Item | Value |
---|---|
geneid | 389197 |
ensemblid | ENSG00000181215.17 |
hgncid | 33766 |
symbol | C4orf50 |
name | chromosome 4 open reading frame 50 |
refseq_nuc | NM_001364689.3 |
refseq_prot | NP_001351618.1 |
ensembl_nuc | ENST00000711657.1 |
ensembl_prot | ENSP00000518823.1 |
mane_status | MANE Select |
chr | chr4 |
start | 5959375 |
end | 6018431 |
strand | - |
ver | v1.2 |
region | chr4:5959375-6018431 |
region5000 | chr4:5954375-6023431 |
regionname0 | C4orf50_chr4_5959375_6018431 |
regionname5000 | C4orf50_chr4_5954375_6023431 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1508 | 67 | 4 | 8 | 48 | 0 | 7 | 28 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0002 | 0/0 | 1508 | 31 | 0 | 5 | 24 | 0 | 2 | 17 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0003 | 1/0 | 1508 | 26 | 0 | 14 | 6 | 3 | 2 | 5 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0004 | 0/0 | 1508 | 22 | 1 | 4 | 10 | 3 | 4 | 7 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0005 | 0/0 | 1508 | 10 | 4 | 0 | 4 | 0 | 2 | 4 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0006 | 0/0 | 1508 | 7 | 0 | 4 | 1 | 0 | 2 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0007 | 0/0 | 1508 | 7 | 0 | 2 | 4 | 0 | 1 | 4 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0008 | 0/0 | 1508 | 7 | 0 | 0 | 7 | 0 | 0 | 4 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0009 | 0/0 | 1508 | 6 | 4 | 0 | 0 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0010 | 0/0 | 1508 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0011 | 0/0 | 1508 | 5 | 0 | 1 | 3 | 0 | 1 | 3 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0012 | 0/1 | 1508 | 5 | 1 | 0 | 1 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0013 | 0/0 | 1508 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0014 | 0/0 | 1508 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0015 | 0/0 | 1508 | 4 | 0 | 2 | 0 | 1 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0016 | 0/0 | 1508 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0017 | 0/0 | 1508 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0018 | 0/0 | 1508 | 4 | 1 | 0 | 0 | 0 | 3 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0019 | 0/0 | 1508 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0020 | 0/0 | 1508 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0021 | 0/0 | 1508 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0022 | 0/0 | 1508 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0023 | 0/0 | 1508 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0024 | 0/0 | 1508 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0025 | 0/0 | 1508 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0026 | 0/0 | 1508 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0027 | 0/0 | 1508 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0028 | 0/0 | 1508 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0029 | 0/0 | 1508 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0030 | 0/0 | 1508 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0031 | 0/0 | 1508 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0032 | 0/0 | 1508 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0033 | 0/0 | 1508 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0034 | 0/0 | 1508 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0035 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0036 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0037 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0038 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0039 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0040 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0041 | 0/0 | 1508 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0042 | 0/0 | 1508 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0043 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0044 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0045 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0046 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0047 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0048 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0049 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0050 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0051 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0052 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0053 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0054 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0055 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0056 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0057 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0058 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0059 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0060 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0061 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0062 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0063 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0064 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0065 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0066 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0067 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0068 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0069 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0070 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0071 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0072 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0073 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0074 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0075 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0076 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0077 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0078 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0079 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0080 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0081 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0082 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0083 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0084 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0085 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0086 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0087 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0088 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0089 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0090 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0091 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0092 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0093 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0094 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0095 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0096 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0097 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0098 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0099 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0100 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0101 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0102 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0103 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0104 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0105 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0106 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0107 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0108 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
a0109 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | MEPTA others(1503): Show |
chr4 | 5954375 | 6023431 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4524 | 65 | 4 | 8 | 46 | 0 | 7 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0001c0084 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0001c0106 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0002c0002 | 0/0 | 4524 | 31 | 0 | 5 | 24 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0003c0004 | 0/0 | 4524 | 18 | 0 | 8 | 6 | 2 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0003c0011 | 1/0 | 4524 | 6 | 0 | 4 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0003c0086 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0003c0090 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0004c0003 | 0/0 | 4524 | 21 | 1 | 3 | 10 | 3 | 4 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0004c0087 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0005c0005 | 0/0 | 4524 | 10 | 4 | 0 | 4 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0006c0006 | 0/0 | 4524 | 7 | 0 | 4 | 1 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0007c0007 | 0/0 | 4524 | 7 | 0 | 2 | 4 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0008c0008 | 0/0 | 4524 | 7 | 0 | 0 | 7 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0009c0010 | 0/0 | 4524 | 6 | 4 | 0 | 0 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0010c0009 | 0/0 | 4524 | 6 | 6 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0011c0014 | 0/0 | 4524 | 5 | 0 | 1 | 3 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0012c0013 | 0/1 | 4524 | 5 | 1 | 0 | 1 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0013c0017 | 0/0 | 4524 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0013c0080 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0014c0012 | 0/0 | 4524 | 5 | 0 | 0 | 0 | 0 | 5 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0015c0018 | 0/0 | 4524 | 4 | 0 | 2 | 0 | 1 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0016c0015 | 0/0 | 4524 | 4 | 3 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0017c0019 | 0/0 | 4524 | 4 | 0 | 2 | 0 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0018c0016 | 0/0 | 4524 | 4 | 1 | 0 | 0 | 0 | 3 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0019c0020 | 0/0 | 4524 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0020c0028 | 0/0 | 4524 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0020c0056 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0021c0024 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0021c0050 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0022c0022 | 0/0 | 4524 | 3 | 2 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0023c0021 | 0/0 | 4524 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0024c0027 | 0/0 | 4524 | 2 | 0 | 0 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0025c0023 | 0/0 | 4524 | 2 | 0 | 0 | 0 | 1 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0026c0042 | 0/0 | 4524 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0027c0038 | 0/0 | 4524 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0028c0031 | 0/0 | 4524 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0029c0030 | 0/0 | 4524 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0030c0026 | 0/0 | 4524 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0031c0032 | 0/0 | 4524 | 2 | 1 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0032c0029 | 0/0 | 4524 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0033c0036 | 0/0 | 4524 | 2 | 0 | 0 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0034c0040 | 0/0 | 4524 | 2 | 0 | 0 | 1 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0035c0037 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0036c0039 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0037c0035 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0038c0034 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0039c0025 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0040c0033 | 0/0 | 4524 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0041c0041 | 0/0 | 4524 | 2 | 0 | 0 | 0 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0042c0043 | 0/0 | 4524 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0043c0075 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0044c0088 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0045c0085 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0046c0077 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0047c0054 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0048c0051 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0049c0053 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0050c0116 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0051c0081 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0052c0108 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0053c0068 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0054c0065 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0055c0057 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0056c0052 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0057c0067 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0058c0083 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0059c0102 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0060c0049 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0061c0089 | 0/0 | 4524 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0062c0082 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0063c0110 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0064c0060 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0065c0115 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0066c0104 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0067c0072 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0068c0109 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0069c0111 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0070c0113 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0071c0046 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0072c0100 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0073c0114 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0074c0071 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0075c0098 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0076c0074 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0077c0097 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0078c0066 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0079c0079 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0080c0045 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0081c0069 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0082c0064 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0083c0047 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0084c0044 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0085c0099 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0086c0073 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0087c0062 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0088c0105 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0089c0091 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0090c0078 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0091c0048 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0092c0096 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0093c0058 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0094c0059 | 0/0 | 4524 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0095c0107 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0096c0076 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0097c0101 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0098c0094 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0099c0103 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0100c0093 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0101c0095 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0102c0112 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0103c0055 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0104c0063 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0105c0092 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0106c0118 | 0/0 | 4524 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0107c0117 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0108c0070 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 | ||
a0109c0061 | 0/0 | 4524 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4519): Show |
chr4 | 5954375 | 6023431 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4527 | 65 | 4 | 8 | 46 | 0 | 7 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0001c0084t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0001c0106t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0002c0002t0001 | 0/0 | 4527 | 31 | 0 | 5 | 24 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0003c0004t0001 | 0/0 | 4527 | 18 | 0 | 8 | 6 | 2 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0003c0011t0001 | 1/0 | 4527 | 6 | 0 | 4 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0003c0086t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0003c0090t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0004c0003t0001 | 0/0 | 4527 | 21 | 1 | 3 | 10 | 3 | 4 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0004c0087t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0005c0005t0001 | 0/0 | 4527 | 10 | 4 | 0 | 4 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0006c0006t0001 | 0/0 | 4527 | 7 | 0 | 4 | 1 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0007c0007t0001 | 0/0 | 4527 | 7 | 0 | 2 | 4 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0008c0008t0001 | 0/0 | 4527 | 7 | 0 | 0 | 7 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0009c0010t0001 | 0/0 | 4527 | 6 | 4 | 0 | 0 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0010c0009t0001 | 0/0 | 4527 | 6 | 6 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0011c0014t0001 | 0/0 | 4527 | 5 | 0 | 1 | 3 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0012c0013t0001 | 0/1 | 4527 | 5 | 1 | 0 | 1 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0013c0017t0001 | 0/0 | 4527 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0013c0080t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0014c0012t0001 | 0/0 | 4527 | 5 | 0 | 0 | 0 | 0 | 5 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0015c0018t0001 | 0/0 | 4527 | 4 | 0 | 2 | 0 | 1 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0016c0015t0001 | 0/0 | 4527 | 4 | 3 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0017c0019t0001 | 0/0 | 4527 | 4 | 0 | 2 | 0 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0018c0016t0001 | 0/0 | 4527 | 4 | 1 | 0 | 0 | 0 | 3 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0019c0020t0001 | 0/0 | 4527 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0020c0028t0001 | 0/0 | 4527 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0020c0056t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0021c0024t0001 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0021c0050t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0022c0022t0001 | 0/0 | 4527 | 3 | 2 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0023c0021t0001 | 0/0 | 4527 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0024c0027t0001 | 0/0 | 4527 | 2 | 0 | 0 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0025c0023t0001 | 0/0 | 4527 | 2 | 0 | 0 | 0 | 1 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0026c0042t0001 | 0/0 | 4527 | 2 | 0 | 1 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0027c0038t0001 | 0/0 | 4527 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0028c0031t0001 | 0/0 | 4527 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0029c0030t0001 | 0/0 | 4527 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0030c0026t0001 | 0/0 | 4527 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0031c0032t0001 | 0/0 | 4527 | 2 | 1 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0032c0029t0001 | 0/0 | 4527 | 2 | 0 | 1 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0033c0036t0001 | 0/0 | 4527 | 2 | 0 | 0 | 0 | 2 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0034c0040t0001 | 0/0 | 4527 | 2 | 0 | 0 | 1 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0035c0037t0001 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0036c0039t0001 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0037c0035t0001 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0038c0034t0001 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0039c0025t0001 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0040c0033t0001 | 0/0 | 4527 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0041c0041t0001 | 0/0 | 4527 | 2 | 0 | 0 | 0 | 0 | 2 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0042c0043t0001 | 0/0 | 4527 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0043c0075t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0044c0088t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0045c0085t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0046c0077t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0047c0054t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0048c0051t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0049c0053t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0050c0116t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0051c0081t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0052c0108t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0053c0068t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0054c0065t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0055c0057t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0056c0052t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0057c0067t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0058c0083t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0059c0102t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0060c0049t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0061c0089t0001 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0062c0082t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0063c0110t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0064c0060t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0065c0115t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0066c0104t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0067c0072t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0068c0109t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0069c0111t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0070c0113t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0071c0046t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0072c0100t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0073c0114t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0074c0071t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0075c0098t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0076c0074t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0077c0097t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0078c0066t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0079c0079t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0080c0045t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0081c0069t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0082c0064t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0083c0047t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0084c0044t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0085c0099t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0086c0073t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0087c0062t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0088c0105t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0089c0091t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0090c0078t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0091c0048t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0092c0096t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0093c0058t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0094c0059t0001 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0095c0107t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0096c0076t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0097c0101t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0098c0094t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0099c0103t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0100c0093t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0101c0095t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0102c0112t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0103c0055t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0104c0063t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0105c0092t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0106c0118t0001 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0107c0117t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0108c0070t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
a0109c0061t0001 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | ATGGA others(4522): Show |
chr4 | 5954375 | 6023431 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0084t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0001c0106t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0011t0001g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0011t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0011t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0011t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0011t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0011t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0086t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0003c0090t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0004c0087t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0005c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0006c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0006c0006t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0006c0006t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0006c0006t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0006c0006t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0006c0006t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0006c0006t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0007c0007t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0007c0007t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0007c0007t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0007c0007t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0007c0007t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0007c0007t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0007c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0008c0008t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0008c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0008c0008t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0008c0008t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0008c0008t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0008c0008t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0009c0010t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0009c0010t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0009c0010t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0009c0010t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0009c0010t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0009c0010t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0010c0009t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0010c0009t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0010c0009t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0010c0009t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0010c0009t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0010c0009t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0011c0014t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0011c0014t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0011c0014t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0011c0014t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0011c0014t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0012c0013t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0012c0013t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0012c0013t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0012c0013t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0012c0013t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0013c0017t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0013c0017t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0013c0017t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0013c0017t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0013c0080t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0014c0012t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0014c0012t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0014c0012t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0014c0012t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0014c0012t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0015c0018t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0015c0018t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0015c0018t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0015c0018t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0016c0015t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0016c0015t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0016c0015t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0016c0015t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0017c0019t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0017c0019t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0017c0019t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0018c0016t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0018c0016t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0018c0016t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0018c0016t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0019c0020t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0019c0020t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0019c0020t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0020c0028t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0020c0028t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0020c0056t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0021c0024t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0021c0024t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0021c0050t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0022c0022t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0022c0022t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0022c0022t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0023c0021t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0023c0021t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0023c0021t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0024c0027t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0024c0027t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0025c0023t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0025c0023t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0026c0042t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0026c0042t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0027c0038t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0028c0031t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0028c0031t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0029c0030t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0030c0026t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0030c0026t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0031c0032t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0031c0032t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0032c0029t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0032c0029t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0033c0036t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0033c0036t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0034c0040t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0034c0040t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0035c0037t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0035c0037t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0036c0039t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0036c0039t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0037c0035t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0037c0035t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0038c0034t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0038c0034t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0039c0025t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0039c0025t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0040c0033t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0040c0033t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0041c0041t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0041c0041t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0042c0043t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0042c0043t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0043c0075t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0044c0088t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0045c0085t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0046c0077t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0047c0054t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0048c0051t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0049c0053t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0050c0116t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0051c0081t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0052c0108t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0053c0068t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0054c0065t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0055c0057t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0056c0052t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0057c0067t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0058c0083t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0059c0102t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0060c0049t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0061c0089t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0062c0082t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0063c0110t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0064c0060t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0065c0115t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0066c0104t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0067c0072t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0068c0109t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0069c0111t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0070c0113t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0071c0046t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0072c0100t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0073c0114t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0074c0071t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0075c0098t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0076c0074t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0077c0097t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0078c0066t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0079c0079t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0080c0045t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0081c0069t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0082c0064t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0083c0047t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0084c0044t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0085c0099t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0086c0073t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0087c0062t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0088c0105t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0089c0091t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0090c0078t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0091c0048t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0092c0096t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0093c0058t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0094c0059t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0095c0107t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0096c0076t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0097c0101t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0098c0094t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0099c0103t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0100c0093t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0101c0095t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0102c0112t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0103c0055t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0104c0063t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0105c0092t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0106c0118t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0107c0117t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0108c0070t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
a0109c0061t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0043 | c0075 | t0001 | g0278 | EUR | GBR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00099 | hp2 | a0004 | c0003 | t0001 | g0316 | EUR | GBR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00140 | hp1 | a0024 | c0027 | t0001 | g0021 | EUR | GBR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00140 | hp2 | a0020 | c0056 | t0001 | g0042 | EUR | GBR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00280 | hp1 | a0004 | c0003 | t0001 | g0288 | EUR | FIN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00280 | hp2 | a0025 | c0023 | t0001 | g0319 | EUR | FIN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00323 | hp1 | a0026 | c0042 | t0001 | g0333 | EUR | FIN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00323 | hp2 | a0024 | c0027 | t0001 | g0041 | EUR | FIN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00597 | hp1 | a0004 | c0003 | t0001 | g0224 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0313 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00639 | hp2 | a0006 | c0006 | t0001 | g0170 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00642 | hp1 | a0027 | c0038 | t0001 | g0002 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00673 | hp2 | a0044 | c0088 | t0001 | g0159 | EAS | CHS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0197 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00735 | hp2 | a0028 | c0031 | t0001 | g0220 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00741 | hp1 | a0027 | c0038 | t0001 | g0002 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG00741 | hp2 | a0045 | c0085 | t0001 | g0119 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01069 | hp1 | a0004 | c0087 | t0001 | g0237 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01069 | hp2 | a0003 | c0004 | t0001 | g0078 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01070 | hp2 | a0004 | c0003 | t0001 | g0009 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01071 | hp1 | a0004 | c0003 | t0001 | g0315 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01071 | hp2 | a0003 | c0004 | t0001 | g0077 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01081 | hp1 | a0003 | c0011 | t0001 | g0236 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01099 | hp1 | a0003 | c0086 | t0001 | g0232 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01099 | hp2 | a0011 | c0014 | t0001 | g0309 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01106 | hp1 | a0046 | c0077 | t0001 | g0263 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01106 | hp2 | a0047 | c0054 | t0001 | g0051 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01109 | hp2 | a0006 | c0006 | t0001 | g0225 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01167 | hp1 | a0016 | c0015 | t0001 | g0043 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01167 | hp2 | a0029 | c0030 | t0001 | g0005 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01168 | hp1 | a0049 | c0053 | t0001 | g0055 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01168 | hp2 | a0003 | c0004 | t0001 | g0305 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01169 | hp1 | a0029 | c0030 | t0001 | g0005 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01169 | hp2 | a0003 | c0004 | t0001 | g0304 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01192 | hp1 | a0006 | c0006 | t0001 | g0128 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01192 | hp2 | a0050 | c0116 | t0001 | g0334 | AMR | PUR | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01255 | hp1 | a0030 | c0026 | t0001 | g0054 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01255 | hp2 | a0031 | c0032 | t0001 | g0025 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01256 | hp1 | a0007 | c0007 | t0001 | g0193 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01256 | hp2 | a0003 | c0011 | t0001 | g0234 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01257 | hp1 | a0017 | c0019 | t0001 | g0008 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01257 | hp2 | a0021 | c0050 | t0001 | g0064 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01258 | hp1 | a0017 | c0019 | t0001 | g0008 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01258 | hp2 | a0007 | c0007 | t0001 | g0195 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01261 | hp1 | a0015 | c0018 | t0001 | g0264 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01261 | hp2 | a0032 | c0029 | t0001 | g0057 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01358 | hp2 | a0022 | c0022 | t0001 | g0052 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01361 | hp1 | a0003 | c0011 | t0001 | g0233 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01433 | hp1 | a0003 | c0011 | t0001 | g0229 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01515 | hp1 | a0020 | c0028 | t0001 | g0024 | EUR | IBS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01515 | hp2 | a0003 | c0004 | t0001 | g0306 | EUR | IBS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01516 | hp1 | a0003 | c0011 | t0001 | g0235 | EUR | IBS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01516 | hp2 | a0033 | c0036 | t0001 | g0265 | EUR | IBS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01517 | hp1 | a0033 | c0036 | t0001 | g0261 | EUR | IBS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01517 | hp2 | a0003 | c0004 | t0001 | g0303 | EUR | IBS | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01884 | hp1 | a0051 | c0081 | t0001 | g0331 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01884 | hp2 | a0023 | c0021 | t0001 | g0168 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01891 | hp1 | a0005 | c0005 | t0001 | g0298 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01891 | hp2 | a0009 | c0010 | t0001 | g0280 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01943 | hp1 | a0028 | c0031 | t0001 | g0218 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01943 | hp2 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01952 | hp2 | a0003 | c0004 | t0001 | g0240 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01975 | hp1 | a0003 | c0004 | t0001 | g0248 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01975 | hp2 | a0052 | c0108 | t0001 | g0290 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01978 | hp1 | a0053 | c0068 | t0001 | g0329 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01978 | hp2 | a0004 | c0003 | t0001 | g0245 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01993 | hp1 | a0020 | c0028 | t0001 | g0023 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01993 | hp2 | a0003 | c0090 | t0001 | g0242 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02004 | hp1 | a0006 | c0006 | t0001 | g0120 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02027 | hp1 | a0054 | c0065 | t0001 | g0219 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02027 | hp2 | a0034 | c0040 | t0001 | g0291 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02055 | hp1 | a0010 | c0009 | t0001 | g0277 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02055 | hp2 | a0055 | c0057 | t0001 | g0039 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02080 | hp2 | a0008 | c0008 | t0001 | g0184 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02083 | hp2 | a0003 | c0004 | t0001 | g0254 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02129 | hp2 | a0012 | c0013 | t0001 | g0231 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02145 | hp1 | a0031 | c0032 | t0001 | g0026 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02145 | hp2 | a0057 | c0067 | t0001 | g0322 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02165 | hp1 | a0008 | c0008 | t0001 | g0003 | EAS | CDX | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02165 | hp2 | a0004 | c0003 | t0001 | g0115 | EAS | CDX | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02257 | hp1 | a0013 | c0017 | t0001 | g0037 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02257 | hp2 | a0036 | c0039 | t0001 | g0157 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02258 | hp1 | a0058 | c0083 | t0001 | g0222 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02258 | hp2 | a0022 | c0022 | t0001 | g0047 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02280 | hp1 | a0035 | c0037 | t0001 | g0293 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02280 | hp2 | a0059 | c0102 | t0001 | g0269 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02293 | hp1 | a0060 | c0049 | t0001 | g0317 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02293 | hp2 | a0061 | c0089 | t0001 | g0238 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02300 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02300 | hp2 | a0026 | c0042 | t0001 | g0332 | AMR | PEL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02451 | hp1 | a0062 | c0082 | t0001 | g0285 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02451 | hp2 | a0037 | c0035 | t0001 | g0214 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02572 | hp1 | a0009 | c0010 | t0001 | g0326 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02572 | hp2 | a0010 | c0009 | t0001 | g0162 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02602 | hp1 | a0011 | c0014 | t0001 | g0302 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02615 | hp1 | a0063 | c0110 | t0001 | g0274 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02615 | hp2 | a0018 | c0016 | t0001 | g0210 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02622 | hp1 | a0037 | c0035 | t0001 | g0223 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02622 | hp2 | a0064 | c0060 | t0001 | g0067 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02647 | hp1 | a0065 | c0115 | t0001 | g0150 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02647 | hp2 | a0010 | c0009 | t0001 | g0167 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02683 | hp1 | a0009 | c0010 | t0001 | g0279 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02683 | hp2 | a0018 | c0016 | t0001 | g0282 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02698 | hp1 | a0004 | c0003 | t0001 | g0289 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02698 | hp2 | a0004 | c0003 | t0001 | g0314 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02717 | hp1 | a0016 | c0015 | t0001 | g0046 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02717 | hp2 | a0066 | c0104 | t0001 | g0296 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02723 | hp1 | a0036 | c0039 | t0001 | g0014 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02723 | hp2 | a0067 | c0072 | t0001 | g0082 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02735 | hp2 | a0014 | c0012 | t0001 | g0216 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02738 | hp1 | a0068 | c0109 | t0001 | g0092 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02738 | hp2 | a0007 | c0007 | t0001 | g0190 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02809 | hp1 | a0069 | c0111 | t0001 | g0094 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02809 | hp2 | a0038 | c0034 | t0001 | g0017 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02818 | hp1 | a0070 | c0113 | t0001 | g0029 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02818 | hp2 | a0009 | c0010 | t0001 | g0267 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02886 | hp1 | a0071 | c0046 | t0001 | g0011 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02886 | hp2 | a0010 | c0009 | t0001 | g0163 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02895 | hp1 | a0013 | c0017 | t0001 | g0038 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02895 | hp2 | a0010 | c0009 | t0001 | g0166 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02896 | hp1 | a0019 | c0020 | t0001 | g0001 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02896 | hp2 | a0013 | c0017 | t0001 | g0031 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02897 | hp1 | a0013 | c0017 | t0001 | g0032 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02897 | hp2 | a0019 | c0020 | t0001 | g0060 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02922 | hp2 | a0039 | c0025 | t0001 | g0206 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02970 | hp1 | a0072 | c0100 | t0001 | g0036 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02970 | hp2 | a0023 | c0021 | t0001 | g0165 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03017 | hp1 | a0025 | c0023 | t0001 | g0318 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03017 | hp2 | a0073 | c0114 | t0001 | g0149 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03041 | hp1 | a0005 | c0005 | t0001 | g0295 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03041 | hp2 | a0040 | c0033 | t0001 | g0294 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03098 | hp1 | a0074 | c0071 | t0001 | g0035 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03098 | hp2 | a0016 | c0015 | t0001 | g0045 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03130 | hp1 | a0075 | c0098 | t0001 | g0272 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03130 | hp2 | a0076 | c0074 | t0001 | g0207 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03139 | hp1 | a0077 | c0097 | t0001 | g0208 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03139 | hp2 | a0078 | c0066 | t0001 | g0018 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03209 | hp1 | a0079 | c0079 | t0001 | g0028 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03209 | hp2 | a0080 | c0045 | t0001 | g0010 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03225 | hp1 | a0081 | c0069 | t0001 | g0325 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03225 | hp2 | a0082 | c0064 | t0001 | g0324 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03239 | hp1 | a0018 | c0016 | t0001 | g0283 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03239 | hp2 | a0005 | c0005 | t0001 | g0138 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03453 | hp1 | a0083 | c0047 | t0001 | g0013 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03453 | hp2 | a0019 | c0020 | t0001 | g0001 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03486 | hp1 | a0022 | c0022 | t0001 | g0068 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03486 | hp2 | a0085 | c0099 | t0001 | g0034 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03490 | hp1 | a0003 | c0004 | t0001 | g0211 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03490 | hp2 | a0014 | c0012 | t0001 | g0215 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03491 | hp1 | a0041 | c0041 | t0001 | g0323 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03491 | hp2 | a0034 | c0040 | t0001 | g0321 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03492 | hp1 | a0041 | c0041 | t0001 | g0299 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03492 | hp2 | a0003 | c0004 | t0001 | g0310 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03516 | hp1 | a0005 | c0005 | t0001 | g0093 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03516 | hp2 | a0086 | c0073 | t0001 | g0153 | AFR | ESN | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03540 | hp1 | a0087 | c0062 | t0001 | g0022 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03540 | hp2 | a0088 | c0105 | t0001 | g0020 | AFR | GWD | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03579 | hp1 | a0038 | c0034 | t0001 | g0330 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03579 | hp2 | a0019 | c0020 | t0001 | g0061 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03654 | hp1 | a0006 | c0006 | t0001 | g0135 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03654 | hp2 | a0005 | c0005 | t0001 | g0136 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03669 | hp1 | a0012 | c0013 | t0001 | g0262 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03669 | hp2 | a0015 | c0018 | t0001 | g0284 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03688 | hp2 | a0017 | c0019 | t0001 | g0308 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03704 | hp2 | a0030 | c0026 | t0001 | g0040 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03710 | hp1 | a0014 | c0012 | t0001 | g0049 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03831 | hp1 | a0089 | c0091 | t0001 | g0070 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03831 | hp2 | a0018 | c0016 | t0001 | g0276 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03834 | hp1 | a0006 | c0006 | t0001 | g0139 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03834 | hp2 | a0090 | c0078 | t0001 | g0311 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03927 | hp1 | a0009 | c0010 | t0001 | g0144 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03927 | hp2 | a0091 | c0048 | t0001 | g0320 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03942 | hp1 | a0014 | c0012 | t0001 | g0050 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03942 | hp2 | a0004 | c0003 | t0001 | g0095 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04115 | hp1 | a0014 | c0012 | t0001 | g0048 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0189 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04184 | hp2 | a0092 | c0096 | t0001 | g0151 | SAS | BEB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04199 | hp1 | a0004 | c0003 | t0001 | g0130 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04199 | hp2 | a0017 | c0019 | t0001 | g0213 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04204 | hp1 | a0012 | c0013 | t0001 | g0059 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04204 | hp2 | a0093 | c0058 | t0001 | g0058 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG04228 | hp2 | a0094 | c0059 | t0001 | g0217 | SAS | STU | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18522 | hp1 | a0095 | c0107 | t0001 | g0286 | AFR | YRI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18522 | hp2 | a0013 | c0080 | t0001 | g0212 | AFR | YRI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18747 | hp1 | a0004 | c0003 | t0001 | g0114 | EAS | CHB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18747 | hp2 | a0008 | c0008 | t0001 | g0003 | EAS | CHB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18906 | hp1 | a0096 | c0076 | t0001 | g0328 | AFR | YRI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18906 | hp2 | a0039 | c0025 | t0001 | g0065 | AFR | YRI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18941 | hp1 | a0097 | c0101 | t0001 | g0089 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18944 | hp2 | a0008 | c0008 | t0001 | g0198 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18945 | hp1 | a0004 | c0003 | t0001 | g0239 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18948 | hp1 | a0011 | c0014 | t0001 | g0145 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18948 | hp2 | a0003 | c0004 | t0001 | g0191 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18960 | hp1 | a0003 | c0004 | t0001 | g0255 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18962 | hp2 | a0098 | c0094 | t0001 | g0180 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18963 | hp1 | a0011 | c0014 | t0001 | g0152 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18964 | hp1 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18964 | hp2 | a0007 | c0007 | t0001 | g0171 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18967 | hp2 | a0004 | c0003 | t0001 | g0131 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18970 | hp1 | a0004 | c0003 | t0001 | g0007 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18970 | hp2 | a0001 | c0084 | t0001 | g0096 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18971 | hp2 | a0007 | c0007 | t0001 | g0203 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18973 | hp1 | a0099 | c0103 | t0001 | g0230 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18979 | hp1 | a0042 | c0043 | t0001 | g0336 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18982 | hp1 | a0001 | c0106 | t0001 | g0246 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18982 | hp2 | a0007 | c0007 | t0001 | g0260 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18986 | hp1 | a0004 | c0003 | t0001 | g0007 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18986 | hp2 | a0008 | c0008 | t0001 | g0076 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18995 | hp1 | a0042 | c0043 | t0001 | g0335 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18995 | hp2 | a0004 | c0003 | t0001 | g0241 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18998 | hp1 | a0004 | c0003 | t0001 | g0083 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19005 | hp1 | a0100 | c0093 | t0001 | g0275 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19007 | hp2 | a0005 | c0005 | t0001 | g0103 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19011 | hp1 | a0011 | c0014 | t0001 | g0227 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19011 | hp2 | a0005 | c0005 | t0001 | g0087 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19012 | hp1 | a0004 | c0003 | t0001 | g0137 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19012 | hp2 | a0101 | c0095 | t0001 | g0266 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19030 | hp1 | a0102 | c0112 | t0001 | g0015 | AFR | LWK | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19030 | hp2 | a0103 | c0055 | t0001 | g0069 | AFR | LWK | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19043 | hp1 | a0104 | c0063 | t0001 | g0071 | AFR | LWK | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19043 | hp2 | a0021 | c0024 | t0001 | g0205 | AFR | LWK | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19056 | hp2 | a0008 | c0008 | t0001 | g0199 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19060 | hp1 | a0007 | c0007 | t0001 | g0172 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19060 | hp2 | a0005 | c0005 | t0001 | g0101 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19064 | hp1 | a0005 | c0005 | t0001 | g0085 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19067 | hp2 | a0105 | c0092 | t0001 | g0243 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19079 | hp2 | a0003 | c0004 | t0001 | g0192 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19080 | hp1 | a0006 | c0006 | t0001 | g0111 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19080 | hp2 | a0003 | c0004 | t0001 | g0249 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19084 | hp2 | a0008 | c0008 | t0001 | g0129 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19090 | hp1 | a0106 | c0118 | t0001 | g0337 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19240 | hp1 | a0107 | c0117 | t0001 | g0019 | AFR | YRI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA19240 | hp2 | a0108 | c0070 | t0001 | g0027 | AFR | YRI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20129 | hp1 | a0040 | c0033 | t0001 | g0273 | AFR | ASW | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20129 | hp2 | a0012 | c0013 | t0001 | g0301 | AFR | ASW | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20805 | hp1 | a0004 | c0003 | t0001 | g0247 | EUR | TSI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20805 | hp2 | a0015 | c0018 | t0001 | g0287 | EUR | TSI | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20905 | hp1 | a0032 | c0029 | t0001 | g0073 | SAS | GIH | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | GIH | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01123 | hp1 | a0048 | c0051 | t0001 | g0053 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG01123 | hp2 | a0015 | c0018 | t0001 | g0300 | AMR | CLM | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02109 | hp1 | a0035 | c0037 | t0001 | g0292 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02109 | hp2 | a0056 | c0052 | t0001 | g0030 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02486 | hp1 | a0004 | c0003 | t0001 | g0009 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02486 | hp2 | a0009 | c0010 | t0001 | g0327 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02559 | hp1 | a0021 | c0024 | t0001 | g0066 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG02559 | hp2 | a0005 | c0005 | t0001 | g0297 | AFR | ACB | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG03471 | hp2 | a0084 | c0044 | t0001 | g0012 | AFR | MSL | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG06807 | hp1 | a0010 | c0009 | t0001 | g0161 | AFR | USA | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | USA | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20300 | hp1 | a0016 | c0015 | t0001 | g0044 | AFR | USA | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA20300 | hp2 | a0023 | c0021 | t0001 | g0164 | AFR | USA | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
NA21309 | hp2 | a0109 | c0061 | t0001 | g0063 | AFR | LWK | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
homoSapiens | chm13v2 | a0012 | c0013 | t0001 | g0072 | REF | REF | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
homoSapiens | grch38p0 | a0003 | c0011 | t0001 | g0062 | REF | REF | C4orf50_chr4_5954375_6023431 | C4orf50 | chr4 | 5954375 | 6023431 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:5959571 | G | A | 1 | a0097 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.4331C>T | p.Thr1444Ile | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 12/12 | 4331/4527 | 4331/4527 | 1444/1508 | chr4 | 5959571 | |||
chr4:5959611 | C | T | 23 | a0010 a0036 a0039 others(20): Show |
30 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(27): Show |
missense_variant | MODERATE | c.4291G>A | p.Val1431Met | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 12/12 | 4291/4527 | 4291/4527 | 1431/1508 | chr4 | 5959611 | |||
chr4:5965044 | C | T | 1 | a0088 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.4255G>A | p.Ala1419Thr | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/12 | 4255/4527 | 4255/4527 | 1419/1508 | chr4 | 5965044 | |||
chr4:5965074 | T | C | 37 | a0004 a0006 a0007 others(34): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
missense_variant | MODERATE | c.4225A>G | p.Ile1409Val | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/12 | 4225/4527 | 4225/4527 | 1409/1508 | chr4 | 5965074 | |||
chr4:5973811 | G | A | 51 | a0001 a0006 a0008 others(48): Show |
160 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(157): Show |
missense_variant | MODERATE | c.3952C>T | p.Arg1318Trp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/12 | 3952/4527 | 3952/4527 | 1318/1508 | chr4 | 5973811 | |||
chr4:5988349 | T | G | 1 | a0095 | 1 | NA18522.hp1 | missense_variant&splice_region_variant | MODERATE | c.3697A>C | p.Met1233Leu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3697/4527 | 3697/4527 | 1233/1508 | chr4 | 5988349 | |||
chr4:5988383 | C | A | 30 | a0001 a0005 a0006 others(27): Show |
118 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(115): Show |
missense_variant | MODERATE | c.3663G>T | p.Gln1221His | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3663/4527 | 3663/4527 | 1221/1508 | chr4 | 5988383 | |||
chr4:5988523 | C | T | 1 | a0099 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.3523G>A | p.Gly1175Ser | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3523/4527 | 3523/4527 | 1175/1508 | chr4 | 5988523 | |||
chr4:5988612 | G | A | 82 | a0001 a0002 a0005 others(79): Show |
243 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(240): Show |
missense_variant | MODERATE | c.3434C>T | p.Ser1145Leu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3434/4527 | 3434/4527 | 1145/1508 | chr4 | 5988612 | |||
chr4:5988618 | A | T | 1 | a0070 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.3428T>A | p.Leu1143Gln | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3428/4527 | 3428/4527 | 1143/1508 | chr4 | 5988618 | |||
chr4:5988653 | G | T | 3 | a0021 a0039 a0081 |
6 | HG01257.hp2 HG02559.hp1 HG02922.hp2 others(3): Show |
missense_variant | MODERATE | c.3393C>A | p.Asp1131Glu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3393/4527 | 3393/4527 | 1131/1508 | chr4 | 5988653 | |||
chr4:5988712 | C | T | 1 | a0071 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.3334G>A | p.Gly1112Arg | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3334/4527 | 3334/4527 | 1112/1508 | chr4 | 5988712 | |||
chr4:5988720 | G | A | 1 | a0095 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.3326C>T | p.Thr1109Met | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3326/4527 | 3326/4527 | 1109/1508 | chr4 | 5988720 | |||
chr4:5988756 | T | A | 1 | a0095 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.3290A>T | p.His1097Leu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3290/4527 | 3290/4527 | 1097/1508 | chr4 | 5988756 | |||
chr4:5988759 | A | G | 2 | a0059 a0080 |
2 | HG02280.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.3287T>C | p.Val1096Ala | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3287/4527 | 3287/4527 | 1096/1508 | chr4 | 5988759 | |||
chr4:5988814 | T | C | 2 | a0059 a0080 |
2 | HG02280.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.3232A>G | p.Ile1078Val | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3232/4527 | 3232/4527 | 1078/1508 | chr4 | 5988814 | |||
chr4:5988853 | C | T | 1 | a0075 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.3193G>A | p.Val1065Ile | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3193/4527 | 3193/4527 | 1065/1508 | chr4 | 5988853 | |||
chr4:5988955 | G | A | 1 | a0095 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.3091C>T | p.Leu1031Phe | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3091/4527 | 3091/4527 | 1031/1508 | chr4 | 5988955 | |||
chr4:5989357 | T | G | 11 | a0019 a0025 a0034 others(8): Show |
16 | HG00099.hp1 HG00280.hp2 HG01123.hp1 others(13): Show |
missense_variant | MODERATE | c.2689A>C | p.Thr897Pro | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2689/4527 | 2689/4527 | 897/1508 | chr4 | 5989357 | |||
chr4:5989494 | C | T | 1 | a0077 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.2552G>A | p.Arg851Lys | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2552/4527 | 2552/4527 | 851/1508 | chr4 | 5989494 | |||
chr4:5989562 | C | A | 1 | a0079 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2484G>T | p.Gln828His | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2484/4527 | 2484/4527 | 828/1508 | chr4 | 5989562 | |||
chr4:5989657 | T | C | 84 | a0001 a0002 a0005 others(81): Show |
254 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(251): Show |
missense_variant | MODERATE | c.2389A>G | p.Asn797Asp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2389/4527 | 2389/4527 | 797/1508 | chr4 | 5989657 | |||
chr4:5989702 | C | T | 3 | a0018 a0057 a0087 |
6 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(3): Show |
missense_variant | MODERATE | c.2344G>A | p.Glu782Lys | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2344/4527 | 2344/4527 | 782/1508 | chr4 | 5989702 | |||
chr4:5989749 | G | A | 67 | a0001 a0002 a0005 others(64): Show |
219 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(216): Show |
missense_variant | MODERATE | c.2297C>T | p.Thr766Ile | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2297/4527 | 2297/4527 | 766/1508 | chr4 | 5989749 | |||
chr4:5989774 | C | T | 1 | a0045 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.2272G>A | p.Glu758Lys | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2272/4527 | 2272/4527 | 758/1508 | chr4 | 5989774 | |||
chr4:5989831 | C | T | 17 | a0010 a0013 a0021 others(14): Show |
33 | HG01257.hp2 HG01884.hp1 HG01884.hp2 others(30): Show |
missense_variant | MODERATE | c.2215G>A | p.Gly739Ser | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2215/4527 | 2215/4527 | 739/1508 | chr4 | 5989831 | |||
chr4:5989887 | C | A | 17 | a0010 a0013 a0021 others(14): Show |
33 | HG01257.hp2 HG01884.hp1 HG01884.hp2 others(30): Show |
missense_variant | MODERATE | c.2159G>T | p.Ser720Ile | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2159/4527 | 2159/4527 | 720/1508 | chr4 | 5989887 | |||
chr4:5989905 | A | G | 1 | a0109 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2141T>C | p.Leu714Pro | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2141/4527 | 2141/4527 | 714/1508 | chr4 | 5989905 | |||
chr4:5990280 | A | T | 32 | a0009 a0010 a0012 others(29): Show |
65 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(62): Show |
missense_variant | MODERATE | c.1766T>A | p.Leu589Gln | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1766/4527 | 1766/4527 | 589/1508 | chr4 | 5990280 | |||
chr4:5990289 | T | C | 1 | a0063 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1757A>G | p.His586Arg | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1757/4527 | 1757/4527 | 586/1508 | chr4 | 5990289 | |||
chr4:5990349 | C | T | 1 | a0071 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1697G>A | p.Gly566Glu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1697/4527 | 1697/4527 | 566/1508 | chr4 | 5990349 | |||
chr4:5990359 | T | C | 20 | a0002 a0007 a0008 others(17): Show |
72 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
missense_variant | MODERATE | c.1687A>G | p.Lys563Glu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1687/4527 | 1687/4527 | 563/1508 | chr4 | 5990359 | |||
chr4:5990487 | C | T | 1 | a0103 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1559G>A | p.Arg520His | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1559/4527 | 1559/4527 | 520/1508 | chr4 | 5990487 | |||
chr4:5990571 | A | G | 24 | a0009 a0010 a0012 others(21): Show |
55 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(52): Show |
missense_variant | MODERATE | c.1475T>C | p.Ile492Thr | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1475/4527 | 1475/4527 | 492/1508 | chr4 | 5990571 | |||
chr4:5990575 | T | G | 27 | a0009 a0010 a0012 others(24): Show |
59 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(56): Show |
missense_variant | MODERATE | c.1471A>C | p.Lys491Gln | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1471/4527 | 1471/4527 | 491/1508 | chr4 | 5990575 | |||
chr4:5990590 | G | A | 2 | a0064 a0070 |
2 | HG02622.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.1456C>T | p.Pro486Ser | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1456/4527 | 1456/4527 | 486/1508 | chr4 | 5990590 | |||
chr4:5990719 | A | G | 25 | a0009 a0010 a0012 others(22): Show |
56 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(53): Show |
missense_variant | MODERATE | c.1327T>C | p.Trp443Arg | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1327/4527 | 1327/4527 | 443/1508 | chr4 | 5990719 | |||
chr4:5990733 | C | G | 24 | a0009 a0010 a0012 others(21): Show |
54 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(51): Show |
missense_variant | MODERATE | c.1313G>C | p.Arg438Pro | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1313/4527 | 1313/4527 | 438/1508 | chr4 | 5990733 | |||
chr4:5990759 | C | G | 13 | a0016 a0018 a0038 others(10): Show |
20 | HG00099.hp1 HG01123.hp1 HG01167.hp1 others(17): Show |
missense_variant | MODERATE | c.1287G>C | p.Glu429Asp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1287/4527 | 1287/4527 | 429/1508 | chr4 | 5990759 | |||
chr4:5992862 | G | C | 1 | a0016 | 4 | HG01167.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.1162C>G | p.Pro388Ala | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/12 | 1162/4527 | 1162/4527 | 388/1508 | chr4 | 5992862 | |||
chr4:5992898 | G | A | 6 | a0031 a0040 a0065 others(3): Show |
8 | HG01255.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
missense_variant | MODERATE | c.1126C>T | p.Arg376Cys | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/12 | 1126/4527 | 1126/4527 | 376/1508 | chr4 | 5992898 | |||
chr4:5994377 | T | C | 23 | a0010 a0016 a0018 others(20): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
missense_variant | MODERATE | c.1063A>G | p.Asn355Asp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/12 | 1063/4527 | 1063/4527 | 355/1508 | chr4 | 5994377 | |||
chr4:6008022 | G | C | 1 | a0073 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.937C>G | p.Gln313Glu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/12 | 937/4527 | 937/4527 | 313/1508 | chr4 | 6008022 | |||
chr4:6008030 | A | G | 3 | a0028 a0029 a0054 |
5 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
missense_variant | MODERATE | c.929T>C | p.Leu310Pro | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/12 | 929/4527 | 929/4527 | 310/1508 | chr4 | 6008030 | |||
chr4:6008273 | C | T | 4 | a0082 a0087 a0104 others(1): Show |
4 | HG03225.hp2 HG03540.hp1 NA19043.hp1 others(1): Show |
missense_variant | MODERATE | c.686G>A | p.Gly229Asp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/12 | 686/4527 | 686/4527 | 229/1508 | chr4 | 6008273 | |||
chr4:6008465 | C | T | 20 | a0010 a0014 a0016 others(17): Show |
44 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(41): Show |
missense_variant | MODERATE | c.494G>A | p.Arg165His | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/12 | 494/4527 | 494/4527 | 165/1508 | chr4 | 6008465 | |||
chr4:6008486 | C | T | 3 | a0025 a0060 a0091 |
4 | HG00280.hp2 HG02293.hp1 HG03017.hp1 others(1): Show |
missense_variant | MODERATE | c.473G>A | p.Arg158Gln | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/12 | 473/4527 | 473/4527 | 158/1508 | chr4 | 6008486 | |||
chr4:6011848 | C | G | 1 | a0083 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.408G>C | p.Gln136His | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/12 | 408/4527 | 408/4527 | 136/1508 | chr4 | 6011848 | |||
chr4:6011855 | G | A | 1 | a0065 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.401C>T | p.Ala134Val | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/12 | 401/4527 | 401/4527 | 134/1508 | chr4 | 6011855 | |||
chr4:6011887 | G | C | 2 | a0026 a0050 |
3 | HG00323.hp1 HG01192.hp2 HG02300.hp2 |
missense_variant | MODERATE | c.369C>G | p.Ser123Arg | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/12 | 369/4527 | 369/4527 | 123/1508 | chr4 | 6011887 | |||
chr4:6011931 | G | A | 1 | a0107 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.325C>T | p.Arg109Trp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/12 | 325/4527 | 325/4527 | 109/1508 | chr4 | 6011931 | |||
chr4:6018158 | C | T | 3 | a0071 a0080 a0084 |
3 | HG02886.hp1 HG03209.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.274G>A | p.Gly92Arg | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/12 | 274/4527 | 274/4527 | 92/1508 | chr4 | 6018158 | |||
chr4:6018232 | G | A | 2 | a0042 a0106 |
3 | NA18979.hp1 NA18995.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.200C>T | p.Ala67Val | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/12 | 200/4527 | 200/4527 | 67/1508 | chr4 | 6018232 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:5973689 | C | G | 1 | a0013c0080 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.4074G>C | p.Thr1358Thr | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/12 | 4074/4527 | 4074/4527 | 1358/1508 | chr4 | 5973689 | |||
chr4:5973728 | C | T | 1 | a0068c0109 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.4035G>A | p.Ala1345Ala | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/12 | 4035/4527 | 4035/4527 | 1345/1508 | chr4 | 5973728 | |||
chr4:5988464 | C | T | 14 | a0013c0017 a0013c0080 a0021c0024 others(11): Show |
21 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(18): Show |
synonymous_variant | LOW | c.3582G>A | p.Leu1194Leu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3582/4527 | 3582/4527 | 1194/1508 | chr4 | 5988464 | |||
chr4:5988794 | G | A | 1 | a0003c0090 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.3252C>T | p.Ala1084Ala | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3252/4527 | 3252/4527 | 1084/1508 | chr4 | 5988794 | |||
chr4:5988824 | G | A | 19 | a0001c0001 a0001c0084 a0001c0106 others(16): Show |
103 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(100): Show |
synonymous_variant | LOW | c.3222C>T | p.Ile1074Ile | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3222/4527 | 3222/4527 | 1074/1508 | chr4 | 5988824 | |||
chr4:5988872 | T | C | 113 | a0001c0001 a0001c0084 a0001c0106 others(110): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
synonymous_variant | LOW | c.3174A>G | p.Thr1058Thr | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 3174/4527 | 3174/4527 | 1058/1508 | chr4 | 5988872 | |||
chr4:5989064 | A | G | 89 | a0001c0001 a0001c0084 a0001c0106 others(86): Show |
249 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(246): Show |
synonymous_variant | LOW | c.2982T>C | p.Asp994Asp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2982/4527 | 2982/4527 | 994/1508 | chr4 | 5989064 | |||
chr4:5989163 | A | G | 1 | a0003c0086 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.2883T>C | p.Leu961Leu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2883/4527 | 2883/4527 | 961/1508 | chr4 | 5989163 | |||
chr4:5989721 | G | A | 1 | a0001c0106 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.2325C>T | p.Ala775Ala | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 2325/4527 | 2325/4527 | 775/1508 | chr4 | 5989721 | |||
chr4:5990210 | G | A | 11 | a0035c0037 a0040c0033 a0041c0041 others(8): Show |
14 | HG02109.hp1 HG02280.hp1 HG02647.hp1 others(11): Show |
synonymous_variant | LOW | c.1836C>T | p.Ala612Ala | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1836/4527 | 1836/4527 | 612/1508 | chr4 | 5990210 | |||
chr4:5990246 | G | A | 7 | a0025c0023 a0034c0040 a0043c0075 others(4): Show |
9 | HG00099.hp1 HG00280.hp2 HG01123.hp1 others(6): Show |
synonymous_variant | LOW | c.1800C>T | p.Asp600Asp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1800/4527 | 1800/4527 | 600/1508 | chr4 | 5990246 | |||
chr4:5990396 | A | G | 2 | a0035c0037 a0069c0111 |
3 | HG02109.hp1 HG02280.hp1 HG02809.hp1 |
synonymous_variant | LOW | c.1650T>C | p.Asn550Asn | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1650/4527 | 1650/4527 | 550/1508 | chr4 | 5990396 | |||
chr4:5990636 | C | T | 1 | a0001c0084 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.1410G>A | p.Pro470Pro | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1410/4527 | 1410/4527 | 470/1508 | chr4 | 5990636 | |||
chr4:5990648 | A | G | 1 | a0035c0037 | 2 | HG02109.hp1 HG02280.hp1 |
synonymous_variant | LOW | c.1398T>C | p.Pro466Pro | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/12 | 1398/4527 | 1398/4527 | 466/1508 | chr4 | 5990648 | |||
chr4:5992854 | C | T | 6 | a0031c0032 a0040c0033 a0065c0115 others(3): Show |
8 | HG01255.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
synonymous_variant | LOW | c.1170G>A | p.Pro390Pro | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/12 | 1170/4527 | 1170/4527 | 390/1508 | chr4 | 5992854 | |||
chr4:5994474 | A | G | 24 | a0010c0009 a0016c0015 a0018c0016 others(21): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
splice_region_variant&synonymous_variant | LOW | c.966T>C | p.Asp322Asp | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/12 | 966/4527 | 966/4527 | 322/1508 | chr4 | 5994474 | |||
chr4:6008041 | C | T | 1 | a0021c0050 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.918G>A | p.Leu306Leu | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/12 | 918/4527 | 918/4527 | 306/1508 | chr4 | 6008041 | |||
chr4:6011905 | G | A | 2 | a0026c0042 a0050c0116 |
3 | HG00323.hp1 HG01192.hp2 HG02300.hp2 |
synonymous_variant | LOW | c.351C>T | p.His117His | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/12 | 351/4527 | 351/4527 | 117/1508 | chr4 | 6011905 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:5959653 | T | C | 15 | a0036c0039t0001g0014 a0039c0025t0001g0206 a0051c0081t0001g0331 others(12): Show |
15 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.4276-27A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959653 | |||||||
chr4:5959660 | G | A | 2 | a0064c0060t0001g0067 a0085c0099t0001g0034 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4276-34C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959660 | |||||||
chr4:5959828 | C | T | 2 | a0013c0017t0001g0031 a0021c0050t0001g0064 |
2 | HG01257.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.4276-202G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959828 | |||||||
chr4:5959835 | G | C | 1 | a0019c0020t0001g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4276-209C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959835 | |||||||
chr4:5959886 | G | T | 2 | a0014c0012t0001g0048 a0060c0049t0001g0317 |
2 | HG02293.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4276-260C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959886 | |||||||
chr4:5959931 | G | A | 8 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(5): Show |
8 | HG02055.hp1 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4276-305C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959931 | |||||||
chr4:5959932 | G | A | 3 | a0004c0003t0001g0083 a0004c0003t0001g0131 a0106c0118t0001g0337 |
3 | NA18967.hp2 NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.4276-306C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959932 | |||||||
chr4:5959960 | G | A | 61 | a0004c0003t0001g0007 a0004c0003t0001g0083 a0004c0003t0001g0095 others(58): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.4276-334C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5959960 | |||||||
chr4:5960099 | A | C | 162 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(159): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.4276-473T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960099 | |||||||
chr4:5960160 | T | C | 170 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(167): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.4276-534A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960160 | |||||||
chr4:5960182 | G | A | 140 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(137): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4276-556C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960182 | |||||||
chr4:5960268 | C | A | 138 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.4276-642G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960268 | |||||||
chr4:5960281 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4276-655G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960281 | |||||||
chr4:5960308 | G | A | 2 | a0002c0002t0001g0200 a0002c0002t0001g0201 |
2 | NA18947.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.4276-682C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960308 | |||||||
chr4:5960404 | T | A | 1 | a0007c0007t0001g0260 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4276-778A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960404 | |||||||
chr4:5960431 | C | T | 1 | a0094c0059t0001g0217 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4276-805G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960431 | |||||||
chr4:5960523 | AGGC | A | 8 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(5): Show |
8 | HG02055.hp1 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4276-900_4276-898d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960523 | |||||||
chr4:5960601 | A | G | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4276-975T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960601 | |||||||
chr4:5960704 | A | G | 174 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(171): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.4276-1078T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960704 | |||||||
chr4:5960744 | C | A | 1 | a0101c0095t0001g0266 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4276-1118G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960744 | |||||||
chr4:5960787 | T | C | 6 | a0059c0102t0001g0269 a0065c0115t0001g0150 a0067c0072t0001g0082 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4276-1161A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960787 | |||||||
chr4:5960860 | T | A | 174 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(171): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.4276-1234A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960860 | |||||||
chr4:5960945 | C | T | 1 | a0069c0111t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4276-1319G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960945 | |||||||
chr4:5960981 | A | G | 174 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(171): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.4276-1355T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960981 | |||||||
chr4:5960992 | G | A | 8 | a0036c0039t0001g0014 a0039c0025t0001g0206 a0055c0057t0001g0039 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.4276-1366C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960992 | |||||||
chr4:5960999 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4276-1373C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5960999 | |||||||
chr4:5961047 | A | C | 1 | a0002c0002t0001g0182 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4276-1421T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961047 | |||||||
chr4:5961048 | AACAAGG | A | 3 | a0021c0024t0001g0205 a0029c0030t0001g0005 a0095c0107t0001g0286 |
4 | HG01167.hp2 HG01169.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4276-1428_4276-142 others(10): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961048 | |||||||
chr4:5961062 | C | A | 8 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(5): Show |
8 | HG02055.hp1 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.4276-1436G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961062 | |||||||
chr4:5961093 | C | A | 180 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(177): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.4276-1467G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961093 | |||||||
chr4:5961114 | C | T | 8 | a0051c0081t0001g0331 a0062c0082t0001g0285 a0074c0071t0001g0035 others(5): Show |
8 | HG01884.hp1 HG02451.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.4276-1488G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961114 | |||||||
chr4:5961223 | G | A | 2 | a0026c0042t0001g0332 a0026c0042t0001g0333 |
2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4276-1597C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961223 | |||||||
chr4:5961307 | T | A | 6 | a0059c0102t0001g0269 a0065c0115t0001g0150 a0067c0072t0001g0082 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4276-1681A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961307 | |||||||
chr4:5961460 | G | A | 1 | a0070c0113t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4276-1834C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961460 | |||||||
chr4:5961467 | G | A | 62 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(59): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.4276-1841C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961467 | |||||||
chr4:5961529 | A | G | 14 | a0036c0039t0001g0014 a0039c0025t0001g0206 a0051c0081t0001g0331 others(11): Show |
14 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.4276-1903T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961529 | |||||||
chr4:5961586 | A | C | 1 | a0016c0015t0001g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4276-1960T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961586 | |||||||
chr4:5961738 | T | C | 173 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4276-2112A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961738 | |||||||
chr4:5961774 | G | T | 1 | a0009c0010t0001g0144 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4276-2148C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961774 | |||||||
chr4:5961820 | C | CT | 23 | a0001c0106t0001g0246 a0036c0039t0001g0014 a0039c0025t0001g0065 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.4276-2195dupA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961820 | |||||||
chr4:5961899 | A | G | 1 | a0006c0006t0001g0111 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4276-2273T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961899 | |||||||
chr4:5961931 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0270 a0002c0002t0001g0196 |
3 | NA18949.hp2 NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.4276-2305G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961931 | |||||||
chr4:5961952 | G | A | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4276-2326C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961952 | |||||||
chr4:5961964 | C | G | 3 | a0009c0010t0001g0279 a0018c0016t0001g0276 a0018c0016t0001g0283 |
3 | HG02683.hp1 HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4276-2338G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5961964 | |||||||
chr4:5962049 | C | T | 170 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(167): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.4276-2423G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962049 | |||||||
chr4:5962155 | T | C | 1 | a0006c0006t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4276-2529A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962155 | |||||||
chr4:5962209 | T | C | 1 | a0101c0095t0001g0266 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4276-2583A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962209 | |||||||
chr4:5962238 | T | C | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4276-2612A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962238 | |||||||
chr4:5962250 | A | G | 1 | a0004c0003t0001g0239 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4276-2624T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962250 | |||||||
chr4:5962325 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4275+2699C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962325 | |||||||
chr4:5962471 | G | A | 1 | a0074c0071t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4275+2553C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962471 | |||||||
chr4:5962574 | T | C | 319 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(316): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.4275+2450A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962574 | |||||||
chr4:5962582 | G | A | 3 | a0004c0003t0001g0288 a0004c0003t0001g0289 a0015c0018t0001g0287 |
3 | HG00280.hp1 HG02698.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4275+2442C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962582 | |||||||
chr4:5962618 | T | C | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+2406A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962618 | |||||||
chr4:5962636 | C | T | 1 | a0008c0008t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4275+2388G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962636 | |||||||
chr4:5962644 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4275+2380C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962644 | |||||||
chr4:5962723 | C | A | 1 | a0060c0049t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4275+2301G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962723 | |||||||
chr4:5962807 | G | T | 6 | a0001c0001t0001g0033 a0005c0005t0001g0093 a0021c0024t0001g0066 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4275+2217C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962807 | |||||||
chr4:5962867 | C | T | 62 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(59): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.4275+2157G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962867 | |||||||
chr4:5962920 | A | G | 8 | a0005c0005t0001g0297 a0005c0005t0001g0298 a0009c0010t0001g0326 others(5): Show |
8 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.4275+2104T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962920 | |||||||
chr4:5962969 | G | A | 87 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(84): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.4275+2055C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962969 | |||||||
chr4:5962990 | T | C | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+2034A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962990 | |||||||
chr4:5962995 | CTTTTCTT others(6): Show |
C | 9 | a0014c0012t0001g0048 a0059c0102t0001g0269 a0060c0049t0001g0317 others(6): Show |
9 | HG02280.hp2 HG02293.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4275+2016_4275+202 others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962995 | |||||||
chr4:5962995 | CTTTTCTT others(7): Show |
C | 163 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(160): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.4275+2015_4275+202 others(18): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5962995 | |||||||
chr4:5963000 | C | CT | 10 | a0001c0001t0001g0033 a0001c0001t0001g0125 a0001c0001t0001g0209 others(7): Show |
10 | HG01109.hp1 HG02083.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.4275+2023dupA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963000 | |||||||
chr4:5963000 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0177 a0002c0002t0001g0090 |
2 | NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.4275+2010_4275+202 others(18): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963000 | |||||||
chr4:5963039 | T | C | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+1985A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963039 | |||||||
chr4:5963057 | A | G | 1 | a0002c0002t0001g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4275+1967T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963057 | |||||||
chr4:5963082 | A | G | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4275+1942T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963082 | |||||||
chr4:5963101 | A | C | 85 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(82): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.4275+1923T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963101 | |||||||
chr4:5963148 | A | G | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+1876T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963148 | |||||||
chr4:5963187 | T | C | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+1837A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963187 | |||||||
chr4:5963287 | G | A | 2 | a0021c0024t0001g0205 a0029c0030t0001g0005 |
3 | HG01167.hp2 HG01169.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4275+1737C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963287 | |||||||
chr4:5963314 | C | A | 9 | a0001c0001t0001g0174 a0002c0002t0001g0112 a0002c0002t0001g0185 others(6): Show |
9 | HG00544.hp2 HG02132.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.4275+1710G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963314 | |||||||
chr4:5963449 | A | G | 6 | a0051c0081t0001g0331 a0062c0082t0001g0285 a0079c0079t0001g0028 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.4275+1575T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963449 | |||||||
chr4:5963476 | C | T | 1 | a0068c0109t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4275+1548G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963476 | |||||||
chr4:5963489 | T | G | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4275+1535A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963489 | |||||||
chr4:5963495 | C | T | 171 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(168): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.4275+1529G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963495 | |||||||
chr4:5963532 | T | C | 165 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(162): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.4275+1492A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963532 | |||||||
chr4:5963583 | T | G | 1 | a0025c0023t0001g0318 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4275+1441A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963583 | |||||||
chr4:5963626 | T | G | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+1398A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963626 | |||||||
chr4:5963657 | C | T | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+1367G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5963657 | |||||||
chr4:5964033 | GT | G | 181 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.4275+990delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964033 | |||||||
chr4:5964105 | T | A | 172 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(169): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.4275+919A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964105 | |||||||
chr4:5964115 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4275+909T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964115 | |||||||
chr4:5964125 | A | G | 2 | a0051c0081t0001g0331 a0083c0047t0001g0013 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4275+899T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964125 | |||||||
chr4:5964182 | A | G | 171 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(168): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.4275+842T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964182 | |||||||
chr4:5964215 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0173 a0002c0002t0001g0259 |
3 | HG02080.hp1 HG02155.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.4275+809C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964215 | |||||||
chr4:5964243 | G | A | 1 | a0017c0019t0001g0308 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4275+781C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964243 | |||||||
chr4:5964282 | T | C | 1 | a0017c0019t0001g0308 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4275+742A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964282 | |||||||
chr4:5964283 | G | A | 2 | a0004c0003t0001g0009 a0004c0003t0001g0315 |
3 | HG01070.hp2 HG01071.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4275+741C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964283 | |||||||
chr4:5964336 | C | CA | 80 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(77): Show |
82 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.4275+687_4275+688i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964336 | |||||||
chr4:5964380 | G | A | 1 | a0073c0114t0001g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4275+644C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964380 | |||||||
chr4:5964411 | A | T | 2 | a0003c0004t0001g0211 a0003c0004t0001g0310 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4275+613T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964411 | |||||||
chr4:5964413 | A | T | 2 | a0007c0007t0001g0203 a0101c0095t0001g0266 |
2 | NA18971.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.4275+611T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964413 | |||||||
chr4:5964435 | GTCA | G | 85 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(82): Show |
87 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.4275+586_4275+588d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964435 | |||||||
chr4:5964468 | C | A | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4275+556G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964468 | |||||||
chr4:5964496 | A | G | 171 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(168): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.4275+528T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964496 | |||||||
chr4:5964683 | G | A | 6 | a0001c0001t0001g0281 a0013c0017t0001g0032 a0013c0017t0001g0038 others(3): Show |
6 | HG01884.hp2 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4275+341C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964683 | |||||||
chr4:5964767 | C | CAAA | 57 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(54): Show |
59 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.4275+254_4275+256d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | C | CAAAA | 14 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0005c0005t0001g0298 others(11): Show |
14 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.4275+253_4275+256d others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | C | CAAAAA | 10 | a0005c0005t0001g0297 a0022c0022t0001g0068 a0033c0036t0001g0261 others(7): Show |
10 | HG01516.hp2 HG01517.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.4275+252_4275+256d others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | CA | C | 135 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(132): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.4275+256delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | CAA | C | 17 | a0001c0001t0001g0175 a0002c0002t0001g0307 a0005c0005t0001g0085 others(14): Show |
17 | HG01168.hp1 HG01257.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.4275+255_4275+256d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | CAAA | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0158 a0005c0005t0001g0093 others(4): Show |
7 | HG01109.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.4275+254_4275+256d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | CAAAAAA | C | 6 | a0010c0009t0001g0162 a0051c0081t0001g0331 a0062c0082t0001g0285 others(3): Show |
6 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.4275+251_4275+256d others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | CAAAAAAA | C | 18 | a0010c0009t0001g0161 a0010c0009t0001g0163 a0010c0009t0001g0166 others(15): Show |
18 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.4275+250_4275+256d others(9): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964767 | CAAAAAAA others(1): Show |
C | 59 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(56): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.4275+249_4275+256d others(10): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964767 | |||||||
chr4:5964847 | T | C | 85 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(82): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.4275+177A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964847 | |||||||
chr4:5964876 | G | C | 3 | a0014c0012t0001g0048 a0060c0049t0001g0317 a0085c0099t0001g0034 |
3 | HG02293.hp1 HG03486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4275+148C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964876 | |||||||
chr4:5964891 | A | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4275+133T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964891 | |||||||
chr4:5964938 | G | A | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4275+86C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 11/11 | chr4 | 5964938 | |||||||
chr4:5965178 | C | T | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4154-33G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965178 | |||||||
chr4:5965216 | T | C | 85 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(82): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.4154-71A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965216 | |||||||
chr4:5965263 | T | C | 1 | a0004c0003t0001g0239 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4154-118A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965263 | |||||||
chr4:5965274 | C | CG | 78 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(75): Show |
82 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.4154-130dupC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965274 | |||||||
chr4:5965320 | A | G | 3 | a0051c0081t0001g0331 a0083c0047t0001g0013 a0086c0073t0001g0153 |
3 | HG01884.hp1 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4154-175T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965320 | |||||||
chr4:5965390 | C | T | 1 | a0064c0060t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4154-245G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965390 | |||||||
chr4:5965396 | C | T | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4154-251G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965396 | |||||||
chr4:5965434 | G | A | 2 | a0003c0004t0001g0211 a0003c0004t0001g0310 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4154-289C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965434 | |||||||
chr4:5965589 | A | G | 179 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4154-444T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965589 | |||||||
chr4:5965624 | A | G | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4154-479T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965624 | |||||||
chr4:5965639 | C | T | 83 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(80): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.4154-494G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965639 | |||||||
chr4:5965692 | T | G | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4154-547A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965692 | |||||||
chr4:5965715 | G | A | 4 | a0059c0102t0001g0269 a0065c0115t0001g0150 a0067c0072t0001g0082 others(1): Show |
4 | HG02280.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.4154-570C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965715 | |||||||
chr4:5965793 | T | G | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4154-648A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965793 | |||||||
chr4:5965809 | G | A | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4154-664C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965809 | |||||||
chr4:5965868 | T | C | 1 | a0007c0007t0001g0172 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4154-723A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965868 | |||||||
chr4:5965879 | A | T | 83 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(80): Show |
85 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.4154-734T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5965879 | |||||||
chr4:5966135 | T | C | 3 | a0021c0024t0001g0205 a0029c0030t0001g0005 a0095c0107t0001g0286 |
4 | HG01167.hp2 HG01169.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4154-990A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966135 | |||||||
chr4:5966159 | A | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4154-1014T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966159 | |||||||
chr4:5966162 | G | C | 1 | a0079c0079t0001g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4154-1017C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966162 | |||||||
chr4:5966225 | C | T | 1 | a0088c0105t0001g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4154-1080G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966225 | |||||||
chr4:5966242 | A | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4154-1097T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966242 | |||||||
chr4:5966251 | G | C | 9 | a0036c0039t0001g0014 a0039c0025t0001g0065 a0039c0025t0001g0206 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4154-1106C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966251 | |||||||
chr4:5966259 | T | C | 3 | a0021c0024t0001g0205 a0029c0030t0001g0005 a0095c0107t0001g0286 |
4 | HG01167.hp2 HG01169.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4154-1114A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966259 | |||||||
chr4:5966367 | C | T | 1 | a0103c0055t0001g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4153+1047G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966367 | |||||||
chr4:5966368 | G | T | 1 | a0103c0055t0001g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4153+1046C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966368 | |||||||
chr4:5966382 | A | G | 169 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(166): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.4153+1032T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966382 | |||||||
chr4:5966387 | A | G | 2 | a0013c0017t0001g0037 a0022c0022t0001g0047 |
2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.4153+1027T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966387 | |||||||
chr4:5966431 | C | T | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4153+983G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966431 | |||||||
chr4:5966435 | T | A | 173 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4153+979A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966435 | |||||||
chr4:5966453 | C | T | 9 | a0036c0039t0001g0014 a0039c0025t0001g0065 a0039c0025t0001g0206 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4153+961G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966453 | |||||||
chr4:5966511 | A | T | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4153+903T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966511 | |||||||
chr4:5966557 | A | T | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4153+857T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966557 | |||||||
chr4:5966658 | G | T | 83 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(80): Show |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.4153+756C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966658 | |||||||
chr4:5966659 | G | GT | 92 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(89): Show |
94 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.4153+754dupA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966659 | |||||||
chr4:5966659 | GT | G | 78 | a0002c0002t0001g0201 a0004c0003t0001g0007 a0004c0003t0001g0009 others(75): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.4153+754delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966659 | |||||||
chr4:5966674 | G | A | 1 | a0004c0003t0001g0241 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4153+740C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966674 | |||||||
chr4:5966713 | T | G | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4153+701A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966713 | |||||||
chr4:5966718 | C | T | 2 | a0079c0079t0001g0028 a0082c0064t0001g0324 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4153+696G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966718 | |||||||
chr4:5966736 | G | A | 3 | a0001c0001t0001g0088 a0003c0004t0001g0249 a0003c0004t0001g0255 |
3 | NA18960.hp1 NA18965.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4153+678C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966736 | |||||||
chr4:5966737 | T | C | 84 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(81): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.4153+677A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966737 | |||||||
chr4:5966777 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0141 a0001c0001t0001g0175 |
3 | HG02015.hp1 NA18947.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.4153+637C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966777 | |||||||
chr4:5966792 | A | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4153+622T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966792 | |||||||
chr4:5966807 | A | G | 173 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(170): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4153+607T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966807 | |||||||
chr4:5966873 | C | T | 1 | a0074c0071t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4153+541G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966873 | |||||||
chr4:5966883 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0228 |
2 | HG00558.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.4153+531G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966883 | |||||||
chr4:5966916 | G | C | 1 | a0080c0045t0001g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4153+498C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966916 | |||||||
chr4:5966916 | G | T | 2 | a0014c0012t0001g0048 a0060c0049t0001g0317 |
2 | HG02293.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4153+498C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966916 | |||||||
chr4:5966983 | T | C | 1 | a0018c0016t0001g0282 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4153+431A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5966983 | |||||||
chr4:5967005 | T | C | 86 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(83): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.4153+409A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5967005 | |||||||
chr4:5967061 | T | C | 86 | a0004c0003t0001g0007 a0004c0003t0001g0009 a0004c0003t0001g0083 others(83): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.4153+353A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5967061 | |||||||
chr4:5967126 | T | G | 2 | a0007c0007t0001g0193 a0007c0007t0001g0195 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.4153+288A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5967126 | |||||||
chr4:5967236 | T | C | 7 | a0005c0005t0001g0297 a0005c0005t0001g0298 a0012c0013t0001g0262 others(4): Show |
7 | HG01516.hp2 HG01517.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.4153+178A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5967236 | |||||||
chr4:5967386 | G | A | 164 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(161): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.4153+28C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 10/11 | chr4 | 5967386 | |||||||
chr4:5967508 | A | G | 179 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4105-46T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967508 | |||||||
chr4:5967525 | A | G | 179 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4105-63T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967525 | |||||||
chr4:5967532 | A | G | 5 | a0051c0081t0001g0331 a0079c0079t0001g0028 a0082c0064t0001g0324 others(2): Show |
5 | HG01884.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4105-70T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967532 | |||||||
chr4:5967565 | C | A | 179 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4105-103G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967565 | |||||||
chr4:5967572 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4105-110G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967572 | |||||||
chr4:5967576 | T | A | 179 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4105-114A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967576 | |||||||
chr4:5967612 | G | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0158 a0021c0024t0001g0066 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4105-150C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967612 | |||||||
chr4:5967620 | T | C | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4105-158A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967620 | |||||||
chr4:5967628 | T | C | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4105-166A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967628 | |||||||
chr4:5967637 | T | C | 179 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4105-175A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967637 | |||||||
chr4:5967651 | C | CA | 179 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4105-190_4105-189i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967651 | |||||||
chr4:5967792 | T | C | 14 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(11): Show |
14 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.4105-330A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967792 | |||||||
chr4:5967814 | C | A | 1 | a0074c0071t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4105-352G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967814 | |||||||
chr4:5967903 | C | T | 132 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(129): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.4105-441G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967903 | |||||||
chr4:5967913 | G | A | 126 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0126 others(123): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.4105-451C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967913 | |||||||
chr4:5967962 | C | T | 1 | a0084c0044t0001g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4105-500G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967962 | |||||||
chr4:5967971 | A | G | 1 | a0062c0082t0001g0285 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4105-509T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5967971 | |||||||
chr4:5968033 | A | G | 4 | a0021c0024t0001g0205 a0029c0030t0001g0005 a0095c0107t0001g0286 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.4105-571T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968033 | |||||||
chr4:5968072 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4105-610G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968072 | |||||||
chr4:5968112 | G | A | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4105-650C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968112 | |||||||
chr4:5968133 | G | A | 2 | a0079c0079t0001g0028 a0082c0064t0001g0324 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4105-671C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968133 | |||||||
chr4:5968242 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4105-780A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968242 | |||||||
chr4:5968259 | T | A | 2 | a0009c0010t0001g0280 a0022c0022t0001g0068 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4105-797A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968259 | |||||||
chr4:5968429 | G | A | 2 | a0013c0017t0001g0037 a0022c0022t0001g0047 |
2 | HG02257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.4105-967C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968429 | |||||||
chr4:5968465 | G | C | 139 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0075 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.4105-1003C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968465 | |||||||
chr4:5968560 | C | T | 8 | a0005c0005t0001g0295 a0019c0020t0001g0001 a0019c0020t0001g0060 others(5): Show |
9 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.4105-1098G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968560 | |||||||
chr4:5968663 | C | T | 11 | a0021c0024t0001g0205 a0036c0039t0001g0014 a0039c0025t0001g0065 others(8): Show |
11 | HG02258.hp1 HG02451.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.4105-1201G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968663 | |||||||
chr4:5968691 | C | T | 4 | a0001c0001t0001g0033 a0021c0024t0001g0066 a0086c0073t0001g0153 others(1): Show |
4 | HG01109.hp1 HG02559.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4105-1229G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968691 | |||||||
chr4:5968758 | G | C | 9 | a0009c0010t0001g0280 a0010c0009t0001g0161 a0010c0009t0001g0162 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4105-1296C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968758 | |||||||
chr4:5968781 | C | T | 164 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0155 others(161): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.4105-1319G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968781 | |||||||
chr4:5968799 | G | A | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4105-1337C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968799 | |||||||
chr4:5968807 | G | C | 7 | a0009c0010t0001g0267 a0023c0021t0001g0164 a0023c0021t0001g0165 others(4): Show |
7 | HG02622.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.4105-1345C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968807 | |||||||
chr4:5968816 | C | T | 3 | a0032c0029t0001g0057 a0047c0054t0001g0051 a0060c0049t0001g0317 |
3 | HG01106.hp2 HG01261.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.4105-1354G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968816 | |||||||
chr4:5968839 | C | G | 27 | a0001c0001t0001g0088 a0001c0001t0001g0177 a0002c0002t0001g0107 others(24): Show |
27 | HG00544.hp2 HG00735.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.4105-1377G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968839 | |||||||
chr4:5968860 | C | G | 38 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0126 others(35): Show |
38 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.4105-1398G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5968860 | |||||||
chr4:5969030 | G | A | 3 | a0032c0029t0001g0057 a0047c0054t0001g0051 a0060c0049t0001g0317 |
3 | HG01106.hp2 HG01261.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.4105-1568C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969030 | |||||||
chr4:5969071 | A | G | 159 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(156): Show |
162 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.4105-1609T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969071 | |||||||
chr4:5969151 | G | A | 1 | a0013c0017t0001g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4105-1689C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969151 | |||||||
chr4:5969188 | C | T | 1 | a0043c0075t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4105-1726G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969188 | |||||||
chr4:5969209 | C | T | 1 | a0077c0097t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4105-1747G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969209 | |||||||
chr4:5969323 | G | T | 6 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0022c0022t0001g0047 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4105-1861C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969323 | |||||||
chr4:5969355 | T | C | 62 | a0001c0001t0001g0033 a0001c0001t0001g0155 a0001c0001t0001g0158 others(59): Show |
63 | HG00099.hp1 HG00280.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.4105-1893A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969355 | |||||||
chr4:5969391 | T | A | 1 | a0007c0007t0001g0190 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4105-1929A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969391 | |||||||
chr4:5969425 | A | G | 44 | a0001c0001t0001g0033 a0001c0001t0001g0155 a0003c0004t0001g0303 others(41): Show |
44 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.4105-1963T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969425 | |||||||
chr4:5969454 | CA | C | 58 | a0001c0001t0001g0033 a0001c0001t0001g0155 a0001c0001t0001g0158 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.4105-1993delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969454 | |||||||
chr4:5969529 | G | A | 9 | a0023c0021t0001g0168 a0029c0030t0001g0005 a0071c0046t0001g0011 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.4105-2067C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969529 | |||||||
chr4:5969758 | A | G | 2 | a0002c0002t0001g0081 a0094c0059t0001g0217 |
2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4105-2296T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969758 | |||||||
chr4:5969769 | C | A | 1 | a0072c0100t0001g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4105-2307G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969769 | |||||||
chr4:5969787 | T | C | 10 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0021c0050t0001g0064 others(7): Show |
10 | HG01257.hp2 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.4105-2325A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969787 | |||||||
chr4:5969816 | T | C | 41 | a0001c0001t0001g0033 a0003c0004t0001g0303 a0003c0004t0001g0304 others(38): Show |
42 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.4105-2354A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969816 | |||||||
chr4:5969907 | A | G | 206 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(203): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.4105-2445T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969907 | |||||||
chr4:5969995 | C | T | 2 | a0057c0067t0001g0322 a0058c0083t0001g0222 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.4105-2533G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969995 | |||||||
chr4:5969996 | G | A | 1 | a0018c0016t0001g0282 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4105-2534C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5969996 | |||||||
chr4:5970020 | G | T | 1 | a0002c0002t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4105-2558C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970020 | |||||||
chr4:5970026 | C | T | 2 | a0042c0043t0001g0335 a0042c0043t0001g0336 |
2 | NA18979.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.4105-2564G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970026 | |||||||
chr4:5970040 | C | G | 70 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0174 others(67): Show |
75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.4105-2578G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970040 | |||||||
chr4:5970055 | G | A | 1 | a0021c0024t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4105-2593C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970055 | |||||||
chr4:5970148 | G | GA | 18 | a0005c0005t0001g0093 a0009c0010t0001g0279 a0009c0010t0001g0327 others(15): Show |
18 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.4105-2687dupT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970148 | |||||||
chr4:5970148 | GA | G | 83 | a0001c0001t0001g0033 a0001c0001t0001g0155 a0001c0001t0001g0173 others(80): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.4105-2687delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970148 | |||||||
chr4:5970172 | G | A | 17 | a0012c0013t0001g0301 a0015c0018t0001g0264 a0017c0019t0001g0213 others(14): Show |
19 | HG00642.hp1 HG00741.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.4105-2710C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970172 | |||||||
chr4:5970215 | G | A | 3 | a0064c0060t0001g0067 a0079c0079t0001g0028 a0085c0099t0001g0034 |
3 | HG02622.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4105-2753C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970215 | |||||||
chr4:5970255 | G | A | 2 | a0003c0004t0001g0249 a0003c0004t0001g0255 |
2 | NA18960.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4105-2793C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970255 | |||||||
chr4:5970265 | A | C | 1 | a0003c0004t0001g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4105-2803T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970265 | |||||||
chr4:5970590 | A | C | 5 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4104+3069T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970590 | |||||||
chr4:5970654 | A | C | 5 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0074c0071t0001g0035 others(2): Show |
5 | HG01891.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4104+3005T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970654 | |||||||
chr4:5970784 | A | G | 266 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(263): Show |
271 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.4104+2875T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970784 | |||||||
chr4:5970793 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4104+2866G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970793 | |||||||
chr4:5970842 | G | A | 1 | a0035c0037t0001g0293 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4104+2817C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970842 | |||||||
chr4:5970905 | G | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0268 a0001c0001t0001g0271 |
3 | NA18963.hp2 NA18989.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4104+2754C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970905 | |||||||
chr4:5970932 | A | G | 1 | a0069c0111t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4104+2727T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970932 | |||||||
chr4:5970977 | T | G | 10 | a0011c0014t0001g0302 a0011c0014t0001g0309 a0012c0013t0001g0301 others(7): Show |
11 | HG01099.hp2 HG01192.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.4104+2682A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970977 | |||||||
chr4:5970990 | C | A | 1 | a0055c0057t0001g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4104+2669G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5970990 | |||||||
chr4:5971070 | G | C | 6 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0013c0017t0001g0037 others(3): Show |
6 | HG01255.hp2 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.4104+2589C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971070 | |||||||
chr4:5971072 | A | G | 142 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(139): Show |
145 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.4104+2587T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971072 | |||||||
chr4:5971106 | G | A | 3 | a0001c0001t0001g0075 a0049c0053t0001g0055 a0068c0109t0001g0092 |
3 | HG01070.hp1 HG01168.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4104+2553C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971106 | |||||||
chr4:5971118 | A | C | 55 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(52): Show |
55 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.4104+2541T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971118 | |||||||
chr4:5971196 | G | A | 1 | a0048c0051t0001g0053 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4104+2463C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971196 | |||||||
chr4:5971228 | G | A | 1 | a0077c0097t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4104+2431C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971228 | |||||||
chr4:5971328 | G | T | 1 | a0002c0002t0001g0160 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4104+2331C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971328 | |||||||
chr4:5971336 | T | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(99): Show |
104 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.4104+2323A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971336 | |||||||
chr4:5971372 | C | T | 1 | a0004c0003t0001g0239 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4104+2287G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971372 | |||||||
chr4:5971437 | A | G | 2 | a0070c0113t0001g0029 a0087c0062t0001g0022 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4104+2222T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971437 | |||||||
chr4:5971467 | C | T | 3 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.4104+2192G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971467 | |||||||
chr4:5971482 | AT | A | 54 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(51): Show |
54 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.4104+2176delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971482 | |||||||
chr4:5971537 | G | A | 330 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(327): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.4104+2122C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971537 | |||||||
chr4:5971585 | C | T | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+2074G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971585 | |||||||
chr4:5971701 | G | A | 4 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0028c0031t0001g0218 others(1): Show |
4 | HG00735.hp2 HG01361.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.4104+1958C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971701 | |||||||
chr4:5971941 | G | A | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+1718C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971941 | |||||||
chr4:5971984 | T | G | 1 | a0077c0097t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4104+1675A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5971984 | |||||||
chr4:5972008 | A | AT | 55 | a0001c0001t0001g0124 a0001c0001t0001g0154 a0001c0001t0001g0228 others(52): Show |
56 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.4104+1650dupA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972008 | |||||||
chr4:5972008 | AT | A | 101 | a0001c0001t0001g0116 a0002c0002t0001g0081 a0002c0002t0001g0090 others(98): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.4104+1650delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972008 | |||||||
chr4:5972162 | G | C | 7 | a0040c0033t0001g0273 a0040c0033t0001g0294 a0064c0060t0001g0067 others(4): Show |
7 | HG02622.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4104+1497C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972162 | |||||||
chr4:5972190 | A | G | 1 | a0016c0015t0001g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4104+1469T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972190 | |||||||
chr4:5972247 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4104+1412A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972247 | |||||||
chr4:5972335 | T | A | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+1324A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972335 | |||||||
chr4:5972501 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(158): Show |
164 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.4104+1158A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972501 | |||||||
chr4:5972578 | G | C | 4 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0077c0097t0001g0208 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4104+1081C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972578 | |||||||
chr4:5972581 | A | T | 1 | a0015c0018t0001g0300 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4104+1078T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972581 | |||||||
chr4:5972587 | C | T | 3 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0077c0097t0001g0208 |
3 | HG01891.hp2 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4104+1072G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972587 | |||||||
chr4:5972591 | G | C | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+1068C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972591 | |||||||
chr4:5972659 | A | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(154): Show |
160 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.4104+1000T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972659 | |||||||
chr4:5972682 | G | A | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+977C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972682 | |||||||
chr4:5972768 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4104+891G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972768 | |||||||
chr4:5972823 | G | A | 1 | a0068c0109t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4104+836C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972823 | |||||||
chr4:5972856 | C | T | 1 | a0006c0006t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4104+803G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972856 | |||||||
chr4:5972857 | G | A | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4104+802C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972857 | |||||||
chr4:5972869 | G | A | 2 | a0004c0003t0001g0224 a0097c0101t0001g0089 |
2 | HG00597.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.4104+790C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972869 | |||||||
chr4:5972875 | G | T | 3 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0077c0097t0001g0208 |
3 | HG01891.hp2 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.4104+784C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972875 | |||||||
chr4:5972972 | C | T | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+687G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5972972 | |||||||
chr4:5973101 | G | A | 1 | a0064c0060t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4104+558C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973101 | |||||||
chr4:5973107 | G | C | 168 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(165): Show |
172 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.4104+552C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973107 | |||||||
chr4:5973116 | G | A | 1 | a0006c0006t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4104+543C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973116 | |||||||
chr4:5973202 | A | G | 253 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(250): Show |
257 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.4104+457T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973202 | |||||||
chr4:5973305 | A | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(158): Show |
164 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.4104+354T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973305 | |||||||
chr4:5973362 | C | T | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+297G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973362 | |||||||
chr4:5973378 | A | G | 1 | a0022c0022t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4104+281T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973378 | |||||||
chr4:5973393 | C | T | 171 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(168): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.4104+266G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973393 | |||||||
chr4:5973403 | C | G | 2 | a0003c0004t0001g0211 a0003c0004t0001g0310 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4104+256G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973403 | |||||||
chr4:5973446 | C | T | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+213G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973446 | |||||||
chr4:5973447 | A | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(166): Show |
173 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(170): Show |
intron_variant | MODIFIER | c.4104+212T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973447 | |||||||
chr4:5973521 | A | G | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4104+138T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973521 | |||||||
chr4:5973526 | G | T | 1 | a0001c0001t0001g0271 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.4104+133C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973526 | |||||||
chr4:5973604 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4104+55C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973604 | |||||||
chr4:5973607 | C | T | 2 | a0016c0015t0001g0043 a0016c0015t0001g0045 |
2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4104+52G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973607 | |||||||
chr4:5973610 | G | A | 1 | a0090c0078t0001g0311 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4104+49C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973610 | |||||||
chr4:5973651 | G | A | 29 | a0002c0002t0001g0081 a0005c0005t0001g0295 a0005c0005t0001g0297 others(26): Show |
30 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.4104+8C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973651 | |||||||
chr4:5973658 | C | T | 1 | a0053c0068t0001g0329 | 1 | HG01978.hp1 | splice_donor_variant&intron_variant | HIGH | c.4104+1G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 9/11 | chr4 | 5973658 | |||||||
chr4:5973988 | A | C | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3922-147T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5973988 | |||||||
chr4:5974002 | C | A | 7 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0013c0017t0001g0037 others(4): Show |
7 | HG01255.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3922-161G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974002 | |||||||
chr4:5974053 | G | A | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3922-212C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974053 | |||||||
chr4:5974057 | T | C | 1 | a0015c0018t0001g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3922-216A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974057 | |||||||
chr4:5974063 | T | G | 1 | a0076c0074t0001g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3922-222A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974063 | |||||||
chr4:5974102 | C | T | 1 | a0088c0105t0001g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3922-261G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974102 | |||||||
chr4:5974168 | A | G | 1 | a0017c0019t0001g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3922-327T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974168 | |||||||
chr4:5974182 | C | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(158): Show |
164 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.3922-341G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974182 | |||||||
chr4:5974212 | C | T | 2 | a0071c0046t0001g0011 a0085c0099t0001g0034 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3922-371G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974212 | |||||||
chr4:5974237 | G | A | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3922-396C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974237 | |||||||
chr4:5974311 | C | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(99): Show |
104 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.3922-470G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974311 | |||||||
chr4:5974373 | C | A | 161 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(158): Show |
164 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.3922-532G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974373 | |||||||
chr4:5974377 | C | T | 37 | a0002c0002t0001g0081 a0005c0005t0001g0295 a0005c0005t0001g0297 others(34): Show |
38 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.3922-536G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974377 | |||||||
chr4:5974391 | C | T | 160 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(157): Show |
163 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.3922-550G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974391 | |||||||
chr4:5974393 | AGCTACCA others(13): Show |
A | 1 | a0075c0098t0001g0272 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3922-572_3922-553d others(22): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974393 | |||||||
chr4:5974449 | G | A | 1 | a0003c0004t0001g0254 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3922-608C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974449 | |||||||
chr4:5974453 | AC | A | 160 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(157): Show |
163 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.3922-613delG | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974453 | |||||||
chr4:5974457 | G | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(157): Show |
163 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.3922-616C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974457 | |||||||
chr4:5974485 | G | A | 2 | a0069c0111t0001g0094 a0074c0071t0001g0035 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3922-644C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974485 | |||||||
chr4:5974487 | G | A | 160 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(157): Show |
163 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.3922-646C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974487 | |||||||
chr4:5974608 | T | G | 1 | a0021c0024t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3922-767A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974608 | |||||||
chr4:5974702 | T | G | 2 | a0069c0111t0001g0094 a0074c0071t0001g0035 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3922-861A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974702 | |||||||
chr4:5974744 | C | A | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3922-903G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974744 | |||||||
chr4:5974801 | T | C | 5 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3922-960A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974801 | |||||||
chr4:5974822 | C | T | 1 | a0076c0074t0001g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3922-981G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974822 | |||||||
chr4:5974825 | GGAGAAAA others(9): Show |
G | 2 | a0003c0011t0001g0229 a0003c0086t0001g0232 |
2 | HG01099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.3922-1000_3922-985 others(19): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974825 | |||||||
chr4:5974913 | G | T | 1 | a0068c0109t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3921+986C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974913 | |||||||
chr4:5974943 | C | T | 75 | a0002c0002t0001g0179 a0003c0004t0001g0006 a0003c0004t0001g0077 others(72): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.3921+956G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974943 | |||||||
chr4:5974967 | C | T | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+932G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974967 | |||||||
chr4:5974995 | C | T | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+904G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5974995 | |||||||
chr4:5975015 | C | A | 3 | a0003c0011t0001g0235 a0003c0011t0001g0236 a0004c0087t0001g0237 |
3 | HG01069.hp1 HG01081.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3921+884G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975015 | |||||||
chr4:5975121 | CAG | C | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+776_3921+777d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975121 | |||||||
chr4:5975139 | C | CA | 33 | a0002c0002t0001g0143 a0002c0002t0001g0187 a0002c0002t0001g0258 others(30): Show |
35 | HG00558.hp2 HG00609.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.3921+759dupT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | C | CAA | 23 | a0002c0002t0001g0090 a0002c0002t0001g0107 a0002c0002t0001g0112 others(20): Show |
24 | HG00140.hp1 HG00544.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.3921+758_3921+759d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | C | CAAA | 18 | a0002c0002t0001g0176 a0002c0002t0001g0183 a0002c0002t0001g0186 others(15): Show |
18 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.3921+757_3921+759d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | C | CAAAA | 5 | a0005c0005t0001g0101 a0027c0038t0001g0002 a0038c0034t0001g0017 others(2): Show |
6 | HG00642.hp1 HG00741.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3921+756_3921+759d others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CA | C | 10 | a0003c0004t0001g0304 a0003c0004t0001g0305 a0010c0009t0001g0162 others(7): Show |
10 | HG01168.hp2 HG01169.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.3921+759delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAA | C | 7 | a0003c0004t0001g0077 a0010c0009t0001g0161 a0010c0009t0001g0166 others(4): Show |
7 | HG01071.hp2 HG01106.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.3921+758_3921+759d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA | C | 11 | a0001c0001t0001g0117 a0001c0001t0001g0221 a0001c0001t0001g0244 others(8): Show |
11 | HG01109.hp2 HG01952.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.3921+753_3921+759d others(9): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(1): Show |
C | 37 | a0001c0001t0001g0056 a0001c0001t0001g0074 a0001c0001t0001g0079 others(34): Show |
37 | HG00642.hp2 HG01168.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.3921+752_3921+759d others(10): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(2): Show |
C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(48): Show |
53 | HG00544.hp1 HG00597.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.3921+751_3921+759d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0177 a0001c0106t0001g0246 |
3 | HG00609.hp1 NA18982.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3921+750_3921+759d others(12): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(4): Show |
C | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3921+749_3921+759d others(13): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(5): Show |
C | 1 | a0042c0043t0001g0335 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3921+748_3921+759d others(14): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(7): Show |
C | 52 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(49): Show |
53 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.3921+746_3921+759d others(16): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(8): Show |
C | 2 | a0005c0005t0001g0136 a0107c0117t0001g0019 |
2 | HG03654.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3921+745_3921+759d others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(15): Show |
C | 2 | a0078c0066t0001g0018 a0102c0112t0001g0015 |
2 | HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3921+738_3921+759d others(24): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975139 | CAAAAAAA others(16): Show |
C | 28 | a0002c0002t0001g0081 a0005c0005t0001g0295 a0005c0005t0001g0297 others(25): Show |
29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.3921+737_3921+759d others(25): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975139 | |||||||
chr4:5975147 | A | C | 1 | a0022c0022t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3921+752T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975147 | |||||||
chr4:5975158 | A | C | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3921+741T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975158 | |||||||
chr4:5975161 | A | C | 1 | a0022c0022t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3921+738T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975161 | |||||||
chr4:5975164 | A | C | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3921+735T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975164 | |||||||
chr4:5975165 | A | C | 1 | a0022c0022t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3921+734T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975165 | |||||||
chr4:5975168 | A | C | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+731T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975168 | |||||||
chr4:5975170 | A | C | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3921+729T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975170 | |||||||
chr4:5975172 | A | C | 56 | a0001c0001t0001g0228 a0009c0010t0001g0267 a0009c0010t0001g0280 others(53): Show |
57 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.3921+727T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975172 | |||||||
chr4:5975180 | T | C | 1 | a0068c0109t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3921+719A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975180 | |||||||
chr4:5975224 | T | C | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+675A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975224 | |||||||
chr4:5975238 | G | A | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+661C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975238 | |||||||
chr4:5975255 | G | A | 1 | a0051c0081t0001g0331 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3921+644C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975255 | |||||||
chr4:5975263 | G | T | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+636C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975263 | |||||||
chr4:5975282 | G | T | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3921+617C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975282 | |||||||
chr4:5975290 | T | C | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+609A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975290 | |||||||
chr4:5975304 | A | C | 1 | a0004c0003t0001g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3921+595T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975304 | |||||||
chr4:5975343 | G | C | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+556C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975343 | |||||||
chr4:5975384 | C | T | 53 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3921+515G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975384 | |||||||
chr4:5975406 | A | C | 36 | a0002c0002t0001g0081 a0005c0005t0001g0295 a0005c0005t0001g0297 others(33): Show |
37 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.3921+493T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975406 | |||||||
chr4:5975495 | T | TTTTTG | 5 | a0003c0004t0001g0254 a0004c0003t0001g0241 a0010c0009t0001g0161 others(2): Show |
5 | HG02055.hp1 HG02083.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3921+399_3921+403d others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975495 | |||||||
chr4:5975495 | TTTTTG | T | 246 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(243): Show |
249 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.3921+399_3921+403d others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975495 | |||||||
chr4:5975495 | TTTTTGTT others(8): Show |
T | 3 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3921+389_3921+403d others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975495 | |||||||
chr4:5975513 | T | C | 1 | a0025c0023t0001g0318 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3921+386A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975513 | |||||||
chr4:5975525 | G | A | 2 | a0005c0005t0001g0295 a0005c0005t0001g0298 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3921+374C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975525 | |||||||
chr4:5975619 | T | C | 54 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(51): Show |
55 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.3921+280A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975619 | |||||||
chr4:5975625 | C | G | 54 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(51): Show |
55 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.3921+274G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975625 | |||||||
chr4:5975657 | C | T | 1 | a0013c0017t0001g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3921+242G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975657 | |||||||
chr4:5975735 | C | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(99): Show |
104 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.3921+164G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975735 | |||||||
chr4:5975826 | T | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(99): Show |
104 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.3921+73A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975826 | |||||||
chr4:5975839 | C | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(188): Show |
195 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.3921+60G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 8/11 | chr4 | 5975839 | |||||||
chr4:5976171 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3865-216G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976171 | |||||||
chr4:5976184 | G | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(99): Show |
104 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.3865-229C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976184 | |||||||
chr4:5976241 | C | T | 5 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865-286G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976241 | |||||||
chr4:5976281 | T | C | 3 | a0003c0011t0001g0235 a0003c0011t0001g0236 a0004c0087t0001g0237 |
3 | HG01069.hp1 HG01081.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3865-326A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976281 | |||||||
chr4:5976315 | G | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(99): Show |
104 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.3865-360C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976315 | |||||||
chr4:5976320 | G | A | 1 | a0011c0014t0001g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3865-365C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976320 | |||||||
chr4:5976328 | C | T | 1 | a0060c0049t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3865-373G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976328 | |||||||
chr4:5976403 | C | A | 6 | a0021c0024t0001g0066 a0021c0024t0001g0205 a0021c0050t0001g0064 others(3): Show |
6 | HG01257.hp2 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3865-448G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976403 | |||||||
chr4:5976426 | A | G | 46 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(43): Show |
47 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.3865-471T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976426 | |||||||
chr4:5976437 | G | C | 254 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(251): Show |
258 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.3865-482C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976437 | |||||||
chr4:5976457 | G | GA | 71 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(68): Show |
71 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.3865-503dupT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976457 | |||||||
chr4:5976457 | G | GAA | 8 | a0002c0002t0001g0189 a0002c0002t0001g0202 a0002c0002t0001g0251 others(5): Show |
8 | HG01891.hp1 HG02109.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.3865-504_3865-503d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976457 | |||||||
chr4:5976457 | GA | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0056 others(94): Show |
99 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.3865-503delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976457 | |||||||
chr4:5976457 | GAA | G | 42 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(39): Show |
43 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.3865-504_3865-503d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976457 | |||||||
chr4:5976457 | GAAAAAAA | G | 10 | a0002c0002t0001g0081 a0024c0027t0001g0041 a0025c0023t0001g0318 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.3865-509_3865-503d others(9): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976457 | |||||||
chr4:5976459 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3865-504T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976459 | |||||||
chr4:5976603 | G | A | 2 | a0009c0010t0001g0267 a0009c0010t0001g0280 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3865-648C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976603 | |||||||
chr4:5976677 | A | C | 1 | a0012c0013t0001g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3865-722T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976677 | |||||||
chr4:5976688 | G | C | 57 | a0001c0001t0001g0228 a0010c0009t0001g0161 a0010c0009t0001g0162 others(54): Show |
59 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.3865-733C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5976688 | |||||||
chr4:5977187 | T | C | 52 | a0001c0001t0001g0228 a0005c0005t0001g0093 a0011c0014t0001g0145 others(49): Show |
53 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(50): Show |
intron_variant | MODIFIER | c.3865-1232A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977187 | |||||||
chr4:5977221 | C | A | 3 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865-1266G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977221 | |||||||
chr4:5977313 | A | T | 58 | a0001c0001t0001g0228 a0010c0009t0001g0161 a0010c0009t0001g0162 others(55): Show |
60 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.3865-1358T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977313 | |||||||
chr4:5977344 | C | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(101): Show |
106 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.3865-1389G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977344 | |||||||
chr4:5977358 | G | A | 1 | a0068c0109t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3865-1403C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977358 | |||||||
chr4:5977416 | G | T | 1 | a0102c0112t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3865-1461C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977416 | |||||||
chr4:5977456 | T | A | 45 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(42): Show |
46 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.3865-1501A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977456 | |||||||
chr4:5977526 | C | G | 46 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(43): Show |
47 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.3865-1571G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977526 | |||||||
chr4:5977601 | GT | G | 46 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(43): Show |
47 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.3865-1647delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977601 | |||||||
chr4:5977738 | C | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(152): Show |
158 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.3865-1783G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977738 | |||||||
chr4:5977747 | A | G | 51 | a0001c0001t0001g0228 a0005c0005t0001g0093 a0011c0014t0001g0145 others(48): Show |
52 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.3865-1792T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977747 | |||||||
chr4:5977846 | G | T | 4 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0031c0032t0001g0025 others(1): Show |
4 | HG01255.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865-1891C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977846 | |||||||
chr4:5977859 | G | A | 6 | a0004c0003t0001g0114 a0004c0003t0001g0115 a0004c0003t0001g0137 others(3): Show |
6 | HG00597.hp1 HG02165.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3865-1904C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977859 | |||||||
chr4:5977916 | T | C | 1 | a0003c0004t0001g0254 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3865-1961A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5977916 | |||||||
chr4:5978036 | C | T | 1 | a0002c0002t0001g0307 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3865-2081G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978036 | |||||||
chr4:5978060 | C | T | 2 | a0071c0046t0001g0011 a0085c0099t0001g0034 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3865-2105G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978060 | |||||||
chr4:5978125 | T | G | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3864+2049A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978125 | |||||||
chr4:5978244 | C | T | 1 | a0022c0022t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3864+1930G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978244 | |||||||
chr4:5978282 | G | T | 4 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0077c0097t0001g0208 others(1): Show |
4 | HG01891.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3864+1892C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978282 | |||||||
chr4:5978283 | AATTAC | A | 45 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(42): Show |
46 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.3864+1886_3864+189 others(9): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978283 | |||||||
chr4:5978325 | A | C | 1 | a0034c0040t0001g0291 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3864+1849T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978325 | |||||||
chr4:5978383 | T | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(95): Show |
100 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.3864+1791A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978383 | |||||||
chr4:5978400 | C | T | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3864+1774G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978400 | |||||||
chr4:5978499 | A | G | 1 | a0068c0109t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3864+1675T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978499 | |||||||
chr4:5978621 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA18941.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.3864+1553G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978621 | |||||||
chr4:5978843 | A | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(94): Show |
99 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.3864+1331T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978843 | |||||||
chr4:5978867 | C | T | 53 | a0001c0001t0001g0228 a0009c0010t0001g0326 a0009c0010t0001g0327 others(50): Show |
54 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.3864+1307G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978867 | |||||||
chr4:5978887 | T | C | 4 | a0005c0005t0001g0093 a0038c0034t0001g0017 a0038c0034t0001g0330 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3864+1287A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978887 | |||||||
chr4:5978970 | G | A | 1 | a0024c0027t0001g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3864+1204C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978970 | |||||||
chr4:5978980 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3864+1194C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978980 | |||||||
chr4:5978988 | T | C | 1 | a0014c0012t0001g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3864+1186A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978988 | |||||||
chr4:5978989 | A | T | 1 | a0014c0012t0001g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3864+1185T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978989 | |||||||
chr4:5978991 | C | A | 1 | a0014c0012t0001g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3864+1183G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978991 | |||||||
chr4:5978992 | G | A | 6 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3864+1182C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5978992 | |||||||
chr4:5979224 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3864+950G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979224 | |||||||
chr4:5979225 | G | A | 7 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0013c0017t0001g0037 others(4): Show |
7 | HG01255.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3864+949C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979225 | |||||||
chr4:5979277 | G | A | 58 | a0001c0001t0001g0228 a0010c0009t0001g0161 a0010c0009t0001g0162 others(55): Show |
60 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.3864+897C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979277 | |||||||
chr4:5979424 | C | G | 66 | a0001c0001t0001g0228 a0009c0010t0001g0326 a0009c0010t0001g0327 others(63): Show |
68 | HG00323.hp1 HG00558.hp1 HG01099.hp2 others(65): Show |
intron_variant | MODIFIER | c.3864+750G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979424 | |||||||
chr4:5979519 | T | C | 1 | a0079c0079t0001g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3864+655A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979519 | |||||||
chr4:5979541 | G | A | 2 | a0018c0016t0001g0210 a0057c0067t0001g0322 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3864+633C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979541 | |||||||
chr4:5979574 | G | A | 7 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0013c0017t0001g0037 others(4): Show |
7 | HG01255.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3864+600C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979574 | |||||||
chr4:5979616 | T | A | 1 | a0089c0091t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3864+558A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979616 | |||||||
chr4:5979722 | T | C | 1 | a0009c0010t0001g0326 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3864+452A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979722 | |||||||
chr4:5979798 | G | A | 2 | a0013c0017t0001g0037 a0051c0081t0001g0331 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3864+376C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5979798 | |||||||
chr4:5980015 | G | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(100): Show |
105 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.3864+159C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5980015 | |||||||
chr4:5980018 | T | G | 1 | a0068c0109t0001g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3864+156A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5980018 | |||||||
chr4:5980062 | G | A | 77 | a0001c0001t0001g0228 a0002c0002t0001g0081 a0005c0005t0001g0295 others(74): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.3864+112C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5980062 | |||||||
chr4:5980122 | C | T | 30 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(27): Show |
31 | HG00558.hp1 HG01099.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.3864+52G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 7/11 | chr4 | 5980122 | |||||||
chr4:5980381 | T | C | 140 | a0001c0001t0001g0228 a0002c0002t0001g0081 a0002c0002t0001g0090 others(137): Show |
143 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.3700-43A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980381 | |||||||
chr4:5980408 | G | T | 127 | a0001c0001t0001g0228 a0002c0002t0001g0090 a0002c0002t0001g0091 others(124): Show |
129 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.3700-70C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980408 | |||||||
chr4:5980431 | G | GT | 11 | a0001c0001t0001g0098 a0001c0001t0001g0105 a0001c0001t0001g0174 others(8): Show |
11 | HG01123.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.3700-94dupA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980431 | |||||||
chr4:5980431 | GT | G | 125 | a0001c0001t0001g0228 a0002c0002t0001g0090 a0002c0002t0001g0091 others(122): Show |
127 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.3700-94delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980431 | |||||||
chr4:5980440 | T | G | 7 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.3700-102A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980440 | |||||||
chr4:5980443 | G | T | 1 | a0001c0106t0001g0246 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3700-105C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980443 | |||||||
chr4:5980580 | A | C | 3 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0077c0097t0001g0208 |
3 | HG01891.hp2 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3700-242T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980580 | |||||||
chr4:5980606 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3700-268C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980606 | |||||||
chr4:5980801 | A | G | 2 | a0071c0046t0001g0011 a0085c0099t0001g0034 |
2 | HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3700-463T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980801 | |||||||
chr4:5980822 | T | A | 41 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(38): Show |
41 | HG00323.hp1 HG01255.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.3700-484A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980822 | |||||||
chr4:5980866 | T | G | 1 | a0032c0029t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3700-528A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980866 | |||||||
chr4:5980919 | C | T | 5 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0013c0080t0001g0212 others(2): Show |
5 | HG01891.hp2 HG02738.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3700-581G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980919 | |||||||
chr4:5980920 | G | A | 2 | a0003c0004t0001g0249 a0003c0004t0001g0255 |
2 | NA18960.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.3700-582C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5980920 | |||||||
chr4:5981207 | C | G | 5 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0013c0080t0001g0212 others(2): Show |
5 | HG01891.hp2 HG02738.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3700-869G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981207 | |||||||
chr4:5981241 | A | T | 5 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0013c0080t0001g0212 others(2): Show |
5 | HG01891.hp2 HG02738.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3700-903T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981241 | |||||||
chr4:5981244 | C | G | 24 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0018c0016t0001g0210 others(21): Show |
24 | HG00323.hp1 HG01255.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.3700-906G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981244 | |||||||
chr4:5981259 | G | A | 1 | a0102c0112t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3700-921C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981259 | |||||||
chr4:5981301 | T | C | 4 | a0012c0013t0001g0262 a0033c0036t0001g0261 a0033c0036t0001g0265 others(1): Show |
4 | HG01106.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.3700-963A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981301 | |||||||
chr4:5981326 | C | T | 41 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(38): Show |
41 | HG00323.hp1 HG01255.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.3700-988G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981326 | |||||||
chr4:5981402 | C | CT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(97): Show |
101 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.3700-1065dupA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981402 | |||||||
chr4:5981402 | C | CTT | 13 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0158 others(10): Show |
14 | HG01167.hp1 HG02071.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.3700-1066_3700-106 others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981402 | |||||||
chr4:5981402 | CT | C | 40 | a0001c0001t0001g0228 a0003c0004t0001g0191 a0005c0005t0001g0093 others(37): Show |
42 | HG00558.hp1 HG01099.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.3700-1065delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981402 | |||||||
chr4:5981402 | CTT | C | 47 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(44): Show |
47 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.3700-1066_3700-106 others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981402 | |||||||
chr4:5981421 | T | C | 1 | a0012c0013t0001g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3700-1083A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981421 | |||||||
chr4:5981470 | C | T | 131 | a0001c0001t0001g0228 a0002c0002t0001g0090 a0002c0002t0001g0091 others(128): Show |
133 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.3700-1132G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981470 | |||||||
chr4:5981481 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3700-1143G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981481 | |||||||
chr4:5981543 | T | A | 11 | a0002c0002t0001g0081 a0024c0027t0001g0041 a0025c0023t0001g0318 others(8): Show |
11 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.3700-1205A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981543 | |||||||
chr4:5981565 | C | T | 1 | a0102c0112t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3700-1227G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981565 | |||||||
chr4:5981623 | C | T | 30 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(27): Show |
31 | HG00558.hp1 HG01099.hp2 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.3700-1285G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981623 | |||||||
chr4:5981639 | G | A | 18 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(15): Show |
19 | HG00558.hp1 HG01099.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.3700-1301C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981639 | |||||||
chr4:5981650 | C | T | 1 | a0073c0114t0001g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3700-1312G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981650 | |||||||
chr4:5981700 | G | A | 2 | a0003c0004t0001g0211 a0003c0004t0001g0310 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3700-1362C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981700 | |||||||
chr4:5981705 | G | A | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3700-1367C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981705 | |||||||
chr4:5981768 | C | A | 1 | a0102c0112t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3700-1430G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981768 | |||||||
chr4:5981829 | T | TC | 86 | a0001c0001t0001g0228 a0002c0002t0001g0090 a0002c0002t0001g0091 others(83): Show |
88 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.3700-1492dupG | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981829 | |||||||
chr4:5981905 | A | G | 2 | a0003c0004t0001g0211 a0003c0004t0001g0310 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3700-1567T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981905 | |||||||
chr4:5981932 | T | A | 97 | a0001c0001t0001g0228 a0002c0002t0001g0090 a0002c0002t0001g0091 others(94): Show |
99 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.3700-1594A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5981932 | |||||||
chr4:5982024 | A | G | 243 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(240): Show |
248 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(245): Show |
intron_variant | MODIFIER | c.3700-1686T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982024 | |||||||
chr4:5982030 | A | C | 12 | a0021c0024t0001g0066 a0021c0024t0001g0205 a0021c0050t0001g0064 others(9): Show |
12 | HG01257.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3700-1692T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982030 | |||||||
chr4:5982033 | T | C | 1 | a0102c0112t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3700-1695A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982033 | |||||||
chr4:5982049 | AT | A | 6 | a0002c0002t0001g0186 a0002c0002t0001g0200 a0002c0002t0001g0201 others(3): Show |
6 | HG02135.hp2 HG02738.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.3700-1712delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982049 | |||||||
chr4:5982143 | G | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0252 others(2): Show |
5 | NA18941.hp2 NA18960.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3700-1805C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982143 | |||||||
chr4:5982163 | G | A | 1 | a0002c0002t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3700-1825C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982163 | |||||||
chr4:5982417 | G | C | 3 | a0069c0111t0001g0094 a0070c0113t0001g0029 a0074c0071t0001g0035 |
3 | HG02809.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3700-2079C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982417 | |||||||
chr4:5982418 | C | T | 77 | a0001c0001t0001g0228 a0002c0002t0001g0090 a0002c0002t0001g0091 others(74): Show |
79 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.3700-2080G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982418 | |||||||
chr4:5982549 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3700-2211G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982549 | |||||||
chr4:5982639 | A | G | 1 | a0014c0012t0001g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3700-2301T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982639 | |||||||
chr4:5982725 | C | T | 1 | a0009c0010t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3700-2387G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982725 | |||||||
chr4:5982814 | A | C | 2 | a0035c0037t0001g0292 a0035c0037t0001g0293 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3700-2476T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982814 | |||||||
chr4:5982911 | G | A | 6 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(3): Show |
6 | HG01891.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.3700-2573C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5982911 | |||||||
chr4:5983002 | C | A | 63 | a0001c0001t0001g0228 a0002c0002t0001g0081 a0002c0002t0001g0090 others(60): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.3700-2664G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983002 | |||||||
chr4:5983003 | C | G | 76 | a0001c0001t0001g0228 a0002c0002t0001g0081 a0002c0002t0001g0090 others(73): Show |
78 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.3700-2665G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983003 | |||||||
chr4:5983088 | T | C | 1 | a0079c0079t0001g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3700-2750A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983088 | |||||||
chr4:5983156 | C | T | 4 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0031c0032t0001g0025 others(1): Show |
4 | HG01255.hp2 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3700-2818G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983156 | |||||||
chr4:5983157 | G | A | 19 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0158 others(16): Show |
19 | HG01109.hp1 HG01167.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3700-2819C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983157 | |||||||
chr4:5983171 | G | A | 15 | a0002c0002t0001g0081 a0013c0017t0001g0031 a0013c0017t0001g0032 others(12): Show |
15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.3700-2833C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983171 | |||||||
chr4:5983177 | C | T | 15 | a0002c0002t0001g0081 a0013c0017t0001g0031 a0013c0017t0001g0032 others(12): Show |
15 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.3700-2839G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983177 | |||||||
chr4:5983189 | C | T | 3 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 |
3 | HG00558.hp1 NA18948.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.3700-2851G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983189 | |||||||
chr4:5983225 | G | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(248): Show |
257 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(254): Show |
intron_variant | MODIFIER | c.3700-2887C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983225 | |||||||
chr4:5983273 | C | T | 52 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(49): Show |
52 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.3700-2935G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983273 | |||||||
chr4:5983275 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(99): Show |
106 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.3700-2937T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983275 | |||||||
chr4:5983323 | C | A | 15 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 others(12): Show |
15 | HG01257.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3700-2985G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983323 | |||||||
chr4:5983372 | G | A | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3700-3034C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983372 | |||||||
chr4:5983450 | G | A | 1 | a0015c0018t0001g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3700-3112C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983450 | |||||||
chr4:5983507 | A | C | 6 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0069c0111t0001g0094 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3700-3169T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983507 | |||||||
chr4:5983614 | T | G | 2 | a0002c0002t0001g0160 a0002c0002t0001g0181 |
2 | NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3700-3276A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983614 | |||||||
chr4:5983647 | A | G | 3 | a0059c0102t0001g0269 a0063c0110t0001g0274 a0080c0045t0001g0010 |
3 | HG02280.hp2 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3700-3309T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983647 | |||||||
chr4:5983698 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3700-3360G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983698 | |||||||
chr4:5983837 | T | C | 2 | a0043c0075t0001g0278 a0048c0051t0001g0053 |
2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.3700-3499A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983837 | |||||||
chr4:5983863 | A | G | 2 | a0013c0017t0001g0037 a0051c0081t0001g0331 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3700-3525T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983863 | |||||||
chr4:5983867 | TC | T | 52 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(49): Show |
52 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.3700-3530delG | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983867 | |||||||
chr4:5983945 | C | G | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3700-3607G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983945 | |||||||
chr4:5983989 | C | G | 1 | a0109c0061t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3700-3651G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5983989 | |||||||
chr4:5984036 | A | C | 1 | a0060c0049t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3700-3698T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984036 | |||||||
chr4:5984099 | C | T | 1 | a0022c0022t0001g0068 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3700-3761G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984099 | |||||||
chr4:5984111 | G | A | 1 | a0054c0065t0001g0219 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3700-3773C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984111 | |||||||
chr4:5984186 | C | T | 1 | a0079c0079t0001g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3700-3848G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984186 | |||||||
chr4:5984234 | A | C | 4 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 others(1): Show |
4 | HG02738.hp1 HG02818.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3700-3896T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984234 | |||||||
chr4:5984325 | A | G | 4 | a0005c0005t0001g0093 a0009c0010t0001g0267 a0009c0010t0001g0280 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3700-3987T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984325 | |||||||
chr4:5984442 | G | A | 2 | a0036c0039t0001g0014 a0083c0047t0001g0013 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3699+3905C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984442 | |||||||
chr4:5984508 | G | A | 3 | a0011c0014t0001g0309 a0032c0029t0001g0057 a0060c0049t0001g0317 |
3 | HG01099.hp2 HG01261.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.3699+3839C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984508 | |||||||
chr4:5984612 | G | C | 12 | a0002c0002t0001g0081 a0024c0027t0001g0041 a0025c0023t0001g0318 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.3699+3735C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984612 | |||||||
chr4:5984850 | T | TA | 18 | a0001c0001t0001g0116 a0001c0001t0001g0228 a0011c0014t0001g0145 others(15): Show |
19 | HG00558.hp1 HG01099.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.3699+3496dupT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984850 | |||||||
chr4:5984850 | TA | T | 73 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.3699+3496delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984850 | |||||||
chr4:5984862 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3699+3485G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984862 | |||||||
chr4:5984907 | A | G | 53 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(50): Show |
53 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.3699+3440T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984907 | |||||||
chr4:5984925 | G | T | 74 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(71): Show |
74 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.3699+3422C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5984925 | |||||||
chr4:5985051 | A | G | 4 | a0038c0034t0001g0017 a0038c0034t0001g0330 a0056c0052t0001g0030 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.3699+3296T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985051 | |||||||
chr4:5985200 | T | C | 1 | a0006c0006t0001g0111 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3699+3147A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985200 | |||||||
chr4:5985216 | A | G | 39 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(36): Show |
39 | HG01257.hp2 HG01884.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.3699+3131T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985216 | |||||||
chr4:5985282 | A | G | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3699+3065T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985282 | |||||||
chr4:5985344 | A | G | 1 | a0002c0002t0001g0257 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3699+3003T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985344 | |||||||
chr4:5985370 | C | T | 70 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.3699+2977G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985370 | |||||||
chr4:5985384 | A | G | 46 | a0002c0002t0001g0090 a0002c0002t0001g0091 a0002c0002t0001g0107 others(43): Show |
46 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.3699+2963T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985384 | |||||||
chr4:5985758 | A | G | 1 | a0071c0046t0001g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3699+2589T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985758 | |||||||
chr4:5985870 | G | T | 1 | a0070c0113t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3699+2477C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985870 | |||||||
chr4:5985955 | C | G | 3 | a0059c0102t0001g0269 a0063c0110t0001g0274 a0080c0045t0001g0010 |
3 | HG02280.hp2 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3699+2392G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985955 | |||||||
chr4:5985964 | G | A | 2 | a0018c0016t0001g0210 a0057c0067t0001g0322 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3699+2383C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5985964 | |||||||
chr4:5986008 | C | T | 66 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.3699+2339G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986008 | |||||||
chr4:5986025 | A | T | 1 | a0066c0104t0001g0296 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3699+2322T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986025 | |||||||
chr4:5986080 | C | T | 2 | a0002c0002t0001g0197 a0002c0002t0001g0313 |
2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.3699+2267G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986080 | |||||||
chr4:5986218 | T | C | 5 | a0001c0001t0001g0221 a0006c0006t0001g0170 a0006c0006t0001g0225 others(2): Show |
6 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.3699+2129A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986218 | |||||||
chr4:5986300 | T | C | 244 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(241): Show |
250 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.3699+2047A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986300 | |||||||
chr4:5986352 | A | G | 203 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(200): Show |
209 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.3699+1995T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986352 | |||||||
chr4:5986401 | CA | C | 206 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(203): Show |
212 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.3699+1945delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986401 | |||||||
chr4:5986420 | T | C | 2 | a0013c0017t0001g0037 a0051c0081t0001g0331 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3699+1927A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986420 | |||||||
chr4:5986469 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3699+1878A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986469 | |||||||
chr4:5986510 | A | G | 205 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(202): Show |
211 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.3699+1837T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986510 | |||||||
chr4:5986521 | C | G | 1 | a0070c0113t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3699+1826G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986521 | |||||||
chr4:5986538 | AT | A | 27 | a0001c0001t0001g0121 a0002c0002t0001g0181 a0003c0004t0001g0248 others(24): Show |
30 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.3699+1808delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986538 | |||||||
chr4:5986538 | ATT | A | 183 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(180): Show |
187 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(184): Show |
intron_variant | MODIFIER | c.3699+1807_3699+180 others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986538 | |||||||
chr4:5986538 | ATTT | A | 18 | a0001c0001t0001g0127 a0001c0001t0001g0252 a0002c0002t0001g0081 others(15): Show |
18 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.3699+1806_3699+180 others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986538 | |||||||
chr4:5986541 | T | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0169 a0001c0001t0001g0256 others(2): Show |
5 | HG03834.hp1 NA18949.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.3699+1806A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986541 | |||||||
chr4:5986603 | A | G | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3699+1744T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986603 | |||||||
chr4:5986619 | A | G | 4 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0069c0111t0001g0094 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3699+1728T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986619 | |||||||
chr4:5986806 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3699+1541C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986806 | |||||||
chr4:5986963 | C | T | 1 | a0006c0006t0001g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3699+1384G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5986963 | |||||||
chr4:5987071 | C | A | 231 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(228): Show |
237 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.3699+1276G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987071 | |||||||
chr4:5987114 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0033 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3699+1233C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987114 | |||||||
chr4:5987129 | G | A | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3699+1218C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987129 | |||||||
chr4:5987135 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0155 |
3 | HG02071.hp2 HG02074.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3699+1212C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987135 | |||||||
chr4:5987240 | G | A | 1 | a0049c0053t0001g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3699+1107C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987240 | |||||||
chr4:5987276 | C | T | 1 | a0008c0008t0001g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3699+1071G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987276 | |||||||
chr4:5987302 | T | C | 17 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0037 others(14): Show |
17 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.3699+1045A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987302 | |||||||
chr4:5987303 | T | C | 20 | a0001c0001t0001g0228 a0011c0014t0001g0145 a0011c0014t0001g0152 others(17): Show |
21 | HG00280.hp2 HG00558.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.3699+1044A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987303 | |||||||
chr4:5987308 | G | C | 2 | a0063c0110t0001g0274 a0080c0045t0001g0010 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3699+1039C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987308 | |||||||
chr4:5987369 | C | T | 13 | a0018c0016t0001g0210 a0018c0016t0001g0276 a0018c0016t0001g0282 others(10): Show |
13 | HG02145.hp2 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3699+978G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987369 | |||||||
chr4:5987412 | C | CA | 8 | a0009c0010t0001g0327 a0030c0026t0001g0054 a0044c0088t0001g0159 others(5): Show |
8 | HG00673.hp2 HG01255.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3699+934dupT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAA | 10 | a0018c0016t0001g0210 a0018c0016t0001g0282 a0018c0016t0001g0283 others(7): Show |
10 | HG02615.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.3699+932_3699+934d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAA | 11 | a0001c0001t0001g0098 a0001c0001t0001g0169 a0001c0001t0001g0252 others(8): Show |
11 | HG00099.hp1 HG00280.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.3699+929_3699+934d others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA | 56 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(53): Show |
59 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.3699+928_3699+934d others(9): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(1): Show |
41 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0080 others(38): Show |
42 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.3699+927_3699+934d others(10): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0079 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG01433.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3699+926_3699+934d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0154 a0002c0002t0001g0081 others(1): Show |
4 | HG00642.hp2 HG02135.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3699+925_3699+934d others(12): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(7): Show |
2 | a0003c0004t0001g0255 a0028c0031t0001g0218 |
2 | HG01943.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.3699+921_3699+934d others(16): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(8): Show |
12 | a0002c0002t0001g0090 a0002c0002t0001g0107 a0002c0002t0001g0112 others(9): Show |
12 | HG00558.hp2 HG00735.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.3699+920_3699+934d others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(9): Show |
18 | a0002c0002t0001g0156 a0002c0002t0001g0176 a0002c0002t0001g0178 others(15): Show |
18 | HG01258.hp2 HG01346.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.3699+919_3699+934d others(18): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(10): Show |
8 | a0002c0002t0001g0091 a0002c0002t0001g0179 a0002c0002t0001g0185 others(5): Show |
8 | HG00544.hp2 HG02083.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.3699+918_3699+934d others(19): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(11): Show |
6 | a0002c0002t0001g0200 a0007c0007t0001g0190 a0038c0034t0001g0330 others(3): Show |
6 | HG01978.hp1 HG02109.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.3699+917_3699+934d others(20): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(12): Show |
2 | a0002c0002t0001g0313 a0096c0076t0001g0328 |
2 | HG00639.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3699+916_3699+934d others(21): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(13): Show |
1 | a0104c0063t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3699+915_3699+934d others(22): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | C | CAAAAAAA others(14): Show |
1 | a0002c0002t0001g0197 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3699+914_3699+934d others(23): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987412 | CAAAA | C | 17 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0037 others(14): Show |
17 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.3699+931_3699+934d others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987412 | |||||||
chr4:5987572 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3699+775C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987572 | |||||||
chr4:5987606 | A | G | 222 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(219): Show |
228 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.3699+741T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987606 | |||||||
chr4:5987659 | C | G | 220 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(217): Show |
226 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(223): Show |
intron_variant | MODIFIER | c.3699+688G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987659 | |||||||
chr4:5987690 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3699+657A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987690 | |||||||
chr4:5987703 | TAGAG | T | 4 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0069c0111t0001g0094 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3699+640_3699+643d others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987703 | |||||||
chr4:5987852 | C | A | 225 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(222): Show |
231 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(228): Show |
intron_variant | MODIFIER | c.3699+495G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5987852 | |||||||
chr4:5988008 | G | A | 1 | a0006c0006t0001g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3699+339C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5988008 | |||||||
chr4:5988062 | TG | T | 21 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0037 others(18): Show |
21 | HG01257.hp2 HG01884.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.3699+284delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5988062 | |||||||
chr4:5988247 | A | G | 5 | a0038c0034t0001g0017 a0038c0034t0001g0330 a0056c0052t0001g0030 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3699+100T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5988247 | |||||||
chr4:5988312 | C | T | 1 | a0036c0039t0001g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3699+35G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 6/11 | chr4 | 5988312 | |||||||
chr4:5990829 | A | G | 203 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(200): Show |
207 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(204): Show |
splice_region_variant&intron_variant | LOW | c.1222-5T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5990829 | |||||||
chr4:5990849 | G | A | 4 | a0059c0102t0001g0269 a0063c0110t0001g0274 a0064c0060t0001g0067 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-25C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5990849 | |||||||
chr4:5990969 | A | AC | 3 | a0002c0002t0001g0160 a0002c0002t0001g0181 a0004c0003t0001g0245 |
3 | HG01978.hp2 NA18979.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1222-146dupG | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5990969 | |||||||
chr4:5991032 | T | C | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1222-208A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991032 | |||||||
chr4:5991055 | T | C | 2 | a0026c0042t0001g0332 a0026c0042t0001g0333 |
2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1222-231A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991055 | |||||||
chr4:5991062 | C | T | 2 | a0069c0111t0001g0094 a0102c0112t0001g0015 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1222-238G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991062 | |||||||
chr4:5991088 | A | T | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1222-264T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991088 | |||||||
chr4:5991103 | C | T | 17 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(14): Show |
17 | HG01257.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1222-279G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991103 | |||||||
chr4:5991119 | C | T | 4 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0068c0109t0001g0092 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1222-295G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991119 | |||||||
chr4:5991173 | C | T | 2 | a0069c0111t0001g0094 a0102c0112t0001g0015 |
2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1222-349G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991173 | |||||||
chr4:5991220 | G | T | 26 | a0009c0010t0001g0144 a0009c0010t0001g0267 a0009c0010t0001g0279 others(23): Show |
26 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1222-396C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991220 | |||||||
chr4:5991230 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1222-406T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991230 | |||||||
chr4:5991260 | T | C | 4 | a0003c0004t0001g0303 a0003c0004t0001g0304 a0003c0004t0001g0305 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-436A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991260 | |||||||
chr4:5991303 | G | A | 17 | a0025c0023t0001g0318 a0025c0023t0001g0319 a0031c0032t0001g0025 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1222-479C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991303 | |||||||
chr4:5991336 | G | A | 31 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(28): Show |
31 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1222-512C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991336 | |||||||
chr4:5991339 | T | C | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1222-515A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991339 | |||||||
chr4:5991347 | T | C | 31 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(28): Show |
31 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.1222-523A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991347 | |||||||
chr4:5991394 | G | C | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1222-570C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991394 | |||||||
chr4:5991406 | T | C | 253 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(250): Show |
258 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1222-582A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991406 | |||||||
chr4:5991411 | C | T | 3 | a0059c0102t0001g0269 a0064c0060t0001g0067 a0070c0113t0001g0029 |
3 | HG02280.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1222-587G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991411 | |||||||
chr4:5991469 | G | A | 10 | a0009c0010t0001g0144 a0025c0023t0001g0318 a0025c0023t0001g0319 others(7): Show |
10 | HG00099.hp1 HG00280.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.1222-645C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991469 | |||||||
chr4:5991530 | T | G | 1 | a0076c0074t0001g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1222-706A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991530 | |||||||
chr4:5991582 | A | G | 39 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(36): Show |
39 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1222-758T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991582 | |||||||
chr4:5991591 | G | C | 9 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0040c0033t0001g0273 others(6): Show |
9 | HG01255.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1222-767C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991591 | |||||||
chr4:5991597 | G | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(194): Show |
202 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1222-773C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991597 | |||||||
chr4:5991631 | G | C | 236 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(233): Show |
241 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1222-807C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991631 | |||||||
chr4:5991685 | A | T | 1 | a0063c0110t0001g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1222-861T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991685 | |||||||
chr4:5991710 | G | A | 8 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0040c0033t0001g0273 others(5): Show |
8 | HG01255.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1222-886C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991710 | |||||||
chr4:5991714 | A | T | 198 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(195): Show |
203 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.1222-890T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991714 | |||||||
chr4:5991762 | G | T | 1 | a0078c0066t0001g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1222-938C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991762 | |||||||
chr4:5991779 | G | T | 38 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(35): Show |
38 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1222-955C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991779 | |||||||
chr4:5991783 | C | T | 38 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(35): Show |
38 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1222-959G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991783 | |||||||
chr4:5991813 | G | T | 38 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(35): Show |
38 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1222-989C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991813 | |||||||
chr4:5991833 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1221+970A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991833 | |||||||
chr4:5991859 | G | A | 2 | a0071c0046t0001g0011 a0080c0045t0001g0010 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1221+944C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991859 | |||||||
chr4:5991898 | G | A | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1221+905C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991898 | |||||||
chr4:5991995 | A | G | 38 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(35): Show |
38 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1221+808T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5991995 | |||||||
chr4:5992098 | C | T | 2 | a0035c0037t0001g0292 a0035c0037t0001g0293 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1221+705G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992098 | |||||||
chr4:5992136 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1221+667C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992136 | |||||||
chr4:5992139 | C | T | 39 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(36): Show |
39 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1221+664G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992139 | |||||||
chr4:5992149 | C | T | 79 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(76): Show |
81 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.1221+654G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992149 | |||||||
chr4:5992150 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1221+653C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992150 | |||||||
chr4:5992170 | A | G | 39 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(36): Show |
39 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1221+633T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992170 | |||||||
chr4:5992193 | A | G | 39 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(36): Show |
39 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1221+610T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992193 | |||||||
chr4:5992208 | T | C | 39 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(36): Show |
39 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1221+595A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992208 | |||||||
chr4:5992274 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1221+529G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992274 | |||||||
chr4:5992297 | C | T | 34 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(31): Show |
34 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.1221+506G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992297 | |||||||
chr4:5992313 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1221+490A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992313 | |||||||
chr4:5992337 | G | A | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01978.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1221+466C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992337 | |||||||
chr4:5992438 | G | T | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1221+365C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992438 | |||||||
chr4:5992549 | G | A | 1 | a0005c0005t0001g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1221+254C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992549 | |||||||
chr4:5992665 | C | A | 26 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(23): Show |
26 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1221+138G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992665 | |||||||
chr4:5992699 | C | G | 4 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0071c0046t0001g0011 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+104G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992699 | |||||||
chr4:5992726 | G | A | 1 | a0005c0005t0001g0138 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1221+77C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 5/11 | chr4 | 5992726 | |||||||
chr4:5992958 | A | G | 8 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0040c0033t0001g0273 others(5): Show |
8 | HG01255.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1094-28T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5992958 | |||||||
chr4:5992989 | C | T | 1 | a0074c0071t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1094-59G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5992989 | |||||||
chr4:5993005 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1094-75C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993005 | |||||||
chr4:5993012 | A | G | 31 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(28): Show |
31 | HG01106.hp1 HG01106.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1094-82T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993012 | |||||||
chr4:5993027 | G | A | 8 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0040c0033t0001g0273 others(5): Show |
8 | HG01255.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1094-97C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993027 | |||||||
chr4:5993030 | A | AC | 40 | a0002c0002t0001g0181 a0002c0002t0001g0257 a0003c0004t0001g0077 others(37): Show |
40 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1094-101dupG | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993030 | |||||||
chr4:5993037 | C | A | 14 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(11): Show |
14 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1094-107G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993037 | |||||||
chr4:5993174 | G | A | 5 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0071c0046t0001g0011 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1094-244C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993174 | |||||||
chr4:5993212 | C | T | 4 | a0038c0034t0001g0017 a0038c0034t0001g0330 a0056c0052t0001g0030 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094-282G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993212 | |||||||
chr4:5993228 | A | G | 33 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(30): Show |
33 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1094-298T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993228 | |||||||
chr4:5993238 | G | A | 8 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0040c0033t0001g0273 others(5): Show |
8 | HG01255.hp2 HG02145.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1094-308C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993238 | |||||||
chr4:5993260 | C | T | 12 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0009c0010t0001g0144 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1094-330G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993260 | |||||||
chr4:5993301 | A | G | 2 | a0071c0046t0001g0011 a0080c0045t0001g0010 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1094-371T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993301 | |||||||
chr4:5993304 | C | T | 24 | a0011c0014t0001g0227 a0016c0015t0001g0043 a0016c0015t0001g0044 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1094-374G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993304 | |||||||
chr4:5993376 | G | T | 1 | a0002c0002t0001g0251 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1094-446C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993376 | |||||||
chr4:5993387 | A | G | 12 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0009c0010t0001g0144 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1094-457T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993387 | |||||||
chr4:5993407 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1094-477A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993407 | |||||||
chr4:5993464 | G | A | 23 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(20): Show |
23 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1094-534C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993464 | |||||||
chr4:5993501 | G | A | 23 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(20): Show |
23 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1094-571C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993501 | |||||||
chr4:5993528 | G | T | 23 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(20): Show |
23 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1094-598C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993528 | |||||||
chr4:5993544 | T | C | 23 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(20): Show |
23 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.1094-614A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993544 | |||||||
chr4:5993580 | T | G | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1094-650A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993580 | |||||||
chr4:5993599 | A | T | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1094-669T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993599 | |||||||
chr4:5993645 | C | T | 12 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0009c0010t0001g0144 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1093+702G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993645 | |||||||
chr4:5993650 | T | C | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+697A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993650 | |||||||
chr4:5993674 | G | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(94): Show |
100 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1093+673C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993674 | |||||||
chr4:5993742 | G | A | 1 | a0075c0098t0001g0272 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1093+605C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993742 | |||||||
chr4:5993744 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1093+603C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993744 | |||||||
chr4:5993778 | C | T | 6 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0071c0046t0001g0011 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093+569G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993778 | |||||||
chr4:5993857 | TA | T | 122 | a0001c0106t0001g0246 a0002c0002t0001g0081 a0002c0002t0001g0090 others(119): Show |
124 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1093+489delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993857 | |||||||
chr4:5993857 | TAAA | T | 23 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(20): Show |
23 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1093+487_1093+489d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993857 | |||||||
chr4:5993861 | A | T | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+486T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993861 | |||||||
chr4:5993870 | G | A | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+477C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993870 | |||||||
chr4:5993871 | A | C | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+476T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993871 | |||||||
chr4:5993882 | T | G | 2 | a0012c0013t0001g0059 a0012c0013t0001g0301 |
2 | HG04204.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1093+465A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993882 | |||||||
chr4:5993916 | C | A | 2 | a0009c0010t0001g0267 a0009c0010t0001g0280 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1093+431G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993916 | |||||||
chr4:5993933 | C | T | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+414G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993933 | |||||||
chr4:5993949 | T | C | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+398A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5993949 | |||||||
chr4:5994015 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1093+332G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994015 | |||||||
chr4:5994025 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0250 |
2 | HG02071.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1093+322A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994025 | |||||||
chr4:5994109 | G | A | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+238C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994109 | |||||||
chr4:5994122 | C | T | 1 | a0063c0110t0001g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1093+225G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994122 | |||||||
chr4:5994188 | T | G | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+159A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994188 | |||||||
chr4:5994240 | C | T | 12 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0009c0010t0001g0144 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.1093+107G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994240 | |||||||
chr4:5994262 | C | T | 24 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(21): Show |
24 | HG01167.hp1 HG01255.hp2 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1093+85G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994262 | |||||||
chr4:5994332 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0270 |
2 | HG02602.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1093+15C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994332 | |||||||
chr4:5994333 | C | T | 1 | a0082c0064t0001g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1093+14G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994333 | |||||||
chr4:5994342 | C | T | 5 | a0009c0010t0001g0279 a0014c0012t0001g0048 a0014c0012t0001g0049 others(2): Show |
5 | HG01106.hp2 HG02683.hp1 HG03710.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1093+5G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 4/11 | chr4 | 5994342 | |||||||
chr4:5994529 | T | C | 41 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(38): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-53A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994529 | |||||||
chr4:5994552 | C | T | 3 | a0002c0002t0001g0179 a0007c0007t0001g0171 a0098c0094t0001g0180 |
3 | NA18962.hp2 NA18964.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.964-76G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994552 | |||||||
chr4:5994560 | C | T | 1 | a0020c0028t0001g0023 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.964-84G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994560 | |||||||
chr4:5994570 | C | A | 1 | a0077c0097t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.964-94G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994570 | |||||||
chr4:5994573 | G | A | 23 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(20): Show |
23 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.964-97C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994573 | |||||||
chr4:5994578 | T | C | 41 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(38): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-102A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994578 | |||||||
chr4:5994591 | A | G | 41 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(38): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-115T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994591 | |||||||
chr4:5994615 | A | G | 41 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(38): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-139T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994615 | |||||||
chr4:5994640 | C | G | 4 | a0013c0017t0001g0037 a0051c0081t0001g0331 a0069c0111t0001g0094 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-164G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994640 | |||||||
chr4:5994678 | C | T | 1 | a0074c0071t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.964-202G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994678 | |||||||
chr4:5994691 | T | C | 41 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(38): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-215A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994691 | |||||||
chr4:5994725 | C | A | 1 | a0040c0033t0001g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.964-249G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994725 | |||||||
chr4:5994778 | GCAGGGTC others(6): Show |
G | 41 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(38): Show |
41 | HG01167.hp1 HG01255.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-315_964-303del others(13): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994778 | |||||||
chr4:5994813 | C | T | 2 | a0009c0010t0001g0267 a0009c0010t0001g0280 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.964-337G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994813 | |||||||
chr4:5994854 | C | T | 1 | a0063c0110t0001g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.964-378G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994854 | |||||||
chr4:5994860 | G | A | 1 | a0032c0029t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.964-384C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994860 | |||||||
chr4:5994868 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.964-392G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5994868 | |||||||
chr4:5995041 | C | A | 2 | a0042c0043t0001g0335 a0042c0043t0001g0336 |
2 | NA18979.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.964-565G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995041 | |||||||
chr4:5995077 | A | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(92): Show |
98 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.964-601T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995077 | |||||||
chr4:5995216 | G | A | 40 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(37): Show |
40 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.964-740C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995216 | |||||||
chr4:5995246 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.964-770G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995246 | |||||||
chr4:5995399 | C | A | 1 | a0080c0045t0001g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.964-923G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995399 | |||||||
chr4:5995474 | A | AAC | 12 | a0001c0001t0001g0074 a0001c0001t0001g0281 a0005c0005t0001g0093 others(9): Show |
12 | HG01168.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.964-1000_964-999du others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACAC | 18 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0204 others(15): Show |
18 | HG00323.hp1 HG00741.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.964-1002_964-999du others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACACAC | 20 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0001g0075 others(17): Show |
20 | HG01070.hp1 HG01192.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.964-1004_964-999du others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACACACA others(1): Show |
35 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0105 others(32): Show |
35 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.964-1006_964-999du others(9): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACACACA others(3): Show |
37 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0098 others(34): Show |
38 | HG00642.hp1 HG00673.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.964-1008_964-999du others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACACACA others(5): Show |
12 | a0001c0001t0001g0004 a0001c0001t0001g0099 a0001c0001t0001g0100 others(9): Show |
12 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.964-1010_964-999du others(13): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACACACA others(7): Show |
2 | a0006c0006t0001g0120 a0029c0030t0001g0005 |
3 | HG01167.hp2 HG01169.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.964-1012_964-999du others(15): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACACACA others(9): Show |
2 | a0001c0001t0001g0106 a0006c0006t0001g0225 |
2 | HG01109.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.964-1014_964-999du others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | AACACACA others(11): Show |
1 | a0001c0001t0001g0118 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.964-1016_964-999du others(19): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.964-999_964-998ins others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | A | ACACACAC others(6): Show |
1 | a0005c0005t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.964-999_964-998ins others(13): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | AAC | A | 55 | a0001c0001t0001g0084 a0001c0001t0001g0209 a0002c0002t0001g0081 others(52): Show |
56 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.964-1000_964-999de others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | AACAC | A | 75 | a0001c0001t0001g0116 a0001c0001t0001g0142 a0001c0001t0001g0244 others(72): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.964-1002_964-999de others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | AACACAC | A | 32 | a0001c0001t0001g0097 a0001c0001t0001g0155 a0001c0084t0001g0096 others(29): Show |
34 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.964-1004_964-999de others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | AACACACA others(1): Show |
A | 9 | a0016c0015t0001g0043 a0016c0015t0001g0045 a0025c0023t0001g0318 others(6): Show |
9 | HG01167.hp1 HG01978.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.964-1006_964-999de others(9): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | AACACACA others(3): Show |
A | 6 | a0018c0016t0001g0210 a0018c0016t0001g0276 a0018c0016t0001g0282 others(3): Show |
6 | HG01884.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-1008_964-999de others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995474 | AACACACA others(9): Show |
A | 1 | a0022c0022t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.964-1014_964-999de others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995474 | |||||||
chr4:5995537 | T | C | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-1061A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995537 | |||||||
chr4:5995541 | G | C | 41 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(38): Show |
41 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-1065C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995541 | |||||||
chr4:5995571 | C | T | 4 | a0038c0034t0001g0017 a0038c0034t0001g0330 a0056c0052t0001g0030 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-1095G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995571 | |||||||
chr4:5995716 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-1240C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995716 | |||||||
chr4:5995741 | C | G | 41 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(38): Show |
41 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.964-1265G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995741 | |||||||
chr4:5995787 | G | T | 56 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(53): Show |
56 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.964-1311C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995787 | |||||||
chr4:5995815 | A | T | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-1339T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995815 | |||||||
chr4:5995858 | A | G | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-1382T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995858 | |||||||
chr4:5995876 | G | T | 31 | a0009c0010t0001g0279 a0012c0013t0001g0059 a0012c0013t0001g0231 others(28): Show |
31 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.964-1400C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5995876 | |||||||
chr4:5996020 | C | T | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.964-1544G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996020 | |||||||
chr4:5996027 | T | C | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-1551A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996027 | |||||||
chr4:5996066 | G | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0059c0102t0001g0269 others(3): Show |
6 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-1590C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996066 | |||||||
chr4:5996096 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0059c0102t0001g0269 others(3): Show |
6 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-1620G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996096 | |||||||
chr4:5996167 | C | T | 33 | a0009c0010t0001g0279 a0012c0013t0001g0059 a0012c0013t0001g0231 others(30): Show |
33 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.964-1691G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996167 | |||||||
chr4:5996192 | C | G | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.964-1716G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996192 | |||||||
chr4:5996260 | C | G | 43 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(40): Show |
43 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.964-1784G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996260 | |||||||
chr4:5996261 | G | A | 43 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(40): Show |
43 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.964-1785C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996261 | |||||||
chr4:5996289 | T | C | 1 | a0004c0003t0001g0289 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.964-1813A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996289 | |||||||
chr4:5996338 | G | A | 78 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(75): Show |
80 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.964-1862C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996338 | |||||||
chr4:5996482 | A | C | 6 | a0011c0014t0001g0152 a0011c0014t0001g0309 a0017c0019t0001g0308 others(3): Show |
6 | HG01099.hp2 HG01261.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-2006T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996482 | |||||||
chr4:5996483 | G | T | 4 | a0035c0037t0001g0292 a0035c0037t0001g0293 a0071c0046t0001g0011 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-2007C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996483 | |||||||
chr4:5996498 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-2022C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996498 | |||||||
chr4:5996562 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0059c0102t0001g0269 others(3): Show |
6 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-2086G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996562 | |||||||
chr4:5996592 | T | C | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-2116A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996592 | |||||||
chr4:5996622 | C | T | 2 | a0071c0046t0001g0011 a0080c0045t0001g0010 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.964-2146G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996622 | |||||||
chr4:5996690 | A | T | 58 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(55): Show |
58 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.964-2214T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996690 | |||||||
chr4:5996736 | G | A | 3 | a0011c0014t0001g0309 a0032c0029t0001g0057 a0060c0049t0001g0317 |
3 | HG01099.hp2 HG01261.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.964-2260C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996736 | |||||||
chr4:5996750 | C | T | 3 | a0004c0003t0001g0009 a0004c0003t0001g0315 a0004c0003t0001g0316 |
4 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-2274G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996750 | |||||||
chr4:5996875 | C | T | 77 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(74): Show |
79 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.964-2399G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996875 | |||||||
chr4:5996966 | AGT | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-2492_964-2491d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5996966 | |||||||
chr4:5997004 | G | A | 1 | a0014c0012t0001g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.964-2528C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997004 | |||||||
chr4:5997016 | C | G | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-2540G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997016 | |||||||
chr4:5997071 | G | A | 3 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.964-2595C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997071 | |||||||
chr4:5997079 | C | T | 12 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0009c0010t0001g0144 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.964-2603G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997079 | |||||||
chr4:5997116 | G | A | 1 | a0010c0009t0001g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.964-2640C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997116 | |||||||
chr4:5997151 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-2675C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997151 | |||||||
chr4:5997176 | A | G | 139 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0002c0002t0001g0081 others(136): Show |
141 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.964-2700T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997176 | |||||||
chr4:5997184 | G | A | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-2708C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997184 | |||||||
chr4:5997185 | T | C | 44 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(41): Show |
44 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.964-2709A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997185 | |||||||
chr4:5997212 | G | C | 26 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0009c0010t0001g0326 others(23): Show |
26 | HG00323.hp1 HG01257.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.964-2736C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997212 | |||||||
chr4:5997240 | C | G | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-2764G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997240 | |||||||
chr4:5997280 | G | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(94): Show |
100 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.964-2804C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997280 | |||||||
chr4:5997322 | G | A | 1 | a0007c0007t0001g0172 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.964-2846C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997322 | |||||||
chr4:5997327 | C | T | 160 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0002c0002t0001g0081 others(157): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.964-2851G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997327 | |||||||
chr4:5997360 | A | G | 15 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(12): Show |
15 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-2884T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997360 | |||||||
chr4:5997444 | C | T | 14 | a0016c0015t0001g0043 a0016c0015t0001g0044 a0016c0015t0001g0045 others(11): Show |
14 | HG01167.hp1 HG01978.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.964-2968G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997444 | |||||||
chr4:5997584 | A | C | 1 | a0011c0014t0001g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.964-3108T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997584 | |||||||
chr4:5997658 | A | G | 1 | a0059c0102t0001g0269 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.964-3182T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997658 | |||||||
chr4:5997703 | T | C | 7 | a0018c0016t0001g0210 a0018c0016t0001g0276 a0018c0016t0001g0282 others(4): Show |
7 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.964-3227A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997703 | |||||||
chr4:5997765 | C | A | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.964-3289G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5997765 | |||||||
chr4:5998011 | A | G | 2 | a0035c0037t0001g0292 a0035c0037t0001g0293 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.964-3535T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998011 | |||||||
chr4:5998082 | A | G | 44 | a0009c0010t0001g0267 a0009c0010t0001g0279 a0009c0010t0001g0280 others(41): Show |
44 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.964-3606T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998082 | |||||||
chr4:5998120 | G | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(94): Show |
100 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.964-3644C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998120 | |||||||
chr4:5998216 | C | T | 161 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0002c0002t0001g0081 others(158): Show |
163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.964-3740G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998216 | |||||||
chr4:5998227 | G | A | 1 | a0031c0032t0001g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.964-3751C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998227 | |||||||
chr4:5998228 | A | G | 95 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(92): Show |
97 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.964-3752T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998228 | |||||||
chr4:5998264 | C | T | 3 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-3788G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998264 | |||||||
chr4:5998272 | A | G | 4 | a0038c0034t0001g0017 a0038c0034t0001g0330 a0056c0052t0001g0030 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-3796T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998272 | |||||||
chr4:5998379 | T | A | 1 | a0012c0013t0001g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.964-3903A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998379 | |||||||
chr4:5998380 | T | A | 138 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(135): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.964-3904A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998380 | |||||||
chr4:5998449 | G | C | 1 | a0007c0007t0001g0171 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.964-3973C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998449 | |||||||
chr4:5998707 | G | T | 9 | a0018c0016t0001g0210 a0018c0016t0001g0282 a0018c0016t0001g0283 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-4231C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998707 | |||||||
chr4:5998754 | A | C | 2 | a0017c0019t0001g0008 a0050c0116t0001g0334 |
3 | HG01192.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.964-4278T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998754 | |||||||
chr4:5998851 | G | A | 5 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0026c0042t0001g0332 others(2): Show |
5 | HG00323.hp1 HG02300.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-4375C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998851 | |||||||
chr4:5998964 | T | C | 257 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(254): Show |
262 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.964-4488A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5998964 | |||||||
chr4:5999049 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.964-4573G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999049 | |||||||
chr4:5999092 | C | T | 1 | a0007c0007t0001g0203 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.964-4616G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999092 | |||||||
chr4:5999160 | A | G | 1 | a0026c0042t0001g0332 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.964-4684T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999160 | |||||||
chr4:5999190 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.964-4714A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999190 | |||||||
chr4:5999320 | G | A | 5 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0026c0042t0001g0332 others(2): Show |
5 | HG00323.hp1 HG02300.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-4844C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999320 | |||||||
chr4:5999416 | A | C | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.964-4940T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999416 | |||||||
chr4:5999437 | C | T | 110 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(107): Show |
112 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.964-4961G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999437 | |||||||
chr4:5999495 | C | T | 1 | a0032c0029t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.964-5019G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999495 | |||||||
chr4:5999536 | T | C | 110 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(107): Show |
112 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.964-5060A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999536 | |||||||
chr4:5999581 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.964-5105C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999581 | |||||||
chr4:5999659 | T | G | 2 | a0035c0037t0001g0292 a0035c0037t0001g0293 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.964-5183A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999659 | |||||||
chr4:5999765 | C | T | 125 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(122): Show |
127 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.964-5289G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999765 | |||||||
chr4:5999954 | T | C | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.964-5478A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 5999954 | |||||||
chr4:6000042 | G | A | 2 | a0071c0046t0001g0011 a0080c0045t0001g0010 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.964-5566C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000042 | |||||||
chr4:6000045 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.964-5569C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000045 | |||||||
chr4:6000108 | A | T | 1 | a0039c0025t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.964-5632T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000108 | |||||||
chr4:6000124 | C | T | 1 | a0082c0064t0001g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.964-5648G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000124 | |||||||
chr4:6000215 | C | G | 2 | a0036c0039t0001g0014 a0083c0047t0001g0013 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.964-5739G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000215 | |||||||
chr4:6000225 | C | T | 1 | a0002c0002t0001g0200 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.964-5749G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000225 | |||||||
chr4:6000292 | C | G | 4 | a0038c0034t0001g0017 a0038c0034t0001g0330 a0056c0052t0001g0030 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-5816G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000292 | |||||||
chr4:6000367 | G | T | 1 | a0012c0013t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.964-5891C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000367 | |||||||
chr4:6000400 | G | C | 8 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0021c0024t0001g0066 others(5): Show |
8 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-5924C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000400 | |||||||
chr4:6000570 | G | A | 4 | a0065c0115t0001g0150 a0067c0072t0001g0082 a0076c0074t0001g0207 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-6094C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000570 | |||||||
chr4:6000954 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0059c0102t0001g0269 others(3): Show |
6 | HG01109.hp1 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-6478G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000954 | |||||||
chr4:6000981 | C | A | 16 | a0009c0010t0001g0279 a0012c0013t0001g0059 a0012c0013t0001g0231 others(13): Show |
16 | HG01106.hp1 HG01106.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.964-6505G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6000981 | |||||||
chr4:6001089 | T | C | 2 | a0026c0042t0001g0332 a0026c0042t0001g0333 |
2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.964-6613A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001089 | |||||||
chr4:6001093 | T | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0035c0037t0001g0292 others(5): Show |
8 | HG01109.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-6617A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001093 | |||||||
chr4:6001103 | C | A | 86 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(83): Show |
88 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.964-6627G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001103 | |||||||
chr4:6001232 | T | G | 1 | a0109c0061t0001g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.964-6756A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001232 | |||||||
chr4:6001312 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.963+6684C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001312 | |||||||
chr4:6001364 | G | C | 1 | a0075c0098t0001g0272 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.963+6632C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001364 | |||||||
chr4:6001441 | C | T | 36 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(33): Show |
36 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.963+6555G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001441 | |||||||
chr4:6001465 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.963+6531A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001465 | |||||||
chr4:6001506 | C | A | 8 | a0001c0001t0001g0088 a0001c0106t0001g0246 a0003c0004t0001g0248 others(5): Show |
8 | HG01975.hp1 HG01978.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+6490G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001506 | |||||||
chr4:6001565 | G | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+6431C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001565 | |||||||
chr4:6001592 | G | A | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.963+6404C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001592 | |||||||
chr4:6001836 | C | T | 2 | a0035c0037t0001g0292 a0035c0037t0001g0293 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.963+6160G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001836 | |||||||
chr4:6001926 | G | C | 5 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+6070C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001926 | |||||||
chr4:6001997 | C | T | 5 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0040c0033t0001g0273 others(2): Show |
5 | HG01255.hp2 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+5999G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6001997 | |||||||
chr4:6002110 | T | A | 7 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(4): Show |
8 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+5886A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002110 | |||||||
chr4:6002125 | C | T | 1 | a0015c0018t0001g0300 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.963+5871G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002125 | |||||||
chr4:6002150 | A | G | 1 | a0002c0002t0001g0112 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.963+5846T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002150 | |||||||
chr4:6002157 | T | C | 1 | a0002c0002t0001g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.963+5839A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002157 | |||||||
chr4:6002170 | T | A | 7 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(4): Show |
8 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+5826A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002170 | |||||||
chr4:6002248 | C | T | 228 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(225): Show |
232 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.963+5748G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002248 | |||||||
chr4:6002258 | T | C | 269 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(266): Show |
274 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.963+5738A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002258 | |||||||
chr4:6002331 | G | C | 2 | a0009c0010t0001g0326 a0009c0010t0001g0327 |
2 | HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.963+5665C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002331 | |||||||
chr4:6002507 | C | T | 5 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+5489G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002507 | |||||||
chr4:6002575 | T | G | 2 | a0059c0102t0001g0269 a0070c0113t0001g0029 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.963+5421A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002575 | |||||||
chr4:6002590 | G | A | 62 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(59): Show |
63 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.963+5406C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002590 | |||||||
chr4:6002706 | G | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(105): Show |
110 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.963+5290C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002706 | |||||||
chr4:6002756 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0132 a0001c0001t0001g0133 others(5): Show |
9 | HG00597.hp2 HG00673.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+5240C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002756 | |||||||
chr4:6002833 | G | A | 7 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(4): Show |
8 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+5163C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6002833 | |||||||
chr4:6003027 | A | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(172): Show |
178 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.963+4969T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003027 | |||||||
chr4:6003103 | G | A | 8 | a0015c0018t0001g0284 a0018c0016t0001g0210 a0018c0016t0001g0276 others(5): Show |
8 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+4893C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003103 | |||||||
chr4:6003194 | G | A | 254 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(251): Show |
258 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.963+4802C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003194 | |||||||
chr4:6003285 | C | T | 29 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
29 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.963+4711G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003285 | |||||||
chr4:6003307 | C | T | 4 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0064c0060t0001g0067 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+4689G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003307 | |||||||
chr4:6003320 | A | C | 5 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
5 | NA18945.hp2 NA18963.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+4676T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003320 | |||||||
chr4:6003379 | T | C | 5 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+4617A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003379 | |||||||
chr4:6003418 | GAGGGTGG others(2): Show |
G | 3 | a0023c0021t0001g0164 a0023c0021t0001g0165 a0108c0070t0001g0027 |
3 | HG02970.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.963+4569_963+4577d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003418 | |||||||
chr4:6003425 | G | A | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.963+4571C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003425 | |||||||
chr4:6003516 | T | C | 1 | a0074c0071t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.963+4480A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003516 | |||||||
chr4:6003533 | T | C | 1 | a0006c0006t0001g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.963+4463A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003533 | |||||||
chr4:6003600 | GTGATGGT others(2): Show |
G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(170): Show |
176 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.963+4387_963+4395d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003600 | |||||||
chr4:6003609 | A | G | 18 | a0009c0010t0001g0279 a0012c0013t0001g0059 a0012c0013t0001g0262 others(15): Show |
18 | HG01106.hp1 HG01106.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.963+4387T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003609 | |||||||
chr4:6003612 | ATGGTGAT others(2): Show |
A | 11 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(8): Show |
11 | HG01167.hp1 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+4375_963+4383d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003612 | |||||||
chr4:6003621 | G | A | 18 | a0009c0010t0001g0279 a0012c0013t0001g0059 a0012c0013t0001g0262 others(15): Show |
18 | HG01106.hp1 HG01106.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.963+4375C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003621 | |||||||
chr4:6003631 | C | T | 178 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(175): Show |
181 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.963+4365G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003631 | |||||||
chr4:6003656 | GTGATGA | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(166): Show |
172 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.963+4334_963+4339d others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003656 | |||||||
chr4:6003665 | GTGATGGT others(11): Show |
G | 11 | a0015c0018t0001g0284 a0018c0016t0001g0210 a0018c0016t0001g0276 others(8): Show |
11 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+4313_963+4330d others(20): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003665 | |||||||
chr4:6003678 | T | C | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4318A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003678 | |||||||
chr4:6003684 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.963+4312A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003684 | |||||||
chr4:6003696 | T | C | 3 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0040c0033t0001g0273 |
3 | HG01255.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.963+4300A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003696 | |||||||
chr4:6003745 | G | A | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4251C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003745 | |||||||
chr4:6003758 | T | TG | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4237dupC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003758 | |||||||
chr4:6003764 | A | G | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4232T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003764 | |||||||
chr4:6003765 | G | C | 1 | a0053c0068t0001g0329 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.963+4231C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003765 | |||||||
chr4:6003768 | ATGATGGT others(8): Show |
A | 4 | a0003c0004t0001g0303 a0003c0004t0001g0304 a0003c0004t0001g0305 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+4213_963+4227d others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003768 | |||||||
chr4:6003772 | TG | T | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4223delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003772 | |||||||
chr4:6003779 | G | A | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4217C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003779 | |||||||
chr4:6003780 | A | G | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4216T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003780 | |||||||
chr4:6003781 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.963+4215A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003781 | |||||||
chr4:6003783 | G | A | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+4213C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003783 | |||||||
chr4:6003801 | ATGG | A | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4192_963+4194d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003801 | |||||||
chr4:6003810 | A | G | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4186T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003810 | |||||||
chr4:6003820 | TG | T | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4175delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003820 | |||||||
chr4:6003822 | GTGA | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(96): Show |
101 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.963+4171_963+4173d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003822 | |||||||
chr4:6003827 | G | A | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4169C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003827 | |||||||
chr4:6003835 | T | TG | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4160dupC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003835 | |||||||
chr4:6003841 | A | G | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4155T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003841 | |||||||
chr4:6003842 | G | A | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4154C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003842 | |||||||
chr4:6003845 | A | G | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4151T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003845 | |||||||
chr4:6003857 | A | G | 11 | a0015c0018t0001g0284 a0018c0016t0001g0210 a0018c0016t0001g0276 others(8): Show |
11 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+4139T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003857 | |||||||
chr4:6003860 | G | A | 11 | a0015c0018t0001g0284 a0018c0016t0001g0210 a0018c0016t0001g0276 others(8): Show |
11 | HG02145.hp2 HG02615.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+4136C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003860 | |||||||
chr4:6003860 | G | GTGA | 9 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0011c0014t0001g0227 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4133_963+4135d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003860 | |||||||
chr4:6003860 | G | GTGATGAT others(20): Show |
2 | a0002c0002t0001g0176 a0002c0002t0001g0196 |
2 | NA18949.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.963+4135_963+4136i others(29): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003860 | |||||||
chr4:6003860 | G | GTGATGGT others(2): Show |
79 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0079 others(76): Show |
80 | HG00323.hp1 HG01081.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.963+4127_963+4135d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003860 | |||||||
chr4:6003860 | G | GTGATGGT others(11): Show |
148 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(145): Show |
151 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.963+4118_963+4135d others(20): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003860 | |||||||
chr4:6003860 | G | GTGATGGT others(26): Show |
3 | a0001c0001t0001g0140 a0001c0001t0001g0169 a0006c0006t0001g0111 |
3 | NA18949.hp1 NA19001.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.963+4135_963+4136i others(35): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003860 | |||||||
chr4:6003874 | G | GGTGATGA others(10): Show |
1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.963+4121_963+4122i others(19): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003874 | |||||||
chr4:6003881 | G | A | 5 | a0012c0013t0001g0059 a0037c0035t0001g0214 a0037c0035t0001g0223 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+4115C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003881 | |||||||
chr4:6003884 | A | G | 5 | a0012c0013t0001g0059 a0037c0035t0001g0214 a0037c0035t0001g0223 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+4112T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003884 | |||||||
chr4:6003886 | T | G | 7 | a0001c0001t0001g0098 a0012c0013t0001g0059 a0032c0029t0001g0073 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+4110A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003886 | |||||||
chr4:6003893 | ATGATG | A | 5 | a0012c0013t0001g0059 a0037c0035t0001g0214 a0037c0035t0001g0223 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+4098_963+4102d others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003893 | |||||||
chr4:6003896 | A | G | 2 | a0001c0001t0001g0098 a0032c0029t0001g0073 |
2 | NA19056.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.963+4100T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003896 | |||||||
chr4:6003897 | T | C | 37 | a0009c0010t0001g0279 a0010c0009t0001g0161 a0010c0009t0001g0162 others(34): Show |
37 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.963+4099A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003897 | |||||||
chr4:6003900 | G | T | 7 | a0001c0001t0001g0098 a0012c0013t0001g0059 a0032c0029t0001g0073 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+4096C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003900 | |||||||
chr4:6003907 | ATGT | A | 47 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(44): Show |
47 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.963+4086_963+4088d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003907 | |||||||
chr4:6003910 | T | A | 7 | a0001c0001t0001g0098 a0012c0013t0001g0059 a0032c0029t0001g0073 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+4086A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003910 | |||||||
chr4:6003911 | T | C | 1 | a0012c0013t0001g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.963+4085A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003911 | |||||||
chr4:6003912 | GA | G | 6 | a0001c0001t0001g0098 a0032c0029t0001g0073 a0037c0035t0001g0214 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+4083delT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003912 | |||||||
chr4:6003916 | ATGG | A | 4 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0064c0060t0001g0067 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+4077_963+4079d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003916 | |||||||
chr4:6003919 | G | A | 1 | a0012c0013t0001g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.963+4077C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003919 | |||||||
chr4:6003919 | GTGGTGAT others(8): Show |
G | 1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.963+4062_963+4076d others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003919 | |||||||
chr4:6003922 | G | A | 6 | a0001c0001t0001g0098 a0032c0029t0001g0073 a0037c0035t0001g0214 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+4074C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003922 | |||||||
chr4:6003925 | A | T | 6 | a0001c0001t0001g0098 a0032c0029t0001g0073 a0037c0035t0001g0214 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+4071T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003925 | |||||||
chr4:6003928 | G | A | 6 | a0012c0013t0001g0059 a0032c0029t0001g0073 a0037c0035t0001g0214 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+4068C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003928 | |||||||
chr4:6003931 | ATGATGG | A | 3 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0009c0010t0001g0144 |
3 | HG01069.hp2 HG01071.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.963+4059_963+4064d others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003931 | |||||||
chr4:6003934 | A | G | 6 | a0012c0013t0001g0059 a0032c0029t0001g0073 a0037c0035t0001g0214 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+4062T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003934 | |||||||
chr4:6003944 | T | A | 4 | a0008c0008t0001g0003 a0008c0008t0001g0076 a0008c0008t0001g0198 others(1): Show |
5 | HG02165.hp1 NA18747.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+4052A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003944 | |||||||
chr4:6003980 | AGTGATGA others(2): Show |
A | 4 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0064c0060t0001g0067 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+4007_963+4015d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003980 | |||||||
chr4:6003980 | AGTGATGA others(25): Show |
A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3984_963+4015d others(34): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6003980 | |||||||
chr4:6004024 | A | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(259): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.963+3972T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004024 | |||||||
chr4:6004027 | G | A | 61 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(58): Show |
62 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.963+3969C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004027 | |||||||
chr4:6004041 | G | A | 12 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0002t0001g0189 others(9): Show |
12 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+3955C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004041 | |||||||
chr4:6004047 | G | GGTGATGA others(422): Show |
1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3948_963+3949i others(431): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004047 | |||||||
chr4:6004048 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3948C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004048 | |||||||
chr4:6004051 | A | G | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3945T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004051 | |||||||
chr4:6004065 | G | GGTGATAG others(389): Show |
4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3930_963+3931i others(398): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004065 | |||||||
chr4:6004072 | GTGA | G | 4 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0064c0060t0001g0067 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+3921_963+3923d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004072 | |||||||
chr4:6004089 | A | ATGATGGT others(38): Show |
1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.963+3862_963+3906d others(47): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004089 | |||||||
chr4:6004102 | T | C | 2 | a0036c0039t0001g0014 a0083c0047t0001g0013 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.963+3894A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004102 | |||||||
chr4:6004104 | G | C | 5 | a0001c0001t0001g0110 a0001c0001t0001g0158 a0001c0001t0001g0281 others(2): Show |
5 | HG00642.hp2 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+3892C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004104 | |||||||
chr4:6004124 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3872T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004124 | |||||||
chr4:6004139 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3857C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004139 | |||||||
chr4:6004139 | GGTGATGA others(17): Show |
G | 11 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(8): Show |
11 | HG01167.hp1 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+3833_963+3856d others(26): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004139 | |||||||
chr4:6004143 | A | ATGATGGT others(182): Show |
4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3852_963+3853i others(191): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004143 | |||||||
chr4:6004163 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3833T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004163 | |||||||
chr4:6004163 | AGTGATGA others(2): Show |
A | 11 | a0013c0017t0001g0037 a0019c0020t0001g0001 a0019c0020t0001g0060 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+3824_963+3832d others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004163 | |||||||
chr4:6004164 | G | A | 1 | a0069c0111t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.963+3832C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004164 | |||||||
chr4:6004167 | A | G | 1 | a0069c0111t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.963+3829T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004167 | |||||||
chr4:6004167 | ATGATGGT others(8): Show |
A | 2 | a0030c0026t0001g0040 a0071c0046t0001g0011 |
2 | HG02886.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.963+3814_963+3828d others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004167 | |||||||
chr4:6004175 | G | T | 1 | a0040c0033t0001g0273 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.963+3821C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004175 | |||||||
chr4:6004176 | A | T | 1 | a0040c0033t0001g0273 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.963+3820T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004176 | |||||||
chr4:6004182 | G | GTGATGGT others(1593): Show |
1 | a0011c0014t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.963+3813_963+3814i others(1602): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004182 | |||||||
chr4:6004193 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3803C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004193 | |||||||
chr4:6004195 | T | C | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3801A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004195 | |||||||
chr4:6004196 | G | GGTGATGG others(7): Show |
104 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(101): Show |
106 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.963+3786_963+3799d others(16): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004196 | |||||||
chr4:6004196 | G | GGTGATGG others(31): Show |
2 | a0009c0010t0001g0267 a0009c0010t0001g0280 |
2 | HG01891.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.963+3799_963+3800i others(40): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004196 | |||||||
chr4:6004197 | G | GTGATGAT others(328): Show |
1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3798_963+3799i others(337): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004197 | |||||||
chr4:6004197 | G | GTGATGGT others(486): Show |
2 | a0043c0075t0001g0278 a0048c0051t0001g0053 |
2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.963+3798_963+3799i others(495): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004197 | |||||||
chr4:6004206 | A | G | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.963+3790T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004206 | |||||||
chr4:6004209 | A | ATGTGATG others(739): Show |
1 | a0002c0002t0001g0176 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.963+3786_963+3787i others(748): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004209 | |||||||
chr4:6004209 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3787T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004209 | |||||||
chr4:6004210 | TG | T | 3 | a0002c0002t0001g0178 a0002c0002t0001g0313 a0102c0112t0001g0015 |
3 | HG00639.hp1 NA19007.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.963+3785delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004210 | |||||||
chr4:6004211 | G | GTGATGGT others(500): Show |
54 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(51): Show |
55 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.963+3784_963+3785i others(509): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004211 | |||||||
chr4:6004212 | G | A | 2 | a0001c0001t0001g0110 a0002c0002t0001g0176 |
2 | HG00642.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.963+3784C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004212 | |||||||
chr4:6004216 | T | TGATGGTG others(2): Show |
4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3779_963+3780i others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004216 | |||||||
chr4:6004223 | G | A | 3 | a0002c0002t0001g0178 a0002c0002t0001g0313 a0102c0112t0001g0015 |
3 | HG00639.hp1 NA19007.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.963+3773C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004223 | |||||||
chr4:6004225 | T | TA | 54 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(51): Show |
55 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.963+3770_963+3771i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004225 | |||||||
chr4:6004226 | G | GA | 3 | a0002c0002t0001g0178 a0002c0002t0001g0313 a0102c0112t0001g0015 |
3 | HG00639.hp1 NA19007.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.963+3769_963+3770i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004226 | |||||||
chr4:6004229 | A | G | 3 | a0002c0002t0001g0178 a0002c0002t0001g0313 a0102c0112t0001g0015 |
3 | HG00639.hp1 NA19007.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.963+3767T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004229 | |||||||
chr4:6004232 | G | A | 57 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(54): Show |
58 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.963+3764C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004232 | |||||||
chr4:6004235 | A | G | 54 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(51): Show |
55 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.963+3761T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004235 | |||||||
chr4:6004237 | G | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(105): Show |
110 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.963+3759C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004237 | |||||||
chr4:6004238 | A | ATGGTGAT others(127): Show |
4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3757_963+3758i others(136): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004238 | |||||||
chr4:6004238 | A | G | 3 | a0002c0002t0001g0178 a0002c0002t0001g0313 a0102c0112t0001g0015 |
3 | HG00639.hp1 NA19007.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.963+3758T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004238 | |||||||
chr4:6004241 | A | T | 2 | a0001c0001t0001g0110 a0002c0002t0001g0176 |
2 | HG00642.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.963+3755T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004241 | |||||||
chr4:6004244 | G | A | 2 | a0001c0001t0001g0110 a0002c0002t0001g0176 |
2 | HG00642.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.963+3752C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004244 | |||||||
chr4:6004250 | A | G | 5 | a0001c0001t0001g0110 a0002c0002t0001g0176 a0002c0002t0001g0178 others(2): Show |
5 | HG00639.hp1 HG00642.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3746T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004250 | |||||||
chr4:6004253 | G | A | 5 | a0001c0001t0001g0110 a0002c0002t0001g0176 a0002c0002t0001g0178 others(2): Show |
5 | HG00639.hp1 HG00642.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3743C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004253 | |||||||
chr4:6004253 | G | GTGATGGT others(8): Show |
5 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+3742_963+3743i others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004253 | |||||||
chr4:6004253 | G | GTGATGGT others(79): Show |
3 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0064c0060t0001g0067 |
3 | HG02486.hp2 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.963+3742_963+3743i others(88): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004253 | |||||||
chr4:6004265 | G | A | 60 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0002c0002t0001g0081 others(57): Show |
61 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.963+3731C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004265 | |||||||
chr4:6004268 | G | A | 110 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(107): Show |
112 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.963+3728C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004268 | |||||||
chr4:6004271 | A | ATGATGT | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3724_963+3725i others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004271 | |||||||
chr4:6004273 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.963+3723C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004273 | |||||||
chr4:6004274 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3722C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004274 | |||||||
chr4:6004280 | G | GTGGTGA | 108 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(105): Show |
110 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.963+3715_963+3716i others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004280 | |||||||
chr4:6004282 | G | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0177 a0001c0001t0001g0209 others(1): Show |
4 | HG00609.hp1 HG02155.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3714C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004282 | |||||||
chr4:6004283 | A | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(105): Show |
110 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.963+3713T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004283 | |||||||
chr4:6004286 | T | A | 170 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(167): Show |
173 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.963+3710A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004286 | |||||||
chr4:6004288 | G | A | 56 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(53): Show |
57 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.963+3708C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004288 | |||||||
chr4:6004288 | G | GGTGATGG others(790): Show |
2 | a0002c0002t0001g0178 a0002c0002t0001g0313 |
2 | HG00639.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.963+3707_963+3708i others(799): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004288 | |||||||
chr4:6004288 | G | GGTGATGG others(796): Show |
1 | a0102c0112t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+3707_963+3708i others(805): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004288 | |||||||
chr4:6004295 | A | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(105): Show |
110 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.963+3701T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004295 | |||||||
chr4:6004298 | G | T | 2 | a0001c0001t0001g0110 a0002c0002t0001g0176 |
2 | HG00642.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.963+3698C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004298 | |||||||
chr4:6004304 | G | A | 61 | a0001c0001t0001g0110 a0002c0002t0001g0081 a0002c0002t0001g0090 others(58): Show |
62 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.963+3692C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004304 | |||||||
chr4:6004306 | G | GATGATA | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3689_963+3690i others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004306 | |||||||
chr4:6004313 | A | G | 59 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.963+3683T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004313 | |||||||
chr4:6004314 | T | TGGTG | 4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3681_963+3682i others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004314 | |||||||
chr4:6004315 | G | GA | 59 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.963+3680_963+3681i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004315 | |||||||
chr4:6004320 | C | G | 212 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(209): Show |
216 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.963+3676G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004320 | |||||||
chr4:6004323 | A | G | 66 | a0001c0001t0001g0110 a0001c0001t0001g0158 a0001c0001t0001g0281 others(63): Show |
67 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.963+3673T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004323 | |||||||
chr4:6004334 | TG | T | 3 | a0002c0002t0001g0178 a0002c0002t0001g0313 a0102c0112t0001g0015 |
3 | HG00639.hp1 NA19007.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.963+3661delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004334 | |||||||
chr4:6004335 | G | A | 2 | a0001c0001t0001g0110 a0002c0002t0001g0176 |
2 | HG00642.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.963+3661C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004335 | |||||||
chr4:6004335 | G | GGTGATGG others(799): Show |
1 | a0011c0014t0001g0145 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.963+3660_963+3661i others(808): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004335 | |||||||
chr4:6004335 | G | GGTGATGG others(1489): Show |
1 | a0040c0033t0001g0273 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.963+3660_963+3661i others(1498): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004335 | |||||||
chr4:6004342 | G | A | 58 | a0001c0001t0001g0110 a0002c0002t0001g0081 a0002c0002t0001g0090 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.963+3654C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004342 | |||||||
chr4:6004345 | A | ATGATGTG others(1442): Show |
2 | a0001c0001t0001g0080 a0006c0006t0001g0139 |
2 | HG03834.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.963+3650_963+3651i others(1451): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004345 | |||||||
chr4:6004345 | A | ATGATGTG others(757): Show |
3 | a0009c0010t0001g0326 a0064c0060t0001g0067 a0085c0099t0001g0034 |
3 | HG02572.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.963+3650_963+3651i others(766): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004345 | |||||||
chr4:6004345 | A | ATGATGTG others(748): Show |
1 | a0009c0010t0001g0327 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.963+3650_963+3651i others(757): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004345 | |||||||
chr4:6004345 | A | ATGATGTG others(554): Show |
1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3650_963+3651i others(563): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004345 | |||||||
chr4:6004345 | A | G | 58 | a0001c0001t0001g0110 a0002c0002t0001g0081 a0002c0002t0001g0090 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.963+3651T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004345 | |||||||
chr4:6004348 | A | ATG | 20 | a0004c0003t0001g0009 a0004c0003t0001g0288 a0004c0003t0001g0289 others(17): Show |
22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.963+3646_963+3647d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(1): Show |
4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3647_963+3648i others(10): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(805): Show |
1 | a0005c0005t0001g0136 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.963+3647_963+3648i others(814): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(805): Show |
3 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.963+3647_963+3648i others(814): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(796): Show |
1 | a0004c0003t0001g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(805): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(790): Show |
1 | a0069c0111t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(799): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(805): Show |
87 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(84): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.963+3647_963+3648i others(814): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(796): Show |
1 | a0011c0014t0001g0227 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(805): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(796): Show |
10 | a0004c0003t0001g0224 a0009c0010t0001g0267 a0009c0010t0001g0280 others(7): Show |
10 | HG00597.hp1 HG01257.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+3647_963+3648i others(805): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(760): Show |
3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.963+3647_963+3648i others(769): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(743): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0033 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.963+3647_963+3648i others(752): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(761): Show |
1 | a0082c0064t0001g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.963+3647_963+3648i others(770): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(734): Show |
2 | a0059c0102t0001g0269 a0070c0113t0001g0029 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.963+3647_963+3648i others(743): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(757): Show |
1 | a0011c0014t0001g0309 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.963+3647_963+3648i others(766): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(751): Show |
1 | a0095c0107t0001g0286 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(760): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(751): Show |
1 | a0078c0066t0001g0018 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.963+3647_963+3648i others(760): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(751): Show |
1 | a0053c0068t0001g0329 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(760): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(742): Show |
29 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(26): Show |
29 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.963+3647_963+3648i others(751): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(742): Show |
3 | a0003c0004t0001g0211 a0003c0004t0001g0310 a0004c0003t0001g0314 |
3 | HG02698.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.963+3647_963+3648i others(751): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(757): Show |
71 | a0001c0001t0001g0142 a0001c0001t0001g0177 a0001c0001t0001g0209 others(68): Show |
74 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.963+3647_963+3648i others(766): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(856): Show |
1 | a0032c0029t0001g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.963+3647_963+3648i others(865): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(772): Show |
1 | a0003c0011t0001g0229 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(781): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(764): Show |
1 | a0001c0001t0001g0088 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(773): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(748): Show |
1 | a0015c0018t0001g0300 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.963+3647_963+3648i others(757): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(742): Show |
10 | a0003c0004t0001g0303 a0003c0004t0001g0304 a0003c0004t0001g0305 others(7): Show |
11 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+3647_963+3648i others(751): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(2283): Show |
1 | a0077c0097t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.963+3647_963+3648i others(2292): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | ATGTGGTG others(754): Show |
1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.963+3647_963+3648i others(763): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004348 | A | G | 1 | a0063c0110t0001g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.963+3648T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004348 | |||||||
chr4:6004351 | A | G | 20 | a0004c0003t0001g0009 a0004c0003t0001g0288 a0004c0003t0001g0289 others(17): Show |
22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.963+3645T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004351 | |||||||
chr4:6004352 | C | CTGTGATG others(737): Show |
1 | a0063c0110t0001g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.963+3643_963+3644i others(746): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004352 | |||||||
chr4:6004352 | C | T | 333 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.963+3644G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004352 | |||||||
chr4:6004358 | T | C | 56 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(53): Show |
57 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.963+3638A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004358 | |||||||
chr4:6004363 | A | ACTG | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3632_963+3633i others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004363 | |||||||
chr4:6004363 | A | ATGGTGAC others(531): Show |
1 | a0004c0003t0001g0288 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.963+3632_963+3633i others(540): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004363 | |||||||
chr4:6004363 | A | ATGGTGAC others(731): Show |
1 | a0020c0056t0001g0042 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.963+3632_963+3633i others(740): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004363 | |||||||
chr4:6004363 | A | ATGGTGAC others(740): Show |
7 | a0004c0003t0001g0009 a0004c0003t0001g0289 a0004c0003t0001g0315 others(4): Show |
8 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+3632_963+3633i others(749): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004363 | |||||||
chr4:6004363 | A | ATGGTGAC others(679): Show |
4 | a0013c0017t0001g0037 a0051c0081t0001g0331 a0072c0100t0001g0036 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3632_963+3633i others(688): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004363 | |||||||
chr4:6004363 | A | ATGGTGAC others(725): Show |
7 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(4): Show |
8 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+3632_963+3633i others(734): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004363 | |||||||
chr4:6004363 | A | G | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3633T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004363 | |||||||
chr4:6004367 | T | A | 1 | a0002c0002t0001g0196 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.963+3629A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004367 | |||||||
chr4:6004367 | TG | T | 60 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(57): Show |
61 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.963+3628delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004367 | |||||||
chr4:6004368 | G | T | 1 | a0002c0002t0001g0196 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.963+3628C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004368 | |||||||
chr4:6004369 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3627C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004369 | |||||||
chr4:6004375 | G | GTGA | 138 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(135): Show |
142 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.963+3618_963+3620d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004375 | |||||||
chr4:6004390 | G | A | 57 | a0001c0001t0001g0256 a0002c0002t0001g0081 a0002c0002t0001g0090 others(54): Show |
58 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.963+3606C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004390 | |||||||
chr4:6004390 | G | GTGA | 19 | a0004c0003t0001g0009 a0004c0003t0001g0288 a0004c0003t0001g0289 others(16): Show |
21 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.963+3605_963+3606i others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004390 | |||||||
chr4:6004390 | G | GTGATGAT others(712): Show |
4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3605_963+3606i others(721): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004390 | |||||||
chr4:6004393 | G | A | 161 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(158): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.963+3603C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004393 | |||||||
chr4:6004399 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(110): Show |
115 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.963+3597C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004399 | |||||||
chr4:6004405 | G | A | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3591C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004405 | |||||||
chr4:6004408 | A | G | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3588T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004408 | |||||||
chr4:6004411 | T | G | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3585A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004411 | |||||||
chr4:6004411 | T | TGATGGTA others(1): Show |
107 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(104): Show |
109 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+3584_963+3585i others(10): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004411 | |||||||
chr4:6004411 | T | TGATGGTA others(995): Show |
3 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.963+3584_963+3585i others(1004): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004411 | |||||||
chr4:6004411 | T | TGATGGTA others(638): Show |
3 | a0021c0024t0001g0205 a0039c0025t0001g0206 a0081c0069t0001g0325 |
3 | HG02922.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.963+3584_963+3585i others(647): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004411 | |||||||
chr4:6004414 | G | A | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3582C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004414 | |||||||
chr4:6004420 | A | G | 142 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(139): Show |
146 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.963+3576T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004420 | |||||||
chr4:6004420 | A | T | 3 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.963+3576T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004420 | |||||||
chr4:6004423 | G | A | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3573C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004423 | |||||||
chr4:6004423 | G | T | 57 | a0001c0001t0001g0256 a0002c0002t0001g0081 a0002c0002t0001g0090 others(54): Show |
58 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.963+3573C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004423 | |||||||
chr4:6004426 | A | G | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3570T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004426 | |||||||
chr4:6004429 | G | A | 200 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(197): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.963+3567C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004429 | |||||||
chr4:6004432 | G | A | 249 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(246): Show |
255 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.963+3564C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004432 | |||||||
chr4:6004435 | A | ATGATGAT others(2): Show |
21 | a0004c0003t0001g0009 a0004c0003t0001g0288 a0004c0003t0001g0289 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.963+3560_963+3561i others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004435 | |||||||
chr4:6004435 | A | ATGATGG | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3560_963+3561i others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004435 | |||||||
chr4:6004435 | A | G | 142 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(139): Show |
146 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.963+3561T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004435 | |||||||
chr4:6004439 | T | TG | 56 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(53): Show |
57 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.963+3556dupC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004439 | |||||||
chr4:6004440 | G | GTGGTGGT others(360): Show |
4 | a0021c0024t0001g0066 a0054c0065t0001g0219 a0065c0115t0001g0150 others(1): Show |
4 | HG02027.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3555_963+3556i others(369): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004440 | |||||||
chr4:6004443 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(100): Show |
105 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.963+3553T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004443 | |||||||
chr4:6004446 | G | GTGATGAT others(538): Show |
1 | a0034c0040t0001g0321 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.963+3549_963+3550i others(547): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGAT others(524): Show |
1 | a0003c0004t0001g0191 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.963+3549_963+3550i others(533): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGAT others(566): Show |
3 | a0003c0004t0001g0146 a0003c0004t0001g0192 a0044c0088t0001g0159 |
3 | HG00673.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.963+3549_963+3550i others(575): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGAT others(542): Show |
1 | a0002c0002t0001g0196 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.963+3549_963+3550i others(551): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGAT others(539): Show |
50 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(47): Show |
51 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.963+3549_963+3550i others(548): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGGT others(228): Show |
1 | a0004c0003t0001g0137 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.963+3549_963+3550i others(237): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGGT others(261): Show |
1 | a0005c0005t0001g0138 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.963+3549_963+3550i others(270): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGGT others(243): Show |
88 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(85): Show |
90 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.963+3549_963+3550i others(252): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004446 | G | GTGATGGT others(243): Show |
1 | a0001c0001t0001g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.963+3549_963+3550i others(252): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004446 | |||||||
chr4:6004448 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(162): Show |
168 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.963+3548T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004448 | |||||||
chr4:6004452 | G | T | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3544C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004452 | |||||||
chr4:6004458 | A | C | 12 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0002c0002t0001g0178 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+3538T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004458 | |||||||
chr4:6004461 | G | A | 12 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0002c0002t0001g0178 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+3535C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004461 | |||||||
chr4:6004464 | A | G | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3532T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004464 | |||||||
chr4:6004467 | G | A | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3529C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004467 | |||||||
chr4:6004470 | A | G | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3526T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004470 | |||||||
chr4:6004471 | T | TGCTGATG others(3): Show |
11 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(8): Show |
11 | HG01167.hp1 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+3524_963+3525i others(12): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004471 | |||||||
chr4:6004473 | A | AT | 162 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(159): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.963+3522_963+3523i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | ATAGT | 86 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(83): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.963+3522_963+3523i others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | ATGATGTG others(285): Show |
1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.963+3522_963+3523i others(294): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | ATGGT | 7 | a0003c0004t0001g0146 a0003c0004t0001g0192 a0021c0024t0001g0066 others(4): Show |
7 | HG00673.hp2 HG02027.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+3522_963+3523i others(6): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | ATGGTGAT others(191): Show |
2 | a0002c0002t0001g0313 a0086c0073t0001g0153 |
2 | HG00639.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.963+3522_963+3523i others(200): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | ATGGTGAT others(238): Show |
1 | a0002c0002t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.963+3522_963+3523i others(247): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | ATGGTGAT others(176): Show |
4 | a0038c0034t0001g0017 a0038c0034t0001g0330 a0056c0052t0001g0030 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3522_963+3523i others(185): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | ATGTGGTG others(109): Show |
3 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.963+3522_963+3523i others(118): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004473 | A | T | 11 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(8): Show |
11 | HG01167.hp1 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+3523T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004473 | |||||||
chr4:6004474 | G | T | 58 | a0001c0001t0001g0109 a0002c0002t0001g0081 a0002c0002t0001g0090 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.963+3522C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004474 | |||||||
chr4:6004475 | A | G | 6 | a0001c0001t0001g0158 a0001c0001t0001g0256 a0001c0001t0001g0281 others(3): Show |
6 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+3521T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004475 | |||||||
chr4:6004475 | AT | A | 58 | a0001c0001t0001g0109 a0002c0002t0001g0081 a0002c0002t0001g0090 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.963+3520delA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004475 | |||||||
chr4:6004477 | G | GTGGTGGT others(2): Show |
8 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0037c0035t0001g0214 others(5): Show |
8 | HG02258.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+3518_963+3519i others(11): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004477 | |||||||
chr4:6004477 | GAGCAC | G | 5 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(2): Show |
5 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+3514_963+3518d others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004477 | |||||||
chr4:6004478 | A | AT | 105 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(102): Show |
107 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.963+3517_963+3518i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004478 | |||||||
chr4:6004478 | A | T | 214 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(211): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.963+3518T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004478 | |||||||
chr4:6004479 | G | T | 9 | a0002c0002t0001g0313 a0013c0017t0001g0031 a0013c0017t0001g0032 others(6): Show |
9 | HG00639.hp1 HG02109.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.963+3517C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004479 | |||||||
chr4:6004479 | GCACAA | G | 147 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(144): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.963+3512_963+3516d others(7): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004479 | |||||||
chr4:6004480 | C | A | 58 | a0001c0001t0001g0109 a0002c0002t0001g0081 a0002c0002t0001g0090 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.963+3516G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004480 | |||||||
chr4:6004480 | C | G | 122 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(119): Show |
124 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.963+3516G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004480 | |||||||
chr4:6004481 | A | T | 180 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(177): Show |
183 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.963+3515T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004481 | |||||||
chr4:6004482 | C | G | 180 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(177): Show |
183 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.963+3514G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004482 | |||||||
chr4:6004483 | A | T | 1 | a0002c0002t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.963+3513T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004483 | |||||||
chr4:6004484 | A | C | 4 | a0021c0024t0001g0066 a0054c0065t0001g0219 a0065c0115t0001g0150 others(1): Show |
4 | HG02027.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3512T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004484 | |||||||
chr4:6004484 | A | T | 182 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(179): Show |
185 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.963+3512T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004484 | |||||||
chr4:6004486 | C | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(84): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.963+3510G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004486 | |||||||
chr4:6004486 | C | G | 91 | a0001c0001t0001g0109 a0001c0001t0001g0158 a0001c0001t0001g0281 others(88): Show |
92 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.963+3510G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004486 | |||||||
chr4:6004486 | C | T | 148 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(145): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.963+3510G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004486 | |||||||
chr4:6004487 | C | G | 148 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(145): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.963+3509G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004487 | |||||||
chr4:6004487 | C | T | 183 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(180): Show |
186 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.963+3509G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004487 | |||||||
chr4:6004488 | C | A | 1 | a0002c0002t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.963+3508G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004488 | |||||||
chr4:6004489 | A | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(84): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.963+3507T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004489 | |||||||
chr4:6004489 | A | T | 148 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(145): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.963+3507T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004489 | |||||||
chr4:6004490 | G | T | 187 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(184): Show |
190 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.963+3506C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004490 | |||||||
chr4:6004491 | G | A | 148 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(145): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.963+3505C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004491 | |||||||
chr4:6004492 | A | AT | 95 | a0001c0001t0001g0109 a0001c0001t0001g0158 a0001c0001t0001g0281 others(92): Show |
96 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.963+3503_963+3504i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004492 | |||||||
chr4:6004492 | A | T | 149 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(146): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.963+3504T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004492 | |||||||
chr4:6004493 | A | G | 214 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(211): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.963+3503T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004493 | |||||||
chr4:6004493 | A | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(89): Show |
94 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.963+3503T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004493 | |||||||
chr4:6004495 | A | AT | 88 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(85): Show |
90 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.963+3500_963+3501i others(3): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004495 | |||||||
chr4:6004497 | A | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(84): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.963+3499T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004497 | |||||||
chr4:6004500 | A | C | 155 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(152): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.963+3496T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004500 | |||||||
chr4:6004500 | A | G | 7 | a0001c0001t0001g0109 a0001c0001t0001g0256 a0021c0024t0001g0066 others(4): Show |
7 | HG01081.hp2 HG02027.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+3496T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004500 | |||||||
chr4:6004503 | A | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(170): Show |
176 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.963+3493T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004503 | |||||||
chr4:6004509 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(113): Show |
118 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.963+3487C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004509 | |||||||
chr4:6004512 | G | A | 217 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(214): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.963+3484C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004512 | |||||||
chr4:6004513 | C | T | 333 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.963+3483G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004513 | |||||||
chr4:6004514 | A | G | 333 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.963+3482T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004514 | |||||||
chr4:6004518 | G | GTGA | 19 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0003c0004t0001g0146 others(16): Show |
19 | HG00673.hp2 HG01167.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+3475_963+3477d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004518 | |||||||
chr4:6004521 | ATGG | A | 6 | a0002c0002t0001g0313 a0038c0034t0001g0017 a0038c0034t0001g0330 others(3): Show |
6 | HG00639.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+3472_963+3474d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004521 | |||||||
chr4:6004523 | G | GAT | 4 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 others(1): Show |
4 | HG01516.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+3472_963+3473i others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004523 | |||||||
chr4:6004524 | G | GTGA | 149 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0080 others(146): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.963+3469_963+3471d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004524 | |||||||
chr4:6004529 | A | G | 178 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(175): Show |
181 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.963+3467T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004529 | |||||||
chr4:6004537 | G | T | 334 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(331): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.963+3459C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004537 | |||||||
chr4:6004538 | G | A | 154 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(151): Show |
157 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.963+3458C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004538 | |||||||
chr4:6004539 | G | GTGATGA | 5 | a0001c0001t0001g0080 a0006c0006t0001g0139 a0021c0024t0001g0205 others(2): Show |
5 | HG02922.hp2 HG03225.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+3456_963+3457i others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(330): Show |
1 | a0040c0033t0001g0273 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.963+3456_963+3457i others(339): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(312): Show |
8 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(5): Show |
8 | HG01167.hp1 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+3456_963+3457i others(321): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(312): Show |
4 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(1): Show |
4 | HG02257.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3456_963+3457i others(321): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(294): Show |
3 | a0016c0015t0001g0044 a0016c0015t0001g0046 a0022c0022t0001g0047 |
3 | HG02258.hp2 HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.963+3456_963+3457i others(303): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(1840): Show |
3 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.963+3456_963+3457i others(1849): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(321): Show |
1 | a0003c0011t0001g0234 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.963+3456_963+3457i others(330): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(336): Show |
81 | a0001c0001t0001g0142 a0001c0001t0001g0177 a0001c0001t0001g0209 others(78): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.963+3456_963+3457i others(345): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(335): Show |
1 | a0001c0001t0001g0088 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.963+3456_963+3457i others(344): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(244): Show |
1 | a0088c0105t0001g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.963+3456_963+3457i others(253): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(1014): Show |
1 | a0002c0002t0001g0176 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.963+3456_963+3457i others(1023): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(345): Show |
1 | a0077c0097t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.963+3456_963+3457i others(354): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(258): Show |
2 | a0071c0046t0001g0011 a0080c0045t0001g0010 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.963+3456_963+3457i others(267): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(351): Show |
46 | a0009c0010t0001g0279 a0010c0009t0001g0161 a0010c0009t0001g0162 others(43): Show |
46 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.963+3456_963+3457i others(360): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(507): Show |
2 | a0104c0063t0001g0071 a0109c0061t0001g0063 |
2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.963+3456_963+3457i others(516): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(342): Show |
3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.963+3456_963+3457i others(351): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | GTGATGAT others(336): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0033 |
2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.963+3456_963+3457i others(345): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004539 | G | T | 4 | a0021c0024t0001g0066 a0054c0065t0001g0219 a0065c0115t0001g0150 others(1): Show |
4 | HG02027.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3457C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004539 | |||||||
chr4:6004541 | G | T | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3455C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004541 | |||||||
chr4:6004542 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(165): Show |
171 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.963+3454C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004542 | |||||||
chr4:6004543 | T | TGATGGTG others(337): Show |
1 | a0003c0004t0001g0255 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.963+3452_963+3453i others(346): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004543 | |||||||
chr4:6004544 | A | G | 334 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(331): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.963+3452T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004544 | |||||||
chr4:6004545 | A | T | 1 | a0003c0004t0001g0255 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.963+3451T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004545 | |||||||
chr4:6004547 | G | A | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3449C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004547 | |||||||
chr4:6004554 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3442T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004554 | |||||||
chr4:6004557 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3439C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004557 | |||||||
chr4:6004561 | T | C | 3 | a0003c0004t0001g0146 a0003c0004t0001g0192 a0044c0088t0001g0159 |
3 | HG00673.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.963+3435A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004561 | |||||||
chr4:6004563 | G | A | 5 | a0021c0024t0001g0066 a0033c0036t0001g0265 a0054c0065t0001g0219 others(2): Show |
5 | HG01516.hp2 HG02027.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+3433C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004563 | |||||||
chr4:6004566 | G | A | 169 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(166): Show |
172 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.963+3430C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004566 | |||||||
chr4:6004566 | G | C | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3430C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004566 | |||||||
chr4:6004569 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3427T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004569 | |||||||
chr4:6004570 | TG | T | 3 | a0003c0004t0001g0146 a0003c0004t0001g0192 a0044c0088t0001g0159 |
3 | HG00673.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.963+3425delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004570 | |||||||
chr4:6004572 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3424C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004572 | |||||||
chr4:6004573 | T | A | 4 | a0013c0017t0001g0031 a0013c0017t0001g0032 a0013c0017t0001g0038 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3423A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004573 | |||||||
chr4:6004577 | G | GATA | 4 | a0021c0024t0001g0066 a0054c0065t0001g0219 a0065c0115t0001g0150 others(1): Show |
4 | HG02027.hp1 HG02559.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+3418_963+3419i others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004577 | |||||||
chr4:6004577 | G | GATATTGA others(389): Show |
3 | a0021c0024t0001g0205 a0039c0025t0001g0206 a0081c0069t0001g0325 |
3 | HG02922.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.963+3418_963+3419i others(398): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004577 | |||||||
chr4:6004577 | G | GATATTGA others(395): Show |
2 | a0001c0001t0001g0080 a0006c0006t0001g0139 |
2 | HG03834.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.963+3418_963+3419i others(404): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004577 | |||||||
chr4:6004578 | G | A | 2 | a0001c0001t0001g0256 a0033c0036t0001g0265 |
2 | HG01516.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.963+3418C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004578 | |||||||
chr4:6004579 | T | A | 161 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0088 others(158): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.963+3417A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004579 | |||||||
chr4:6004581 | A | G | 2 | a0001c0001t0001g0256 a0033c0036t0001g0265 |
2 | HG01516.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.963+3415T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004581 | |||||||
chr4:6004583 | G | GATGGTGA others(400): Show |
1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.963+3412_963+3413i others(409): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GATGGTGA others(400): Show |
3 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 |
3 | HG02258.hp1 HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.963+3412_963+3413i others(409): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GATGGTGA others(407): Show |
3 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0064c0060t0001g0067 |
3 | HG02486.hp2 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.963+3412_963+3413i others(416): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GATGGTGA others(404): Show |
1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.963+3412_963+3413i others(413): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GATGGTGA others(641): Show |
1 | a0086c0073t0001g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.963+3412_963+3413i others(650): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GGTA | 5 | a0001c0001t0001g0080 a0006c0006t0001g0139 a0021c0024t0001g0205 others(2): Show |
5 | HG02922.hp2 HG03225.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+3412_963+3413i others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GGTGATGA others(813): Show |
1 | a0002c0002t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.963+3412_963+3413i others(822): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GGTGATGG others(862): Show |
2 | a0038c0034t0001g0017 a0038c0034t0001g0330 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.963+3412_963+3413i others(871): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004583 | G | GGTGATGG others(862): Show |
2 | a0056c0052t0001g0030 a0096c0076t0001g0328 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.963+3412_963+3413i others(871): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004583 | |||||||
chr4:6004584 | T | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(171): Show |
177 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.963+3412A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004584 | |||||||
chr4:6004584 | T | TTGGTGAT others(31): Show |
5 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(2): Show |
6 | HG02109.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+3411_963+3412i others(40): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004584 | |||||||
chr4:6004585 | T | A | 1 | a0003c0004t0001g0255 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.963+3411A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004585 | |||||||
chr4:6004586 | G | A | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3410C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004586 | |||||||
chr4:6004595 | G | A | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.963+3401C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004595 | |||||||
chr4:6004599 | A | ATGATGGA others(770): Show |
1 | a0025c0023t0001g0318 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.963+3396_963+3397i others(779): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(775): Show |
1 | a0005c0005t0001g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.963+3396_963+3397i others(784): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(790): Show |
1 | a0001c0001t0001g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.963+3396_963+3397i others(799): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(796): Show |
1 | a0001c0001t0001g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.963+3396_963+3397i others(805): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(775): Show |
1 | a0102c0112t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+3396_963+3397i others(784): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(790): Show |
5 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0021c0050t0001g0064 others(2): Show |
5 | HG01257.hp2 HG01891.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3396_963+3397i others(799): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(796): Show |
56 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0075 others(53): Show |
58 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.963+3396_963+3397i others(805): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(799): Show |
3 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0069c0111t0001g0094 |
3 | HG01255.hp2 HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.963+3396_963+3397i others(808): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(787): Show |
4 | a0001c0001t0001g0097 a0001c0001t0001g0204 a0001c0084t0001g0096 others(1): Show |
4 | HG00544.hp1 HG00597.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+3396_963+3397i others(796): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(802): Show |
16 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
16 | HG01358.hp2 HG02080.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.963+3396_963+3397i others(811): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(808): Show |
1 | a0001c0001t0001g0140 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.963+3396_963+3397i others(817): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(779): Show |
1 | a0001c0001t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.963+3396_963+3397i others(788): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(778): Show |
1 | a0004c0003t0001g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.963+3396_963+3397i others(787): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(760): Show |
48 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(45): Show |
49 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+3396_963+3397i others(769): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(759): Show |
3 | a0002c0002t0001g0194 a0007c0007t0001g0193 a0007c0007t0001g0195 |
3 | HG01256.hp1 HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.963+3396_963+3397i others(768): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(760): Show |
1 | a0002c0002t0001g0196 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.963+3396_963+3397i others(769): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004599 | A | ATGATGGT others(766): Show |
2 | a0025c0023t0001g0319 a0052c0108t0001g0290 |
2 | HG00280.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.963+3396_963+3397i others(775): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004599 | |||||||
chr4:6004602 | G | A | 146 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(143): Show |
149 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.963+3394C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004602 | |||||||
chr4:6004602 | G | GTGA | 19 | a0001c0001t0001g0080 a0002c0002t0001g0313 a0006c0006t0001g0139 others(16): Show |
19 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.963+3391_963+3393d others(5): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004602 | |||||||
chr4:6004602 | G | GTGATGAT others(713): Show |
3 | a0003c0004t0001g0146 a0003c0004t0001g0192 a0044c0088t0001g0159 |
3 | HG00673.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.963+3393_963+3394i others(722): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004602 | |||||||
chr4:6004602 | G | GTGATGAT others(659): Show |
1 | a0021c0024t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.963+3393_963+3394i others(668): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004602 | |||||||
chr4:6004602 | G | GTGATGAT others(659): Show |
1 | a0054c0065t0001g0219 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.963+3393_963+3394i others(668): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004602 | |||||||
chr4:6004602 | G | GTGATGAT others(668): Show |
2 | a0065c0115t0001g0150 a0067c0072t0001g0082 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.963+3393_963+3394i others(677): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004602 | |||||||
chr4:6004602 | G | GTGGTGAT others(34): Show |
156 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0088 others(153): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.963+3393_963+3394i others(43): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004602 | |||||||
chr4:6004616 | G | A | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3380C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004616 | |||||||
chr4:6004622 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3374C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004622 | |||||||
chr4:6004633 | TGTGATG | T | 12 | a0003c0004t0001g0077 a0003c0004t0001g0078 a0009c0010t0001g0144 others(9): Show |
12 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+3357_963+3362d others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004633 | |||||||
chr4:6004642 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3354C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004642 | |||||||
chr4:6004651 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3345A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004651 | |||||||
chr4:6004661 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3335T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004661 | |||||||
chr4:6004663 | G | GATGATGA others(157): Show |
1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3332_963+3333i others(166): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004663 | |||||||
chr4:6004664 | T | G | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3332A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004664 | |||||||
chr4:6004668 | G | A | 333 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.963+3328C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004668 | |||||||
chr4:6004675 | T | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3321A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004675 | |||||||
chr4:6004684 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3312C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004684 | |||||||
chr4:6004687 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3309C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004687 | |||||||
chr4:6004698 | A | G | 2 | a0001c0001t0001g0256 a0033c0036t0001g0265 |
2 | HG01516.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.963+3298T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004698 | |||||||
chr4:6004708 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3288C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004708 | |||||||
chr4:6004708 | G | GCGATGAT others(23): Show |
1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3287_963+3288i others(32): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004708 | |||||||
chr4:6004714 | A | G | 8 | a0025c0023t0001g0318 a0025c0023t0001g0319 a0034c0040t0001g0291 others(5): Show |
8 | HG00099.hp1 HG00280.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+3282T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004714 | |||||||
chr4:6004732 | T | A | 1 | a0025c0023t0001g0318 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.963+3264A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004732 | |||||||
chr4:6004758 | G | A | 1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3238C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004758 | |||||||
chr4:6004765 | C | T | 2 | a0001c0001t0001g0256 a0033c0036t0001g0265 |
2 | HG01516.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.963+3231G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004765 | |||||||
chr4:6004766 | A | G | 2 | a0001c0001t0001g0256 a0033c0036t0001g0265 |
2 | HG01516.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.963+3230T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004766 | |||||||
chr4:6004773 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3223T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004773 | |||||||
chr4:6004774 | C | T | 2 | a0001c0001t0001g0256 a0033c0036t0001g0265 |
2 | HG01516.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.963+3222G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004774 | |||||||
chr4:6004776 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3220C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004776 | |||||||
chr4:6004777 | C | T | 3 | a0001c0001t0001g0256 a0033c0036t0001g0265 a0078c0066t0001g0018 |
3 | HG01516.hp2 HG03139.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.963+3219G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004777 | |||||||
chr4:6004779 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3217T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004779 | |||||||
chr4:6004781 | G | GGTGATGG others(1111): Show |
1 | a0033c0036t0001g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.963+3214_963+3215i others(1120): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004781 | |||||||
chr4:6004782 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3214C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004782 | |||||||
chr4:6004788 | GTGGTGA | G | 4 | a0008c0008t0001g0003 a0008c0008t0001g0076 a0008c0008t0001g0198 others(1): Show |
5 | HG02165.hp1 NA18747.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3202_963+3207d others(8): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004788 | |||||||
chr4:6004791 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3205C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004791 | |||||||
chr4:6004809 | T | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3187A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004809 | |||||||
chr4:6004818 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3178T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004818 | |||||||
chr4:6004821 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3175C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004821 | |||||||
chr4:6004833 | A | T | 1 | a0053c0068t0001g0329 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.963+3163T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004833 | |||||||
chr4:6004838 | A | ATGGTGAT others(8): Show |
2 | a0002c0002t0001g0197 a0002c0002t0001g0313 |
2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.963+3157_963+3158i others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004838 | |||||||
chr4:6004838 | A | ATGGTGAT others(8): Show |
75 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(72): Show |
76 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.963+3143_963+3157d others(17): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004838 | |||||||
chr4:6004844 | A | ATGGTGAT others(11): Show |
1 | a0025c0023t0001g0318 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.963+3151_963+3152i others(20): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004844 | |||||||
chr4:6004853 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3143C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004853 | |||||||
chr4:6004855 | G | GGTGATGG others(425): Show |
1 | a0001c0001t0001g0256 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.963+3140_963+3141i others(434): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004855 | |||||||
chr4:6004910 | C | T | 5 | a0010c0009t0001g0162 a0010c0009t0001g0163 a0041c0041t0001g0299 others(2): Show |
5 | HG02572.hp2 HG02738.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3086G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004910 | |||||||
chr4:6004911 | G | A | 1 | a0079c0079t0001g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.963+3085C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6004911 | |||||||
chr4:6005119 | C | T | 2 | a0036c0039t0001g0014 a0083c0047t0001g0013 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.963+2877G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005119 | |||||||
chr4:6005141 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.963+2855C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005141 | |||||||
chr4:6005242 | A | G | 3 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0064c0060t0001g0067 |
3 | HG02486.hp2 HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.963+2754T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005242 | |||||||
chr4:6005257 | G | C | 70 | a0002c0002t0001g0081 a0002c0002t0001g0090 a0002c0002t0001g0091 others(67): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.963+2739C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005257 | |||||||
chr4:6005258 | G | A | 1 | a0043c0075t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.963+2738C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005258 | |||||||
chr4:6005277 | A | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(96): Show |
101 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.963+2719T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005277 | |||||||
chr4:6005673 | T | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(97): Show |
102 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.963+2323A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005673 | |||||||
chr4:6005815 | C | T | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.963+2181G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005815 | |||||||
chr4:6005864 | A | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(259): Show |
266 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.963+2132T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005864 | |||||||
chr4:6005865 | G | T | 1 | a0063c0110t0001g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.963+2131C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005865 | |||||||
chr4:6005919 | T | C | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+2077A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005919 | |||||||
chr4:6005920 | G | A | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+2076C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005920 | |||||||
chr4:6005991 | T | G | 171 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(168): Show |
174 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.963+2005A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6005991 | |||||||
chr4:6006003 | A | G | 6 | a0001c0001t0001g0158 a0001c0001t0001g0281 a0022c0022t0001g0068 others(3): Show |
6 | HG02257.hp2 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+1993T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006003 | |||||||
chr4:6006012 | T | G | 1 | a0085c0099t0001g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.963+1984A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006012 | |||||||
chr4:6006015 | G | C | 2 | a0035c0037t0001g0292 a0035c0037t0001g0293 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.963+1981C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006015 | |||||||
chr4:6006122 | G | C | 1 | a0077c0097t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.963+1874C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006122 | |||||||
chr4:6006215 | T | C | 31 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(28): Show |
31 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.963+1781A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006215 | |||||||
chr4:6006263 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.963+1733A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006263 | |||||||
chr4:6006424 | A | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(112): Show |
117 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.963+1572T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006424 | |||||||
chr4:6006461 | G | T | 4 | a0037c0035t0001g0214 a0037c0035t0001g0223 a0058c0083t0001g0222 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1535C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006461 | |||||||
chr4:6006543 | T | C | 32 | a0005c0005t0001g0295 a0005c0005t0001g0297 a0005c0005t0001g0298 others(29): Show |
32 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.963+1453A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006543 | |||||||
chr4:6006548 | A | G | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.963+1448T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006548 | |||||||
chr4:6006812 | G | A | 1 | a0002c0002t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.963+1184C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006812 | |||||||
chr4:6006813 | A | G | 1 | a0002c0002t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.963+1183T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006813 | |||||||
chr4:6006814 | C | A | 1 | a0002c0002t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.963+1182G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006814 | |||||||
chr4:6006911 | G | A | 1 | a0007c0007t0001g0171 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.963+1085C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6006911 | |||||||
chr4:6007021 | T | C | 8 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0021c0024t0001g0066 others(5): Show |
8 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+975A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007021 | |||||||
chr4:6007032 | G | A | 5 | a0013c0017t0001g0037 a0051c0081t0001g0331 a0072c0100t0001g0036 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+964C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007032 | |||||||
chr4:6007048 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.963+948C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007048 | |||||||
chr4:6007119 | A | T | 12 | a0009c0010t0001g0267 a0009c0010t0001g0280 a0021c0024t0001g0066 others(9): Show |
12 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.963+877T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007119 | |||||||
chr4:6007130 | T | C | 2 | a0063c0110t0001g0274 a0102c0112t0001g0015 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.963+866A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007130 | |||||||
chr4:6007208 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.963+788T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007208 | |||||||
chr4:6007366 | G | A | 3 | a0079c0079t0001g0028 a0085c0099t0001g0034 a0102c0112t0001g0015 |
3 | HG03209.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.963+630C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007366 | |||||||
chr4:6007432 | A | T | 3 | a0041c0041t0001g0299 a0041c0041t0001g0323 a0068c0109t0001g0092 |
3 | HG02738.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.963+564T>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007432 | |||||||
chr4:6007755 | G | A | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.963+241C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007755 | |||||||
chr4:6007816 | G | C | 1 | a0101c0095t0001g0266 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.963+180C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007816 | |||||||
chr4:6007882 | A | G | 174 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0074 others(171): Show |
180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.963+114T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007882 | |||||||
chr4:6007995 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | splice_donor_variant&intron_variant | HIGH | c.963+1G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 3/11 | chr4 | 6007995 | |||||||
chr4:6008717 | G | A | 59 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0173 others(56): Show |
59 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.427-185C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6008717 | |||||||
chr4:6008723 | A | G | 1 | a0002c0002t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.427-191T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6008723 | |||||||
chr4:6008854 | G | A | 2 | a0013c0017t0001g0037 a0072c0100t0001g0036 |
2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.427-322C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6008854 | |||||||
chr4:6008911 | G | C | 1 | a0038c0034t0001g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.427-379C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6008911 | |||||||
chr4:6008969 | C | A | 1 | a0032c0029t0001g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.427-437G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6008969 | |||||||
chr4:6009149 | G | A | 3 | a0071c0046t0001g0011 a0080c0045t0001g0010 a0084c0044t0001g0012 |
3 | HG02886.hp1 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.427-617C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009149 | |||||||
chr4:6009230 | C | T | 1 | a0018c0016t0001g0276 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.427-698G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009230 | |||||||
chr4:6009231 | G | A | 1 | a0104c0063t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.427-699C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009231 | |||||||
chr4:6009434 | A | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0074 others(138): Show |
145 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.427-902T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009434 | |||||||
chr4:6009470 | G | C | 1 | a0070c0113t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.427-938C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009470 | |||||||
chr4:6009547 | T | C | 16 | a0001c0001t0001g0158 a0006c0006t0001g0170 a0021c0024t0001g0066 others(13): Show |
16 | HG00639.hp2 HG01257.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.427-1015A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009547 | |||||||
chr4:6009571 | G | A | 1 | a0032c0029t0001g0057 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.427-1039C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009571 | |||||||
chr4:6009643 | C | T | 1 | a0010c0009t0001g0161 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.427-1111G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009643 | |||||||
chr4:6009726 | G | C | 3 | a0026c0042t0001g0332 a0026c0042t0001g0333 a0050c0116t0001g0334 |
3 | HG00323.hp1 HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.427-1194C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009726 | |||||||
chr4:6009727 | G | A | 3 | a0026c0042t0001g0332 a0026c0042t0001g0333 a0050c0116t0001g0334 |
3 | HG00323.hp1 HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.427-1195C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009727 | |||||||
chr4:6009896 | G | A | 1 | a0100c0093t0001g0275 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.427-1364C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6009896 | |||||||
chr4:6010118 | C | T | 3 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 |
4 | HG02896.hp1 HG02897.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.427-1586G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010118 | |||||||
chr4:6010178 | G | A | 1 | a0084c0044t0001g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.427-1646C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010178 | |||||||
chr4:6010205 | T | A | 1 | a0070c0113t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.426+1625A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010205 | |||||||
chr4:6010251 | G | A | 1 | a0005c0005t0001g0298 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.426+1579C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010251 | |||||||
chr4:6010301 | CTGAAGTT others(27): Show |
C | 1 | a0092c0096t0001g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.426+1495_426+1528d others(36): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010301 | |||||||
chr4:6010330 | T | A | 2 | a0074c0071t0001g0035 a0085c0099t0001g0034 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.426+1500A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010330 | |||||||
chr4:6010384 | C | G | 2 | a0036c0039t0001g0014 a0083c0047t0001g0013 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.426+1446G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010384 | |||||||
chr4:6010656 | G | A | 333 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.426+1174C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010656 | |||||||
chr4:6010707 | C | G | 3 | a0026c0042t0001g0332 a0026c0042t0001g0333 a0050c0116t0001g0334 |
3 | HG00323.hp1 HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.426+1123G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010707 | |||||||
chr4:6010708 | C | T | 2 | a0007c0007t0001g0171 a0044c0088t0001g0159 |
2 | HG00673.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.426+1122G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010708 | |||||||
chr4:6010934 | A | C | 2 | a0051c0081t0001g0331 a0088c0105t0001g0020 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.426+896T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010934 | |||||||
chr4:6010943 | T | C | 2 | a0051c0081t0001g0331 a0088c0105t0001g0020 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.426+887A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6010943 | |||||||
chr4:6011034 | G | C | 29 | a0001c0001t0001g0281 a0004c0003t0001g0288 a0004c0003t0001g0289 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.426+796C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011034 | |||||||
chr4:6011050 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.426+780G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011050 | |||||||
chr4:6011067 | C | A | 2 | a0051c0081t0001g0331 a0088c0105t0001g0020 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.426+763G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011067 | |||||||
chr4:6011067 | C | T | 1 | a0012c0013t0001g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.426+763G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011067 | |||||||
chr4:6011240 | G | A | 1 | a0012c0013t0001g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.426+590C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011240 | |||||||
chr4:6011286 | T | G | 2 | a0074c0071t0001g0035 a0085c0099t0001g0034 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.426+544A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011286 | |||||||
chr4:6011289 | G | A | 1 | a0030c0026t0001g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.426+541C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011289 | |||||||
chr4:6011300 | G | A | 3 | a0071c0046t0001g0011 a0080c0045t0001g0010 a0084c0044t0001g0012 |
3 | HG02886.hp1 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.426+530C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011300 | |||||||
chr4:6011303 | G | A | 1 | a0089c0091t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.426+527C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011303 | |||||||
chr4:6011343 | C | G | 2 | a0036c0039t0001g0014 a0083c0047t0001g0013 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.426+487G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011343 | |||||||
chr4:6011393 | A | G | 2 | a0051c0081t0001g0331 a0088c0105t0001g0020 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.426+437T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011393 | |||||||
chr4:6011459 | G | C | 320 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(317): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.426+371C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011459 | |||||||
chr4:6011473 | G | A | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.426+357C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011473 | |||||||
chr4:6011475 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.426+355G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011475 | |||||||
chr4:6011538 | C | T | 4 | a0019c0020t0001g0001 a0019c0020t0001g0060 a0019c0020t0001g0061 others(1): Show |
5 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.426+292G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011538 | |||||||
chr4:6011693 | G | T | 2 | a0051c0081t0001g0331 a0088c0105t0001g0020 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.426+137C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 2/11 | chr4 | 6011693 | |||||||
chr4:6012003 | G | C | 4 | a0025c0023t0001g0318 a0025c0023t0001g0319 a0060c0049t0001g0317 others(1): Show |
4 | HG00280.hp2 HG02293.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.288-35C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012003 | |||||||
chr4:6012017 | G | A | 1 | a0038c0034t0001g0330 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.288-49C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012017 | |||||||
chr4:6012049 | T | G | 37 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(34): Show |
37 | HG00544.hp2 HG00673.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.288-81A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012049 | |||||||
chr4:6012110 | C | A | 36 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(33): Show |
36 | HG00544.hp2 HG00673.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.288-142G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012110 | |||||||
chr4:6012148 | G | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(280): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.288-180C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012148 | |||||||
chr4:6012178 | G | T | 1 | a0051c0081t0001g0331 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.288-210C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012178 | |||||||
chr4:6012303 | A | G | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.288-335T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012303 | |||||||
chr4:6012507 | T | C | 1 | a0087c0062t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.288-539A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012507 | |||||||
chr4:6012524 | G | C | 187 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(184): Show |
193 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.288-556C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012524 | |||||||
chr4:6012551 | C | CTGCATTA others(27): Show |
1 | a0092c0096t0001g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.288-617_288-584dup others(34): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012551 | |||||||
chr4:6012625 | A | G | 115 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(112): Show |
118 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.288-657T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012625 | |||||||
chr4:6012651 | C | A | 1 | a0087c0062t0001g0022 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.288-683G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012651 | |||||||
chr4:6012681 | T | C | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.288-713A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012681 | |||||||
chr4:6012698 | G | A | 1 | a0034c0040t0001g0321 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.288-730C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012698 | |||||||
chr4:6012746 | G | C | 1 | a0082c0064t0001g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.288-778C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6012746 | |||||||
chr4:6013030 | T | C | 3 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0108c0070t0001g0027 |
3 | HG01255.hp2 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.288-1062A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013030 | |||||||
chr4:6013118 | A | C | 1 | a0082c0064t0001g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.288-1150T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013118 | |||||||
chr4:6013237 | G | A | 2 | a0018c0016t0001g0210 a0057c0067t0001g0322 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.288-1269C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013237 | |||||||
chr4:6013347 | G | C | 2 | a0013c0017t0001g0037 a0072c0100t0001g0036 |
2 | HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.288-1379C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013347 | |||||||
chr4:6013366 | A | G | 1 | a0037c0035t0001g0214 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288-1398T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013366 | |||||||
chr4:6013460 | C | G | 1 | a0017c0019t0001g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.288-1492G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013460 | |||||||
chr4:6013509 | C | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(276): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.288-1541G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013509 | |||||||
chr4:6013730 | G | A | 1 | a0093c0058t0001g0058 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.288-1762C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013730 | |||||||
chr4:6013784 | T | C | 24 | a0001c0001t0001g0056 a0012c0013t0001g0059 a0014c0012t0001g0048 others(21): Show |
24 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.288-1816A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013784 | |||||||
chr4:6013798 | T | A | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.288-1830A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013798 | |||||||
chr4:6013799 | C | G | 1 | a0107c0117t0001g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.288-1831G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013799 | |||||||
chr4:6013999 | TTG | T | 16 | a0001c0001t0001g0033 a0009c0010t0001g0326 a0009c0010t0001g0327 others(13): Show |
16 | HG00323.hp1 HG01109.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.288-2033_288-2032d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6013999 | |||||||
chr4:6014004 | T | TG | 15 | a0001c0001t0001g0281 a0004c0003t0001g0288 a0009c0010t0001g0279 others(12): Show |
15 | HG00099.hp1 HG00280.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.288-2037dupC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014004 | |||||||
chr4:6014004 | TG | T | 24 | a0001c0001t0001g0056 a0014c0012t0001g0048 a0014c0012t0001g0049 others(21): Show |
24 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.288-2037delC | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014004 | |||||||
chr4:6014005 | G | GT | 33 | a0001c0001t0001g0075 a0001c0001t0001g0174 a0001c0001t0001g0175 others(30): Show |
33 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.288-2038dupA | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014005 | |||||||
chr4:6014005 | G | GTT | 92 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0079 others(89): Show |
95 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.288-2039_288-2038d others(4): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014005 | |||||||
chr4:6014005 | G | T | 1 | a0022c0022t0001g0052 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.288-2037C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014005 | |||||||
chr4:6014006 | T | G | 138 | a0001c0001t0001g0016 a0001c0001t0001g0204 a0001c0001t0001g0209 others(135): Show |
144 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.288-2038A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014006 | |||||||
chr4:6014007 | T | G | 1 | a0041c0041t0001g0323 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.288-2039A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014007 | |||||||
chr4:6014070 | T | C | 1 | a0104c0063t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.288-2102A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014070 | |||||||
chr4:6014115 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.288-2147C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014115 | |||||||
chr4:6014128 | G | A | 5 | a0026c0042t0001g0332 a0026c0042t0001g0333 a0050c0116t0001g0334 others(2): Show |
5 | HG00323.hp1 HG01192.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-2160C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014128 | |||||||
chr4:6014219 | C | G | 1 | a0013c0080t0001g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.288-2251G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014219 | |||||||
chr4:6014337 | T | A | 24 | a0001c0001t0001g0056 a0012c0013t0001g0059 a0014c0012t0001g0048 others(21): Show |
24 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.288-2369A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014337 | |||||||
chr4:6014377 | G | A | 2 | a0051c0081t0001g0331 a0079c0079t0001g0028 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.288-2409C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014377 | |||||||
chr4:6014400 | T | C | 6 | a0026c0042t0001g0332 a0026c0042t0001g0333 a0038c0034t0001g0330 others(3): Show |
6 | HG00323.hp1 HG01192.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.288-2432A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014400 | |||||||
chr4:6014453 | T | G | 2 | a0038c0034t0001g0017 a0078c0066t0001g0018 |
2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.288-2485A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014453 | |||||||
chr4:6014706 | CTCATCTG others(27): Show |
C | 1 | a0003c0004t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288-2772_288-2739d others(36): Show |
C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014706 | |||||||
chr4:6014742 | C | G | 1 | a0003c0004t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288-2774G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014742 | |||||||
chr4:6014743 | A | G | 1 | a0003c0004t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.288-2775T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014743 | |||||||
chr4:6014872 | G | A | 130 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0221 others(127): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.288-2904C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014872 | |||||||
chr4:6014887 | C | A | 6 | a0001c0001t0001g0016 a0038c0034t0001g0017 a0071c0046t0001g0011 others(3): Show |
6 | HG02809.hp2 HG02886.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.288-2919G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014887 | |||||||
chr4:6014972 | G | T | 2 | a0003c0004t0001g0077 a0003c0004t0001g0078 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.288-3004C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014972 | |||||||
chr4:6014987 | A | G | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(280): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.288-3019T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6014987 | |||||||
chr4:6015010 | G | C | 3 | a0026c0042t0001g0332 a0026c0042t0001g0333 a0050c0116t0001g0334 |
3 | HG00323.hp1 HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.288-3042C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015010 | |||||||
chr4:6015105 | C | T | 10 | a0010c0009t0001g0161 a0010c0009t0001g0162 a0010c0009t0001g0163 others(7): Show |
10 | HG01884.hp2 HG02572.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+3040G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015105 | |||||||
chr4:6015156 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.287+2989G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015156 | |||||||
chr4:6015221 | T | G | 129 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0221 others(126): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.287+2924A>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015221 | |||||||
chr4:6015285 | G | A | 3 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0108c0070t0001g0027 |
3 | HG01255.hp2 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.287+2860C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015285 | |||||||
chr4:6015350 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.287+2795C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015350 | |||||||
chr4:6015361 | A | G | 138 | a0001c0001t0001g0204 a0001c0001t0001g0209 a0001c0001t0001g0221 others(135): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.287+2784T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015361 | |||||||
chr4:6015441 | C | T | 2 | a0021c0024t0001g0205 a0039c0025t0001g0206 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.287+2704G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015441 | |||||||
chr4:6015518 | G | GA | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(280): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.287+2626dupT | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015518 | |||||||
chr4:6015563 | G | C | 1 | a0082c0064t0001g0324 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.287+2582C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015563 | |||||||
chr4:6015817 | C | T | 320 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0033 others(317): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.287+2328G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015817 | |||||||
chr4:6015866 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.287+2279G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6015866 | |||||||
chr4:6016043 | A | G | 3 | a0051c0081t0001g0331 a0079c0079t0001g0028 a0088c0105t0001g0020 |
3 | HG01884.hp1 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.287+2102T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016043 | |||||||
chr4:6016060 | T | C | 1 | a0007c0007t0001g0203 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.287+2085A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016060 | |||||||
chr4:6016291 | A | G | 1 | a0056c0052t0001g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.287+1854T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016291 | |||||||
chr4:6016301 | C | T | 3 | a0051c0081t0001g0331 a0079c0079t0001g0028 a0088c0105t0001g0020 |
3 | HG01884.hp1 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.287+1844G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016301 | |||||||
chr4:6016409 | C | T | 1 | a0070c0113t0001g0029 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.287+1736G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016409 | |||||||
chr4:6016421 | C | T | 3 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0108c0070t0001g0027 |
3 | HG01255.hp2 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.287+1724G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016421 | |||||||
chr4:6016463 | C | T | 3 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0108c0070t0001g0027 |
3 | HG01255.hp2 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.287+1682G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016463 | |||||||
chr4:6016514 | A | C | 142 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(139): Show |
145 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.287+1631T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016514 | |||||||
chr4:6016580 | T | A | 3 | a0009c0010t0001g0326 a0009c0010t0001g0327 a0081c0069t0001g0325 |
3 | HG02486.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.287+1565A>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016580 | |||||||
chr4:6016630 | A | G | 283 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(280): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.287+1515T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016630 | |||||||
chr4:6016853 | G | T | 3 | a0031c0032t0001g0025 a0031c0032t0001g0026 a0108c0070t0001g0027 |
3 | HG01255.hp2 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.287+1292C>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016853 | |||||||
chr4:6016901 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.287+1244G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016901 | |||||||
chr4:6016959 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287+1186G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6016959 | |||||||
chr4:6017039 | T | C | 1 | a0096c0076t0001g0328 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.287+1106A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017039 | |||||||
chr4:6017046 | A | G | 2 | a0020c0028t0001g0023 a0020c0028t0001g0024 |
2 | HG01515.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.287+1099T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017046 | |||||||
chr4:6017064 | G | C | 1 | a0053c0068t0001g0329 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.287+1081C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017064 | |||||||
chr4:6017078 | G | A | 2 | a0051c0081t0001g0331 a0088c0105t0001g0020 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.287+1067C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017078 | |||||||
chr4:6017139 | C | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0075 others(85): Show |
91 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.287+1006G>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017139 | |||||||
chr4:6017164 | C | T | 276 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(273): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.287+981G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017164 | |||||||
chr4:6017245 | G | A | 3 | a0002c0002t0001g0156 a0051c0081t0001g0331 a0088c0105t0001g0020 |
3 | HG01884.hp1 HG02056.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.287+900C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017245 | |||||||
chr4:6017269 | T | C | 3 | a0001c0001t0001g0158 a0036c0039t0001g0157 a0088c0105t0001g0020 |
3 | HG02257.hp2 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.287+876A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017269 | |||||||
chr4:6017280 | A | G | 1 | a0044c0088t0001g0159 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.287+865T>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017280 | |||||||
chr4:6017292 | C | T | 3 | a0071c0046t0001g0011 a0080c0045t0001g0010 a0084c0044t0001g0012 |
3 | HG02886.hp1 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.287+853G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017292 | |||||||
chr4:6017319 | C | T | 281 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0074 others(278): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.287+826G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017319 | |||||||
chr4:6017687 | C | T | 2 | a0036c0039t0001g0014 a0083c0047t0001g0013 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.287+458G>A | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017687 | |||||||
chr4:6017853 | A | C | 1 | a0024c0027t0001g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.287+292T>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017853 | |||||||
chr4:6017889 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0074 a0001c0001t0001g0075 others(86): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.287+256C>T | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017889 | |||||||
chr4:6017903 | C | G | 8 | a0001c0001t0001g0016 a0036c0039t0001g0014 a0038c0034t0001g0017 others(5): Show |
8 | HG02723.hp1 HG02809.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.287+242G>C | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6017903 | |||||||
chr4:6018016 | G | C | 181 | a0001c0001t0001g0169 a0001c0001t0001g0173 a0001c0001t0001g0174 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.287+129C>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6018016 | |||||||
chr4:6018031 | T | C | 3 | a0026c0042t0001g0332 a0026c0042t0001g0333 a0050c0116t0001g0334 |
3 | HG00323.hp1 HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.287+114A>G | C4orf50 | ENSG00000181215.17 | transcript | ENST00000711657.1 | protein_coding | 1/11 | chr4 | 6018031 |