3): Show |
G | 7 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(4): Show |
7 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+838_673+847del others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32890241 | ||||||
chr20:32890488 | G | C | 1 | a0002c0011t0001g0246 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.673+1082G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890488 | |||||||
chr20:32890494 | A | AACCTCCA others(2): Show |
141 | a0001c0001t0001g0126 a0001c0001t0002g0030 a0001c0001t0002g0054 others(138): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.673+1089_673+1090i others(11): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32890494 | ||||||
chr20:32890647 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0108 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.673+1241A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890647 | |||||||
chr20:32890658 | T | C | 43 | a0001c0001t0001g0108 a0001c0001t0001g0148 a0001c0001t0001g0173 others(40): Show |
43 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+1252T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890658 | |||||||
chr20:32890880 | G | T | 36 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(33): Show |
38 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.674-1333G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890880 | |||||||
chr20:32890932 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.674-1281A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890932 | |||||||
chr20:32891169 | G | A | 7 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(4): Show |
7 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-1044G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891169 | |||||||
chr20:32891178 | C | T | 3 | a0019c0017t0007g0219 a0019c0017t0007g0229 a0019c0017t0007g0230 |
3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.674-1035C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891178 | |||||||
chr20:32891203 | G | A | 35 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(32): Show |
35 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.674-1010G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891203 | |||||||
chr20:32891217 | C | T | 104 | a0001c0001t0002g0059 a0001c0001t0005g0257 a0001c0001t0005g0258 others(101): Show |
104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.674-996C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891217 | |||||||
chr20:32891277 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0002g0059 a0001c0001t0005g0257 others(102): Show |
106 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.674-936A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891277 | |||||||
chr20:32891300 | T | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.674-913T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891300 | |||||||
chr20:32891325 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-888C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891325 | |||||||
chr20:32891547 | A | G | 1 | a0026c0028t0002g0020 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.674-666A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891547 | |||||||
chr20:32891640 | G | A | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-573G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891640 | |||||||
chr20:32891650 | G | A | 4 | a0002c0002t0001g0095 a0002c0002t0004g0103 a0002c0002t0004g0104 others(1): Show |
4 | HG02630.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-563G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891650 | |||||||
chr20:32891660 | A | T | 1 | a0005c0035t0001g0097 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.674-553A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891660 | |||||||
chr20:32891762 | A | G | 148 | a0001c0001t0001g0126 a0001c0001t0001g0242 a0001c0001t0001g0243 others(145): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.674-451A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891762 | |||||||
chr20:32891808 | G | A | 1 | a0007c0006t0001g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.674-405G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891808 | |||||||
chr20:32891827 | G | GT | 10 | a0001c0001t0001g0063 a0012c0012t0004g0096 a0012c0012t0004g0110 others(7): Show |
10 | HG00621.hp2 HG01243.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.674-371dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32891827 | ||||||
chr20:32891827 | GT | G | 50 | a0001c0001t0001g0173 a0004c0004t0001g0091 a0004c0004t0003g0060 others(47): Show |
50 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.674-371delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32891827 | ||||||
chr20:32891922 | A | G | 147 | a0001c0001t0001g0126 a0001c0001t0001g0242 a0001c0001t0001g0243 others(144): Show |
147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.674-291A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891922 | |||||||
chr20:32892073 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.674-140C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32892073 | |||||||
chr20:32892137 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.674-76A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32892137 | |||||||
chr20:32892831 | C | CT | 8 | a0001c0001t0001g0126 a0001c0001t0001g0148 a0002c0002t0002g0027 others(5): Show |
8 | HG01109.hp2 HG01175.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-327dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr20 | 32892831 | ||||||
chr20:32892831 | CT | C | 14 | a0001c0001t0005g0257 a0002c0002t0001g0236 a0003c0003t0001g0280 others(11): Show |
14 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.759-327delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr20 | 32892831 | ||||||
chr20:32892847 | T | C | 1 | a0002c0002t0001g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.759-327T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892847 | |||||||
chr20:32892848 | C | CT | 12 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0270 others(9): Show |
14 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.759-318dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr20 | 32892848 | ||||||
chr20:32892848 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.759-326C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892848 | |||||||
chr20:32892959 | G | A | 1 | a0004c0004t0003g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.759-215G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892959 | |||||||
chr20:32892982 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(136): Show |
140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.759-192T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892982 | |||||||
chr20:32892989 | C | T | 1 | a0002c0002t0003g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.759-185C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892989 | |||||||
chr20:32893032 | G | A | 3 | a0005c0035t0001g0097 a0009c0023t0001g0127 a0020c0025t0001g0195 |
3 | HG01123.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.759-142G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893032 | |||||||
chr20:32893130 | C | T | 57 | a0001c0001t0002g0059 a0002c0002t0002g0005 a0002c0002t0002g0006 others(54): Show |
57 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.759-44C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893130 | |||||||
chr20:32893132 | C | T | 49 | a0002c0002t0001g0263 a0004c0004t0001g0091 a0004c0004t0003g0060 others(46): Show |
49 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.759-42C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893132 | |||||||
chr20:32893155 | C | T | 139 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0002g0059 others(136): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.759-19C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893155 | |||||||
chr20:32893470 | G | A | 59 | a0001c0001t0002g0059 a0002c0002t0002g0005 a0002c0002t0002g0006 others(56): Show |
59 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.883+172G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893470 | |||||||
chr20:32893721 | G | A | 55 | a0001c0001t0002g0059 a0002c0002t0002g0005 a0002c0002t0002g0006 others(52): Show |
55 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.883+423G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893721 | |||||||
chr20:32893767 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.883+469C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893767 | |||||||
chr20:32893844 | C | T | 1 | a0002c0002t0002g0039 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.883+546C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893844 | |||||||
chr20:32893845 | G | A | 3 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 |
3 | HG02572.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.883+547G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893845 | |||||||
chr20:32894059 | G | A | 1 | a0011c0009t0004g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883+761G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894059 | |||||||
chr20:32894078 | C | T | 26 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0242 others(23): Show |
26 | HG00099.hp2 HG00642.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.883+780C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894078 | |||||||
chr20:32894091 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.883+793C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894091 | |||||||
chr20:32894213 | A | G | 55 | a0001c0001t0002g0059 a0002c0002t0002g0005 a0002c0002t0002g0006 others(52): Show |
55 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.883+915A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894213 | |||||||
chr20:32894295 | T | C | 137 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0002g0059 others(134): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.883+997T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894295 | |||||||
chr20:32894295 | T | G | 1 | a0009c0023t0001g0127 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+997T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894295 | |||||||
chr20:32894328 | G | A | 36 | a0002c0002t0001g0192 a0004c0004t0001g0091 a0004c0004t0003g0060 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.883+1030G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894328 | |||||||
chr20:32894386 | G | A | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.883+1088G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894386 | |||||||
chr20:32894489 | A | G | 88 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0002g0059 others(85): Show |
88 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.883+1191A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894489 | |||||||
chr20:32894619 | T | C | 177 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0002g0059 others(174): Show |
179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.883+1321T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894619 | |||||||
chr20:32894746 | G | A | 1 | a0019c0017t0007g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.883+1448G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894746 | |||||||
chr20:32894820 | T | C | 1 | a0004c0004t0003g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.883+1522T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894820 | |||||||
chr20:32895106 | C | T | 54 | a0001c0001t0002g0059 a0002c0002t0002g0005 a0002c0002t0002g0006 others(51): Show |
54 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.884-1348C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895106 | |||||||
chr20:32895148 | C | T | 14 | a0002c0002t0001g0095 a0002c0002t0001g0130 a0002c0002t0001g0131 others(11): Show |
14 | HG02451.hp2 HG02630.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.884-1306C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895148 | |||||||
chr20:32895313 | A | AT | 13 | a0001c0001t0001g0166 a0001c0001t0001g0213 a0002c0002t0001g0269 others(10): Show |
13 | HG01109.hp1 HG01358.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.884-1119dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | ||||||
chr20:32895313 | A | ATT | 16 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0121 others(13): Show |
16 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-1120_884-1119d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | ||||||
chr20:32895313 | AT | A | 66 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0150 others(63): Show |
66 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.884-1119delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | ||||||
chr20:32895313 | ATT | A | 48 | a0002c0002t0001g0192 a0004c0004t0001g0091 a0004c0004t0003g0060 others(45): Show |
48 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-1120_884-1119d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | ||||||
chr20:32895364 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.884-1090G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895364 | |||||||
chr20:32895571 | C | CT | 21 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0121 others(18): Show |
21 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.884-880dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895571 | ||||||
chr20:32895571 | C | CTT | 6 | a0003c0003t0001g0125 a0003c0003t0001g0167 a0003c0003t0001g0203 others(3): Show |
6 | HG01981.hp2 NA18966.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.884-881_884-880dup others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895571 | ||||||
chr20:32895575 | C | T | 29 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0121 others(26): Show |
29 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.884-879C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895575 | |||||||
chr20:32895579 | T | C | 1 | a0038c0044t0002g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.884-875T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895579 | |||||||
chr20:32895608 | A | G | 171 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0002g0059 others(168): Show |
173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.884-846A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895608 | |||||||
chr20:32895633 | G | A | 2 | a0011c0009t0004g0252 a0026c0028t0005g0260 |
2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.884-821G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895633 | |||||||
chr20:32895672 | AG | A | 8 | a0004c0004t0003g0061 a0004c0004t0003g0068 a0004c0004t0003g0074 others(5): Show |
8 | HG00741.hp2 HG01255.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-781delG | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895672 | |||||||
chr20:32895732 | C | T | 1 | a0004c0004t0003g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.884-722C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895732 | |||||||
chr20:32895847 | A | C | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-607A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895847 | |||||||
chr20:32895861 | G | A | 6 | a0002c0002t0001g0121 a0003c0003t0001g0125 a0003c0003t0001g0167 others(3): Show |
6 | NA18966.hp1 NA19007.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.884-593G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895861 | |||||||
chr20:32895900 | G | T | 89 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0002g0059 others(86): Show |
89 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.884-554G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895900 | |||||||
chr20:32896174 | C | T | 68 | a0001c0001t0002g0059 a0002c0002t0001g0263 a0002c0002t0002g0005 others(65): Show |
68 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(65): Show |
intron_variant | MODIFIER | c.884-280C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896174 | |||||||
chr20:32896283 | G | A | 3 | a0007c0006t0001g0238 a0007c0006t0001g0249 a0007c0006t0004g0201 |
3 | HG03041.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.884-171G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896283 | |||||||
chr20:32896289 | C | T | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.884-165C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896289 | |||||||
chr20:32896380 | C | T | 13 | a0014c0019t0005g0221 a0014c0019t0005g0233 a0014c0019t0005g0234 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.884-74C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896380 | |||||||
chr20:32896611 | T | A | 36 | a0002c0002t0001g0192 a0004c0004t0001g0091 a0004c0004t0003g0060 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.957+84T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896611 | |||||||
chr20:32896713 | G | A | 1 | a0025c0027t0003g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.957+186G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896713 | |||||||
chr20:32896765 | G | T | 13 | a0014c0019t0005g0221 a0014c0019t0005g0233 a0014c0019t0005g0234 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+238G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896765 | |||||||
chr20:32896941 | G | A | 13 | a0014c0019t0005g0221 a0014c0019t0005g0233 a0014c0019t0005g0234 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+414G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896941 | |||||||
chr20:32897137 | T | C | 1 | a0005c0035t0001g0097 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.957+610T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897137 | |||||||
chr20:32897302 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.957+775G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897302 | |||||||
chr20:32897308 | G | A | 13 | a0014c0019t0005g0221 a0014c0019t0005g0233 a0014c0019t0005g0234 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+781G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897308 | |||||||
chr20:32897344 | C | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(8): Show |
13 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.957+817C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897344 | |||||||
chr20:32897348 | G | A | 22 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0121 others(19): Show |
22 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.957+821G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897348 | |||||||
chr20:32897430 | C | T | 1 | a0004c0004t0003g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.957+903C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897430 | |||||||
chr20:32897434 | A | G | 5 | a0014c0019t0005g0233 a0014c0019t0005g0234 a0017c0018t0005g0231 others(2): Show |
5 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+907A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897434 | |||||||
chr20:32897439 | C | CT | 62 | a0001c0001t0001g0156 a0001c0001t0002g0059 a0002c0002t0002g0005 others(59): Show |
62 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.957+929dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr20 | 32897439 | ||||||
chr20:32897439 | CT | C | 12 | a0001c0001t0001g0126 a0001c0001t0001g0188 a0001c0001t0002g0030 others(9): Show |
12 | HG00423.hp1 HG00621.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.957+929delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr20 | 32897439 | ||||||
chr20:32897473 | T | G | 60 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0121 others(57): Show |
60 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.957+946T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897473 | |||||||
chr20:32897526 | T | G | 1 | a0014c0019t0005g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-967T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897526 | |||||||
chr20:32897529 | A | G | 2 | a0003c0003t0001g0175 a0003c0003t0001g0176 |
2 | NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.958-964A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897529 | |||||||
chr20:32897591 | A | C | 2 | a0002c0046t0003g0235 a0041c0049t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.958-902A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897591 | |||||||
chr20:32897770 | G | A | 6 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(3): Show |
6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-723G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897770 | |||||||
chr20:32897811 | G | C | 2 | a0003c0003t0001g0132 a0007c0030t0004g0129 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.958-682G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897811 | |||||||
chr20:32897814 | A | G | 3 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0075 |
3 | HG01175.hp1 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.958-679A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897814 | |||||||
chr20:32898034 | C | A | 167 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0002 others(164): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.958-459C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898034 | |||||||
chr20:32898035 | G | A | 1 | a0001c0052t0001g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.958-458G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898035 | |||||||
chr20:32898052 | A | G | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-441A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898052 | |||||||
chr20:32898154 | A | G | 3 | a0007c0006t0001g0238 a0007c0006t0001g0249 a0007c0006t0004g0201 |
3 | HG03041.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.958-339A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898154 | |||||||
chr20:32898206 | G | A | 13 | a0014c0019t0005g0221 a0014c0019t0005g0233 a0014c0019t0005g0234 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.958-287G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898206 | |||||||
chr20:32898221 | C | T | 1 | a0035c0058t0002g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.958-272C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898221 | |||||||
chr20:32898245 | C | T | 148 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0002 others(145): Show |
150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.958-248C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898245 | |||||||
chr20:32898263 | A | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.958-230A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898263 | |||||||
chr20:32898400 | A | G | 148 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0002 others(145): Show |
150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.958-93A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898400 | |||||||
chr20:32898657 | G | A | 1 | a0009c0015t0001g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1088+34G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32898657 | |||||||
chr20:32898753 | T | C | 64 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0002c0002t0001g0121 others(61): Show |
64 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1088+130T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32898753 | |||||||
chr20:32898802 | C | T | 13 | a0002c0002t0001g0263 a0003c0003t0001g0132 a0007c0030t0004g0129 others(10): Show |
13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1088+179C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32898802 | |||||||
chr20:32899022 | A | G | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+399A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899022 | |||||||
chr20:32899107 | C | G | 1 | a0050c0038t0002g0262 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1088+484C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899107 | |||||||
chr20:32899107 | C | T | 1 | a0016c0051t0003g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1088+484C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899107 | |||||||
chr20:32899162 | G | A | 2 | a0002c0011t0001g0102 a0043c0050t0002g0220 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1088+539G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899162 | |||||||
chr20:32899229 | C | CAAT | 24 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(21): Show |
24 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1088+631_1088+633d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32899229 | ||||||
chr20:32899229 | CAAT | C | 81 | a0002c0002t0001g0095 a0002c0002t0001g0130 a0002c0002t0001g0131 others(78): Show |
81 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.1088+631_1088+633d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32899229 | ||||||
chr20:32899266 | G | A | 1 | a0035c0058t0002g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1088+643G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899266 | |||||||
chr20:32899297 | C | T | 3 | a0002c0046t0003g0235 a0016c0026t0001g0281 a0041c0049t0001g0199 |
3 | HG01109.hp2 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1088+674C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899297 | |||||||
chr20:32899338 | G | A | 1 | a0004c0004t0003g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1088+715G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899338 | |||||||
chr20:32899404 | C | CA | 74 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0192 others(71): Show |
76 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1088+798dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32899404 | ||||||
chr20:32899417 | A | G | 14 | a0002c0002t0001g0121 a0002c0002t0001g0263 a0003c0003t0001g0125 others(11): Show |
14 | HG01109.hp2 HG01123.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1088+794A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899417 | |||||||
chr20:32899423 | A | G | 1 | a0002c0002t0004g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1088+800A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899423 | |||||||
chr20:32899622 | T | C | 2 | a0002c0011t0001g0102 a0043c0050t0002g0220 |
2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1088+999T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899622 | |||||||
chr20:32899637 | C | T | 1 | a0014c0019t0005g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1088+1014C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899637 | |||||||
chr20:32899735 | C | T | 33 | a0002c0002t0001g0192 a0004c0004t0001g0091 a0004c0004t0003g0060 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1088+1112C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899735 | |||||||
chr20:32900415 | C | G | 4 | a0004c0004t0003g0078 a0006c0005t0003g0077 a0006c0005t0003g0079 others(1): Show |
4 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088+1792C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900415 | |||||||
chr20:32900517 | T | C | 161 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(158): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1088+1894T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900517 | |||||||
chr20:32900555 | A | C | 1 | a0021c0062t0001g0073 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1088+1932A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900555 | |||||||
chr20:32900590 | C | T | 80 | a0002c0002t0001g0095 a0002c0002t0001g0130 a0002c0002t0001g0131 others(77): Show |
80 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.1088+1967C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900590 | |||||||
chr20:32900615 | G | A | 1 | a0011c0009t0004g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1088+1992G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900615 | |||||||
chr20:32900654 | C | T | 12 | a0002c0002t0003g0273 a0002c0002t0003g0274 a0014c0019t0005g0221 others(9): Show |
12 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1088+2031C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900654 | |||||||
chr20:32900660 | G | A | 33 | a0002c0002t0001g0192 a0004c0004t0001g0091 a0004c0004t0003g0060 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1088+2037G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900660 | |||||||
chr20:32900790 | G | A | 3 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 |
3 | HG02486.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1088+2167G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900790 | |||||||
chr20:32900848 | G | C | 102 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(99): Show |
104 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.1088+2225G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900848 | |||||||
chr20:32900859 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1088+2236T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900859 | |||||||
chr20:32900991 | C | T | 54 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0008 others(51): Show |
54 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1088+2368C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900991 | |||||||
chr20:32901102 | G | A | 1 | a0002c0002t0003g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1088+2479G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901102 | |||||||
chr20:32901174 | T | A | 1 | a0004c0004t0003g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1088+2551T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901174 | |||||||
chr20:32901182 | G | C | 12 | a0002c0002t0003g0273 a0002c0002t0003g0274 a0014c0019t0005g0221 others(9): Show |
12 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1088+2559G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901182 | |||||||
chr20:32901488 | TCCTGATG others(64): Show |
T | 3 | a0019c0017t0007g0219 a0019c0017t0007g0229 a0019c0017t0007g0230 |
3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1088+2869_1088+293 others(75): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32901488 | ||||||
chr20:32901521 | C | T | 1 | a0003c0003t0002g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1088+2898C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901521 | |||||||
chr20:32901573 | A | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1088+2950A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901573 | |||||||
chr20:32901837 | G | A | 2 | a0002c0002t0002g0112 a0002c0002t0002g0136 |
2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1088+3214G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901837 | |||||||
chr20:32901908 | C | G | 168 | a0001c0001t0001g0215 a0002c0002t0001g0002 a0002c0002t0001g0003 others(165): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1088+3285C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901908 | |||||||
chr20:32901929 | G | A | 3 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0266 |
3 | HG02965.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1088+3306G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901929 | |||||||
chr20:32901931 | C | G | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+3308C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901931 | |||||||
chr20:32901958 | T | C | 2 | a0003c0003t0002g0137 a0003c0003t0002g0138 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1088+3335T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901958 | |||||||
chr20:32901966 | G | A | 1 | a0021c0061t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1088+3343G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901966 | |||||||
chr20:32902101 | G | A | 1 | a0002c0002t0002g0024 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1088+3478G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902101 | |||||||
chr20:32902124 | A | G | 8 | a0002c0011t0001g0102 a0003c0003t0001g0277 a0003c0003t0001g0280 others(5): Show |
8 | HG01358.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1088+3501A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902124 | |||||||
chr20:32902164 | G | A | 1 | a0001c0056t0001g0123 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1088+3541G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902164 | |||||||
chr20:32902293 | G | A | 1 | a0002c0002t0001g0270 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1088+3670G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902293 | |||||||
chr20:32902328 | G | C | 11 | a0002c0002t0001g0121 a0003c0003t0001g0125 a0003c0003t0001g0167 others(8): Show |
11 | HG01123.hp2 HG02257.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1088+3705G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902328 | |||||||
chr20:32902358 | G | T | 1 | a0041c0049t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088+3735G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902358 | |||||||
chr20:32902411 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1088+3788G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902411 | |||||||
chr20:32902419 | GACAGAGC others(10): Show |
G | 1 | a0003c0003t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1088+3797_1088+381 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902419 | |||||||
chr20:32902458 | C | A | 1 | a0035c0058t0002g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1088+3835C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902458 | |||||||
chr20:32902493 | T | C | 1 | a0035c0058t0002g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1088+3870T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902493 | |||||||
chr20:32902766 | C | T | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-3796C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902766 | |||||||
chr20:32902818 | T | C | 167 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(164): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1089-3744T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902818 | |||||||
chr20:32902828 | C | T | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-3734C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902828 | |||||||
chr20:32902878 | G | A | 2 | a0042c0067t0004g0193 a0051c0068t0004g0218 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1089-3684G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902878 | |||||||
chr20:32902922 | C | T | 1 | a0011c0009t0004g0124 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1089-3640C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902922 | |||||||
chr20:32903172 | C | T | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-3390C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903172 | |||||||
chr20:32903279 | C | T | 1 | a0018c0014t0002g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1089-3283C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903279 | |||||||
chr20:32903305 | A | C | 1 | a0003c0003t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-3257A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903305 | |||||||
chr20:32903353 | C | T | 3 | a0001c0001t0005g0222 a0005c0036t0004g0183 a0046c0054t0004g0101 |
3 | HG03471.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1089-3209C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903353 | |||||||
chr20:32903368 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1089-3194C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903368 | |||||||
chr20:32903433 | C | T | 1 | a0010c0010t0006g0051 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1089-3129C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903433 | |||||||
chr20:32903495 | G | C | 34 | a0002c0002t0001g0192 a0004c0004t0001g0091 a0004c0004t0003g0060 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1089-3067G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903495 | |||||||
chr20:32903551 | G | A | 1 | a0011c0009t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1089-3011G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903551 | |||||||
chr20:32903605 | C | T | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-2957C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903605 | |||||||
chr20:32903712 | G | C | 2 | a0002c0011t0001g0247 a0002c0011t0001g0248 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1089-2850G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903712 | |||||||
chr20:32903785 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1089-2777A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903785 | |||||||
chr20:32903813 | A | G | 4 | a0004c0004t0003g0078 a0006c0005t0003g0077 a0006c0005t0003g0079 others(1): Show |
4 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2749A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903813 | |||||||
chr20:32903933 | C | T | 1 | a0018c0014t0002g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1089-2629C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903933 | |||||||
chr20:32904019 | G | T | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-2543G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904019 | |||||||
chr20:32904166 | A | T | 1 | a0003c0003t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-2396A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904166 | |||||||
chr20:32904318 | G | T | 13 | a0002c0002t0001g0121 a0002c0002t0001g0263 a0003c0003t0001g0125 others(10): Show |
13 | HG01123.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1089-2244G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904318 | |||||||
chr20:32904375 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0244 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1089-2187A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904375 | |||||||
chr20:32904567 | G | A | 167 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(164): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1089-1995G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904567 | |||||||
chr20:32904603 | C | CT | 23 | a0001c0001t0001g0108 a0002c0002t0001g0002 a0002c0002t0001g0003 others(20): Show |
25 | HG01243.hp1 HG01346.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1089-1938dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32904603 | ||||||
chr20:32904603 | CT | C | 102 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0146 others(99): Show |
102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1089-1938delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32904603 | ||||||
chr20:32904629 | C | CG | 3 | a0002c0002t0001g0121 a0007c0030t0004g0129 a0010c0010t0006g0032 |
3 | HG03098.hp1 NA19058.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1089-1931dupG | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32904629 | ||||||
chr20:32904635 | C | G | 1 | a0002c0002t0001g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1089-1927C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904635 | |||||||
chr20:32904636 | G | C | 69 | a0002c0002t0001g0095 a0002c0002t0001g0130 a0002c0002t0001g0131 others(66): Show |
69 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.1089-1926G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904636 | |||||||
chr20:32904642 | G | A | 1 | a0002c0002t0003g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1089-1920G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904642 | |||||||
chr20:32904712 | C | T | 1 | a0009c0023t0001g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1089-1850C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904712 | |||||||
chr20:32904713 | A | G | 168 | a0001c0001t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(165): Show |
171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1089-1849A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904713 | |||||||
chr20:32904815 | C | T | 1 | a0002c0002t0002g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1089-1747C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904815 | |||||||
chr20:32904847 | G | T | 1 | a0002c0002t0002g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1089-1715G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904847 | |||||||
chr20:32904869 | C | T | 2 | a0018c0014t0002g0044 a0048c0039t0002g0045 |
2 | NA18950.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1089-1693C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904869 | |||||||
chr20:32904906 | C | T | 1 | a0008c0007t0003g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1089-1656C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904906 | |||||||
chr20:32904941 | A | T | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-1621A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904941 | |||||||
chr20:32904965 | G | A | 1 | a0008c0007t0003g0279 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1089-1597G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904965 | |||||||
chr20:32905137 | C | T | 3 | a0001c0001t0005g0222 a0005c0036t0004g0183 a0046c0054t0004g0101 |
3 | HG03471.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1089-1425C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905137 | |||||||
chr20:32905439 | T | C | 1 | a0035c0058t0002g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1089-1123T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905439 | |||||||
chr20:32905444 | C | T | 1 | a0003c0003t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-1118C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905444 | |||||||
chr20:32905445 | T | C | 1 | a0003c0003t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-1117T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905445 | |||||||
chr20:32905614 | G | A | 58 | a0002c0002t0001g0192 a0002c0011t0001g0102 a0002c0042t0001g0200 others(55): Show |
58 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1089-948G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905614 | |||||||
chr20:32905637 | G | C | 1 | a0007c0006t0001g0184 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1089-925G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905637 | |||||||
chr20:32905759 | C | CAA | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-790_1089-789d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | ||||||
chr20:32905759 | C | CAAAAAAA others(6): Show |
32 | a0002c0002t0001g0095 a0002c0002t0001g0130 a0002c0002t0001g0131 others(29): Show |
32 | HG01168.hp1 HG01243.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1089-801_1089-789d others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | ||||||
chr20:32905759 | C | CAAAAAAA others(7): Show |
61 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0271 others(58): Show |
63 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1089-802_1089-789d others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | ||||||
chr20:32905759 | C | CAAAAAAA others(8): Show |
45 | a0002c0002t0001g0192 a0002c0002t0001g0263 a0002c0002t0001g0269 others(42): Show |
45 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1089-789_1089-788i others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | ||||||
chr20:32905759 | C | CAAAAAAA others(9): Show |
17 | a0002c0002t0001g0121 a0003c0003t0001g0167 a0004c0004t0003g0086 others(14): Show |
17 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1089-789_1089-788i others(18): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | ||||||
chr20:32905759 | C | CAAAAAAA others(10): Show |
3 | a0003c0003t0001g0125 a0003c0003t0001g0203 a0009c0023t0001g0127 |
3 | HG02886.hp2 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1089-789_1089-788i others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | ||||||
chr20:32905759 | C | CAAAAAAA others(11): Show |
2 | a0005c0035t0001g0097 a0020c0025t0001g0195 |
2 | HG01123.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1089-789_1089-788i others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | ||||||
chr20:32905793 | G | A | 1 | a0004c0004t0003g0060 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1089-769G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905793 | |||||||
chr20:32905802 | T | C | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-760T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905802 | |||||||
chr20:32905911 | A | G | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-651A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905911 | |||||||
chr20:32905960 | T | A | 1 | a0003c0003t0001g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-602T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905960 | |||||||
chr20:32906202 | C | T | 9 | a0014c0019t0005g0221 a0014c0019t0005g0233 a0014c0019t0005g0234 others(6): Show |
9 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1089-360C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32906202 | |||||||
chr20:32906354 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1089-208C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32906354 | |||||||
chr20:32906558 | G | A | 1 | a0002c0002t0002g0049 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.1089-4G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32906558 | |||||||
chr20:32907109 | G | C | 54 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0008 others(51): Show |
54 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1308+115G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907109 | |||||||
chr20:32907119 | G | A | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+125G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907119 | |||||||
chr20:32907148 | C | T | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+154C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907148 | |||||||
chr20:32907157 | T | C | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+163T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907157 | |||||||
chr20:32907350 | G | A | 6 | a0002c0042t0001g0200 a0009c0015t0001g0098 a0009c0015t0001g0100 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+356G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907350 | |||||||
chr20:32907375 | G | A | 1 | a0015c0020t0003g0256 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1308+381G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907375 | |||||||
chr20:32907441 | C | A | 1 | a0001c0001t0002g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1308+447C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907441 | |||||||
chr20:32907519 | G | A | 1 | a0002c0002t0002g0019 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1308+525G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907519 | |||||||
chr20:32907796 | C | G | 39 | a0002c0002t0001g0192 a0002c0042t0001g0200 a0004c0004t0001g0091 others(36): Show |
39 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1309-479C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907796 | |||||||
chr20:32907904 | G | T | 6 | a0002c0002t0001g0121 a0003c0003t0001g0125 a0003c0003t0001g0167 others(3): Show |
6 | NA18966.hp1 NA19007.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-371G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907904 | |||||||
chr20:32908167 | C | T | 1 | a0044c0045t0007g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1309-108C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908167 | |||||||
chr20:32908171 | C | T | 33 | a0002c0002t0001g0192 a0004c0004t0001g0091 a0004c0004t0003g0060 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1309-104C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908171 | |||||||
chr20:32908202 | C | T | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1309-73C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908202 | |||||||
chr20:32908257 | C | G | 14 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(11): Show |
16 | HG01261.hp2 HG01361.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1309-18C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908257 | |||||||
chr20:32908528 | C | T | 10 | a0002c0002t0001g0121 a0003c0003t0001g0125 a0003c0003t0001g0167 others(7): Show |
10 | HG01123.hp2 HG02257.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1446+116C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908528 | |||||||
chr20:32908602 | G | T | 1 | a0007c0030t0004g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1446+190G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908602 | |||||||
chr20:32908691 | G | A | 2 | a0002c0002t0002g0112 a0002c0002t0002g0136 |
2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1446+279G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908691 | |||||||
chr20:32908864 | G | A | 1 | a0018c0014t0002g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1446+452G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908864 | |||||||
chr20:32908996 | G | T | 1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1446+584G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908996 | |||||||
chr20:32909012 | G | T | 5 | a0002c0002t0001g0121 a0005c0013t0004g0099 a0009c0041t0001g0253 others(2): Show |
5 | HG01109.hp2 HG02109.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+600G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909012 | |||||||
chr20:32909094 | G | A | 147 | a0001c0001t0001g0174 a0001c0001t0005g0222 a0002c0002t0001g0121 others(144): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1446+682G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909094 | |||||||
chr20:32909125 | C | T | 37 | a0002c0002t0001g0192 a0002c0002t0002g0008 a0002c0002t0002g0014 others(34): Show |
37 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1447-696C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909125 | |||||||
chr20:32909221 | G | C | 3 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 |
3 | HG02486.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1447-600G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909221 | |||||||
chr20:32909465 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1447-356A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909465 | |||||||
chr20:32909515 | G | A | 1 | a0041c0049t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1447-306G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909515 | |||||||
chr20:32909562 | G | A | 19 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(16): Show |
19 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1447-259G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909562 | |||||||
chr20:32909577 | C | CTTGGAA | 7 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0266 others(4): Show |
7 | HG02145.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1447-241_1447-236d others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr20 | 32909577 | ||||||
chr20:32909606 | G | T | 1 | a0004c0004t0003g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1447-215G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909606 | |||||||
chr20:32909719 | C | T | 5 | a0012c0012t0004g0096 a0023c0024t0005g0043 a0023c0024t0005g0113 others(2): Show |
5 | HG01243.hp1 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-102C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909719 | |||||||
chr20:32909783 | C | G | 1 | a0002c0002t0002g0024 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1447-38C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909783 | |||||||
chr20:32910071 | G | A | 2 | a0017c0018t0004g0149 a0017c0018t0004g0194 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1557+140G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910071 | |||||||
chr20:32910141 | C | T | 1 | a0016c0051t0003g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1557+210C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910141 | |||||||
chr20:32910149 | A | G | 1 | a0008c0007t0003g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1557+218A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910149 | |||||||
chr20:32910205 | C | T | 1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+274C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910205 | |||||||
chr20:32910214 | G | C | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1557+283G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910214 | |||||||
chr20:32910226 | T | G | 3 | a0035c0058t0002g0259 a0045c0055t0001g0276 a0047c0057t0004g0251 |
3 | HG01261.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1557+295T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910226 | |||||||
chr20:32910354 | C | A | 144 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(141): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1557+423C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910354 | |||||||
chr20:32910654 | A | G | 1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+723A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910654 | |||||||
chr20:32910738 | C | CT | 42 | a0001c0001t0001g0106 a0001c0001t0001g0150 a0001c0001t0001g0164 others(39): Show |
42 | HG00423.hp1 HG00741.hp1 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.1558-720dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | ||||||
chr20:32910738 | C | CTT | 53 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(50): Show |
55 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.1558-721_1558-720d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | ||||||
chr20:32910738 | C | CTTT | 10 | a0002c0002t0001g0271 a0002c0002t0004g0104 a0003c0003t0002g0137 others(7): Show |
10 | HG00323.hp1 HG01123.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558-722_1558-720d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | ||||||
chr20:32910738 | CT | C | 12 | a0001c0001t0001g0090 a0001c0001t0001g0157 a0001c0001t0001g0244 others(9): Show |
12 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1558-720delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | ||||||
chr20:32910738 | CTTTTTTT others(5): Show |
C | 1 | a0002c0042t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-731_1558-720d others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | ||||||
chr20:32910771 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1558-709C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910771 | |||||||
chr20:32910780 | G | A | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1558-700G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910780 | |||||||
chr20:32910792 | G | A | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1558-688G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910792 | |||||||
chr20:32910841 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1558-639G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910841 | |||||||
chr20:32911013 | C | T | 32 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(29): Show |
32 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1558-467C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911013 | |||||||
chr20:32911020 | G | A | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1558-460G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911020 | |||||||
chr20:32911164 | C | T | 4 | a0004c0004t0003g0087 a0035c0058t0002g0259 a0045c0055t0001g0276 others(1): Show |
4 | HG01123.hp1 HG01261.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-316C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911164 | |||||||
chr20:32911385 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1558-95T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911385 | |||||||
chr20:32911393 | G | T | 3 | a0035c0058t0002g0259 a0045c0055t0001g0276 a0047c0057t0004g0251 |
3 | HG01261.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1558-87G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911393 | |||||||
chr20:32911739 | C | T | 1 | a0002c0042t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1785+32C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32911739 | |||||||
chr20:32911769 | T | A | 3 | a0035c0058t0002g0259 a0045c0055t0001g0276 a0047c0057t0004g0251 |
3 | HG01261.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1785+62T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32911769 | |||||||
chr20:32911897 | G | A | 3 | a0002c0002t0001g0223 a0002c0002t0001g0236 a0002c0002t0001g0237 |
3 | HG02451.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1785+190G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32911897 | |||||||
chr20:32912000 | A | G | 4 | a0002c0002t0003g0264 a0002c0002t0003g0265 a0002c0002t0003g0267 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785+293A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912000 | |||||||
chr20:32912004 | G | A | 1 | a0004c0004t0003g0255 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1785+297G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912004 | |||||||
chr20:32912147 | G | A | 2 | a0009c0015t0001g0100 a0009c0015t0001g0114 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1785+440G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912147 | |||||||
chr20:32912301 | C | T | 12 | a0002c0002t0003g0273 a0002c0002t0003g0274 a0002c0011t0001g0102 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1786-493C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912301 | |||||||
chr20:32912386 | C | T | 2 | a0002c0011t0001g0247 a0002c0011t0001g0248 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1786-408C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912386 | |||||||
chr20:32912398 | C | T | 2 | a0022c0031t0002g0198 a0022c0031t0002g0232 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1786-396C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912398 | |||||||
chr20:32912430 | C | CA | 27 | a0001c0001t0002g0139 a0003c0003t0001g0147 a0003c0003t0001g0175 others(24): Show |
27 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1786-349dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr20 | 32912430 | ||||||
chr20:32912444 | AAG | A | 74 | a0002c0002t0001g0121 a0002c0002t0001g0192 a0002c0002t0002g0005 others(71): Show |
74 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1786-348_1786-347d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr20 | 32912444 | ||||||
chr20:32912445 | AG | A | 61 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(58): Show |
63 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(60): Show |
intron_variant | MODIFIER | c.1786-348delG | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912445 | |||||||
chr20:32912446 | G | A | 33 | a0002c0011t0001g0102 a0002c0042t0001g0200 a0005c0013t0001g0202 others(30): Show |
33 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1786-348G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912446 | |||||||
chr20:32912449 | G | A | 143 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(140): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1786-345G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912449 | |||||||
chr20:32912572 | A | G | 1 | a0002c0042t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1786-222A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912572 | |||||||
chr20:32912613 | C | G | 2 | a0004c0004t0003g0069 a0036c0059t0003g0072 |
2 | HG01516.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1786-181C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912613 | |||||||
chr20:32912755 | G | A | 1 | a0041c0049t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1786-39G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912755 | |||||||
chr20:32912918 | C | T | 3 | a0014c0019t0005g0221 a0042c0067t0004g0193 a0051c0068t0004g0218 |
3 | HG01884.hp2 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1856+54C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32912918 | |||||||
chr20:32913016 | C | A | 1 | a0007c0006t0004g0144 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1856+152C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913016 | |||||||
chr20:32913018 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1856+154T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913018 | |||||||
chr20:32913314 | A | C | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1856+450A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913314 | |||||||
chr20:32913365 | G | T | 1 | a0014c0019t0005g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1856+501G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913365 | |||||||
chr20:32913473 | G | A | 1 | a0034c0063t0004g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1856+609G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913473 | |||||||
chr20:32913479 | A | G | 46 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(43): Show |
48 | HG00323.hp1 HG01123.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1856+615A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913479 | |||||||
chr20:32913573 | C | G | 3 | a0001c0001t0004g0050 a0003c0003t0001g0125 a0005c0008t0004g0207 |
3 | NA18968.hp1 NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1856+709C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913573 | |||||||
chr20:32913678 | AAATGCCC others(27): Show |
A | 32 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(29): Show |
34 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1856+816_1856+849d others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32913678 | ||||||
chr20:32913998 | G | T | 1 | a0004c0004t0003g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1856+1134G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913998 | |||||||
chr20:32914255 | T | C | 2 | a0008c0007t0006g0015 a0008c0007t0006g0046 |
2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1856+1391T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914255 | |||||||
chr20:32914336 | G | A | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1856+1472G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914336 | |||||||
chr20:32914526 | A | C | 72 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(69): Show |
74 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1856+1662A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914526 | |||||||
chr20:32914553 | G | C | 164 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(161): Show |
166 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1856+1689G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914553 | |||||||
chr20:32914591 | A | C | 1 | a0038c0044t0002g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1856+1727A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914591 | |||||||
chr20:32914601 | G | A | 6 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1856+1737G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914601 | |||||||
chr20:32914751 | A | C | 161 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(158): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1856+1887A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914751 | |||||||
chr20:32914900 | A | AT | 34 | a0002c0002t0003g0273 a0002c0002t0003g0274 a0002c0011t0001g0102 others(31): Show |
34 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1856+2046dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32914900 | ||||||
chr20:32914900 | A | ATT | 14 | a0011c0009t0001g0250 a0011c0009t0004g0122 a0011c0009t0004g0124 others(11): Show |
14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1856+2045_1856+204 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32914900 | ||||||
chr20:32915076 | A | T | 155 | a0001c0001t0001g0117 a0001c0001t0001g0171 a0002c0002t0001g0002 others(152): Show |
157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1856+2212A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915076 | |||||||
chr20:32915077 | T | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0009g0116 |
3 | HG01070.hp2 NA18951.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1856+2213T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915077 | |||||||
chr20:32915158 | C | T | 2 | a0001c0001t0001g0162 a0005c0008t0001g0216 |
2 | NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1857-2143C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915158 | |||||||
chr20:32915193 | C | T | 1 | a0008c0007t0003g0279 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1857-2108C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915193 | |||||||
chr20:32915307 | T | C | 12 | a0002c0002t0003g0273 a0002c0002t0003g0274 a0002c0011t0001g0102 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1857-1994T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915307 | |||||||
chr20:32915559 | C | T | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-1742C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915559 | |||||||
chr20:32915569 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1857-1732C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915569 | |||||||
chr20:32915637 | C | T | 75 | a0002c0002t0001g0121 a0002c0002t0001g0192 a0002c0002t0002g0005 others(72): Show |
75 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1857-1664C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915637 | |||||||
chr20:32915672 | C | CT | 23 | a0001c0001t0001g0163 a0001c0001t0002g0054 a0006c0005t0003g0066 others(20): Show |
23 | HG00423.hp1 HG00423.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1857-1612dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32915672 | ||||||
chr20:32915672 | CT | C | 17 | a0001c0001t0001g0106 a0001c0001t0001g0169 a0001c0001t0001g0214 others(14): Show |
17 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1857-1612delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32915672 | ||||||
chr20:32915676 | T | C | 4 | a0001c0001t0001g0146 a0001c0001t0001g0158 a0001c0001t0001g0178 others(1): Show |
4 | HG00323.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857-1625T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915676 | |||||||
chr20:32915760 | G | A | 3 | a0020c0025t0001g0195 a0022c0031t0002g0198 a0022c0031t0002g0232 |
3 | HG01167.hp2 HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1857-1541G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915760 | |||||||
chr20:32915765 | G | A | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-1536G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915765 | |||||||
chr20:32915879 | G | A | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1857-1422G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915879 | |||||||
chr20:32915917 | C | T | 4 | a0004c0004t0003g0255 a0008c0007t0006g0015 a0008c0007t0006g0018 others(1): Show |
4 | HG00733.hp1 HG01168.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857-1384C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915917 | |||||||
chr20:32915965 | C | T | 3 | a0002c0002t0001g0095 a0002c0002t0004g0103 a0002c0002t0004g0104 |
3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1857-1336C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915965 | |||||||
chr20:32915999 | C | T | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-1302C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915999 | |||||||
chr20:32916490 | C | T | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1857-811C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32916490 | |||||||
chr20:32916661 | G | A | 1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1857-640G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32916661 | |||||||
chr20:32917013 | C | G | 1 | a0002c0002t0002g0041 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1857-288C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917013 | |||||||
chr20:32917014 | C | G | 1 | a0003c0003t0001g0212 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1857-287C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917014 | |||||||
chr20:32917032 | T | G | 1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1857-269T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917032 | |||||||
chr20:32917206 | C | T | 41 | a0002c0002t0001g0121 a0002c0002t0001g0192 a0002c0002t0002g0005 others(38): Show |
41 | HG01099.hp2 HG01258.hp1 HG01515.hp1 others(38): Show |
intron_variant | MODIFIER | c.1857-95C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917206 | |||||||
chr20:32917226 | G | A | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-75G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917226 | |||||||
chr20:32917548 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2061+43C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917548 | |||||||
chr20:32917718 | C | T | 1 | a0004c0004t0001g0091 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2061+213C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917718 | |||||||
chr20:32917942 | G | A | 3 | a0001c0001t0001g0162 a0005c0008t0001g0216 a0016c0026t0001g0281 |
3 | HG01109.hp2 NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2062-420G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917942 | |||||||
chr20:32917969 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2062-393C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917969 | |||||||
chr20:32918234 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2062-128G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32918234 | |||||||
chr20:32918309 | A | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2062-53A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32918309 | |||||||
chr20:32918623 | G | A | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2274+49G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918623 | |||||||
chr20:32918626 | G | A | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2274+52G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918626 | |||||||
chr20:32918858 | C | G | 1 | a0006c0005t0003g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2274+284C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918858 | |||||||
chr20:32918883 | A | G | 1 | a0002c0046t0003g0235 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2274+309A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918883 | |||||||
chr20:32918916 | G | T | 1 | a0002c0002t0001g0121 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2274+342G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918916 | |||||||
chr20:32919056 | C | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0211 a0001c0052t0001g0187 |
3 | HG01071.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2274+482C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919056 | |||||||
chr20:32919087 | G | A | 23 | a0002c0042t0001g0200 a0011c0009t0001g0250 a0011c0009t0004g0122 others(20): Show |
23 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.2274+513G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919087 | |||||||
chr20:32919091 | A | C | 4 | a0023c0024t0005g0043 a0023c0024t0005g0113 a0034c0063t0004g0083 others(1): Show |
4 | HG01243.hp1 HG01346.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2274+517A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919091 | |||||||
chr20:32919125 | C | T | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2274+551C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919125 | |||||||
chr20:32919341 | A | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-737A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919341 | |||||||
chr20:32919468 | G | A | 1 | a0021c0061t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2275-610G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919468 | |||||||
chr20:32919566 | C | T | 10 | a0011c0009t0004g0122 a0011c0009t0004g0124 a0011c0009t0004g0252 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2275-512C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919566 | |||||||
chr20:32919640 | G | A | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-438G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919640 | |||||||
chr20:32919669 | T | C | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2275-409T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919669 | |||||||
chr20:32919824 | G | T | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-254G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919824 | |||||||
chr20:32919956 | C | G | 162 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(159): Show |
164 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2275-122C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919956 | |||||||
chr20:32919979 | T | C | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-99T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919979 | |||||||
chr20:32920025 | A | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-53A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32920025 | |||||||
chr20:32920346 | T | G | 19 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(16): Show |
19 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.2412+131T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920346 | |||||||
chr20:32920403 | G | T | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+188G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920403 | |||||||
chr20:32920419 | G | A | 1 | a0002c0002t0002g0029 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2412+204G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920419 | |||||||
chr20:32920483 | T | C | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+268T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920483 | |||||||
chr20:32920526 | G | A | 1 | a0014c0019t0005g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2412+311G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920526 | |||||||
chr20:32920563 | A | G | 1 | a0005c0008t0001g0004 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2412+348A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920563 | |||||||
chr20:32920580 | CGGAAACC others(3): Show |
C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0154 |
2 | HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2412+367_2412+376d others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32920580 | ||||||
chr20:32920605 | A | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+390A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920605 | |||||||
chr20:32920648 | G | A | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+433G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920648 | |||||||
chr20:32920720 | A | G | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+505A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920720 | |||||||
chr20:32920747 | C | G | 2 | a0008c0007t0006g0015 a0008c0007t0006g0046 |
2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2412+532C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920747 | |||||||
chr20:32921009 | A | C | 19 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(16): Show |
19 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.2412+794A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921009 | |||||||
chr20:32921153 | G | A | 1 | a0010c0010t0006g0032 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2412+938G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921153 | |||||||
chr20:32921196 | CTCT | C | 14 | a0011c0009t0001g0250 a0011c0009t0004g0122 a0011c0009t0004g0124 others(11): Show |
14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2412+982_2412+984d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921196 | |||||||
chr20:32921201 | C | CTT | 6 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(3): Show |
6 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2412+994_2412+995d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921201 | ||||||
chr20:32921201 | C | T | 14 | a0011c0009t0001g0250 a0011c0009t0004g0122 a0011c0009t0004g0124 others(11): Show |
14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2412+986C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921201 | |||||||
chr20:32921222 | G | A | 14 | a0011c0009t0001g0250 a0011c0009t0004g0122 a0011c0009t0004g0124 others(11): Show |
14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2412+1007G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921222 | |||||||
chr20:32921230 | G | A | 1 | a0043c0050t0002g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2412+1015G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921230 | |||||||
chr20:32921267 | C | T | 40 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(37): Show |
42 | HG00323.hp1 HG00741.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.2412+1052C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921267 | |||||||
chr20:32921361 | T | TTG | 37 | a0001c0001t0004g0050 a0002c0002t0001g0002 a0002c0002t0001g0003 others(34): Show |
39 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.2412+1176_2412+117 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921361 | T | TTGTG | 28 | a0002c0002t0003g0264 a0002c0002t0003g0265 a0002c0002t0003g0267 others(25): Show |
28 | HG00733.hp1 HG00741.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+1174_2412+117 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921361 | T | TTGTGTG | 26 | a0002c0002t0003g0273 a0002c0002t0003g0274 a0003c0003t0001g0132 others(23): Show |
26 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2412+1172_2412+117 others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921361 | T | TTGTGTGT others(1): Show |
26 | a0004c0004t0001g0091 a0004c0004t0003g0087 a0004c0004t0003g0088 others(23): Show |
26 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2412+1170_2412+117 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921361 | T | TTGTGTGT others(3): Show |
4 | a0004c0004t0003g0069 a0008c0007t0003g0278 a0008c0007t0003g0279 others(1): Show |
4 | HG01516.hp1 HG01975.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2412+1168_2412+117 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921361 | T | TTGTGTGT others(5): Show |
5 | a0004c0004t0003g0060 a0006c0005t0003g0077 a0006c0005t0003g0079 others(2): Show |
5 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2412+1166_2412+117 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921361 | TTG | T | 5 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(2): Show |
5 | HG01433.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.2412+1176_2412+117 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921361 | TTGTGTGT others(1): Show |
T | 40 | a0002c0002t0001g0121 a0002c0002t0001g0192 a0002c0002t0002g0005 others(37): Show |
40 | HG01099.hp2 HG01258.hp1 HG01515.hp1 others(37): Show |
intron_variant | MODIFIER | c.2412+1170_2412+117 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | ||||||
chr20:32921391 | G | T | 1 | a0003c0003t0002g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2412+1176G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921391 | |||||||
chr20:32921393 | T | G | 51 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0130 others(48): Show |
53 | HG00323.hp1 HG00741.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.2412+1178T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921393 | |||||||
chr20:32921394 | T | G | 1 | a0002c0002t0001g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2412+1179T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921394 | |||||||
chr20:32921416 | A | G | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+1201A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921416 | |||||||
chr20:32921431 | G | T | 159 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(156): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.2412+1216G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921431 | |||||||
chr20:32921573 | T | G | 3 | a0002c0002t0001g0223 a0002c0002t0001g0236 a0002c0002t0001g0237 |
3 | HG02451.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2412+1358T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921573 | |||||||
chr20:32921574 | A | G | 1 | a0008c0007t0003g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2412+1359A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921574 | |||||||
chr20:32921700 | C | CTT | 161 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0095 others(158): Show |
163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2412+1496_2412+149 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921700 | ||||||
chr20:32921828 | A | G | 1 | a0011c0009t0004g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2412+1613A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921828 | |||||||
chr20:32921831 | C | CT | 127 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0121 others(124): Show |
129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2412+1633dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921831 | ||||||
chr20:32921831 | CT | C | 7 | a0001c0001t0001g0120 a0001c0001t0001g0142 a0001c0001t0001g0214 others(4): Show |
7 | HG01167.hp2 HG01261.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2412+1633delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921831 | ||||||
chr20:32921832 | T | C | 1 | a0038c0044t0002g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2412+1617T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921832 | |||||||
chr20:32921836 | T | C | 1 | a0027c0029t0003g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2412+1621T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921836 | |||||||
chr20:32921853 | C | T | 1 | a0021c0062t0001g0073 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2412+1638C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921853 | |||||||
chr20:32921882 | G | A | 6 | a0005c0037t0004g0185 a0010c0010t0003g0143 a0010c0010t0006g0011 others(3): Show |
6 | HG01261.hp1 HG01943.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.2412+1667G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921882 | |||||||
chr20:32921894 | G | A | 1 | a0005c0033t0008g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2412+1679G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921894 | |||||||
chr20:32921983 | C | A | 1 | a0015c0020t0003g0081 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2412+1768C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921983 | |||||||
chr20:32922310 | G | A | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+2095G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32922310 | |||||||
chr20:32922393 | T | C | 2 | a0036c0059t0003g0072 a0047c0057t0004g0251 |
2 | HG01975.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2412+2178T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32922393 | |||||||
chr20:32922444 | C | T | 140 | a0001c0001t0001g0245 a0002c0002t0001g0002 a0002c0002t0001g0003 others(137): Show |
142 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.2412+2229C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32922444 | |||||||
chr20:32922813 | T | TTC | 26 | a0002c0002t0001g0227 a0002c0002t0001g0263 a0006c0005t0003g0066 others(23): Show |
26 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2412+2612_2412+261 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32922813 | ||||||
chr20:32923029 | A | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+2814A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923029 | |||||||
chr20:32923150 | C | T | 1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2412+2935C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923150 | |||||||
chr20:32923166 | A | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+2951A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923166 | |||||||
chr20:32923303 | C | T | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2412+3088C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923303 | |||||||
chr20:32923314 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+3099C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923314 | |||||||
chr20:32923763 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0244 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2412+3548G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923763 | |||||||
chr20:32923772 | G | A | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2412+3557G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923772 | |||||||
chr20:32923896 | A | C | 78 | a0002c0002t0001g0192 a0002c0002t0002g0005 a0002c0002t0002g0006 others(75): Show |
78 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.2412+3681A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923896 | |||||||
chr20:32923974 | C | G | 26 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(23): Show |
28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+3759C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923974 | |||||||
chr20:32924106 | T | C | 1 | a0008c0007t0006g0018 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2412+3891T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924106 | |||||||
chr20:32924129 | T | C | 32 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(29): Show |
34 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.2412+3914T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924129 | |||||||
chr20:32924366 | A | C | 1 | a0027c0029t0003g0241 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2412+4151A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924366 | |||||||
chr20:32924457 | C | G | 26 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(23): Show |
28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+4242C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924457 | |||||||
chr20:32924479 | G | A | 26 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(23): Show |
28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+4264G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924479 | |||||||
chr20:32924632 | A | G | 26 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(23): Show |
28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+4417A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924632 | |||||||
chr20:32924698 | C | T | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2412+4483C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924698 | |||||||
chr20:32924821 | G | A | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2412+4606G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924821 | |||||||
chr20:32924923 | T | G | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2412+4708T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924923 | |||||||
chr20:32925572 | C | T | 1 | a0002c0002t0002g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2413-4826C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925572 | |||||||
chr20:32925719 | C | T | 1 | a0024c0032t0004g0275 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2413-4679C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925719 | |||||||
chr20:32925779 | C | T | 80 | a0001c0001t0005g0222 a0001c0001t0005g0257 a0001c0001t0005g0258 others(77): Show |
82 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.2413-4619C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925779 | |||||||
chr20:32925960 | G | T | 1 | a0006c0005t0003g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2413-4438G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925960 | |||||||
chr20:32926045 | C | T | 1 | a0002c0002t0002g0058 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2413-4353C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926045 | |||||||
chr20:32926073 | C | T | 7 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0001c0056t0001g0123 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2413-4325C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926073 | |||||||
chr20:32926098 | C | T | 72 | a0002c0002t0001g0192 a0002c0002t0002g0005 a0002c0002t0002g0006 others(69): Show |
72 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.2413-4300C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926098 | |||||||
chr20:32926218 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2413-4180T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926218 | |||||||
chr20:32926236 | T | G | 1 | a0009c0015t0001g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2413-4162T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926236 | |||||||
chr20:32926446 | T | C | 1 | a0033c0065t0001g0062 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2413-3952T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926446 | |||||||
chr20:32926489 | A | C | 9 | a0005c0033t0008g0115 a0019c0017t0007g0219 a0019c0017t0007g0229 others(6): Show |
9 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2413-3909A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926489 | |||||||
chr20:32926520 | T | TA | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2413-3878_2413-387 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926520 | |||||||
chr20:32926520 | T | TTA | 53 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0227 others(50): Show |
53 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.2413-3877_2413-387 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32926520 | ||||||
chr20:32926599 | C | T | 15 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0011c0009t0001g0250 others(12): Show |
15 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2413-3799C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926599 | |||||||
chr20:32926654 | TC | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-3738delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32926654 | ||||||
chr20:32926660 | C | G | 1 | a0002c0002t0002g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2413-3738C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926660 | |||||||
chr20:32926666 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG01943.hp1 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413-3732C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926666 | |||||||
chr20:32926756 | C | T | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-3642C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926756 | |||||||
chr20:32926758 | G | A | 1 | a0002c0002t0002g0008 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2413-3640G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926758 | |||||||
chr20:32926907 | T | C | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-3491T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926907 | |||||||
chr20:32926915 | G | C | 7 | a0002c0002t0003g0225 a0002c0002t0003g0264 a0002c0002t0003g0265 others(4): Show |
7 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2413-3483G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926915 | |||||||
chr20:32926960 | G | A | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-3438G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926960 | |||||||
chr20:32927405 | C | T | 3 | a0011c0009t0001g0250 a0014c0019t0005g0233 a0014c0019t0005g0234 |
3 | HG00741.hp1 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2413-2993C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927405 | |||||||
chr20:32927489 | T | C | 5 | a0005c0033t0008g0115 a0019c0017t0007g0219 a0019c0017t0007g0229 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2413-2909T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927489 | |||||||
chr20:32927591 | C | T | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2413-2807C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927591 | |||||||
chr20:32927805 | T | G | 1 | a0024c0032t0004g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2413-2593T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927805 | |||||||
chr20:32928240 | A | AT | 29 | a0001c0001t0001g0210 a0001c0001t0005g0222 a0002c0002t0001g0002 others(26): Show |
31 | HG00323.hp1 HG01123.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.2413-2145dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32928240 | ||||||
chr20:32928246 | T | A | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2413-2152T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928246 | |||||||
chr20:32928246 | T | TA | 38 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0227 others(35): Show |
38 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2413-2152_2413-215 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928246 | |||||||
chr20:32928298 | C | T | 28 | a0004c0004t0003g0060 a0004c0004t0003g0061 a0004c0004t0003g0068 others(25): Show |
28 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.2413-2100C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928298 | |||||||
chr20:32928396 | T | C | 1 | a0025c0027t0003g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2413-2002T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928396 | |||||||
chr20:32928404 | A | G | 46 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0002c0002t0001g0227 others(43): Show |
46 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.2413-1994A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928404 | |||||||
chr20:32928514 | C | G | 29 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(26): Show |
29 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2413-1884C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928514 | |||||||
chr20:32928540 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0170 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2413-1858G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928540 | |||||||
chr20:32928596 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2413-1802G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928596 | |||||||
chr20:32928597 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2413-1801C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928597 | |||||||
chr20:32928893 | AT | A | 23 | a0001c0001t0001g0117 a0001c0001t0001g0168 a0001c0001t0004g0050 others(20): Show |
23 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2413-1493delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32928893 | ||||||
chr20:32928935 | T | C | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-1463T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928935 | |||||||
chr20:32928940 | T | C | 38 | a0005c0033t0008g0115 a0006c0005t0003g0066 a0006c0005t0003g0067 others(35): Show |
38 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.2413-1458T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928940 | |||||||
chr20:32929019 | A | G | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-1379A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929019 | |||||||
chr20:32929138 | CT | C | 16 | a0001c0001t0001g0117 a0001c0001t0005g0257 a0001c0001t0005g0258 others(13): Show |
16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2413-1249delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929138 | ||||||
chr20:32929143 | T | G | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-1255T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929143 | |||||||
chr20:32929321 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2413-1077A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929321 | |||||||
chr20:32929379 | T | A | 2 | a0038c0044t0002g0204 a0043c0050t0002g0220 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2413-1019T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929379 | |||||||
chr20:32929445 | T | A | 1 | a0009c0041t0001g0253 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2413-953T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929445 | |||||||
chr20:32929454 | T | TCCCTCCC others(3): Show |
6 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(3): Show |
8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2413-940_2413-939i others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929454 | ||||||
chr20:32929459 | T | C | 6 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(3): Show |
8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2413-939T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929459 | |||||||
chr20:32929459 | T | TCCCTCCC others(3): Show |
11 | a0001c0001t0005g0222 a0002c0002t0001g0095 a0002c0002t0004g0103 others(8): Show |
11 | HG00323.hp1 HG01123.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2413-922_2413-913d others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929459 | ||||||
chr20:32929502 | G | GT | 31 | a0002c0002t0003g0265 a0005c0033t0008g0115 a0006c0005t0003g0066 others(28): Show |
31 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.2413-881dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929502 | ||||||
chr20:32929589 | G | A | 1 | a0044c0045t0007g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2413-809G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929589 | |||||||
chr20:32929594 | G | A | 19 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(16): Show |
19 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2413-804G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929594 | |||||||
chr20:32929768 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2413-630C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929768 | |||||||
chr20:32929786 | T | G | 1 | a0008c0007t0003g0278 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2413-612T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929786 | |||||||
chr20:32929857 | C | G | 8 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-541C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929857 | |||||||
chr20:32929983 | A | G | 3 | a0007c0006t0004g0144 a0007c0030t0004g0129 a0007c0030t0004g0268 |
3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2413-415A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929983 | |||||||
chr20:32930008 | C | T | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-390C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930008 | |||||||
chr20:32930035 | C | T | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-363C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930035 | |||||||
chr20:32930143 | C | T | 4 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0027 others(1): Show |
4 | NA18946.hp2 NA18950.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413-255C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930143 | |||||||
chr20:32930154 | G | T | 17 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(14): Show |
17 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2413-244G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930154 | |||||||
chr20:32930189 | C | T | 1 | a0002c0002t0002g0005 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2413-209C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930189 | |||||||
chr20:32930746 | C | G | 165 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(162): Show |
167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2631+130C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930746 | |||||||
chr20:32930747 | G | A | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2631+131G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930747 | |||||||
chr20:32930787 | C | T | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2631+171C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930787 | |||||||
chr20:32930951 | T | G | 30 | a0005c0033t0008g0115 a0006c0005t0003g0066 a0006c0005t0003g0067 others(27): Show |
30 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2632-227T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930951 | |||||||
chr20:32930978 | C | T | 1 | a0008c0007t0006g0018 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2632-200C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930978 | |||||||
chr20:32931484 | C | T | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+148C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931484 | |||||||
chr20:32931633 | T | C | 1 | a0041c0049t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2790+297T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931633 | |||||||
chr20:32931673 | G | T | 13 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(10): Show |
13 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2790+337G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931673 | |||||||
chr20:32931761 | AAAGAAAA others(6): Show |
A | 32 | a0004c0004t0003g0060 a0004c0004t0003g0061 a0004c0004t0003g0068 others(29): Show |
32 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2790+427_2790+439d others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32931761 | ||||||
chr20:32931972 | T | C | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+636T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931972 | |||||||
chr20:32932337 | G | A | 1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2790+1001G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932337 | |||||||
chr20:32932376 | C | CA | 169 | a0001c0001t0001g0117 a0001c0001t0001g0208 a0001c0001t0001g0213 others(166): Show |
171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.2790+1051dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32932376 | ||||||
chr20:32932481 | C | T | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+1145C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932481 | |||||||
chr20:32932665 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2790+1329A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932665 | |||||||
chr20:32932914 | A | G | 47 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(44): Show |
49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2790+1578A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932914 | |||||||
chr20:32933057 | T | C | 172 | a0001c0001t0001g0117 a0001c0001t0001g0208 a0001c0001t0001g0213 others(169): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2790+1721T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933057 | |||||||
chr20:32933071 | TC | T | 5 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2790+1736delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933071 | |||||||
chr20:32933177 | T | C | 1 | a0002c0002t0002g0056 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2790+1841T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933177 | |||||||
chr20:32933197 | A | G | 2 | a0002c0002t0002g0008 a0002c0002t0002g0019 |
2 | HG04204.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2790+1861A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933197 | |||||||
chr20:32933379 | C | T | 171 | a0001c0001t0001g0117 a0001c0001t0001g0208 a0001c0001t0001g0213 others(168): Show |
173 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(170): Show |
intron_variant | MODIFIER | c.2790+2043C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933379 | |||||||
chr20:32933453 | C | G | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2790+2117C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933453 | |||||||
chr20:32933587 | A | AC | 13 | a0001c0001t0001g0108 a0001c0001t0001g0158 a0001c0001t0001g0170 others(10): Show |
13 | HG01109.hp2 HG01175.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.2790+2255dupC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32933587 | ||||||
chr20:32933608 | C | T | 1 | a0004c0004t0003g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2790+2272C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933608 | |||||||
chr20:32933633 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2790+2297C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933633 | |||||||
chr20:32933645 | G | A | 5 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2790+2309G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933645 | |||||||
chr20:32933703 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2790+2367G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933703 | |||||||
chr20:32933750 | G | T | 2 | a0024c0032t0004g0064 a0024c0032t0004g0275 |
2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2790+2414G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933750 | |||||||
chr20:32933849 | G | A | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+2513G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933849 | |||||||
chr20:32933971 | C | T | 8 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+2635C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933971 | |||||||
chr20:32934013 | C | CT | 147 | a0001c0001t0001g0117 a0001c0001t0001g0158 a0001c0001t0001g0208 others(144): Show |
149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2790+2692dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934013 | ||||||
chr20:32934013 | C | CTT | 27 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(24): Show |
27 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2790+2691_2790+269 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934013 | ||||||
chr20:32934279 | A | AT | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+2951dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934279 | ||||||
chr20:32934287 | T | TC | 40 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(37): Show |
40 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.2790+2952dupC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934287 | ||||||
chr20:32934298 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2790+2962G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934298 | |||||||
chr20:32934454 | T | C | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2790+3118T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934454 | |||||||
chr20:32934547 | G | A | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+3211G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934547 | |||||||
chr20:32934617 | A | G | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2790+3281A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934617 | |||||||
chr20:32934642 | G | A | 2 | a0002c0002t0001g0130 a0002c0002t0001g0131 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2790+3306G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934642 | |||||||
chr20:32934656 | G | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01346.hp2 HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2790+3320G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934656 | |||||||
chr20:32934771 | C | T | 22 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(19): Show |
24 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.2790+3435C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934771 | |||||||
chr20:32934945 | T | C | 1 | a0014c0019t0005g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2790+3609T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934945 | |||||||
chr20:32934965 | T | C | 31 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2790+3629T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934965 | |||||||
chr20:32935098 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2790+3762C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935098 | |||||||
chr20:32935116 | G | A | 26 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(23): Show |
28 | HG00323.hp1 HG01123.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.2790+3780G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935116 | |||||||
chr20:32935172 | TTTTC | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+3856_2790+385 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935172 | ||||||
chr20:32935185 | T | TTTC | 6 | a0004c0004t0003g0060 a0004c0004t0003g0069 a0004c0004t0003g0087 others(3): Show |
6 | HG00733.hp1 HG01123.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2790+3852_2790+385 others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935185 | ||||||
chr20:32935188 | C | CT | 4 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0036 others(1): Show |
4 | HG01515.hp1 NA18946.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.2790+3855dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTT | 24 | a0001c0001t0001g0117 a0002c0002t0001g0192 a0002c0002t0002g0008 others(21): Show |
24 | HG01099.hp2 HG01169.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.2790+3854_2790+385 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTCT | 4 | a0004c0004t0003g0078 a0004c0004t0003g0191 a0027c0029t0003g0241 others(1): Show |
4 | HG00280.hp2 HG00642.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2790+3854_2790+385 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTT | 19 | a0002c0002t0002g0027 a0002c0002t0002g0035 a0002c0002t0002g0041 others(16): Show |
19 | HG01167.hp1 HG01168.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+3853_2790+385 others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTT | 12 | a0004c0004t0003g0086 a0004c0004t0003g0088 a0008c0007t0003g0196 others(9): Show |
12 | HG00741.hp2 HG01261.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTT | 7 | a0002c0002t0003g0273 a0002c0002t0003g0274 a0004c0004t0001g0091 others(4): Show |
7 | HG00280.hp1 HG01496.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(9): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(3): Show |
1 | a0019c0017t0007g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(4): Show |
3 | a0019c0017t0007g0219 a0019c0017t0007g0230 a0044c0045t0007g0135 |
3 | HG02145.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(5): Show |
1 | a0005c0033t0008g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(6): Show |
2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(9): Show |
3 | a0002c0002t0003g0264 a0002c0002t0003g0265 a0035c0058t0002g0259 |
3 | HG01261.hp2 HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(10): Show |
2 | a0002c0002t0003g0225 a0002c0002t0003g0267 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(22): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(23): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | C | CTTTTTTT others(17): Show |
1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | CTTTCTTT | C | 17 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+3856_2790+386 others(11): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | CTTTCTTT others(2): Show |
C | 7 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0248 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2790+3856_2790+386 others(13): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935188 | CTTTCTTT others(3): Show |
C | 1 | a0002c0011t0001g0247 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2790+3856_2790+386 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | ||||||
chr20:32935192 | C | CT | 20 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0148 others(17): Show |
20 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2790+3881dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTT | 12 | a0006c0005t0003g0067 a0006c0005t0003g0071 a0006c0005t0003g0077 others(9): Show |
12 | HG00639.hp2 HG01071.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2790+3878_2790+388 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTT | 6 | a0006c0005t0003g0066 a0006c0005t0003g0075 a0006c0005t0003g0076 others(3): Show |
6 | HG01175.hp1 HG02148.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.2790+3877_2790+388 others(9): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(3): Show |
1 | a0002c0002t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2790+3872_2790+388 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0005g0258 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2790+3871_2790+388 others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0005g0257 a0011c0009t0004g0252 |
2 | HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2790+3870_2790+388 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(6): Show |
1 | a0026c0028t0005g0260 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2790+3869_2790+388 others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(8): Show |
1 | a0014c0019t0005g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2790+3867_2790+388 others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(9): Show |
2 | a0011c0009t0001g0250 a0024c0032t0004g0064 |
2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2790+3866_2790+388 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(10): Show |
4 | a0011c0009t0004g0122 a0024c0032t0004g0275 a0042c0067t0004g0193 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2790+3865_2790+388 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(11): Show |
1 | a0014c0019t0005g0234 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2790+3864_2790+388 others(22): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(12): Show |
1 | a0011c0009t0005g0009 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2790+3863_2790+388 others(23): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | CTTTTTTT others(15): Show |
1 | a0014c0019t0005g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2790+3860_2790+388 others(26): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935192 | C | T | 96 | a0001c0001t0001g0117 a0001c0001t0001g0208 a0001c0001t0001g0213 others(93): Show |
96 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.2790+3856C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935192 | |||||||
chr20:32935192 | CT | C | 11 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0154 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.2790+3881delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | ||||||
chr20:32935288 | C | T | 1 | a0043c0050t0002g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2790+3952C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935288 | |||||||
chr20:32935314 | C | A | 1 | a0008c0007t0003g0278 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2790+3978C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935314 | |||||||
chr20:32935327 | A | T | 2 | a0002c0002t0002g0048 a0002c0002t0002g0049 |
2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2790+3991A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935327 | |||||||
chr20:32935388 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2790+4052C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935388 | |||||||
chr20:32935446 | C | T | 1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2790+4110C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935446 | |||||||
chr20:32935491 | C | T | 1 | a0003c0003t0002g0007 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2790+4155C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935491 | |||||||
chr20:32935656 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2790+4320G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935656 | |||||||
chr20:32935742 | G | A | 37 | a0001c0001t0001g0117 a0002c0002t0001g0192 a0002c0002t0002g0005 others(34): Show |
37 | HG01099.hp2 HG01258.hp1 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.2790+4406G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935742 | |||||||
chr20:32935922 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+4586C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935922 | |||||||
chr20:32936014 | A | ATTTATT | 3 | a0002c0002t0001g0223 a0002c0002t0001g0236 a0002c0002t0001g0237 |
3 | HG02451.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2790+4700_2790+470 others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32936014 | ||||||
chr20:32936020 | T | A | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2790+4684T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936020 | |||||||
chr20:32936032 | T | G | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2790+4696T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936032 | |||||||
chr20:32936192 | C | T | 17 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(14): Show |
17 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2790+4856C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936192 | |||||||
chr20:32936278 | C | A | 6 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(3): Show |
8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2790+4942C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936278 | |||||||
chr20:32936625 | G | A | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2790+5289G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936625 | |||||||
chr20:32937152 | G | C | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2790+5816G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937152 | |||||||
chr20:32937163 | A | G | 1 | a0007c0006t0001g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2790+5827A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937163 | |||||||
chr20:32937168 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+5832C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937168 | |||||||
chr20:32937223 | G | T | 1 | a0034c0063t0004g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2790+5887G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937223 | |||||||
chr20:32937344 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2790+6008C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937344 | |||||||
chr20:32937345 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2790+6009A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937345 | |||||||
chr20:32937624 | CT | C | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-6003delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32937624 | ||||||
chr20:32937640 | A | G | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-5996A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937640 | |||||||
chr20:32937670 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2791-5966G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937670 | |||||||
chr20:32937680 | GTGATCTT others(3880): Show |
G | 27 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(24): Show |
27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-5955_2791-206 others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937680 | |||||||
chr20:32937762 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2791-5874G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937762 | |||||||
chr20:32937793 | A | G | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2791-5843A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937793 | |||||||
chr20:32937979 | C | T | 2 | a0022c0031t0002g0198 a0022c0031t0002g0232 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2791-5657C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937979 | |||||||
chr20:32938204 | C | A | 1 | a0018c0014t0002g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2791-5432C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938204 | |||||||
chr20:32938433 | A | T | 8 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-5203A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938433 | |||||||
chr20:32938511 | A | G | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2791-5125A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938511 | |||||||
chr20:32938526 | A | G | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2791-5110A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938526 | |||||||
chr20:32938753 | A | G | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2791-4883A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938753 | |||||||
chr20:32938983 | CCCTT | C | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2791-4638_2791-463 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32938983 | ||||||
chr20:32939014 | TTCCC | T | 19 | a0001c0001t0001g0245 a0001c0001t0005g0222 a0002c0002t0001g0002 others(16): Show |
21 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.2791-4606_2791-460 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939014 | ||||||
chr20:32939051 | C | CTCTT | 3 | a0002c0002t0001g0130 a0002c0002t0001g0131 a0002c0002t0001g0266 |
3 | HG02965.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2791-4573_2791-457 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939051 | ||||||
chr20:32939051 | CTCTT | C | 20 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.2791-4573_2791-457 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939051 | ||||||
chr20:32939104 | CCTTTCTT others(27): Show |
C | 1 | a0018c0014t0002g0042 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2791-4521_2791-448 others(38): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939104 | ||||||
chr20:32939104 | CCTTTCTT others(31): Show |
C | 1 | a0018c0014t0002g0016 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2791-4521_2791-448 others(42): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939104 | ||||||
chr20:32939115 | CTCTTTCT others(19): Show |
C | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2791-4509_2791-448 others(30): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939115 | ||||||
chr20:32939116 | T | C | 1 | a0003c0003t0001g0212 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2791-4520T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939116 | |||||||
chr20:32939119 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2791-4517T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939119 | |||||||
chr20:32939123 | TTCTCTTT others(17): Show |
T | 1 | a0019c0017t0007g0229 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2791-4511_2791-448 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939123 | ||||||
chr20:32939125 | C | CCCTT | 3 | a0002c0002t0002g0006 a0002c0002t0002g0049 a0027c0029t0003g0241 |
3 | HG03688.hp1 HG03688.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.2791-4511_2791-451 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | |||||||
chr20:32939125 | C | CCCTTTCT others(1): Show |
7 | a0002c0002t0002g0024 a0002c0002t0002g0029 a0002c0022t0002g0017 others(4): Show |
7 | HG00741.hp2 HG01255.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791-4511_2791-451 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | |||||||
chr20:32939125 | C | CCCTTTCT others(5): Show |
1 | a0004c0004t0003g0061 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | |||||||
chr20:32939125 | C | CCCTTTCT others(9): Show |
1 | a0004c0004t0003g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | |||||||
chr20:32939125 | C | CCCTTTCT others(13): Show |
1 | a0036c0059t0003g0072 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | |||||||
chr20:32939125 | C | CCCTTTCT others(25): Show |
1 | a0004c0004t0003g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | |||||||
chr20:32939125 | C | CTCTT | 14 | a0001c0001t0001g0160 a0001c0001t0001g0168 a0001c0001t0001g0171 others(11): Show |
14 | HG00642.hp2 HG01071.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2791-4436_2791-443 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | C | CTCTTTCT others(1): Show |
8 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0161 others(5): Show |
8 | HG00423.hp1 HG00621.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-4440_2791-443 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | C | CTCTTTCT others(5): Show |
3 | a0001c0001t0001g0146 a0003c0003t0001g0212 a0003c0003t0002g0138 |
3 | HG00323.hp2 HG02071.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2791-4444_2791-443 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | C | CTCTTTCT others(9): Show |
2 | a0001c0001t0001g0063 a0003c0003t0001g0176 |
2 | HG04204.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2791-4448_2791-443 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | C | CTCTTTCT others(13): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0215 |
2 | HG02071.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2791-4452_2791-443 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | C | CTCTTTCT others(17): Show |
2 | a0001c0001t0001g0157 a0003c0003t0001g0147 |
2 | HG00621.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2791-4456_2791-443 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | C | T | 2 | a0001c0001t0001g0169 a0049c0040t0002g0261 |
2 | NA18992.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2791-4511C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | |||||||
chr20:32939125 | CTCTT | C | 28 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0126 others(25): Show |
28 | HG00733.hp1 HG01167.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.2791-4436_2791-443 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(1): Show |
C | 22 | a0001c0001t0001g0118 a0001c0001t0001g0133 a0001c0001t0001g0189 others(19): Show |
22 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2791-4440_2791-443 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(5): Show |
C | 29 | a0001c0001t0001g0134 a0001c0001t0001g0141 a0001c0001t0001g0153 others(26): Show |
29 | HG00280.hp1 HG01099.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2791-4444_2791-443 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(9): Show |
C | 27 | a0001c0001t0001g0140 a0001c0001t0001g0190 a0001c0001t0001g0208 others(24): Show |
27 | HG00639.hp2 HG01099.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-4448_2791-443 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(13): Show |
C | 19 | a0001c0001t0001g0164 a0002c0002t0001g0223 a0002c0002t0001g0237 others(16): Show |
19 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2791-4452_2791-443 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(17): Show |
C | 21 | a0001c0001t0001g0120 a0001c0001t0001g0162 a0002c0002t0001g0002 others(18): Show |
22 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2791-4456_2791-443 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(21): Show |
C | 6 | a0001c0001t0001g0142 a0002c0002t0001g0269 a0002c0002t0001g0270 others(3): Show |
6 | HG01361.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2791-4460_2791-443 others(32): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(25): Show |
C | 1 | a0001c0001t0005g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2791-4464_2791-443 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(29): Show |
C | 1 | a0020c0025t0002g0021 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2791-4468_2791-443 others(40): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939125 | CTCTTTCT others(33): Show |
C | 2 | a0005c0035t0001g0097 a0020c0025t0001g0195 |
2 | HG01123.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2791-4472_2791-443 others(44): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | ||||||
chr20:32939126 | T | C | 11 | a0002c0002t0002g0025 a0002c0002t0002g0027 a0002c0002t0002g0055 others(8): Show |
11 | HG00642.hp1 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2791-4510T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939126 | |||||||
chr20:32939127 | CTTTCTTT others(10): Show |
C | 1 | a0032c0060t0001g0080 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2791-4506_2791-449 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939127 | ||||||
chr20:32939127 | CTTTCTTT others(22): Show |
C | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2791-4506_2791-447 others(33): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939127 | ||||||
chr20:32939130 | T | C | 9 | a0002c0002t0002g0047 a0002c0002t0002g0048 a0002c0011t0001g0246 others(6): Show |
9 | HG00733.hp1 HG02083.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2791-4506T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939130 | |||||||
chr20:32939134 | T | C | 13 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0002c0002t0001g0192 others(10): Show |
13 | HG01109.hp1 HG01258.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.2791-4502T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939134 | |||||||
chr20:32939138 | T | C | 13 | a0001c0001t0001g0214 a0002c0002t0002g0014 a0002c0002t0002g0019 others(10): Show |
13 | HG00280.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2791-4498T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939138 | |||||||
chr20:32939142 | T | C | 15 | a0001c0001t0001g0208 a0002c0002t0002g0005 a0002c0002t0002g0053 others(12): Show |
15 | HG01099.hp2 HG02135.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2791-4494T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939142 | |||||||
chr20:32939146 | T | C | 7 | a0002c0002t0002g0035 a0002c0002t0002g0038 a0002c0002t0003g0225 others(4): Show |
7 | HG00280.hp2 HG01943.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791-4490T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939146 | |||||||
chr20:32939149 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2791-4487T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939149 | |||||||
chr20:32939150 | T | C | 4 | a0002c0002t0003g0274 a0007c0030t0004g0129 a0008c0007t0003g0279 others(1): Show |
4 | HG02976.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2791-4486T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939150 | |||||||
chr20:32939152 | T | TTTCTTTC others(18): Show |
1 | a0002c0002t0002g0027 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2791-4463_2791-446 others(29): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939152 | ||||||
chr20:32939154 | T | C | 1 | a0002c0002t0003g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2791-4482T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939154 | |||||||
chr20:32939179 | CTTTCTTT others(14): Show |
C | 1 | a0016c0026t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2791-4454_2791-443 others(25): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939179 | ||||||
chr20:32939188 | TTTCTTTC others(8): Show |
T | 2 | a0001c0001t0001g0163 a0009c0015t0001g0100 |
2 | HG00423.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2791-4447_2791-443 others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939188 | |||||||
chr20:32939200 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0242 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939200 | ||||||
chr20:32939201 | T | TTCTTTCT others(7): Show |
1 | a0004c0004t0003g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(18): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939201 | ||||||
chr20:32939203 | C | CCT | 8 | a0001c0001t0001g0146 a0001c0001t0001g0178 a0001c0001t0001g0179 others(5): Show |
8 | HG00323.hp2 HG00621.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2791-4410_2791-440 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939203 | ||||||
chr20:32939203 | C | CTTTCTTT others(3): Show |
1 | a0013c0016t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939203 | |||||||
chr20:32939203 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0002g0030 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(18): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939203 | |||||||
chr20:32939203 | C | CTTTCTTT others(16): Show |
1 | a0005c0034t0002g0033 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(27): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939203 | |||||||
chr20:32939203 | CCTCT | C | 36 | a0002c0002t0001g0192 a0002c0002t0002g0005 a0002c0002t0002g0006 others(33): Show |
36 | HG01099.hp2 HG01258.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.2791-4412_2791-440 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939203 | ||||||
chr20:32939204 | C | T | 1 | a0002c0022t0002g0010 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2791-4432C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939204 | |||||||
chr20:32939207 | T | C | 1 | a0002c0002t0002g0055 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2791-4429T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939207 | |||||||
chr20:32939242 | G | C | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2791-4394G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939242 | |||||||
chr20:32939289 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0170 |
2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2791-4347G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939289 | |||||||
chr20:32939290 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2791-4346T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939290 | |||||||
chr20:32939484 | T | C | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2791-4152T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939484 | |||||||
chr20:32939518 | T | C | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2791-4118T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939518 | |||||||
chr20:32939804 | C | T | 7 | a0002c0002t0003g0225 a0002c0002t0003g0264 a0002c0002t0003g0265 others(4): Show |
7 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791-3832C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939804 | |||||||
chr20:32939820 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2791-3816G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939820 | |||||||
chr20:32939928 | C | T | 1 | a0002c0002t0001g0223 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2791-3708C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939928 | |||||||
chr20:32939985 | G | GTGCC | 3 | a0001c0001t0001g0142 a0001c0001t0001g0214 a0003c0003t0001g0147 |
3 | HG00621.hp1 NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2791-3633_2791-363 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939985 | ||||||
chr20:32939999 | G | C | 1 | a0002c0002t0002g0019 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2791-3637G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939999 | |||||||
chr20:32939999 | G | GCCTCCCT others(1): Show |
16 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(13): Show |
16 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2791-3634_2791-363 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | ||||||
chr20:32939999 | G | GCCTCCCT others(5): Show |
3 | a0004c0004t0003g0087 a0010c0010t0003g0143 a0016c0026t0001g0281 |
3 | HG01109.hp2 HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2791-3634_2791-363 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | ||||||
chr20:32939999 | G | GCCTCCCT others(9): Show |
1 | a0025c0027t0003g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2791-3634_2791-363 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | ||||||
chr20:32939999 | G | GCCTCCCT others(17): Show |
1 | a0016c0026t0003g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2791-3634_2791-363 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | ||||||
chr20:32940003 | G | C | 25 | a0002c0002t0002g0019 a0004c0004t0003g0087 a0006c0005t0003g0066 others(22): Show |
25 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2791-3633G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940003 | |||||||
chr20:32940003 | G | GCCTC | 25 | a0001c0001t0001g0118 a0001c0001t0001g0146 a0001c0001t0001g0155 others(22): Show |
25 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2791-3613_2791-361 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(1): Show |
20 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0208 others(17): Show |
20 | HG01109.hp1 HG01943.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.2791-3617_2791-361 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(5): Show |
8 | a0002c0002t0002g0006 a0002c0002t0002g0035 a0002c0002t0002g0039 others(5): Show |
8 | HG01516.hp1 HG01516.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2791-3621_2791-361 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(9): Show |
15 | a0002c0002t0002g0027 a0002c0002t0002g0036 a0002c0002t0002g0049 others(12): Show |
15 | HG01261.hp1 HG02040.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.2791-3625_2791-361 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(13): Show |
14 | a0002c0002t0001g0192 a0004c0004t0003g0074 a0004c0004t0003g0082 others(11): Show |
14 | HG00733.hp1 HG01099.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2791-3629_2791-361 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(17): Show |
1 | a0002c0002t0002g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(21): Show |
4 | a0004c0004t0003g0060 a0004c0004t0003g0061 a0005c0033t0008g0115 others(1): Show |
4 | HG00642.hp1 HG01496.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(32): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(25): Show |
6 | a0004c0004t0003g0068 a0004c0004t0003g0086 a0005c0013t0004g0099 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(29): Show |
1 | a0019c0017t0007g0219 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(40): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940003 | G | GCCTCCCT others(37): Show |
1 | a0004c0004t0003g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(48): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | ||||||
chr20:32940007 | C | G | 3 | a0001c0001t0001g0188 a0001c0001t0001g0205 a0001c0001t0001g0211 |
3 | HG03491.hp1 HG03492.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.2791-3629C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940007 | |||||||
chr20:32940023 | C | CCCTCCCT others(25): Show |
1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTCCCT others(21): Show |
2 | a0035c0058t0002g0259 a0041c0049t0001g0199 |
2 | HG01261.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(32): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTCCCT others(9): Show |
1 | a0002c0046t0003g0235 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTCCCT others(9): Show |
2 | a0001c0001t0002g0139 a0032c0060t0001g0080 |
2 | HG00733.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTT | 18 | a0001c0001t0001g0133 a0001c0001t0001g0154 a0001c0001t0001g0158 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.2791-3556_2791-355 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTTCCT others(1): Show |
12 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0148 others(9): Show |
12 | HG00423.hp1 HG01081.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2791-3560_2791-355 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTTCCT others(5): Show |
3 | a0001c0001t0001g0107 a0002c0002t0001g0130 a0003c0003t0002g0007 |
3 | NA18946.hp1 NA19043.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2791-3564_2791-355 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0188 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2791-3568_2791-355 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | CCCTTCCT others(13): Show |
1 | a0001c0001t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2791-3572_2791-355 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | C | T | 3 | a0001c0001t0001g0161 a0002c0042t0001g0200 a0003c0003t0001g0147 |
3 | HG00621.hp1 HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2791-3613C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940023 | |||||||
chr20:32940023 | CCCTT | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0152 others(24): Show |
28 | HG00639.hp1 HG01123.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.2791-3556_2791-355 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | CCCTTCCT others(1): Show |
C | 7 | a0001c0001t0001g0244 a0002c0002t0002g0038 a0002c0002t0004g0104 others(4): Show |
7 | HG00323.hp1 HG01167.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2791-3560_2791-355 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | CCCTTCCT others(5): Show |
C | 15 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0005g0222 others(12): Show |
17 | HG01071.hp2 HG01243.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.2791-3564_2791-355 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940023 | CCCTTCCT others(9): Show |
C | 2 | a0003c0003t0001g0280 a0007c0006t0001g0249 |
2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2791-3568_2791-355 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | ||||||
chr20:32940027 | T | C | 118 | a0001c0001t0001g0063 a0001c0001t0001g0106 a0001c0001t0001g0117 others(115): Show |
118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2791-3609T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940027 | |||||||
chr20:32940031 | T | C | 90 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0001c0001t0001g0215 others(87): Show |
90 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.2791-3605T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940031 | |||||||
chr20:32940035 | T | C | 81 | a0002c0002t0001g0192 a0002c0002t0002g0005 a0002c0002t0002g0006 others(78): Show |
81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.2791-3601T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940035 | |||||||
chr20:32940038 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2791-3598T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940038 | |||||||
chr20:32940039 | T | C | 70 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(67): Show |
72 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.2791-3597T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940039 | |||||||
chr20:32940043 | T | C | 50 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(47): Show |
52 | HG00323.hp1 HG01099.hp2 HG01258.hp1 others(49): Show |
intron_variant | MODIFIER | c.2791-3593T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940043 | |||||||
chr20:32940047 | T | C | 8 | a0002c0002t0002g0014 a0002c0002t0002g0029 a0002c0002t0002g0038 others(5): Show |
8 | HG02055.hp1 HG02083.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-3589T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940047 | |||||||
chr20:32940049 | C | T | 19 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(16): Show |
19 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2791-3587C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940049 | |||||||
chr20:32940051 | T | C | 4 | a0002c0002t0002g0038 a0002c0002t0002g0041 a0002c0002t0002g0058 others(1): Show |
4 | NA18964.hp2 NA18998.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.2791-3585T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940051 | |||||||
chr20:32940243 | A | G | 6 | a0005c0033t0008g0115 a0019c0017t0007g0219 a0019c0017t0007g0229 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2791-3393A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940243 | |||||||
chr20:32940270 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2791-3366C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940270 | |||||||
chr20:32940396 | T | G | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2791-3240T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940396 | |||||||
chr20:32940505 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2791-3131T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940505 | |||||||
chr20:32940748 | C | T | 1 | a0043c0050t0002g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2791-2888C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940748 | |||||||
chr20:32940751 | G | A | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-2885G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940751 | |||||||
chr20:32941054 | C | A | 1 | a0002c0002t0002g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2791-2582C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941054 | |||||||
chr20:32941144 | C | T | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-2492C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941144 | |||||||
chr20:32941145 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0244 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2791-2491G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941145 | |||||||
chr20:32941169 | T | C | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2791-2467T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941169 | |||||||
chr20:32941423 | A | G | 1 | a0002c0002t0001g0002 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2791-2213A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941423 | |||||||
chr20:32941568 | A | G | 27 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(24): Show |
27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2068A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941568 | |||||||
chr20:32941572 | AT | A | 27 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(24): Show |
27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2063delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941572 | |||||||
chr20:32941575 | A | T | 27 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(24): Show |
27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2061A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941575 | |||||||
chr20:32941577 | CCTTGAA | C | 27 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(24): Show |
27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2058_2791-205 others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941577 | |||||||
chr20:32941722 | G | T | 78 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0002c0002t0001g0192 others(75): Show |
78 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.2791-1914G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941722 | |||||||
chr20:32941841 | G | A | 29 | a0005c0033t0008g0115 a0006c0005t0003g0066 a0006c0005t0003g0067 others(26): Show |
29 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2791-1795G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941841 | |||||||
chr20:32941989 | A | T | 2 | a0002c0002t0001g0227 a0002c0002t0001g0263 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2791-1647A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941989 | |||||||
chr20:32942028 | T | C | 29 | a0005c0033t0008g0115 a0006c0005t0003g0066 a0006c0005t0003g0067 others(26): Show |
29 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2791-1608T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942028 | |||||||
chr20:32942157 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2791-1479C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942157 | |||||||
chr20:32942273 | T | C | 1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2791-1363T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942273 | |||||||
chr20:32942533 | C | A | 2 | a0002c0002t0001g0227 a0002c0002t0001g0263 |
2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2791-1103C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942533 | |||||||
chr20:32942630 | G | C | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2791-1006G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942630 | |||||||
chr20:32942893 | C | G | 2 | a0017c0018t0004g0149 a0017c0018t0004g0194 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2791-743C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942893 | |||||||
chr20:32942894 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0009g0116 others(2): Show |
5 | HG01070.hp2 NA18951.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2791-742C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942894 | |||||||
chr20:32943344 | TAGTCATA others(4): Show |
T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-271_2791-261d others(13): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32943344 | ||||||
chr20:32943363 | T | G | 31 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2791-273T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32943363 | |||||||
chr20:32943479 | G | A | 3 | a0017c0018t0004g0149 a0017c0018t0004g0194 a0017c0018t0005g0231 |
3 | HG01167.hp1 HG01169.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2791-157G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32943479 | |||||||
chr20:32943889 | A | G | 1 | a0010c0010t0006g0051 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2959+85A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32943889 | |||||||
chr20:32943985 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2959+181T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32943985 | |||||||
chr20:32944250 | C | T | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2959+446C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944250 | |||||||
chr20:32944320 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG01071.hp2 HG01346.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2959+516C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944320 | |||||||
chr20:32944356 | T | C | 1 | a0002c0046t0003g0235 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2959+552T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944356 | |||||||
chr20:32944471 | A | T | 11 | a0007c0006t0004g0144 a0007c0030t0004g0129 a0007c0030t0004g0268 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2959+667A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944471 | |||||||
chr20:32944501 | G | T | 1 | a0002c0002t0002g0039 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2959+697G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944501 | |||||||
chr20:32944518 | A | G | 8 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+714A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944518 | |||||||
chr20:32944521 | G | A | 8 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+717G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944521 | |||||||
chr20:32944847 | T | C | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2959+1043T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944847 | |||||||
chr20:32944972 | G | A | 3 | a0001c0001t0001g0156 a0013c0016t0001g0145 a0013c0016t0001g0181 |
3 | HG00099.hp1 HG04184.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2959+1168G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944972 | |||||||
chr20:32944990 | TAA | T | 6 | a0005c0033t0008g0115 a0019c0017t0007g0219 a0019c0017t0007g0229 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2959+1187_2959+118 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944990 | |||||||
chr20:32945474 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2959+1670A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945474 | |||||||
chr20:32945551 | G | A | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+1747G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945551 | |||||||
chr20:32945594 | T | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0148 a0001c0001t0001g0161 others(1): Show |
4 | HG01175.hp2 HG01255.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2959+1790T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945594 | |||||||
chr20:32945779 | G | A | 6 | a0011c0009t0001g0250 a0014c0019t0005g0221 a0014c0019t0005g0233 others(3): Show |
6 | HG00741.hp1 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2959+1975G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945779 | |||||||
chr20:32945997 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2959+2193G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945997 | |||||||
chr20:32946308 | G | A | 1 | a0006c0005t0003g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2959+2504G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946308 | |||||||
chr20:32946328 | A | C | 19 | a0006c0005t0003g0066 a0006c0005t0003g0067 a0006c0005t0003g0070 others(16): Show |
19 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2959+2524A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946328 | |||||||
chr20:32946397 | T | C | 10 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0002c0002t0003g0225 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2959+2593T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946397 | |||||||
chr20:32946505 | G | A | 1 | a0014c0019t0005g0221 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2959+2701G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946505 | |||||||
chr20:32946766 | A | C | 1 | a0038c0044t0002g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2959+2962A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946766 | |||||||
chr20:32946836 | T | C | 3 | a0007c0006t0004g0144 a0007c0030t0004g0129 a0007c0030t0004g0268 |
3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2959+3032T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946836 | |||||||
chr20:32946844 | A | G | 31 | a0004c0004t0001g0091 a0004c0004t0003g0060 a0004c0004t0003g0061 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2959+3040A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946844 | |||||||
chr20:32946852 | G | A | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+3048G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946852 | |||||||
chr20:32946895 | G | A | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2959+3091G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946895 | |||||||
chr20:32946928 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2959+3124A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946928 | |||||||
chr20:32947041 | G | A | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+3237G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947041 | |||||||
chr20:32947085 | G | A | 2 | a0035c0058t0002g0259 a0045c0055t0001g0276 |
2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2959+3281G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947085 | |||||||
chr20:32947175 | A | G | 78 | a0001c0001t0001g0208 a0001c0001t0001g0213 a0002c0002t0001g0192 others(75): Show |
78 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.2959+3371A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947175 | |||||||
chr20:32947379 | A | C | 1 | a0047c0057t0004g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2959+3575A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947379 | |||||||
chr20:32947459 | C | A | 165 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(162): Show |
167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2959+3655C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947459 | |||||||
chr20:32947668 | TA | T | 8 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+3866delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32947668 | ||||||
chr20:32947764 | T | A | 165 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(162): Show |
167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2959+3960T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947764 | |||||||
chr20:32947903 | T | TA | 9 | a0004c0004t0003g0078 a0009c0015t0001g0098 a0009c0015t0001g0100 others(6): Show |
9 | HG00280.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2959+4114dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32947903 | ||||||
chr20:32947903 | TA | T | 15 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0004c0004t0001g0091 others(12): Show |
15 | HG00280.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2959+4114delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32947903 | ||||||
chr20:32948065 | T | C | 1 | a0009c0015t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2959+4261T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948065 | |||||||
chr20:32948315 | G | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+4511G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948315 | |||||||
chr20:32948437 | C | T | 47 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(44): Show |
49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2959+4633C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948437 | |||||||
chr20:32948524 | A | AAAAG | 41 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0126 others(38): Show |
41 | HG00280.hp2 HG00323.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.2959+4776_2959+477 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | A | AAAAGAAA others(1): Show |
15 | a0001c0001t0001g0063 a0001c0001t0001g0210 a0001c0001t0005g0222 others(12): Show |
15 | HG00642.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2959+4772_2959+477 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | A | AAAAGAAA others(5): Show |
3 | a0001c0001t0001g0213 a0034c0063t0004g0083 a0043c0050t0002g0220 |
3 | HG01109.hp1 HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2959+4768_2959+477 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | AAAAG | A | 61 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0148 others(58): Show |
62 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2959+4776_2959+477 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | AAAAGAAA others(1): Show |
A | 47 | a0001c0001t0001g0090 a0001c0001t0001g0174 a0001c0001t0001g0209 others(44): Show |
48 | HG00323.hp1 HG00733.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2959+4772_2959+477 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | AAAAGAAA others(5): Show |
A | 16 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0003c0003t0001g0272 others(13): Show |
16 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2959+4768_2959+477 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | AAAAGAAA others(9): Show |
A | 1 | a0028c0021t0002g0013 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2959+4764_2959+477 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0001g0245 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2959+4760_2959+477 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948524 | AAAAGAAA others(17): Show |
A | 2 | a0025c0027t0003g0128 a0035c0058t0002g0259 |
2 | HG01261.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.2959+4756_2959+477 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | ||||||
chr20:32948570 | A | AAG | 3 | a0002c0011t0001g0247 a0002c0011t0001g0248 a0021c0061t0001g0240 |
3 | HG02486.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2959+4768_2959+476 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948570 | ||||||
chr20:32948570 | A | AAGAAAGA others(3): Show |
2 | a0007c0006t0004g0144 a0007c0030t0004g0268 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2959+4768_2959+477 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948570 | ||||||
chr20:32948580 | G | GAAAGAAA others(3): Show |
1 | a0020c0025t0001g0195 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2959+4779_2959+478 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948580 | ||||||
chr20:32948808 | A | G | 6 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0269 others(3): Show |
8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2959+5004A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948808 | |||||||
chr20:32949213 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2959+5409C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949213 | |||||||
chr20:32949641 | A | G | 7 | a0002c0002t0003g0225 a0002c0002t0003g0264 a0002c0002t0003g0265 others(4): Show |
7 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2959+5837A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949641 | |||||||
chr20:32949705 | C | G | 11 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(8): Show |
11 | HG01891.hp2 HG02630.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.2959+5901C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949705 | |||||||
chr20:32949721 | A | G | 168 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(165): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.2959+5917A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949721 | |||||||
chr20:32949931 | C | T | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2959+6127C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949931 | |||||||
chr20:32949954 | C | T | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+6150C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949954 | |||||||
chr20:32949995 | G | A | 2 | a0019c0017t0007g0219 a0019c0017t0007g0230 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2959+6191G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949995 | |||||||
chr20:32950001 | A | AAAAC | 84 | a0002c0002t0001g0192 a0002c0002t0002g0005 a0002c0002t0002g0006 others(81): Show |
84 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.2959+6205_2959+620 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32950001 | ||||||
chr20:32950012 | A | AC | 74 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(71): Show |
76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6208_2959+620 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950012 | |||||||
chr20:32950014 | C | A | 74 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(71): Show |
76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6210C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950014 | |||||||
chr20:32950019 | AAAC | A | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+6233_2959+623 others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32950019 | ||||||
chr20:32950020 | A | C | 74 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(71): Show |
76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6216A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950020 | |||||||
chr20:32950022 | C | A | 74 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(71): Show |
76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6218C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950022 | |||||||
chr20:32950053 | A | C | 2 | a0002c0011t0001g0247 a0002c0011t0001g0248 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2959+6249A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950053 | |||||||
chr20:32950515 | C | T | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2959+6711C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950515 | |||||||
chr20:32950650 | G | A | 2 | a0001c0001t0001g0217 a0002c0002t0002g0057 |
2 | NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2959+6846G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950650 | |||||||
chr20:32950664 | C | T | 11 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(8): Show |
11 | HG01891.hp2 HG02630.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.2959+6860C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950664 | |||||||
chr20:32950918 | G | A | 27 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(24): Show |
27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2959+7114G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950918 | |||||||
chr20:32950927 | C | T | 1 | a0002c0011t0001g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2959+7123C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950927 | |||||||
chr20:32950989 | A | G | 1 | a0044c0045t0007g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2959+7185A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950989 | |||||||
chr20:32951024 | A | T | 1 | a0002c0011t0001g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2959+7220A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951024 | |||||||
chr20:32951138 | G | A | 29 | a0005c0033t0008g0115 a0006c0005t0003g0066 a0006c0005t0003g0067 others(26): Show |
29 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2960-7283G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951138 | |||||||
chr20:32951245 | T | C | 1 | a0020c0025t0002g0021 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2960-7176T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951245 | |||||||
chr20:32951302 | T | C | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2960-7119T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951302 | |||||||
chr20:32951414 | G | A | 1 | a0005c0008t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2960-7007G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951414 | |||||||
chr20:32951547 | TA | T | 3 | a0017c0018t0004g0149 a0017c0018t0004g0194 a0017c0018t0005g0231 |
3 | HG01167.hp1 HG01169.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2960-6873delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951547 | |||||||
chr20:32952400 | C | T | 3 | a0017c0018t0004g0149 a0017c0018t0004g0194 a0017c0018t0005g0231 |
3 | HG01167.hp1 HG01169.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2960-6021C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952400 | |||||||
chr20:32952449 | A | T | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-5972A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952449 | |||||||
chr20:32952606 | A | G | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-5815A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952606 | |||||||
chr20:32952659 | C | T | 1 | a0013c0016t0001g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2960-5762C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952659 | |||||||
chr20:32952715 | A | G | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2960-5706A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952715 | |||||||
chr20:32953027 | C | T | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2960-5394C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953027 | |||||||
chr20:32953118 | A | C | 2 | a0003c0003t0001g0175 a0003c0003t0001g0176 |
2 | NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2960-5303A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953118 | |||||||
chr20:32953501 | T | C | 17 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(14): Show |
17 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2960-4920T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953501 | |||||||
chr20:32953613 | A | G | 17 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(14): Show |
17 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2960-4808A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953613 | |||||||
chr20:32953913 | C | T | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2960-4508C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953913 | |||||||
chr20:32953935 | C | T | 1 | a0008c0007t0003g0196 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2960-4486C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953935 | |||||||
chr20:32953936 | G | T | 1 | a0024c0032t0004g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2960-4485G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953936 | |||||||
chr20:32953942 | C | T | 2 | a0018c0014t0002g0016 a0018c0014t0002g0042 |
2 | HG01515.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2960-4479C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953942 | |||||||
chr20:32954054 | C | T | 47 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(44): Show |
49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2960-4367C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954054 | |||||||
chr20:32954478 | T | C | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-3943T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954478 | |||||||
chr20:32954509 | C | T | 1 | a0005c0034t0002g0033 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2960-3912C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954509 | |||||||
chr20:32954684 | T | G | 1 | a0003c0003t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2960-3737T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954684 | |||||||
chr20:32954718 | A | G | 165 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(162): Show |
167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2960-3703A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954718 | |||||||
chr20:32954772 | C | G | 1 | a0024c0032t0004g0275 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2960-3649C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954772 | |||||||
chr20:32955291 | G | A | 3 | a0007c0006t0004g0144 a0007c0030t0004g0129 a0007c0030t0004g0268 |
3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2960-3130G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955291 | |||||||
chr20:32955358 | T | C | 168 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(165): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.2960-3063T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955358 | |||||||
chr20:32955374 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2960-3047T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955374 | |||||||
chr20:32955412 | C | T | 3 | a0007c0006t0004g0144 a0007c0030t0004g0129 a0007c0030t0004g0268 |
3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2960-3009C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955412 | |||||||
chr20:32955497 | G | A | 1 | a0002c0011t0001g0102 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2960-2924G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955497 | |||||||
chr20:32955673 | G | A | 1 | a0003c0003t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2960-2748G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955673 | |||||||
chr20:32955716 | C | T | 2 | a0022c0031t0002g0198 a0022c0031t0002g0232 |
2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2960-2705C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955716 | |||||||
chr20:32955846 | C | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0214 |
2 | NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2960-2575C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955846 | |||||||
chr20:32955984 | A | AC | 8 | a0012c0012t0004g0096 a0012c0012t0004g0110 a0012c0012t0004g0111 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-2437_2960-243 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955984 | |||||||
chr20:32956089 | A | T | 166 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(163): Show |
168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2960-2332A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956089 | |||||||
chr20:32956097 | G | A | 4 | a0002c0011t0001g0246 a0002c0011t0001g0247 a0002c0011t0001g0248 others(1): Show |
4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2960-2324G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956097 | |||||||
chr20:32956125 | G | A | 75 | a0002c0002t0001g0192 a0002c0002t0002g0005 a0002c0002t0002g0006 others(72): Show |
75 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.2960-2296G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956125 | |||||||
chr20:32956223 | G | A | 2 | a0002c0002t0001g0095 a0007c0006t0001g0249 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2960-2198G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956223 | |||||||
chr20:32956284 | C | T | 165 | a0001c0001t0004g0050 a0001c0001t0005g0222 a0001c0001t0005g0257 others(162): Show |
167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2960-2137C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956284 | |||||||
chr20:32956530 | C | T | 27 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(24): Show |
27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2960-1891C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956530 | |||||||
chr20:32956943 | C | CT | 8 | a0002c0011t0001g0102 a0002c0011t0001g0246 a0002c0011t0001g0247 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-1464dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32956943 | ||||||
chr20:32956943 | CT | C | 31 | a0001c0001t0001g0161 a0002c0002t0001g0227 a0002c0002t0001g0263 others(28): Show |
31 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.2960-1464delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32956943 | ||||||
chr20:32956958 | C | T | 16 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(13): Show |
16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-1463C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956958 | |||||||
chr20:32956959 | A | C | 16 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(13): Show |
16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-1462A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956959 | |||||||
chr20:32956959 | AT | A | 11 | a0002c0002t0001g0227 a0002c0002t0001g0263 a0011c0009t0001g0250 others(8): Show |
11 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.2960-1454delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32956959 | ||||||
chr20:32956960 | T | A | 16 | a0001c0001t0004g0050 a0001c0001t0005g0257 a0001c0001t0005g0258 others(13): Show |
16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-1461T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956960 | |||||||
chr20:32957099 | A | T | 47 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(44): Show |
49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2960-1322A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957099 | |||||||
chr20:32957287 | C | T | 5 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2960-1134C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957287 | |||||||
chr20:32957318 | TA | T | 20 | a0002c0002t0002g0041 a0002c0002t0003g0273 a0002c0002t0003g0274 others(17): Show |
20 | HG01261.hp2 HG02109.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2960-1091delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32957318 | ||||||
chr20:32957319 | A | T | 2 | a0002c0042t0001g0200 a0009c0041t0001g0253 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2960-1102A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957319 | |||||||
chr20:32957330 | AC | A | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2960-1088delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32957330 | ||||||
chr20:32957494 | G | T | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2960-927G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957494 | |||||||
chr20:32957542 | C | T | 2 | a0032c0060t0001g0080 a0033c0065t0001g0062 |
2 | HG00733.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2960-879C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957542 | |||||||
chr20:32957735 | C | G | 1 | a0043c0050t0002g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2960-686C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957735 | |||||||
chr20:32957757 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.2960-664C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957757 | |||||||
chr20:32957824 | A | T | 2 | a0004c0004t0003g0069 a0036c0059t0003g0072 |
2 | HG01516.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.2960-597A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957824 | |||||||
chr20:32958208 | G | T | 2 | a0008c0007t0006g0015 a0008c0007t0006g0046 |
2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2960-213G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32958208 | |||||||
chr20:32958326 | T | A | 1 | a0045c0055t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2960-95T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32958326 | |||||||
chr20:32958404 | G | A | 4 | a0006c0005t0003g0076 a0006c0005t0003g0084 a0006c0005t0003g0093 others(1): Show |
4 | HG01361.hp1 HG02602.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.2960-17G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32958404 | |||||||
chr20:32958678 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0156 |
2 | HG02735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3089+128G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32958678 | |||||||
chr20:32958804 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3089+254C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32958804 | |||||||
chr20:32958833 | G | T | 1 | a0020c0025t0001g0195 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3089+283G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32958833 | |||||||
chr20:32959102 | G | A | 1 | a0016c0026t0003g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3089+552G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959102 | |||||||
chr20:32959227 | ATG | A | 5 | a0005c0033t0008g0115 a0019c0017t0007g0219 a0019c0017t0007g0229 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3090-548_3090-547d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr20 | 32959227 | ||||||
chr20:32959312 | G | A | 18 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(15): Show |
20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.3090-466G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959312 | |||||||
chr20:32959353 | A | G | 1 | a0005c0036t0004g0183 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3090-425A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959353 | |||||||
chr20:32959482 | T | C | 3 | a0002c0002t0001g0227 a0002c0002t0001g0263 a0002c0002t0002g0041 |
3 | HG01884.hp1 HG02809.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.3090-296T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959482 | |||||||
chr20:32960216 | C | T | 8 | a0009c0015t0001g0098 a0009c0015t0001g0100 a0009c0015t0001g0114 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3393+55C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960216 | |||||||
chr20:32960275 | C | T | 1 | a0006c0005t0003g0084 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3393+114C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960275 | |||||||
chr20:32960307 | A | G | 1 | a0006c0005t0003g0084 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3393+146A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960307 | |||||||
chr20:32960724 | A | G | 55 | a0001c0001t0005g0222 a0002c0002t0001g0002 a0002c0002t0001g0003 others(52): Show |
57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.3394-412A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960724 | |||||||
chr20:32960743 | C | T | 1 | a0002c0002t0003g0264 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3394-393C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960743 | |||||||
chr20:32960857 | G | A | 1 | a0006c0005t0003g0093 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3394-279G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960857 | |||||||
chr20:32960974 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3394-162C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960974 | |||||||
chr20:32961012 | G | A | 1 | a0005c0013t0004g0099 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3394-124G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32961012 | |||||||
chr20:32961096 | A | G | 1 | a0019c0017t0007g0230 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3394-40A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32961096 |