geneid | 113828 |
---|---|
ensemblid | ENSG00000133477.17 |
hgncid | 25148 |
symbol | FAM83F |
name | family with sequence similarity 83 member F |
refseq_nuc | NM_138435.4 |
refseq_prot | NP_612444.2 |
ensembl_nuc | ENST00000333407.11 |
ensembl_prot | ENSP00000330432.5 |
mane_status | MANE Select |
chr | chr22 |
start | 39994954 |
end | 40043534 |
strand | + |
ver | v1.2 |
region | chr22:39994954-40043534 |
region5000 | chr22:39989954-40048534 |
regionname0 | FAM83F_chr22_39994954_40043534 |
regionname5000 | FAM83F_chr22_39989954_40048534 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 500 | 146 | 44 | 34 | 38 | 5 | 23 | 21 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002 | 0/0 | 500 | 67 | 27 | 11 | 10 | 2 | 17 | 5 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0003 | 0/0 | 500 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0004 | 0/0 | 500 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0005 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0006 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0007 | 0/0 | 500 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0008 | 0/0 | 500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0009 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0010 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0011 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0012 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1503 | 144 | 43 | 34 | 37 | 5 | 23 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0002 | 0/0 | 1503 | 66 | 27 | 11 | 10 | 2 | 16 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0003 | 0/0 | 1503 | 7 | 7 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0004 | 0/0 | 1503 | 6 | 0 | 2 | 0 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0005 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0006 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0007 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0008 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0009 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0010 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0011 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0012 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0013 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0014 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
c0015 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 14059 | 28 | 12 | 6 | 2 | 1 | 7 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0002 | 1/0 | 14059 | 23 | 1 | 6 | 7 | 1 | 7 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0003 | 0/0 | 14059 | 22 | 2 | 7 | 8 | 1 | 4 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0004 | 0/0 | 14059 | 16 | 0 | 7 | 5 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0005 | 0/0 | 14060 | 8 | 0 | 3 | 3 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0006 | 0/0 | 14059 | 7 | 6 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0007 | 0/0 | 14059 | 6 | 1 | 2 | 1 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0008 | 0/0 | 14071 | 5 | 4 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0009 | 0/0 | 14057 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0010 | 0/0 | 14059 | 5 | 0 | 3 | 0 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0011 | 0/0 | 14059 | 5 | 0 | 0 | 0 | 0 | 5 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0012 | 0/0 | 14071 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0013 | 0/0 | 14059 | 4 | 0 | 0 | 3 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0014 | 0/0 | 14059 | 4 | 0 | 0 | 3 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0015 | 0/0 | 14071 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0016 | 0/0 | 14059 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0017 | 0/0 | 14059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0018 | 0/0 | 14059 | 2 | 0 | 0 | 0 | 1 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0019 | 0/0 | 14067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0020 | 0/0 | 14059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0021 | 0/0 | 14059 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0022 | 0/0 | 14059 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0023 | 0/0 | 14059 | 2 | 1 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0024 | 0/0 | 14060 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0025 | 0/0 | 14067 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0026 | 0/0 | 14058 | 2 | 0 | 0 | 0 | 2 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0027 | 0/0 | 14067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0028 | 0/0 | 14059 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0029 | 0/0 | 14059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0030 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0031 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0032 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0033 | 0/0 | 14071 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0034 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0035 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0036 | 0/0 | 14071 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0037 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0038 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0039 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0040 | 0/0 | 14079 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0041 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0042 | 0/0 | 14071 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0043 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0044 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0045 | 0/0 | 14042 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0046 | 0/0 | 14042 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0047 | 0/0 | 14042 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0048 | 0/0 | 14067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0049 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0050 | 0/0 | 14060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0051 | 0/1 | 14059 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0052 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0053 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0054 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0055 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0056 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0057 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0058 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0059 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0060 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0061 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0062 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0063 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0064 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0065 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0066 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0067 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0068 | 0/0 | 14059 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0069 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0070 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0071 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0072 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0073 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0074 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0075 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0076 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0077 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0078 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0079 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0080 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0081 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0082 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0083 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0084 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0085 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0086 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0087 | 0/0 | 14057 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0088 | 0/0 | 14060 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0089 | 0/0 | 14059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0090 | 0/0 | 14059 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
t0091 | 0/0 | 14059 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0002 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1503 | 144 | 43 | 34 | 37 | 5 | 23 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0009 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0014 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002 | 0/0 | 1503 | 66 | 27 | 11 | 10 | 2 | 16 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0010 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0003c0003 | 0/0 | 1503 | 7 | 7 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0004c0004 | 0/0 | 1503 | 6 | 0 | 2 | 0 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0005c0013 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0006c0012 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0007c0008 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0008c0006 | 0/0 | 1503 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0009c0007 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0010c0011 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0011c0015 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0012c0005 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 15561 | 21 | 0 | 5 | 7 | 1 | 7 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0003 | 0/0 | 15561 | 20 | 2 | 7 | 6 | 1 | 4 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0004 | 0/0 | 15561 | 15 | 0 | 7 | 4 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0005 | 0/0 | 15562 | 8 | 0 | 3 | 3 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0006 | 0/0 | 15561 | 7 | 6 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0008 | 0/0 | 15573 | 5 | 4 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0012 | 0/0 | 15573 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0013 | 0/0 | 15561 | 4 | 0 | 0 | 3 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0016 | 0/0 | 15561 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0017 | 0/0 | 15561 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0020 | 0/0 | 15561 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0021 | 0/0 | 15561 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0022 | 0/0 | 15561 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0023 | 0/0 | 15561 | 2 | 1 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0024 | 0/0 | 15562 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0025 | 0/0 | 15569 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0026 | 0/0 | 15560 | 2 | 0 | 0 | 0 | 2 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0027 | 0/0 | 15569 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0028 | 0/0 | 15561 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0029 | 0/0 | 15561 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0032 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0033 | 0/0 | 15573 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0036 | 0/0 | 15573 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0037 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0038 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0039 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0040 | 0/0 | 15581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0041 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0042 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0047 | 0/0 | 15544 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0048 | 0/0 | 15569 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0049 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0050 | 0/0 | 15562 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0051 | 0/1 | 15561 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0052 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0053 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0054 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0055 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0056 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0070 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0071 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0072 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0076 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0077 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0078 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0080 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0081 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0082 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0083 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0084 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0085 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0086 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0087 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0088 | 0/0 | 15562 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0090 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0001t0091 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0009t0046 | 0/0 | 15544 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0001c0014t0004 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0001 | 0/0 | 15561 | 22 | 12 | 4 | 2 | 0 | 4 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0007 | 0/0 | 15561 | 6 | 1 | 2 | 1 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0010 | 0/0 | 15561 | 4 | 0 | 3 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0011 | 0/0 | 15561 | 5 | 0 | 0 | 0 | 0 | 5 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0014 | 0/0 | 15561 | 4 | 0 | 0 | 3 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0015 | 0/0 | 15573 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0018 | 0/0 | 15561 | 2 | 0 | 0 | 0 | 1 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0019 | 0/0 | 15569 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0031 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0034 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0035 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0057 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0058 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0059 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0060 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0061 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0062 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0063 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0064 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0065 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0066 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0067 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0068 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0069 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0073 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0074 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0002t0075 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0002c0010t0010 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0003c0003t0009 | 0/0 | 15559 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0003c0003t0043 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0003c0003t0044 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0004c0004t0001 | 0/0 | 15561 | 6 | 0 | 2 | 0 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0005c0013t0045 | 0/0 | 15544 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0006c0012t0030 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0007c0008t0079 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0008c0006t0002 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0009c0007t0003 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0010c0011t0002 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0011c0015t0003 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
a0012c0005t0089 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | copy fasta | chr22 | 39989954 | 40048534 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0016g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0016g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0017g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0021g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0022g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0022g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0023g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0023g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0024g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0025g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0025g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0026g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0026g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0027g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0027g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0028g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0028g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0032g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0033g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0036g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0037g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0038g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0039g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0040g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0041g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0042g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0047g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0048g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0049g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0050g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0051g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0052g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0053g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0054g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0055g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0056g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0070g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0071g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0072g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0076g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0077g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0078g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0080g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0081g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0082g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0083g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0084g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0085g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0086g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0087g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0088g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0090g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0091g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0009t0046g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0014t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0010g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0010g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0010g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0018g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0018g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0031g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0034g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0035g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0057g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0058g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0059g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0060g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0061g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0062g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0063g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0064g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0065g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0066g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0067g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0068g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0069g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0073g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0074g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0075g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0010t0010g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0043g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0044g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0005c0013t0045g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0006c0012t0030g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0007c0008t0079g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0008c0006t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0009c0007t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0010c0011t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0011c0015t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0012c0005t0089g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0018 | g0188 | EUR | GBR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00280 | hp2 | a0004 | c0004 | t0001 | g0145 | EUR | FIN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0077 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0065 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00673 | hp2 | a0001 | c0001 | t0013 | g0093 | EAS | CHS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0056 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01069 | hp1 | a0002 | c0002 | t0010 | g0009 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01071 | hp1 | a0002 | c0002 | t0010 | g0009 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01106 | hp1 | a0002 | c0002 | t0007 | g0157 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0153 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01109 | hp2 | a0001 | c0001 | t0025 | g0139 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01168 | hp2 | a0001 | c0001 | t0028 | g0042 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01169 | hp2 | a0001 | c0001 | t0028 | g0047 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01175 | hp2 | a0004 | c0004 | t0001 | g0149 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01243 | hp1 | a0001 | c0001 | t0036 | g0217 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01243 | hp2 | a0002 | c0002 | t0068 | g0082 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01257 | hp1 | a0002 | c0002 | t0065 | g0199 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01257 | hp2 | a0001 | c0001 | t0021 | g0005 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01258 | hp1 | a0001 | c0001 | t0021 | g0005 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01258 | hp2 | a0002 | c0002 | t0007 | g0155 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01346 | hp1 | a0001 | c0001 | t0054 | g0106 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01346 | hp2 | a0002 | c0002 | t0010 | g0161 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01433 | hp1 | a0008 | c0006 | t0002 | g0007 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0183 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01515 | hp1 | a0001 | c0001 | t0026 | g0002 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0092 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01517 | hp1 | a0001 | c0001 | t0026 | g0063 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01517 | hp2 | a0002 | c0002 | t0073 | g0212 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01884 | hp1 | a0001 | c0001 | t0087 | g0013 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0133 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01891 | hp1 | a0002 | c0002 | t0061 | g0162 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01891 | hp2 | a0002 | c0002 | t0031 | g0143 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01934 | hp2 | a0001 | c0001 | t0033 | g0123 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01978 | hp1 | a0001 | c0001 | t0016 | g0109 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02015 | hp1 | a0001 | c0001 | t0056 | g0046 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02015 | hp2 | a0002 | c0002 | t0014 | g0168 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02027 | hp2 | a0001 | c0001 | t0050 | g0117 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02040 | hp1 | a0001 | c0001 | t0082 | g0044 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02056 | hp1 | a0001 | c0001 | t0083 | g0038 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02056 | hp2 | a0002 | c0002 | t0014 | g0170 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02074 | hp1 | a0002 | c0002 | t0014 | g0169 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02080 | hp1 | a0001 | c0001 | t0077 | g0055 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02080 | hp2 | a0001 | c0001 | t0013 | g0095 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02132 | hp2 | a0002 | c0002 | t0067 | g0172 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02135 | hp1 | a0002 | c0002 | t0059 | g0171 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02135 | hp2 | a0001 | c0001 | t0013 | g0219 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02145 | hp1 | a0003 | c0003 | t0009 | g0083 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02145 | hp2 | a0010 | c0011 | t0002 | g0053 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02155 | hp1 | a0001 | c0001 | t0090 | g0021 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02155 | hp2 | a0001 | c0014 | t0004 | g0024 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02165 | hp1 | a0009 | c0007 | t0003 | g0121 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02165 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02257 | hp1 | a0001 | c0001 | t0020 | g0134 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02257 | hp2 | a0002 | c0002 | t0007 | g0158 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02258 | hp2 | a0001 | c0001 | t0055 | g0081 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0070 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02572 | hp2 | a0001 | c0001 | t0085 | g0068 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02622 | hp1 | a0001 | c0001 | t0029 | g0136 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02622 | hp2 | a0003 | c0003 | t0009 | g0088 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02630 | hp1 | a0002 | c0002 | t0060 | g0073 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02630 | hp2 | a0001 | c0001 | t0070 | g0203 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02647 | hp1 | a0001 | c0001 | t0048 | g0091 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02683 | hp1 | a0004 | c0004 | t0001 | g0156 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02698 | hp2 | a0001 | c0001 | t0013 | g0103 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02717 | hp1 | a0002 | c0002 | t0035 | g0098 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0197 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02735 | hp1 | a0004 | c0004 | t0001 | g0150 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02738 | hp1 | a0002 | c0002 | t0011 | g0198 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02738 | hp2 | a0002 | c0002 | t0010 | g0159 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02818 | hp1 | a0001 | c0001 | t0041 | g0193 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02818 | hp2 | a0003 | c0003 | t0009 | g0087 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02886 | hp2 | a0001 | c0001 | t0047 | g0090 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02895 | hp1 | a0001 | c0001 | t0037 | g0003 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02895 | hp2 | a0001 | c0001 | t0027 | g0137 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02896 | hp1 | a0001 | c0001 | t0017 | g0014 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02896 | hp2 | a0002 | c0002 | t0019 | g0208 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02897 | hp1 | a0002 | c0002 | t0019 | g0206 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02897 | hp2 | a0001 | c0001 | t0027 | g0138 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02965 | hp1 | a0001 | c0001 | t0023 | g0069 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0184 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02970 | hp1 | a0002 | c0002 | t0057 | g0213 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02970 | hp2 | a0001 | c0001 | t0038 | g0216 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02976 | hp1 | a0001 | c0001 | t0078 | g0067 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02976 | hp2 | a0001 | c0001 | t0042 | g0130 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03017 | hp1 | a0002 | c0002 | t0011 | g0154 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03017 | hp2 | a0001 | c0001 | t0016 | g0111 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0076 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0003 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03098 | hp1 | a0002 | c0002 | t0063 | g0211 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0075 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03139 | hp2 | a0012 | c0005 | t0089 | g0131 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03195 | hp1 | a0001 | c0001 | t0029 | g0135 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03195 | hp2 | a0005 | c0013 | t0045 | g0132 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03209 | hp1 | a0002 | c0002 | t0064 | g0141 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0191 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03225 | hp1 | a0002 | c0002 | t0069 | g0209 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03225 | hp2 | a0003 | c0003 | t0009 | g0086 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03239 | hp1 | a0002 | c0002 | t0011 | g0202 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03453 | hp1 | a0001 | c0001 | t0084 | g0025 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03453 | hp2 | a0002 | c0002 | t0015 | g0100 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03486 | hp1 | a0001 | c0001 | t0071 | g0215 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03490 | hp1 | a0002 | c0002 | t0018 | g0186 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0050 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0049 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0080 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03540 | hp1 | a0001 | c0001 | t0025 | g0140 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03540 | hp2 | a0001 | c0001 | t0086 | g0012 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0195 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03579 | hp2 | a0003 | c0003 | t0044 | g0089 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03669 | hp1 | a0001 | c0001 | t0023 | g0016 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0144 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03710 | hp1 | a0002 | c0002 | t0007 | g0166 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03831 | hp1 | a0002 | c0010 | t0010 | g0160 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03831 | hp2 | a0002 | c0002 | t0011 | g0200 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03834 | hp1 | a0004 | c0004 | t0001 | g0142 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03834 | hp2 | a0002 | c0002 | t0011 | g0201 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03942 | hp1 | a0001 | c0001 | t0091 | g0125 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03942 | hp2 | a0001 | c0001 | t0049 | g0113 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04115 | hp2 | a0002 | c0002 | t0066 | g0189 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04184 | hp1 | a0001 | c0001 | t0022 | g0064 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04184 | hp2 | a0001 | c0001 | t0052 | g0105 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04199 | hp2 | a0002 | c0002 | t0007 | g0176 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04204 | hp2 | a0007 | c0008 | t0079 | g0043 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04228 | hp1 | a0002 | c0002 | t0062 | g0167 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0026 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18747 | hp2 | a0011 | c0015 | t0003 | g0220 | EAS | CHB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0182 | AFR | YRI | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18906 | hp2 | a0003 | c0003 | t0043 | g0084 | AFR | YRI | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18979 | hp2 | a0001 | c0001 | t0088 | g0029 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18993 | hp2 | a0002 | c0002 | t0075 | g0174 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18994 | hp2 | a0001 | c0001 | t0053 | g0112 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18995 | hp1 | a0001 | c0001 | t0080 | g0004 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18997 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19005 | hp1 | a0001 | c0001 | t0076 | g0062 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19005 | hp2 | a0002 | c0002 | t0007 | g0173 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19011 | hp2 | a0001 | c0001 | t0081 | g0002 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19030 | hp1 | a0002 | c0002 | t0015 | g0097 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19030 | hp2 | a0001 | c0009 | t0046 | g0127 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19043 | hp1 | a0001 | c0001 | t0039 | g0194 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0190 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19079 | hp1 | a0001 | c0001 | t0072 | g0037 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19079 | hp2 | a0002 | c0002 | t0074 | g0165 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20129 | hp1 | a0001 | c0001 | t0040 | g0192 | AFR | ASW | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | ASW | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20905 | hp1 | a0002 | c0002 | t0014 | g0175 | SAS | GIH | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | GIH | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02559 | hp1 | a0003 | c0003 | t0009 | g0085 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03471 | hp1 | a0002 | c0002 | t0034 | g0099 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20300 | hp1 | a0001 | c0001 | t0032 | g0124 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20300 | hp2 | a0002 | c0002 | t0058 | g0187 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA21309 | hp1 | a0001 | c0001 | t0017 | g0015 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA21309 | hp2 | a0006 | c0012 | t0030 | g0003 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0051 | g0116 | REF | REF | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0061 | REF | REF | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995166
|
G | A | 1 | a0012 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.124G>A | p.Gly42Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 213/15561 | 124/1503 | 42/500 | chr22 | 39995166 | ||
chr22:39995328
|
C | T | 1 | a0011 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.286C>T | p.Pro96Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 375/15561 | 286/1503 | 96/500 | chr22 | 39995328 | ||
chr22:39995366
|
G | C | 1 | a0012 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.324G>C | p.Trp108Cys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 413/15561 | 324/1503 | 108/500 | chr22 | 39995366 | ||
chr22:40019899
|
C | T | 1 | a0005 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.670C>T | p.Arg224Cys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 759/15561 | 670/1503 | 224/500 | chr22 | 40019899 | ||
chr22:40019926
|
A | C | 1 | a0006 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.697A>C | p.Met233Leu | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 786/15561 | 697/1503 | 233/500 | chr22 | 40019926 | ||
chr22:40019964
|
G | T | 1 | a0003 | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.735G>T | p.Arg245Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 824/15561 | 735/1503 | 245/500 | chr22 | 40019964 | ||
chr22:40019984
|
A | G | 1 | a0010 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.755A>G | p.Asp252Gly | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 844/15561 | 755/1503 | 252/500 | chr22 | 40019984 | ||
chr22:40021567
|
G | A | 1 | a0004 | 6 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
missense_variant | MODERATE | c.1057G>A | p.Gly353Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1146/15561 | 1057/1503 | 353/500 | chr22 | 40021567 | ||
chr22:40021816
|
A | G | 2 | a0002a0004 | 73 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(70): Show |
missense_variant | MODERATE | c.1306A>G | p.Arg436Gly | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1395/15561 | 1306/1503 | 436/500 | chr22 | 40021816 | ||
chr22:40021819
|
C | T | 1 | a0007 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1309C>T | p.Arg437Cys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1398/15561 | 1309/1503 | 437/500 | chr22 | 40021819 | ||
chr22:40021871
|
A | G | 1 | a0009 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1361A>G | p.Asn454Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1450/15561 | 1361/1503 | 454/500 | chr22 | 40021871 | ||
chr22:40021939
|
G | A | 1 | a0008 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1429G>A | p.Glu477Lys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1518/15561 | 1429/1503 | 477/500 | chr22 | 40021939 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995327
|
G | T | 1 | a0011c0015 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.285G>T | p.Ala95Ala | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 374/15561 | 285/1503 | 95/500 | chr22 | 39995327 | ||
chr22:40019260
|
C | T | 1 | a0001c0014 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.582C>T | p.Ile194Ile | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/5 | 671/15561 | 582/1503 | 194/500 | chr22 | 40019260 | ||
chr22:40021491
|
C | T | 1 | a0003c0003 | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
synonymous_variant | LOW | c.981C>T | p.Tyr327Tyr | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1070/15561 | 981/1503 | 327/500 | chr22 | 40021491 | ||
chr22:40021776
|
C | T | 6 | a0001c0009a0002c0002a0002c0010others(3): Show | 82 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(79): Show |
synonymous_variant | LOW | c.1266C>T | p.Asn422Asn | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1355/15561 | 1266/1503 | 422/500 | chr22 | 40021776 | ||
chr22:40021923
|
G | A | 1 | a0002c0010 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.1413G>A | p.Thr471Thr | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1502/15561 | 1413/1503 | 471/500 | chr22 | 40021923 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995005
|
G | GGGGCCGG others(5): Show |
15 | a0001c0001t0008a0001c0001t0012a0001c0001t0032others(12): Show | 23 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-26_-15dupAGGGCCGG others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 14 | INFO_REALIGN_3_PRIME | chr22 | 39995005 | ||||
chr22:39995017
|
A | AGGGCCGG others(5): Show |
1 | a0001c0001t0042 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15_-4dupCGGGGCCGG others(3): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 3 | INFO_REALIGN_3_PRIME | chr22 | 39995017 | ||||
chr22:40029591
|
G | A | 1 | a0006c0012t0030 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 26 | chr22 | 40029591 | |||||
chr22:40029621
|
T | C | 6 | a0001c0001t0047a0001c0009t0046a0003c0003t0009others(3): Show | 10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*56T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 56 | chr22 | 40029621 | |||||
chr22:40029870
|
T | C | 7 | a0001c0001t0047a0001c0001t0048a0001c0009t0046others(4): Show | 11 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 305 | chr22 | 40029870 | |||||
chr22:40029970
|
G | A | 13 | a0001c0001t0003a0001c0001t0006a0001c0001t0013others(10): Show | 42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*405G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 405 | chr22 | 40029970 | |||||
chr22:40030089
|
G | A | 1 | a0001c0001t0056 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 524 | chr22 | 40030089 | |||||
chr22:40030278
|
C | T | 2 | a0001c0001t0040a0001c0001t0041 | 2 | HG02818.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*713C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 713 | chr22 | 40030278 | |||||
chr22:40030291
|
T | C | 7 | a0001c0001t0017a0001c0001t0047a0001c0009t0046others(4): Show | 12 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 726 | chr22 | 40030291 | |||||
chr22:40030302
|
T | C | 61 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(58): Show | 146 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*737T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 737 | chr22 | 40030302 | |||||
chr22:40030539
|
T | C | 1 | a0002c0002t0057 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*974T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 974 | chr22 | 40030539 | |||||
chr22:40031018
|
TGAG | T | 3 | a0003c0003t0009a0003c0003t0043a0003c0003t0044 | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1457_*1459delGAG | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1457 | INFO_REALIGN_3_PRIME | chr22 | 40031018 | ||||
chr22:40031253
|
G | C | 1 | a0001c0001t0072 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1688G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1688 | chr22 | 40031253 | |||||
chr22:40031339
|
C | G | 10 | a0001c0001t0020a0001c0001t0047a0001c0001t0048others(7): Show | 15 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1774C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1774 | chr22 | 40031339 | |||||
chr22:40031399
|
C | T | 10 | a0001c0001t0020a0001c0001t0047a0001c0001t0048others(7): Show | 15 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1834C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1834 | chr22 | 40031399 | |||||
chr22:40031713
|
AAGGCAGG others(7): Show |
A | 3 | a0001c0001t0047a0001c0009t0046a0005c0013t0045 | 3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2156_*2169delAGTG others(10): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2156 | INFO_REALIGN_3_PRIME | chr22 | 40031713 | ||||
chr22:40031869
|
A | G | 1 | a0001c0001t0029 | 2 | HG02622.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2304A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2304 | chr22 | 40031869 | |||||
chr22:40032014
|
C | T | 1 | a0001c0001t0091 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2449C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2449 | chr22 | 40032014 | |||||
chr22:40032027
|
C | T | 1 | a0001c0001t0028 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2462C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2462 | chr22 | 40032027 | |||||
chr22:40032047
|
GGGT | G | 3 | a0001c0001t0047a0001c0009t0046a0005c0013t0045 | 3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2485_*2487delTGG | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2485 | INFO_REALIGN_3_PRIME | chr22 | 40032047 | ||||
chr22:40032051
|
G | A | 3 | a0001c0001t0047a0001c0009t0046a0005c0013t0045 | 3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2486G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2486 | chr22 | 40032051 | |||||
chr22:40032190
|
C | T | 1 | a0001c0001t0027 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2625C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2625 | chr22 | 40032190 | |||||
chr22:40032260
|
C | T | 1 | a0001c0001t0090 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2695C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2695 | chr22 | 40032260 | |||||
chr22:40032324
|
A | G | 4 | a0001c0001t0047a0001c0009t0046a0005c0013t0045others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2759A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2759 | chr22 | 40032324 | |||||
chr22:40032429
|
G | A | 26 | a0001c0001t0032a0001c0001t0033a0002c0002t0001others(23): Show | 69 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2864G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2864 | chr22 | 40032429 | |||||
chr22:40032560
|
C | CT | 4 | a0001c0001t0088a0003c0003t0009a0003c0003t0043others(1): Show | 8 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3007dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3008 | INFO_REALIGN_3_PRIME | chr22 | 40032560 | ||||
chr22:40032568
|
T | G | 2 | a0002c0002t0015a0002c0002t0068 | 3 | HG01243.hp2 HG03453.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3003T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3003 | chr22 | 40032568 | |||||
chr22:40032606
|
T | C | 2 | a0001c0001t0020a0001c0001t0070 | 3 | HG01884.hp2 HG02257.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3041T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3041 | chr22 | 40032606 | |||||
chr22:40032661
|
C | T | 1 | a0001c0001t0026 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3096C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3096 | chr22 | 40032661 | |||||
chr22:40032702
|
A | G | 51 | a0001c0001t0008a0001c0001t0012a0001c0001t0017others(48): Show | 108 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3137A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3137 | chr22 | 40032702 | |||||
chr22:40032783
|
T | A | 27 | a0001c0001t0013a0001c0001t0021a0001c0001t0036others(24): Show | 66 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3218T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3218 | chr22 | 40032783 | |||||
chr22:40032790
|
T | C | 27 | a0001c0001t0013a0001c0001t0021a0001c0001t0036others(24): Show | 66 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3225T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3225 | chr22 | 40032790 | |||||
chr22:40032812
|
G | A | 12 | a0001c0001t0004a0001c0001t0005a0001c0001t0037others(9): Show | 33 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3247G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3247 | chr22 | 40032812 | |||||
chr22:40032820
|
T | C | 1 | a0001c0001t0051 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3255T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3255 | chr22 | 40032820 | |||||
chr22:40033092
|
G | GT | 3 | a0001c0001t0005a0001c0001t0024a0001c0001t0050 | 11 | HG00642.hp2 HG00733.hp2 HG01070.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3537dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3538 | INFO_REALIGN_3_PRIME | chr22 | 40033092 | ||||
chr22:40033107
|
C | G | 1 | a0002c0002t0064 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3542 | chr22 | 40033107 | |||||
chr22:40033316
|
C | T | 2 | a0001c0001t0039a0001c0001t0047 | 2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3751C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3751 | chr22 | 40033316 | |||||
chr22:40033361
|
A | G | 25 | a0001c0001t0008a0001c0001t0017a0001c0001t0023others(22): Show | 64 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3796A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3796 | chr22 | 40033361 | |||||
chr22:40033494
|
T | C | 20 | a0001c0001t0025a0001c0001t0027a0001c0001t0039others(17): Show | 23 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3929T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3929 | chr22 | 40033494 | |||||
chr22:40033729
|
C | G | 1 | a0001c0001t0041 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4164C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4164 | chr22 | 40033729 | |||||
chr22:40033832
|
C | T | 8 | a0001c0001t0025a0001c0001t0027a0001c0001t0040others(5): Show | 11 | HG01109.hp2 HG01884.hp1 HG02647.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4267C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4267 | chr22 | 40033832 | |||||
chr22:40033839
|
G | A | 1 | a0002c0002t0018 | 2 | HG00140.hp1 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4274G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4274 | chr22 | 40033839 | |||||
chr22:40034026
|
C | T | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4461C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4461 | chr22 | 40034026 | |||||
chr22:40034347
|
A | G | 14 | a0001c0001t0032a0001c0001t0033a0001c0001t0039others(11): Show | 14 | HG01891.hp1 HG01934.hp2 HG02572.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4782A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4782 | chr22 | 40034347 | |||||
chr22:40034598
|
C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5033C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5033 | chr22 | 40034598 | |||||
chr22:40034613
|
C | T | 2 | a0001c0001t0020a0001c0001t0087 | 3 | HG01884.hp1 HG01884.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5048C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5048 | chr22 | 40034613 | |||||
chr22:40034763
|
T | C | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5198T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5198 | chr22 | 40034763 | |||||
chr22:40034923
|
G | C | 1 | a0007c0008t0079 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5358G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5358 | chr22 | 40034923 | |||||
chr22:40035022
|
G | T | 2 | a0001c0001t0039a0001c0001t0047 | 2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5457G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5457 | chr22 | 40035022 | |||||
chr22:40035137
|
G | A | 1 | a0001c0001t0070 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5572G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5572 | chr22 | 40035137 | |||||
chr22:40035170
|
TA | T | 1 | a0001c0001t0026 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5606delA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5606 | chr22 | 40035170 | |||||
chr22:40035195
|
C | A | 1 | a0002c0002t0064 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5630C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5630 | chr22 | 40035195 | |||||
chr22:40035248
|
A | G | 1 | a0001c0001t0033 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5683A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5683 | chr22 | 40035248 | |||||
chr22:40035260
|
G | A | 1 | a0002c0002t0067 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5695G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5695 | chr22 | 40035260 | |||||
chr22:40035410
|
C | T | 1 | a0002c0002t0035 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5845C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5845 | chr22 | 40035410 | |||||
chr22:40035444
|
C | T | 4 | a0001c0001t0025a0001c0001t0027a0001c0001t0048others(1): Show | 7 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5879C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5879 | chr22 | 40035444 | |||||
chr22:40035498
|
C | A | 1 | a0002c0002t0074 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5933C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5933 | chr22 | 40035498 | |||||
chr22:40035621
|
G | A | 1 | a0001c0001t0016 | 2 | HG01978.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6056G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6056 | chr22 | 40035621 | |||||
chr22:40035625
|
G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6060G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6060 | chr22 | 40035625 | |||||
chr22:40035626
|
G | C | 7 | a0001c0001t0025a0001c0001t0027a0001c0001t0048others(4): Show | 10 | HG01109.hp2 HG01884.hp1 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6061G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6061 | chr22 | 40035626 | |||||
chr22:40035674
|
A | C | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6109A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6109 | chr22 | 40035674 | |||||
chr22:40035805
|
A | G | 5 | a0001c0001t0012a0001c0001t0037a0001c0001t0070others(2): Show | 8 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6240A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6240 | chr22 | 40035805 | |||||
chr22:40035848
|
T | G | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6283T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6283 | chr22 | 40035848 | |||||
chr22:40035944
|
T | C | 1 | a0001c0001t0052 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6379T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6379 | chr22 | 40035944 | |||||
chr22:40036219
|
A | G | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6654A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6654 | chr22 | 40036219 | |||||
chr22:40036306
|
A | G | 1 | a0002c0002t0061 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6741A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6741 | chr22 | 40036306 | |||||
chr22:40036314
|
G | A | 1 | a0002c0002t0060 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6749G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6749 | chr22 | 40036314 | |||||
chr22:40036343
|
C | T | 1 | a0005c0013t0045 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6778C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6778 | chr22 | 40036343 | |||||
chr22:40036351
|
A | G | 1 | a0001c0001t0070 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6786A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6786 | chr22 | 40036351 | |||||
chr22:40036653
|
A | T | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7088A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7088 | chr22 | 40036653 | |||||
chr22:40036664
|
C | T | 3 | a0001c0001t0086a0001c0001t0087a0001c0009t0046 | 3 | HG01884.hp1 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7099C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7099 | chr22 | 40036664 | |||||
chr22:40036764
|
C | T | 1 | a0001c0001t0087 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7199C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7199 | chr22 | 40036764 | |||||
chr22:40036777
|
G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7212G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7212 | chr22 | 40036777 | |||||
chr22:40036791
|
G | A | 1 | a0001c0001t0022 | 2 | HG00639.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7226G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7226 | chr22 | 40036791 | |||||
chr22:40036844
|
C | T | 1 | a0002c0002t0019 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7279C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7279 | chr22 | 40036844 | |||||
chr22:40036926
|
C | T | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7361C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7361 | chr22 | 40036926 | |||||
chr22:40037065
|
A | G | 2 | a0001c0001t0039a0001c0001t0047 | 2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7500A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7500 | chr22 | 40037065 | |||||
chr22:40037090
|
G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7525G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7525 | chr22 | 40037090 | |||||
chr22:40037095
|
G | C | 1 | a0001c0001t0026 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7530G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7530 | chr22 | 40037095 | |||||
chr22:40037278
|
G | A | 1 | a0001c0001t0053 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7713G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7713 | chr22 | 40037278 | |||||
chr22:40037281
|
G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7716G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7716 | chr22 | 40037281 | |||||
chr22:40037333
|
C | T | 23 | a0001c0001t0017a0001c0001t0025a0001c0001t0027others(20): Show | 27 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7768C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7768 | chr22 | 40037333 | |||||
chr22:40037480
|
C | T | 2 | a0001c0001t0006a0001c0001t0055 | 8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7915C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7915 | chr22 | 40037480 | |||||
chr22:40037510
|
C | T | 1 | a0001c0001t0048 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7945C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7945 | chr22 | 40037510 | |||||
chr22:40038168
|
G | T | 1 | a0001c0001t0028 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8603G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8603 | chr22 | 40038168 | |||||
chr22:40038189
|
C | A | 1 | a0002c0002t0064 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8624C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8624 | chr22 | 40038189 | |||||
chr22:40038290
|
G | A | 1 | a0001c0001t0024 | 2 | HG02165.hp2 NA18997.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8725G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8725 | chr22 | 40038290 | |||||
chr22:40038290
|
G | T | 5 | a0001c0001t0025a0001c0001t0027a0001c0001t0040others(2): Show | 8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8725G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8725 | chr22 | 40038290 | |||||
chr22:40038412
|
C | T | 3 | a0001c0001t0012a0001c0001t0037a0006c0012t0030 | 6 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8847C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8847 | chr22 | 40038412 | |||||
chr22:40038752
|
C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9187C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9187 | chr22 | 40038752 | |||||
chr22:40038753
|
A | G | 54 | a0001c0001t0008a0001c0001t0012a0001c0001t0017others(51): Show | 104 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*9188A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9188 | chr22 | 40038753 | |||||
chr22:40038763
|
ACT | A | 2 | a0001c0001t0086a0001c0001t0087 | 2 | HG01884.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9203_*9204delCT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9203 | INFO_REALIGN_3_PRIME | chr22 | 40038763 | ||||
chr22:40039316
|
A | G | 2 | a0001c0001t0039a0001c0001t0047 | 2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9751A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9751 | chr22 | 40039316 | |||||
chr22:40039374
|
G | A | 11 | a0001c0001t0039a0001c0001t0041a0001c0001t0042others(8): Show | 11 | HG01891.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9809G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9809 | chr22 | 40039374 | |||||
chr22:40039386
|
G | A | 4 | a0001c0001t0012a0001c0001t0037a0001c0001t0070others(1): Show | 7 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9821G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9821 | chr22 | 40039386 | |||||
chr22:40039419
|
G | T | 18 | a0001c0001t0017a0001c0001t0025a0001c0001t0027others(15): Show | 22 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*9854G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9854 | chr22 | 40039419 | |||||
chr22:40039642
|
G | A | 1 | a0001c0001t0080 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10077G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10077 | chr22 | 40039642 | |||||
chr22:40039649
|
G | A | 1 | a0002c0002t0062 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10084G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10084 | chr22 | 40039649 | |||||
chr22:40039974
|
C | G | 1 | a0001c0001t0083 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10409C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10409 | chr22 | 40039974 | |||||
chr22:40040202
|
C | G | 3 | a0001c0001t0086a0001c0001t0087a0001c0009t0046 | 3 | HG01884.hp1 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10637C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10637 | chr22 | 40040202 | |||||
chr22:40040355
|
G | C | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10790G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10790 | chr22 | 40040355 | |||||
chr22:40040365
|
G | T | 3 | a0001c0001t0042a0002c0002t0034a0002c0002t0035 | 3 | HG02717.hp1 HG02976.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10800G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10800 | chr22 | 40040365 | |||||
chr22:40040486
|
C | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10921C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10921 | chr22 | 40040486 | |||||
chr22:40040571
|
C | T | 2 | a0003c0003t0043a0003c0003t0044 | 2 | HG03579.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11006C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11006 | chr22 | 40040571 | |||||
chr22:40040925
|
A | G | 13 | a0001c0001t0032a0001c0001t0033a0001c0001t0039others(10): Show | 13 | HG01891.hp1 HG01934.hp2 HG02572.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*11360A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11360 | chr22 | 40040925 | |||||
chr22:40040969
|
G | C | 20 | a0001c0001t0023a0001c0001t0036a0001c0001t0038others(17): Show | 53 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*11404G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11404 | chr22 | 40040969 | |||||
chr22:40041191
|
G | A | 2 | a0001c0001t0072a0001c0001t0077 | 2 | HG02080.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11626G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11626 | chr22 | 40041191 | |||||
chr22:40041633
|
G | A | 1 | a0007c0008t0079 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12068G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12068 | chr22 | 40041633 | |||||
chr22:40041653
|
C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12088C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12088 | chr22 | 40041653 | |||||
chr22:40042003
|
C | T | 2 | a0001c0001t0056a0001c0001t0082 | 2 | HG02015.hp1 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12438C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12438 | chr22 | 40042003 | |||||
chr22:40042018
|
G | A | 4 | a0001c0001t0012a0001c0001t0037a0001c0001t0070others(1): Show | 7 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12453G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12453 | chr22 | 40042018 | |||||
chr22:40042071
|
T | A | 18 | a0001c0001t0017a0001c0001t0025a0001c0001t0027others(15): Show | 22 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*12506T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12506 | chr22 | 40042071 | |||||
chr22:40042350
|
C | T | 1 | a0002c0002t0061 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12785C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12785 | chr22 | 40042350 | |||||
chr22:40042398
|
C | CGTAAGTC others(1): Show |
5 | a0001c0001t0025a0001c0001t0027a0001c0001t0040others(2): Show | 8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12836_*12837insAG others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12837 | INFO_REALIGN_3_PRIME | chr22 | 40042398 | ||||
chr22:40042402
|
G | A | 5 | a0001c0001t0025a0001c0001t0027a0001c0001t0040others(2): Show | 8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12837G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12837 | chr22 | 40042402 | |||||
chr22:40042495
|
G | A | 4 | a0001c0001t0012a0001c0001t0037a0001c0001t0070others(1): Show | 7 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12930G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12930 | chr22 | 40042495 | |||||
chr22:40042507
|
A | T | 1 | a0001c0001t0053 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12942A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12942 | chr22 | 40042507 | |||||
chr22:40042588
|
C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13023C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13023 | chr22 | 40042588 | |||||
chr22:40042606
|
G | T | 1 | a0001c0001t0081 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13041G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13041 | chr22 | 40042606 | |||||
chr22:40042662
|
A | G | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13097A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13097 | chr22 | 40042662 | |||||
chr22:40042854
|
A | G | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13289A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13289 | chr22 | 40042854 | |||||
chr22:40042858
|
A | G | 1 | a0001c0009t0046 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13293A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13293 | chr22 | 40042858 | |||||
chr22:40043086
|
C | T | 1 | a0001c0001t0054 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13521C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13521 | chr22 | 40043086 | |||||
chr22:40043123
|
A | T | 16 | a0001c0001t0025a0001c0001t0027a0001c0001t0039others(13): Show | 19 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*13558A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13558 | chr22 | 40043123 | |||||
chr22:40043439
|
G | A | 1 | a0002c0002t0063 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13874G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13874 | chr22 | 40043439 | |||||
chr22:40043521
|
C | T | 5 | a0001c0001t0025a0001c0001t0027a0001c0001t0040others(2): Show | 8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13956C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13956 | chr22 | 40043521 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995624
|
G | A | 2 | a0001c0001t0086g0012a0001c0001t0087g0013 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.489+93G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995624 | ||||||
chr22:39995640
|
G | A | 2 | a0001c0001t0017g0014a0001c0001t0017g0015 | 2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+109G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995640 | ||||||
chr22:39995972
|
C | T | 3 | a0001c0001t0003g0218a0001c0001t0013g0219a0011c0015t0003g0220 | 3 | HG02135.hp2 NA18747.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.489+441C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995972 | ||||||
chr22:39995973
|
G | T | 2 | a0001c0001t0036g0217a0001c0001t0038g0216 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.489+442G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995973 | ||||||
chr22:39995990
|
G | A | 2 | a0001c0001t0002g0017a0001c0001t0023g0016 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.489+459G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995990 | ||||||
chr22:39996600
|
A | G | 150 | a0001c0001t0002g0120a0001c0001t0002g0128a0001c0001t0002g0129others(147): Show | 154 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(151): Show |
intron_variant | MODIFIER | c.489+1069A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39996600 | ||||||
chr22:39996719
|
T | C | 52 | a0001c0001t0002g0120a0001c0001t0002g0128a0001c0001t0002g0129others(49): Show | 53 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.489+1188T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39996719 | ||||||
chr22:39997008
|
T | C | 8 | a0002c0002t0068g0082a0003c0003t0009g0083a0003c0003t0009g0085others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+1477T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997008 | ||||||
chr22:39997474
|
G | A | 2 | a0001c0001t0047g0090a0001c0001t0048g0091 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+1943G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997474 | ||||||
chr22:39997536
|
ACAAATGC others(3732): Show |
A | 1 | a0001c0001t0004g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.489+2011_489+5749d others(2): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 39997536 | |||||
chr22:39997592
|
T | A | 1 | a0001c0001t0023g0016 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.489+2061T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997592 | ||||||
chr22:39997628
|
T | C | 1 | a0001c0001t0042g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489+2097T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997628 | ||||||
chr22:39997836
|
C | T | 1 | a0001c0001t0071g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.489+2305C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997836 | ||||||
chr22:39998009
|
G | T | 1 | a0002c0002t0001g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.489+2478G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998009 | ||||||
chr22:39998041
|
C | A | 15 | a0001c0001t0017g0014a0001c0001t0017g0015a0001c0001t0020g0133others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2510C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998041 | ||||||
chr22:39998095
|
C | T | 11 | a0001c0001t0017g0014a0001c0001t0017g0015a0001c0001t0025g0139others(8): Show | 11 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+2564C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998095 | ||||||
chr22:39998264
|
C | A | 1 | a0001c0001t0017g0014 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.489+2733C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998264 | ||||||
chr22:39998571
|
C | A | 1 | a0012c0005t0089g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489+3040C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998571 | ||||||
chr22:39998606
|
G | A | 8 | a0002c0002t0068g0082a0003c0003t0009g0083a0003c0003t0009g0085others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3075G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998606 | ||||||
chr22:39998613
|
C | T | 1 | a0002c0002t0057g0213 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.489+3082C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998613 | ||||||
chr22:39998793
|
G | C | 147 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0092others(144): Show | 151 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(148): Show |
intron_variant | MODIFIER | c.489+3262G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998793 | ||||||
chr22:39998899
|
C | T | 8 | a0002c0002t0001g0205a0002c0002t0001g0207a0002c0002t0001g0210others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3368C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998899 | ||||||
chr22:39999074
|
A | G | 1 | a0002c0002t0001g0204 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.489+3543A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999074 | ||||||
chr22:39999080
|
T | C | 135 | a0001c0001t0002g0120a0001c0001t0002g0128a0001c0001t0003g0008others(132): Show | 139 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.489+3549T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999080 | ||||||
chr22:39999284
|
A | G | 3 | a0001c0001t0047g0090a0001c0001t0048g0091a0001c0001t0070g0203 | 3 | HG02630.hp2 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+3753A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999284 | ||||||
chr22:39999343
|
A | G | 1 | a0001c0001t0055g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.489+3812A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999343 | ||||||
chr22:39999361
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.489+3830G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999361 | ||||||
chr22:39999443
|
C | T | 12 | a0001c0001t0047g0090a0001c0001t0048g0091a0001c0001t0071g0215others(9): Show | 12 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+3912C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999443 | ||||||
chr22:39999444
|
G | A | 1 | a0004c0004t0001g0142 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+3913G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999444 | ||||||
chr22:39999492
|
C | T | 5 | a0002c0002t0011g0198a0002c0002t0011g0200a0002c0002t0011g0201others(2): Show | 5 | HG01257.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3961C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999492 | ||||||
chr22:39999526
|
C | G | 76 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0074others(73): Show | 77 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.489+3995C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999526 | ||||||
chr22:39999846
|
A | C | 11 | a0001c0001t0025g0139a0001c0001t0025g0140a0001c0001t0047g0090others(8): Show | 11 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+4315A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999846 | ||||||
chr22:40000024
|
C | T | 6 | a0002c0002t0001g0011a0002c0002t0001g0096a0002c0002t0018g0186others(3): Show | 7 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+4493C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000024 | ||||||
chr22:40000241
|
G | T | 9 | a0001c0001t0047g0090a0001c0001t0048g0091a0003c0003t0009g0083others(6): Show | 9 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+4710G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000241 | ||||||
chr22:40000394
|
C | T | 1 | a0001c0001t0004g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.489+4863C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000394 | ||||||
chr22:40000405
|
A | T | 69 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0074others(66): Show | 70 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.489+4874A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000405 | ||||||
chr22:40000608
|
C | CA | 69 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0074others(66): Show | 70 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.489+5084dupA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40000608 | |||||
chr22:40000616
|
C | A | 1 | a0001c0001t0003g0218 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.489+5085C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000616 | ||||||
chr22:40000630
|
GTA | G | 6 | a0002c0002t0001g0010a0002c0002t0001g0177a0002c0002t0001g0178others(3): Show | 7 | HG02258.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5101_489+5102d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40000630 | |||||
chr22:40000739
|
C | T | 4 | a0001c0001t0025g0139a0001c0001t0025g0140a0001c0001t0027g0137others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+5208C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000739 | ||||||
chr22:40000902
|
G | A | 3 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203 | 3 | HG01884.hp2 HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.489+5371G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000902 | ||||||
chr22:40000925
|
C | G | 1 | a0003c0003t0044g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.489+5394C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000925 | ||||||
chr22:40001088
|
T | C | 9 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+5557T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001088 | ||||||
chr22:40001102
|
C | T | 9 | a0001c0001t0047g0090a0001c0001t0048g0091a0003c0003t0009g0083others(6): Show | 9 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+5571C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001102 | ||||||
chr22:40001106
|
T | C | 1 | a0001c0001t0090g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.489+5575T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001106 | ||||||
chr22:40001241
|
C | T | 1 | a0001c0001t0004g0070 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.489+5710C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001241 | ||||||
chr22:40001304
|
G | A | 4 | a0001c0001t0004g0022a0001c0001t0004g0023a0001c0001t0004g0072others(1): Show | 4 | HG02155.hp2 NA18969.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+5773G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001304 | ||||||
chr22:40001519
|
A | G | 155 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0074others(152): Show | 159 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.489+5988A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001519 | ||||||
chr22:40001899
|
C | T | 1 | a0001c0001t0036g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+6368C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001899 | ||||||
chr22:40001927
|
C | G | 2 | a0001c0001t0086g0012a0001c0001t0087g0013 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.489+6396C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001927 | ||||||
chr22:40001961
|
C | T | 1 | a0001c0001t0004g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.489+6430C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001961 | ||||||
chr22:40002033
|
G | A | 2 | a0001c0009t0046g0127a0005c0013t0045g0132 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+6502G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002033 | ||||||
chr22:40002038
|
C | CCGAGCTG others(4): Show |
7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+6510_489+6520d others(13): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40002038 | |||||
chr22:40002108
|
C | T | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+6577C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002108 | ||||||
chr22:40002344
|
C | T | 1 | a0002c0002t0015g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.489+6813C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002344 | ||||||
chr22:40002496
|
C | T | 4 | a0001c0001t0025g0139a0001c0001t0025g0140a0001c0001t0027g0137others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+6965C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002496 | ||||||
chr22:40002507
|
A | G | 3 | a0001c0001t0023g0069a0001c0001t0078g0067a0001c0001t0085g0068 | 3 | HG02572.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.489+6976A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002507 | ||||||
chr22:40002581
|
C | T | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+7050C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002581 | ||||||
chr22:40002608
|
G | A | 1 | a0002c0002t0015g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.489+7077G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002608 | ||||||
chr22:40002743
|
G | A | 22 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(19): Show | 22 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.489+7212G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002743 | ||||||
chr22:40002841
|
A | G | 133 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(130): Show | 137 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.489+7310A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002841 | ||||||
chr22:40002841
|
A | T | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+7310A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002841 | ||||||
chr22:40002866
|
C | T | 1 | a0002c0002t0060g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.489+7335C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002866 | ||||||
chr22:40002867
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.489+7336G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002867 | ||||||
chr22:40002922
|
C | A | 1 | a0001c0001t0084g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.489+7391C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002922 | ||||||
chr22:40003085
|
G | A | 1 | a0003c0003t0009g0083 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.489+7554G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003085 | ||||||
chr22:40003289
|
G | C | 1 | a0001c0001t0004g0026 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.489+7758G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003289 | ||||||
chr22:40003394
|
C | T | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+7863C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003394 | ||||||
chr22:40003444
|
A | G | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+7913A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003444 | ||||||
chr22:40003539
|
C | T | 1 | a0002c0002t0007g0176 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.489+8008C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003539 | ||||||
chr22:40003546
|
A | AG | 61 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(58): Show | 62 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.489+8022dupG | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40003546 | |||||
chr22:40003769
|
T | C | 1 | a0001c0001t0070g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.489+8238T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003769 | ||||||
chr22:40003823
|
C | T | 61 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(58): Show | 62 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.489+8292C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003823 | ||||||
chr22:40003832
|
C | T | 1 | a0001c0001t0012g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.489+8301C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003832 | ||||||
chr22:40003893
|
G | A | 1 | a0001c0001t0004g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.489+8362G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003893 | ||||||
chr22:40004021
|
G | T | 1 | a0002c0002t0014g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.489+8490G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004021 | ||||||
chr22:40004160
|
G | A | 3 | a0001c0001t0003g0102a0001c0001t0003g0104a0001c0001t0013g0103 | 3 | HG00733.hp1 HG01255.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.489+8629G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004160 | ||||||
chr22:40004267
|
A | AATTTT | 19 | a0001c0001t0002g0004a0001c0001t0002g0028a0001c0001t0002g0128others(16): Show | 20 | HG00673.hp1 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.489+8782_489+8786d others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
A | AATTTTAT others(3): Show |
9 | a0001c0001t0008g0183a0001c0001t0008g0184a0001c0001t0008g0195others(6): Show | 9 | HG01496.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+8777_489+8786d others(12): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
A | AATTTTAT others(8): Show |
17 | a0001c0001t0003g0094a0001c0001t0003g0185a0001c0001t0006g0071others(14): Show | 17 | HG00639.hp1 HG01243.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+8772_489+8786d others(17): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
A | AATTTTAT others(13): Show |
6 | a0001c0001t0003g0122a0001c0001t0041g0193a0001c0001t0042g0130others(3): Show | 6 | HG02165.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+8767_489+8786d others(22): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
A | AATTTTAT others(18): Show |
7 | a0001c0001t0002g0120a0001c0001t0003g0104a0001c0001t0003g0119others(4): Show | 7 | HG01255.hp2 HG02698.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+8762_489+8786d others(27): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
A | AATTTTAT others(23): Show |
20 | a0001c0001t0003g0008a0001c0001t0003g0092a0001c0001t0003g0102others(17): Show | 21 | HG00733.hp1 HG00735.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.489+8757_489+8786d others(32): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
A | AATTTTAT others(28): Show |
8 | a0001c0001t0003g0066a0001c0001t0003g0101a0001c0001t0003g0107others(5): Show | 8 | HG00673.hp2 HG01346.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.489+8752_489+8786d others(37): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
A | AATTTTAT others(38): Show |
1 | a0001c0001t0003g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.489+8742_489+8786d others(47): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
AATTTT | A | 60 | a0001c0001t0032g0124a0001c0001t0033g0123a0001c0001t0071g0215others(57): Show | 62 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.489+8782_489+8786d others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004267
|
AATTTTAT others(8): Show |
A | 3 | a0001c0001t0047g0090a0001c0001t0048g0091a0002c0002t0001g0214 | 3 | HG02647.hp1 HG02683.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489+8772_489+8786d others(17): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | |||||
chr22:40004289
|
T | TTTTATTT others(17): Show |
1 | a0001c0001t0052g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.489+8762_489+8785d others(26): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004289 | |||||
chr22:40004328
|
G | A | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.489+8797G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004328 | ||||||
chr22:40004406
|
G | A | 1 | a0002c0002t0065g0199 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.489+8875G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004406 | ||||||
chr22:40004731
|
C | A | 42 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(39): Show | 43 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.489+9200C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004731 | ||||||
chr22:40004908
|
A | G | 61 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(58): Show | 62 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.489+9377A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004908 | ||||||
chr22:40005000
|
A | G | 6 | a0001c0001t0012g0003a0001c0001t0012g0190a0001c0001t0012g0191others(3): Show | 6 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+9469A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005000 | ||||||
chr22:40005160
|
A | G | 1 | a0012c0005t0089g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489+9629A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005160 | ||||||
chr22:40005236
|
C | T | 2 | a0001c0001t0022g0064a0001c0001t0022g0065 | 2 | HG00639.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.489+9705C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005236 | ||||||
chr22:40005265
|
CACCA | C | 2 | a0001c0001t0025g0139a0001c0001t0025g0140 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.489+9739_489+9742d others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40005265 | |||||
chr22:40005775
|
A | C | 19 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(16): Show | 19 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.489+10244A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005775 | ||||||
chr22:40005825
|
T | C | 2 | a0001c0009t0046g0127a0005c0013t0045g0132 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+10294T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005825 | ||||||
chr22:40005891
|
A | C | 42 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(39): Show | 43 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.489+10360A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005891 | ||||||
chr22:40005961
|
C | T | 2 | a0001c0001t0047g0090a0001c0001t0048g0091 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+10430C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005961 | ||||||
chr22:40006069
|
G | A | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+10538G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006069 | ||||||
chr22:40006124
|
C | T | 1 | a0002c0002t0007g0176 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.489+10593C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006124 | ||||||
chr22:40006239
|
CA | C | 47 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(44): Show | 48 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.489+10723delA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40006239 | |||||
chr22:40006315
|
G | C | 2 | a0001c0009t0046g0127a0005c0013t0045g0132 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+10784G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006315 | ||||||
chr22:40006403
|
A | G | 6 | a0002c0002t0007g0173a0002c0002t0014g0168a0002c0002t0014g0169others(3): Show | 6 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+10872A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006403 | ||||||
chr22:40006544
|
C | G | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+11013C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006544 | ||||||
chr22:40006606
|
C | T | 1 | a0002c0002t0031g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+11075C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006606 | ||||||
chr22:40006637
|
A | G | 1 | a0001c0001t0076g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.489+11106A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006637 | ||||||
chr22:40006755
|
A | G | 42 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(39): Show | 43 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.489+11224A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006755 | ||||||
chr22:40006767
|
C | T | 2 | a0001c0001t0023g0069a0001c0001t0078g0067 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.489+11236C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006767 | ||||||
chr22:40006777
|
G | T | 17 | a0002c0002t0001g0146a0002c0002t0001g0147a0002c0002t0001g0148others(14): Show | 17 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+11246G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006777 | ||||||
chr22:40006782
|
G | A | 4 | a0002c0002t0011g0198a0002c0002t0011g0200a0002c0002t0011g0201others(1): Show | 4 | HG02738.hp1 HG03239.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11251G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006782 | ||||||
chr22:40006808
|
T | G | 1 | a0002c0002t0075g0174 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.489+11277T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006808 | ||||||
chr22:40006809
|
G | T | 1 | a0002c0002t0075g0174 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.489+11278G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006809 | ||||||
chr22:40006813
|
T | G | 68 | a0001c0001t0029g0135a0001c0001t0032g0124a0001c0001t0033g0123others(65): Show | 71 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.489+11282T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006813 | ||||||
chr22:40007109
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.489+11578C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007109 | ||||||
chr22:40007159
|
A | C | 1 | a0001c0001t0036g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+11628A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007159 | ||||||
chr22:40007167
|
C | T | 79 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(76): Show | 80 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.489+11636C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007167 | ||||||
chr22:40007172
|
T | C | 1 | a0002c0002t0014g0168 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.489+11641T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007172 | ||||||
chr22:40007251
|
C | T | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11720C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007251 | ||||||
chr22:40007267
|
C | CTCCTCCT others(448): Show |
1 | a0001c0001t0040g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.489+11736_489+1173 others(459): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007267 | ||||||
chr22:40007267
|
C | CTCCTCCT others(449): Show |
1 | a0001c0001t0041g0193 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.489+11736_489+1173 others(460): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007267 | ||||||
chr22:40007270
|
C | T | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11739C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007270 | ||||||
chr22:40007273
|
T | C | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11742T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007273 | ||||||
chr22:40007280
|
T | TCTC | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11749_489+1175 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007280 | ||||||
chr22:40007301
|
T | C | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11770T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007301 | ||||||
chr22:40007303
|
G | C | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11772G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007303 | ||||||
chr22:40007319
|
C | T | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11788C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007319 | ||||||
chr22:40007323
|
G | C | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11792G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007323 | ||||||
chr22:40007327
|
T | TCCTCTCC others(91): Show |
2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11797_489+1179 others(102): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(559): Show |
2 | a0001c0001t0020g0133a0001c0001t0020g0134 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(570): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(551): Show |
1 | a0009c0007t0003g0121 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(562): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(551): Show |
4 | a0001c0001t0008g0195a0001c0001t0008g0196a0001c0001t0036g0217others(1): Show | 4 | HG01243.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(562): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(571): Show |
1 | a0001c0001t0003g0218 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(572): Show |
1 | a0001c0001t0012g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(583): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(573): Show |
22 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(19): Show | 23 | HG00733.hp1 HG01069.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(584): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(578): Show |
1 | a0001c0001t0003g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(589): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(573): Show |
6 | a0001c0001t0008g0183a0001c0001t0008g0184a0001c0001t0012g0003others(3): Show | 6 | HG01496.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(584): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(573): Show |
6 | a0001c0001t0006g0071a0001c0001t0006g0075a0001c0001t0006g0076others(3): Show | 6 | HG00639.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(584): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(574): Show |
4 | a0001c0001t0003g0115a0001c0001t0013g0093a0001c0001t0013g0095others(1): Show | 4 | HG00673.hp2 HG00735.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(574): Show |
2 | a0001c0001t0008g0182a0001c0001t0033g0123 | 2 | HG01934.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(574): Show |
1 | a0001c0001t0055g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(552): Show |
1 | a0001c0001t0039g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(563): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(574): Show |
5 | a0001c0001t0003g0094a0001c0001t0003g0104a0001c0001t0050g0117others(2): Show | 5 | HG01255.hp2 HG02027.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(574): Show |
1 | a0001c0001t0012g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(574): Show |
1 | a0001c0001t0006g0080 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(575): Show |
1 | a0001c0001t0032g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(586): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(574): Show |
1 | a0001c0001t0042g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(556): Show |
2 | a0001c0001t0070g0203a0001c0001t0071g0215 | 2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(567): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(608): Show |
2 | a0001c0009t0046g0127a0005c0013t0045g0132 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(619): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(570): Show |
1 | a0001c0001t0002g0031 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(569): Show |
1 | a0001c0001t0005g0020 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(580): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(569): Show |
9 | a0001c0001t0025g0139a0001c0001t0025g0140a0001c0001t0027g0137others(6): Show | 9 | HG01109.hp2 HG01175.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(580): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(553): Show |
1 | a0002c0002t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(564): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(571): Show |
1 | a0001c0001t0076g0062 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(571): Show |
1 | a0002c0002t0074g0165 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(570): Show |
1 | a0002c0002t0075g0174 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(570): Show |
2 | a0001c0001t0086g0012a0001c0001t0087g0013 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(570): Show |
65 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0019others(62): Show | 67 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(570): Show |
68 | a0001c0001t0017g0014a0001c0001t0017g0015a0001c0001t0029g0135others(65): Show | 71 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(571): Show |
2 | a0001c0001t0002g0017a0001c0001t0023g0016 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(571): Show |
1 | a0002c0002t0061g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(566): Show |
1 | a0003c0003t0009g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(577): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007327
|
T | TCTCCTCC others(567): Show |
6 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0087others(3): Show | 6 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(578): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | |||||
chr22:40007431
|
TCTCCTCC others(9): Show |
T | 1 | a0001c0001t0003g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.490-11714_490-1169 others(20): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007431 | |||||
chr22:40007439
|
TCTCCTCT others(4): Show |
T | 45 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(42): Show | 46 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.490-11717_490-1170 others(15): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007439 | |||||
chr22:40007442
|
CCTCTCCT others(11): Show |
C | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11722_490-1170 others(22): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007442 | |||||
chr22:40007447
|
C | CCT | 18 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(15): Show | 18 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-11719_490-1171 others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007447 | |||||
chr22:40007454
|
C | T | 1 | a0001c0001t0040g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11714C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007454 | ||||||
chr22:40007455
|
T | C | 1 | a0001c0001t0040g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11713T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007455 | ||||||
chr22:40007459
|
C | T | 1 | a0001c0001t0040g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11709C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007459 | ||||||
chr22:40007460
|
T | C | 1 | a0001c0001t0040g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11708T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007460 | ||||||
chr22:40007460
|
T | TCTC | 18 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(15): Show | 18 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-11701_490-1169 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007460 | |||||
chr22:40007527
|
TCTCCTCC others(4): Show |
T | 1 | a0001c0001t0003g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.490-11615_490-1160 others(15): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007527 | |||||
chr22:40007535
|
T | TCTC | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-11623_490-1162 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007535 | |||||
chr22:40007541
|
CCTCCTCT others(9): Show |
C | 146 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0017others(143): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.490-11591_490-1157 others(20): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007541 | |||||
chr22:40007546
|
TCTCCTCC others(12): Show |
T | 1 | a0001c0001t0002g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.490-11612_490-1159 others(23): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007546 | |||||
chr22:40007553
|
C | CTCCTCTC others(4): Show |
5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11614_490-1160 others(15): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007553 | |||||
chr22:40007553
|
CTCCTCTC others(20): Show |
C | 5 | a0002c0002t0014g0168a0002c0002t0014g0169a0002c0002t0014g0170others(2): Show | 5 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-11614_490-1158 others(31): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007553 | ||||||
chr22:40007621
|
CCTCCTCT others(3): Show |
C | 1 | a0001c0001t0006g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-11534_490-1152 others(14): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007621 | |||||
chr22:40007645
|
C | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0110a0001c0001t0003g0115others(2): Show | 6 | HG00735.hp1 HG01069.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-11523C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007645 | ||||||
chr22:40007667
|
TCTC | T | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11494_490-1149 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007667 | |||||
chr22:40007984
|
G | A | 2 | a0004c0004t0001g0145a0004c0004t0001g0150 | 2 | HG00280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.490-11184G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007984 | ||||||
chr22:40008031
|
C | T | 2 | a0001c0001t0086g0012a0001c0001t0087g0013 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.490-11137C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008031 | ||||||
chr22:40008045
|
T | C | 5 | a0002c0002t0015g0097a0002c0002t0015g0100a0002c0002t0034g0099others(2): Show | 5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11123T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008045 | ||||||
chr22:40008051
|
T | C | 2 | a0002c0002t0001g0151a0002c0002t0001g0152 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.490-11117T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008051 | ||||||
chr22:40008112
|
C | T | 4 | a0002c0002t0010g0009a0002c0002t0010g0159a0002c0002t0010g0161others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11056C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008112 | ||||||
chr22:40008151
|
G | A | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-11017G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008151 | ||||||
chr22:40008286
|
C | T | 8 | a0001c0001t0006g0071a0001c0001t0006g0075a0001c0001t0006g0076others(5): Show | 8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-10882C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008286 | ||||||
chr22:40008287
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.490-10881G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008287 | ||||||
chr22:40008289
|
G | C | 34 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(31): Show | 35 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-10879G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008289 | ||||||
chr22:40008330
|
G | A | 1 | a0001c0001t0054g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.490-10838G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008330 | ||||||
chr22:40008408
|
G | C | 1 | a0001c0001t0047g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-10760G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008408 | ||||||
chr22:40008416
|
A | AC | 5 | a0001c0001t0002g0033a0001c0001t0003g0115a0001c0001t0013g0093others(2): Show | 5 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-10750dupC | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40008416 | |||||
chr22:40008600
|
G | C | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-10568G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008600 | ||||||
chr22:40008608
|
C | G | 1 | a0002c0002t0074g0165 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.490-10560C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008608 | ||||||
chr22:40008608
|
C | T | 1 | a0001c0001t0004g0026 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.490-10560C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008608 | ||||||
chr22:40008687
|
C | T | 30 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(27): Show | 30 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.490-10481C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008687 | ||||||
chr22:40008768
|
A | G | 2 | a0001c0001t0002g0060a0002c0002t0073g0212 | 2 | HG01433.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.490-10400A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008768 | ||||||
chr22:40008792
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-10376T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008792 | ||||||
chr22:40008819
|
T | C | 19 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(16): Show | 19 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-10349T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008819 | ||||||
chr22:40009056
|
T | G | 1 | a0001c0001t0047g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-10112T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009056 | ||||||
chr22:40009216
|
A | T | 1 | a0001c0001t0002g0059 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-9952A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009216 | ||||||
chr22:40009543
|
C | A | 8 | a0001c0001t0006g0071a0001c0001t0006g0075a0001c0001t0006g0076others(5): Show | 8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-9625C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009543 | ||||||
chr22:40009629
|
G | A | 3 | a0001c0001t0020g0133a0001c0009t0046g0127a0005c0013t0045g0132 | 3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-9539G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009629 | ||||||
chr22:40009759
|
G | A | 72 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(69): Show | 73 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.490-9409G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009759 | ||||||
chr22:40009894
|
A | G | 42 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(39): Show | 43 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.490-9274A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009894 | ||||||
chr22:40009927
|
C | T | 62 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(59): Show | 63 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.490-9241C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009927 | ||||||
chr22:40010140
|
G | A | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-9028G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010140 | ||||||
chr22:40010264
|
C | T | 1 | a0001c0001t0004g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.490-8904C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010264 | ||||||
chr22:40010268
|
C | G | 1 | a0005c0013t0045g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.490-8900C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010268 | ||||||
chr22:40010268
|
C | T | 6 | a0002c0002t0001g0011a0002c0002t0001g0096a0002c0002t0018g0186others(3): Show | 7 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-8900C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010268 | ||||||
chr22:40010293
|
G | C | 3 | a0001c0001t0020g0133a0001c0009t0046g0127a0005c0013t0045g0132 | 3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-8875G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010293 | ||||||
chr22:40010346
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.490-8822G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010346 | ||||||
chr22:40010458
|
A | G | 6 | a0002c0002t0001g0151a0002c0002t0001g0152a0002c0002t0010g0009others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-8710A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010458 | ||||||
chr22:40010599
|
C | T | 1 | a0001c0001t0039g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-8569C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010599 | ||||||
chr22:40010699
|
A | T | 8 | a0001c0001t0006g0071a0001c0001t0006g0075a0001c0001t0006g0076others(5): Show | 8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-8469A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010699 | ||||||
chr22:40010859
|
T | C | 1 | a0001c0001t0032g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.490-8309T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010859 | ||||||
chr22:40010946
|
T | C | 1 | a0001c0001t0003g0008 | 2 | HG01069.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.490-8222T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010946 | ||||||
chr22:40011286
|
G | A | 1 | a0001c0001t0055g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-7882G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011286 | ||||||
chr22:40011293
|
G | A | 1 | a0001c0001t0020g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-7875G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011293 | ||||||
chr22:40011426
|
G | A | 2 | a0002c0002t0001g0151a0002c0002t0001g0152 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.490-7742G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011426 | ||||||
chr22:40011570
|
C | T | 34 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(31): Show | 35 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.490-7598C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011570 | ||||||
chr22:40011814
|
C | G | 1 | a0001c0001t0084g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.490-7354C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011814 | ||||||
chr22:40012023
|
T | TTTTGGAT others(34): Show |
7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-7117_490-7077d others(43): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40012023 | |||||
chr22:40012260
|
G | A | 1 | a0001c0001t0004g0034 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.490-6908G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012260 | ||||||
chr22:40012372
|
T | G | 1 | a0002c0002t0001g0205 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-6796T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012372 | ||||||
chr22:40012382
|
G | A | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-6786G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012382 | ||||||
chr22:40012490
|
C | T | 1 | a0002c0002t0007g0176 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-6678C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012490 | ||||||
chr22:40012616
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-6552A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012616 | ||||||
chr22:40012676
|
A | G | 3 | a0001c0001t0020g0133a0001c0009t0046g0127a0005c0013t0045g0132 | 3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-6492A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012676 | ||||||
chr22:40012685
|
G | A | 3 | a0001c0001t0002g0120a0001c0001t0016g0109a0001c0001t0016g0111 | 3 | HG01978.hp1 HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.490-6483G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012685 | ||||||
chr22:40012801
|
C | T | 63 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0074others(60): Show | 64 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.490-6367C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012801 | ||||||
chr22:40012848
|
C | T | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-6320C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012848 | ||||||
chr22:40012889
|
C | T | 1 | a0001c0001t0047g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-6279C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012889 | ||||||
chr22:40012891
|
G | T | 1 | a0001c0001t0005g0020 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.490-6277G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012891 | ||||||
chr22:40012917
|
C | CA | 24 | a0001c0001t0002g0035a0001c0001t0003g0115a0001c0001t0005g0020others(21): Show | 24 | HG00639.hp1 HG00735.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.490-6235dupA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40012917 | |||||
chr22:40013082
|
C | CA | 28 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0039others(25): Show | 28 | HG01106.hp2 HG01109.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.490-6061dupA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | |||||
chr22:40013082
|
C | CAA | 10 | a0001c0001t0002g0036a0001c0001t0020g0133a0001c0009t0046g0127others(7): Show | 10 | HG01175.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-6062_490-6061d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | |||||
chr22:40013082
|
C | CAAAA | 22 | a0001c0001t0006g0071a0001c0001t0006g0076a0001c0001t0006g0077others(19): Show | 22 | HG00639.hp1 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.490-6064_490-6061d others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | |||||
chr22:40013082
|
C | CAAAAA | 25 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0092others(22): Show | 26 | HG00733.hp1 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-6065_490-6061d others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | |||||
chr22:40013082
|
C | CAAAAAA | 7 | a0001c0001t0003g0074a0001c0001t0003g0119a0001c0001t0016g0111others(4): Show | 7 | HG02257.hp1 HG03017.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-6066_490-6061d others(8): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | |||||
chr22:40013082
|
C | CAAAAAAA | 6 | a0001c0001t0002g0120a0001c0001t0003g0122a0001c0001t0013g0095others(3): Show | 6 | HG01978.hp1 HG02080.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-6067_490-6061d others(9): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | |||||
chr22:40013135
|
C | T | 74 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(71): Show | 75 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-6033C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40013135 | ||||||
chr22:40013384
|
G | A | 4 | a0001c0001t0025g0139a0001c0001t0025g0140a0001c0001t0027g0137others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-5784G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40013384 | ||||||
chr22:40013645
|
T | A | 2 | a0001c0001t0017g0014a0001c0001t0017g0015 | 2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-5523T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40013645 | ||||||
chr22:40013923
|
CCTTTTTT | C | 3 | a0001c0001t0020g0133a0001c0009t0046g0127a0005c0013t0045g0132 | 3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-5240_490-5234d others(9): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013923 | |||||
chr22:40014131
|
C | CT | 83 | a0001c0001t0003g0110a0001c0001t0003g0218a0001c0001t0005g0057others(80): Show | 86 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.490-5020dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40014131 | |||||
chr22:40014131
|
C | CTT | 54 | a0001c0001t0002g0060a0001c0001t0002g0120a0001c0001t0003g0008others(51): Show | 55 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.490-5021_490-5020d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40014131 | |||||
chr22:40014131
|
C | CTTT | 5 | a0001c0001t0003g0101a0001c0001t0013g0093a0001c0001t0020g0133others(2): Show | 5 | HG00673.hp2 HG01884.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-5022_490-5020d others(5): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40014131 | |||||
chr22:40014446
|
G | A | 2 | a0003c0003t0043g0084a0003c0003t0044g0089 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.490-4722G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014446 | ||||||
chr22:40014625
|
A | G | 2 | a0002c0002t0060g0073a0002c0002t0061g0162 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.490-4543A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014625 | ||||||
chr22:40014870
|
G | C | 1 | a0001c0001t0048g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.490-4298G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014870 | ||||||
chr22:40014974
|
A | G | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-4194A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014974 | ||||||
chr22:40015086
|
G | A | 1 | a0001c0001t0039g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-4082G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015086 | ||||||
chr22:40015231
|
G | C | 1 | a0012c0005t0089g0131 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-3937G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015231 | ||||||
chr22:40015419
|
C | G | 1 | a0002c0002t0073g0212 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.490-3749C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015419 | ||||||
chr22:40015508
|
C | G | 1 | a0001c0001t0071g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-3660C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015508 | ||||||
chr22:40015565
|
C | T | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-3603C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015565 | ||||||
chr22:40015566
|
G | T | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-3602G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015566 | ||||||
chr22:40015584
|
C | T | 2 | a0002c0002t0001g0204a0002c0002t0001g0214 | 2 | HG00642.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.490-3584C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015584 | ||||||
chr22:40015649
|
T | G | 1 | a0001c0001t0090g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.490-3519T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015649 | ||||||
chr22:40015907
|
T | C | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-3261T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015907 | ||||||
chr22:40015997
|
A | G | 3 | a0001c0001t0003g0094a0001c0001t0003g0126a0001c0001t0003g0185 | 3 | HG03492.hp1 HG03669.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.490-3171A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015997 | ||||||
chr22:40016033
|
A | G | 1 | a0001c0001t0003g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.490-3135A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016033 | ||||||
chr22:40016042
|
C | T | 1 | a0001c0001t0004g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-3126C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016042 | ||||||
chr22:40016185
|
C | CGTT | 72 | a0001c0001t0032g0124a0001c0001t0033g0123a0002c0002t0001g0010others(69): Show | 75 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-2970_490-2968d others(5): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40016185 | |||||
chr22:40016201
|
T | G | 92 | a0001c0001t0002g0041a0001c0001t0008g0182a0001c0001t0008g0183others(89): Show | 95 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.490-2967T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016201 | ||||||
chr22:40016352
|
G | T | 1 | a0001c0001t0012g0197 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.490-2816G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016352 | ||||||
chr22:40016353
|
C | G | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-2815C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016353 | ||||||
chr22:40016547
|
G | C | 156 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0074others(153): Show | 160 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(157): Show |
intron_variant | MODIFIER | c.490-2621G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016547 | ||||||
chr22:40016622
|
G | A | 9 | a0001c0009t0046g0127a0003c0003t0009g0083a0003c0003t0009g0085others(6): Show | 9 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-2546G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016622 | ||||||
chr22:40016883
|
C | T | 2 | a0001c0001t0086g0012a0001c0001t0087g0013 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.490-2285C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016883 | ||||||
chr22:40016960
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.490-2208G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016960 | ||||||
chr22:40016964
|
G | C | 1 | a0001c0001t0006g0076 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.490-2204G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016964 | ||||||
chr22:40016990
|
G | T | 2 | a0002c0002t0001g0010a0002c0002t0001g0177 | 3 | HG02258.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.490-2178G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016990 | ||||||
chr22:40017030
|
CTT | C | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2131_490-2130d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017030 | |||||
chr22:40017035
|
T | C | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2133T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017035 | ||||||
chr22:40017176
|
C | T | 1 | a0001c0001t0005g0056 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.490-1992C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017176 | ||||||
chr22:40017225
|
C | CT | 85 | a0001c0001t0003g0074a0001c0001t0003g0094a0001c0001t0006g0080others(82): Show | 88 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.490-1923dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017225 | |||||
chr22:40017225
|
C | CTT | 8 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0032g0124others(5): Show | 8 | HG01884.hp2 HG02132.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-1924_490-1923d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017225 | |||||
chr22:40017254
|
G | C | 2 | a0001c0009t0046g0127a0005c0013t0045g0132 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-1914G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017254 | ||||||
chr22:40017335
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.490-1833C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017335 | ||||||
chr22:40017360
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.490-1808G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017360 | ||||||
chr22:40017526
|
C | A | 1 | a0001c0001t0006g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.490-1642C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017526 | ||||||
chr22:40017616
|
G | T | 1 | a0001c0001t0071g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-1552G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017616 | ||||||
chr22:40017681
|
G | A | 1 | a0005c0013t0045g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.490-1487G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017681 | ||||||
chr22:40017848
|
A | AAC | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-1318_490-1317d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017848 | |||||
chr22:40018317
|
A | G | 3 | a0001c0001t0002g0120a0001c0001t0016g0109a0001c0001t0016g0111 | 3 | HG01978.hp1 HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.490-851A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018317 | ||||||
chr22:40018526
|
T | C | 71 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0074others(68): Show | 72 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.490-642T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018526 | ||||||
chr22:40018605
|
A | AT | 72 | a0001c0001t0013g0219a0001c0001t0032g0124a0001c0001t0033g0123others(69): Show | 75 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-547dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40018605 | |||||
chr22:40018605
|
AT | A | 26 | a0001c0001t0004g0027a0001c0001t0008g0182a0001c0001t0008g0183others(23): Show | 26 | HG01168.hp2 HG01243.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-547delT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40018605 | |||||
chr22:40018622
|
C | T | 2 | a0001c0009t0046g0127a0005c0013t0045g0132 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-546C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018622 | ||||||
chr22:40018654
|
G | C | 2 | a0001c0001t0020g0133a0001c0001t0020g0134 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.490-514G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018654 | ||||||
chr22:40019018
|
C | T | 5 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-150C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40019018 | ||||||
chr22:40019023
|
G | T | 2 | a0001c0009t0046g0127a0005c0013t0045g0132 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-145G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40019023 | ||||||
chr22:40019136
|
C | T | 71 | a0001c0001t0032g0124a0001c0001t0033g0123a0002c0002t0001g0010others(68): Show | 74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.490-32C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40019136 | ||||||
chr22:40019458
|
A | G | 1 | a0001c0001t0008g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657+123A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019458 | ||||||
chr22:40019465
|
T | C | 1 | a0001c0001t0017g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.657+130T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019465 | ||||||
chr22:40019491
|
A | T | 1 | a0002c0002t0001g0164 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.657+156A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019491 | ||||||
chr22:40019613
|
T | C | 51 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(48): Show | 52 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.658-274T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019613 | ||||||
chr22:40019651
|
T | A | 1 | a0007c0008t0079g0043 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.658-236T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019651 | ||||||
chr22:40019705
|
G | A | 71 | a0001c0001t0032g0124a0001c0001t0033g0123a0002c0002t0001g0010others(68): Show | 74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.658-182G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019705 | ||||||
chr22:40019760
|
C | T | 1 | a0001c0001t0048g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.658-127C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019760 | ||||||
chr22:40020021
|
G | A | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.779+13G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020021 | ||||||
chr22:40020081
|
C | T | 30 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(27): Show | 30 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.779+73C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020081 | ||||||
chr22:40020084
|
A | C | 4 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.779+76A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020084 | ||||||
chr22:40020221
|
G | A | 21 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(18): Show | 21 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.779+213G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020221 | ||||||
chr22:40020357
|
A | AT | 65 | a0001c0001t0002g0054a0001c0001t0002g0120a0001c0001t0003g0008others(62): Show | 66 | HG00639.hp1 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.779+372dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 40020357 | |||||
chr22:40020357
|
AT | A | 9 | a0001c0001t0002g0045a0001c0001t0004g0022a0001c0001t0004g0023others(6): Show | 9 | HG01168.hp2 HG02040.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.779+372delT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 40020357 | |||||
chr22:40020399
|
G | A | 1 | a0001c0001t0071g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.779+391G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020399 | ||||||
chr22:40020691
|
C | T | 2 | a0001c0001t0040g0192a0001c0001t0041g0193 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.780-599C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020691 | ||||||
chr22:40020855
|
A | G | 1 | a0002c0002t0007g0176 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.780-435A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020855 | ||||||
chr22:40020918
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.780-372G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020918 | ||||||
chr22:40021227
|
G | A | 1 | a0002c0002t0007g0158 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.780-63G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40021227 | ||||||
chr22:40022097
|
C | T | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.1453+134C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022097 | ||||||
chr22:40022135
|
C | T | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453+172C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022135 | ||||||
chr22:40022416
|
C | T | 1 | a0001c0001t0090g0021 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1453+453C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022416 | ||||||
chr22:40022502
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1453+539C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022502 | ||||||
chr22:40022506
|
G | A | 1 | a0001c0001t0055g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1453+543G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022506 | ||||||
chr22:40022649
|
C | T | 3 | a0001c0001t0023g0069a0001c0001t0078g0067a0001c0001t0085g0068 | 3 | HG02572.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1453+686C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022649 | ||||||
chr22:40022657
|
T | C | 1 | a0001c0001t0039g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1453+694T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022657 | ||||||
chr22:40022812
|
G | T | 1 | a0001c0001t0002g0045 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1453+849G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022812 | ||||||
chr22:40022900
|
C | T | 1 | a0002c0002t0014g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1453+937C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022900 | ||||||
chr22:40022927
|
G | C | 1 | a0001c0001t0091g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1453+964G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022927 | ||||||
chr22:40023084
|
C | T | 1 | a0002c0002t0007g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1453+1121C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023084 | ||||||
chr22:40023119
|
T | C | 57 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0074others(54): Show | 58 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1453+1156T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023119 | ||||||
chr22:40023150
|
C | G | 41 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0074others(38): Show | 42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1453+1187C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023150 | ||||||
chr22:40023170
|
C | T | 1 | a0002c0002t0001g0205 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1453+1207C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023170 | ||||||
chr22:40023328
|
C | G | 2 | a0002c0002t0074g0165a0002c0002t0075g0174 | 2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1453+1365C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023328 | ||||||
chr22:40023366
|
GCTC | G | 71 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0074others(68): Show | 72 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1453+1406_1453+140 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40023366 | |||||
chr22:40023613
|
C | T | 41 | a0001c0001t0003g0008a0001c0001t0003g0066a0001c0001t0003g0074others(38): Show | 42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1453+1650C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023613 | ||||||
chr22:40023651
|
G | A | 2 | a0001c0001t0086g0012a0001c0001t0087g0013 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1453+1688G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023651 | ||||||
chr22:40023801
|
G | A | 1 | a0001c0001t0049g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1453+1838G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023801 | ||||||
chr22:40023812
|
G | A | 70 | a0001c0001t0032g0124a0001c0001t0033g0123a0002c0002t0001g0010others(67): Show | 73 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1453+1849G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023812 | ||||||
chr22:40024256
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1453+2293C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024256 | ||||||
chr22:40024385
|
G | A | 1 | a0001c0001t0071g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1453+2422G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024385 | ||||||
chr22:40024514
|
C | T | 2 | a0001c0001t0002g0017a0001c0001t0023g0016 | 2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1453+2551C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024514 | ||||||
chr22:40024520
|
C | T | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.1453+2557C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024520 | ||||||
chr22:40024571
|
C | T | 2 | a0001c0001t0020g0133a0001c0001t0070g0203 | 2 | HG01884.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1453+2608C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024571 | ||||||
chr22:40024782
|
C | G | 13 | a0001c0001t0004g0007a0001c0001t0004g0018a0001c0001t0004g0027others(10): Show | 13 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1453+2819C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024782 | ||||||
chr22:40025061
|
C | T | 10 | a0001c0001t0071g0215a0001c0009t0046g0127a0003c0003t0009g0083others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1453+3098C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025061 | ||||||
chr22:40025484
|
A | G | 55 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(52): Show | 56 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1453+3521A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025484 | ||||||
chr22:40025912
|
G | A | 4 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-3604G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025912 | ||||||
chr22:40025936
|
C | T | 2 | a0001c0001t0036g0217a0001c0001t0038g0216 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1454-3580C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025936 | ||||||
chr22:40026046
|
G | A | 1 | a0002c0002t0065g0199 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1454-3470G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026046 | ||||||
chr22:40026117
|
C | T | 1 | a0001c0001t0039g0194 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1454-3399C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026117 | ||||||
chr22:40026210
|
C | T | 1 | a0001c0001t0091g0125 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1454-3306C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026210 | ||||||
chr22:40026211
|
G | A | 1 | a0001c0001t0047g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1454-3305G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026211 | ||||||
chr22:40026244
|
G | A | 17 | a0001c0001t0008g0182a0001c0001t0008g0183a0001c0001t0008g0184others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.1454-3272G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026244 | ||||||
chr22:40026291
|
T | G | 10 | a0001c0001t0047g0090a0001c0009t0046g0127a0003c0003t0009g0083others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-3225T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026291 | ||||||
chr22:40026416
|
A | G | 3 | a0001c0001t0002g0120a0001c0001t0016g0109a0001c0001t0016g0111 | 3 | HG01978.hp1 HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1454-3100A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026416 | ||||||
chr22:40026466
|
G | T | 1 | a0002c0002t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1454-3050G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026466 | ||||||
chr22:40026540
|
AC | A | 7 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0047g0090others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1454-2975delC | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026540 | ||||||
chr22:40026541
|
C | A | 7 | a0003c0003t0009g0083a0003c0003t0009g0085a0003c0003t0009g0086others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1454-2975C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026541 | ||||||
chr22:40026595
|
C | T | 1 | a0001c0001t0052g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1454-2921C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026595 | ||||||
chr22:40026683
|
C | T | 1 | a0001c0001t0040g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1454-2833C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026683 | ||||||
chr22:40026803
|
C | G | 10 | a0001c0001t0047g0090a0001c0009t0046g0127a0003c0003t0009g0083others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-2713C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026803 | ||||||
chr22:40026854
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1454-2662G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026854 | ||||||
chr22:40026929
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1454-2587C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026929 | ||||||
chr22:40027064
|
A | G | 1 | a0002c0002t0014g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1454-2452A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027064 | ||||||
chr22:40027340
|
C | G | 71 | a0001c0001t0032g0124a0001c0001t0033g0123a0002c0002t0001g0010others(68): Show | 74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1454-2176C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027340 | ||||||
chr22:40027343
|
G | A | 4 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-2173G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027343 | ||||||
chr22:40027435
|
G | A | 3 | a0001c0001t0047g0090a0001c0009t0046g0127a0005c0013t0045g0132 | 3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-2081G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027435 | ||||||
chr22:40027435
|
G | C | 42 | a0001c0001t0002g0120a0001c0001t0003g0008a0001c0001t0003g0066others(39): Show | 43 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1454-2081G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027435 | ||||||
chr22:40027447
|
G | A | 3 | a0001c0001t0047g0090a0001c0009t0046g0127a0005c0013t0045g0132 | 3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-2069G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027447 | ||||||
chr22:40027544
|
T | C | 11 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203others(8): Show | 11 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1454-1972T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027544 | ||||||
chr22:40027560
|
C | G | 3 | a0001c0001t0005g0051a0001c0001t0005g0052a0001c0001t0005g0056 | 3 | HG00642.hp2 HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1454-1956C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027560 | ||||||
chr22:40027592
|
C | G | 71 | a0001c0001t0032g0124a0001c0001t0033g0123a0002c0002t0001g0010others(68): Show | 74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1454-1924C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027592 | ||||||
chr22:40027645
|
T | C | 3 | a0001c0001t0047g0090a0001c0009t0046g0127a0005c0013t0045g0132 | 3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-1871T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027645 | ||||||
chr22:40027884
|
C | T | 2 | a0001c0001t0047g0090a0001c0009t0046g0127 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-1632C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027884 | ||||||
chr22:40027889
|
C | T | 2 | a0001c0001t0022g0064a0001c0001t0022g0065 | 2 | HG00639.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1454-1627C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027889 | ||||||
chr22:40027897
|
GT | G | 3 | a0002c0002t0007g0155a0002c0002t0007g0157a0002c0002t0007g0158 | 3 | HG01106.hp1 HG01258.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1454-1616delT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40027897 | |||||
chr22:40028071
|
A | T | 71 | a0001c0001t0032g0124a0001c0001t0033g0123a0002c0002t0001g0010others(68): Show | 74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1454-1445A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028071 | ||||||
chr22:40028098
|
G | A | 4 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-1418G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028098 | ||||||
chr22:40028221
|
G | C | 1 | a0002c0002t0061g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1454-1295G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028221 | ||||||
chr22:40028262
|
T | A | 4 | a0001c0001t0020g0133a0001c0001t0020g0134a0001c0001t0070g0203others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-1254T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028262 | ||||||
chr22:40028389
|
A | T | 3 | a0001c0001t0023g0069a0001c0001t0078g0067a0001c0001t0085g0068 | 3 | HG02572.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1454-1127A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028389 | ||||||
chr22:40028608
|
C | T | 4 | a0001c0001t0025g0139a0001c0001t0025g0140a0001c0001t0027g0137others(1): Show | 4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-908C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028608 | ||||||
chr22:40028611
|
G | A | 1 | a0002c0002t0010g0009 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1454-905G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028611 | ||||||
chr22:40028690
|
A | G | 10 | a0001c0001t0047g0090a0001c0009t0046g0127a0003c0003t0009g0083others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-826A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028690 | ||||||
chr22:40028776
|
C | T | 1 | a0001c0001t0048g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1454-740C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028776 | ||||||
chr22:40028788
|
G | A | 1 | a0002c0002t0069g0209 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1454-728G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028788 | ||||||
chr22:40028855
|
C | T | 10 | a0001c0001t0047g0090a0001c0009t0046g0127a0003c0003t0009g0083others(7): Show | 10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-661C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028855 | ||||||
chr22:40028901
|
G | A | 1 | a0002c0002t0001g0205 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1454-615G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028901 | ||||||
chr22:40028918
|
G | A | 6 | a0004c0004t0001g0142a0004c0004t0001g0145a0004c0004t0001g0149others(3): Show | 6 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454-598G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028918 | ||||||
chr22:40029058
|
A | G | 1 | a0002c0002t0010g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1454-458A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029058 | ||||||
chr22:40029075
|
C | T | 1 | a0001c0001t0003g0108 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1454-441C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029075 | ||||||
chr22:40029078
|
GAC | G | 3 | a0001c0001t0025g0139a0001c0001t0027g0137a0001c0001t0027g0138 | 3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1454-437_1454-436d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029078 | ||||||
chr22:40029078
|
GACGTGTG others(3): Show |
G | 2 | a0001c0001t0086g0012a0001c0001t0087g0013 | 2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1454-437_1454-428d others(12): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029078 | ||||||
chr22:40029078
|
GACGTGTG others(7): Show |
G | 2 | a0001c0001t0029g0135a0001c0001t0029g0136 | 2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1454-437_1454-424d others(16): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029078 | ||||||
chr22:40029079
|
A | G | 1 | a0001c0001t0025g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1454-437A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029079 | ||||||
chr22:40029080
|
C | CGT | 3 | a0002c0002t0034g0099a0002c0002t0062g0167a0002c0002t0069g0209 | 3 | HG03225.hp1 HG03471.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1454-384_1454-383d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
C | T | 1 | a0001c0001t0025g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1454-436C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029080 | ||||||
chr22:40029080
|
CGT | C | 35 | a0001c0001t0002g0035a0001c0001t0003g0094a0001c0001t0004g0002others(32): Show | 36 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1454-384_1454-383d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGT | C | 49 | a0001c0001t0002g0032a0001c0001t0002g0039a0001c0001t0002g0041others(46): Show | 53 | HG00733.hp2 HG01069.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1454-386_1454-383d others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGTGT | C | 35 | a0001c0001t0002g0006a0001c0001t0002g0059a0001c0001t0003g0101others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1454-388_1454-383d others(8): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGTGTG others(1): Show |
C | 26 | a0001c0001t0003g0008a0001c0001t0003g0074a0001c0001t0003g0107others(23): Show | 27 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1454-390_1454-383d others(10): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGTGTG others(3): Show |
C | 12 | a0001c0001t0002g0054a0001c0001t0003g0066a0001c0001t0023g0069others(9): Show | 12 | HG01255.hp1 HG01346.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1454-392_1454-383d others(12): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGTGTG others(5): Show |
C | 10 | a0001c0001t0002g0028a0001c0001t0004g0027a0001c0001t0006g0080others(7): Show | 10 | HG00673.hp1 HG01496.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454-394_1454-383d others(14): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGTGTG others(7): Show |
C | 13 | a0001c0001t0002g0019a0001c0001t0002g0031a0001c0001t0004g0023others(10): Show | 13 | HG02015.hp1 HG02040.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454-396_1454-383d others(16): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGTGTG others(9): Show |
C | 4 | a0001c0001t0006g0077a0002c0002t0019g0206a0002c0002t0019g0208others(1): Show | 4 | HG00639.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454-398_1454-383d others(18): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029080
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0004g0070 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1454-400_1454-383d others(20): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | |||||
chr22:40029132
|
T | A | 1 | a0002c0002t0001g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1454-384T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029132 | ||||||
chr22:40029167
|
A | C | 1 | a0001c0001t0008g0182 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1454-349A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029167 | ||||||
chr22:40029311
|
C | T | 1 | a0005c0013t0045g0132 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1454-205C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029311 |