geneid | 152877 |
---|---|
ensemblid | ENSG00000174137.14 |
hgncid | 31860 |
symbol | FAM53A |
name | family with sequence similarity 53 member A |
refseq_nuc | NM_001174070.3 |
refseq_prot | NP_001167541.1 |
ensembl_nuc | ENST00000308132.11 |
ensembl_prot | ENSP00000310057.6 |
mane_status | MANE Select |
chr | chr4 |
start | 1639887 |
end | 1684313 |
strand | - |
ver | v1.2 |
region | chr4:1639887-1684313 |
region5000 | chr4:1634887-1689313 |
regionname0 | FAM53A_chr4_1639887_1684313 |
regionname5000 | FAM53A_chr4_1634887_1689313 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 398 | 286 | 56 | 68 | 109 | 10 | 41 | 72 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002 | 0/0 | 398 | 48 | 31 | 8 | 9 | 0 | 0 | 7 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0003 | 0/0 | 398 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0004 | 0/0 | 398 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0005 | 0/0 | 398 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0006 | 0/0 | 398 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0007 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0008 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0009 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0010 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0011 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0012 | 0/0 | 398 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0013 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1197 | 229 | 50 | 51 | 97 | 6 | 23 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0002 | 0/0 | 1197 | 53 | 6 | 17 | 9 | 4 | 17 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0003 | 0/0 | 1197 | 48 | 31 | 8 | 9 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0004 | 0/0 | 1197 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0005 | 0/0 | 1197 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0006 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0007 | 0/0 | 1197 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0008 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0009 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0010 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0011 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0012 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0013 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0014 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0015 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0016 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0017 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
c0018 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1652 | 92 | 8 | 21 | 48 | 2 | 12 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0002 | 0/0 | 1595 | 24 | 11 | 3 | 10 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0003 | 0/0 | 1595 | 22 | 1 | 4 | 12 | 0 | 5 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0004 | 0/0 | 1782 | 20 | 2 | 8 | 1 | 2 | 7 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0005 | 1/0 | 1652 | 18 | 0 | 3 | 12 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0006 | 0/0 | 1652 | 16 | 0 | 3 | 7 | 3 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0007 | 0/0 | 1652 | 16 | 0 | 13 | 0 | 0 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0008 | 0/0 | 1652 | 14 | 0 | 4 | 7 | 0 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0009 | 0/0 | 1595 | 13 | 12 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0010 | 0/0 | 1652 | 11 | 0 | 0 | 11 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0011 | 0/0 | 1652 | 7 | 6 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0012 | 0/0 | 1652 | 6 | 6 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0013 | 0/0 | 1652 | 6 | 0 | 0 | 6 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0014 | 0/0 | 1652 | 5 | 0 | 3 | 0 | 1 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0015 | 0/0 | 1782 | 5 | 0 | 3 | 0 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0016 | 0/0 | 1652 | 5 | 5 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0017 | 0/0 | 1782 | 5 | 2 | 0 | 0 | 2 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0018 | 0/0 | 1595 | 4 | 1 | 2 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0019 | 0/0 | 1652 | 4 | 4 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0020 | 0/0 | 1595 | 4 | 2 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0021 | 0/0 | 1652 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0022 | 0/0 | 1595 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0023 | 0/0 | 1714 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0024 | 0/0 | 1714 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0025 | 0/0 | 1595 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0026 | 0/0 | 1656 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0027 | 0/0 | 1471 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0028 | 0/0 | 1652 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0029 | 0/0 | 1652 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0030 | 0/0 | 1533 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0031 | 0/0 | 1594 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0032 | 0/0 | 1595 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0033 | 0/0 | 1652 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0034 | 0/0 | 1652 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0035 | 0/0 | 1652 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0036 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0037 | 0/0 | 1535 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0038 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0039 | 0/0 | 1595 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0040 | 0/0 | 1656 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0041 | 0/0 | 1595 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0042 | 0/0 | 1652 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0043 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0044 | 0/0 | 1595 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0045 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0046 | 0/0 | 1594 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0047 | 0/0 | 1594 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0048 | 0/0 | 1652 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0049 | 0/0 | 1595 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0050 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0051 | 0/0 | 1652 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0052 | 0/0 | 1590 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0053 | 0/0 | 1652 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0054 | 0/0 | 1652 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0055 | 0/0 | 1652 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0056 | 0/0 | 1714 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0057 | 0/0 | 1714 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0058 | 0/0 | 1652 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0059 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0060 | 0/0 | 1658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
t0061 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1197 | 229 | 50 | 51 | 97 | 6 | 23 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002 | 0/0 | 1197 | 53 | 6 | 17 | 9 | 4 | 17 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0010 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0013 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0014 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0017 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003 | 0/0 | 1197 | 48 | 31 | 8 | 9 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0003c0004 | 0/0 | 1197 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0004c0007 | 0/0 | 1197 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0005c0006 | 0/0 | 1197 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0006c0005 | 0/0 | 1197 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0007c0015 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0008c0016 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0009c0018 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0010c0011 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0011c0012 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0012c0009 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0013c0008 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2848 | 89 | 8 | 21 | 45 | 2 | 12 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0003 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0005 | 1/0 | 2848 | 18 | 0 | 3 | 12 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0006 | 0/0 | 2848 | 16 | 0 | 3 | 7 | 3 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0007 | 0/0 | 2848 | 16 | 0 | 13 | 0 | 0 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0008 | 0/0 | 2848 | 14 | 0 | 4 | 7 | 0 | 3 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0009 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0010 | 0/0 | 2848 | 10 | 0 | 0 | 10 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0011 | 0/0 | 2848 | 6 | 5 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0012 | 0/0 | 2848 | 6 | 6 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0013 | 0/0 | 2848 | 5 | 0 | 0 | 5 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0014 | 0/0 | 2848 | 4 | 0 | 3 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0016 | 0/0 | 2848 | 5 | 5 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0019 | 0/0 | 2848 | 4 | 4 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0021 | 0/0 | 2848 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0023 | 0/0 | 2910 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0024 | 0/0 | 2910 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0026 | 0/0 | 2852 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0027 | 0/0 | 2667 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0028 | 0/0 | 2848 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0029 | 0/0 | 2848 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0031 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0033 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0034 | 0/0 | 2848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0035 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0037 | 0/0 | 2731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0040 | 0/0 | 2852 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0042 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0043 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0046 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0047 | 0/0 | 2790 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0048 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0051 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0052 | 0/0 | 2786 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0053 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0054 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0055 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0056 | 0/0 | 2910 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0057 | 0/0 | 2910 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0001t0058 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0003 | 0/0 | 2791 | 18 | 0 | 4 | 9 | 0 | 5 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0004 | 0/0 | 2978 | 18 | 2 | 8 | 0 | 2 | 6 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0015 | 0/0 | 2978 | 5 | 0 | 3 | 0 | 0 | 2 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0017 | 0/0 | 2978 | 5 | 2 | 0 | 0 | 2 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0032 | 0/0 | 2791 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0036 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0041 | 0/0 | 2791 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0049 | 0/0 | 2791 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0050 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0059 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0002t0060 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0010t0001 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0013t0013 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0014t0001 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0001c0017t0004 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0002 | 0/0 | 2791 | 22 | 11 | 3 | 8 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0009 | 0/0 | 2791 | 12 | 11 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0011 | 0/0 | 2848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0018 | 0/0 | 2791 | 4 | 1 | 2 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0020 | 0/0 | 2791 | 3 | 1 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0025 | 0/0 | 2791 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0030 | 0/0 | 2729 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0039 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0002c0003t0044 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0003c0004t0022 | 0/0 | 2791 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0004c0007t0003 | 0/0 | 2791 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0005c0006t0038 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0005c0006t0061 | 0/0 | 2911 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0006c0005t0002 | 0/0 | 2791 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0007c0015t0001 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0008c0016t0003 | 0/0 | 2791 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0009c0018t0004 | 0/0 | 2978 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0010c0011t0045 | 0/0 | 2792 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0011c0012t0010 | 0/0 | 2848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0012c0009t0014 | 0/0 | 2848 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
a0013c0008t0020 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | copy fasta | chr4 | 1634887 | 1689313 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0008g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0011g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0011g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0011g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0012g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0013g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0013g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0013g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0013g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0014g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0014g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0014g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0014g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0016g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0016g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0016g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0019g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0021g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0021g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0021g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0023g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0023g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0024g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0024g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0026g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0026g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0027g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0027g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0028g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0028g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0029g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0029g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0031g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0033g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0034g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0035g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0037g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0040g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0042g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0043g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0046g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0047g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0048g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0051g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0052g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0053g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0054g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0055g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0056g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0057g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0001t0058g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0015g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0015g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0015g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0015g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0015g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0017g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0017g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0017g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0017g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0032g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0036g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0041g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0049g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0050g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0059g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0002t0060g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0010t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0013t0013g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0014t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0001c0017t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0018g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0018g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0018g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0018g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0020g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0020g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0020g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0025g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0025g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0030g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0030g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0039g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0002c0003t0044g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0003c0004t0022g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0003c0004t0022g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0003c0004t0022g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0004c0007t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0004c0007t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0005c0006t0038g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0005c0006t0061g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0006c0005t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0007c0015t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0008c0016t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0009c0018t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0010c0011t0045g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0011c0012t0010g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0012c0009t0014g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
a0013c0008t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00099 | hp2 | a0001 | c0002 | t0017 | g0003 | EUR | GBR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00280 | hp1 | a0001 | c0002 | t0004 | g0309 | EUR | FIN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0047 | EUR | FIN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00408 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00423 | hp1 | a0001 | c0001 | t0021 | g0103 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00423 | hp2 | a0001 | c0001 | t0008 | g0257 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00438 | hp1 | a0001 | c0010 | t0001 | g0243 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00438 | hp2 | a0001 | c0001 | t0051 | g0192 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0271 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00558 | hp1 | a0001 | c0001 | t0010 | g0029 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00609 | hp1 | a0001 | c0013 | t0013 | g0252 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00609 | hp2 | a0001 | c0001 | t0013 | g0258 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0330 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00621 | hp2 | a0001 | c0001 | t0010 | g0034 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00639 | hp1 | a0001 | c0002 | t0004 | g0302 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0303 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00673 | hp2 | a0001 | c0001 | t0008 | g0233 | EAS | CHS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00733 | hp1 | a0002 | c0003 | t0018 | g0021 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00735 | hp1 | a0001 | c0002 | t0004 | g0266 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00735 | hp2 | a0001 | c0001 | t0034 | g0053 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0161 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG00738 | hp2 | a0001 | c0001 | t0014 | g0019 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0121 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01070 | hp2 | a0001 | c0002 | t0003 | g0200 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0120 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01074 | hp2 | a0001 | c0002 | t0015 | g0016 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0072 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01106 | hp2 | a0001 | c0002 | t0004 | g0326 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01109 | hp1 | a0002 | c0003 | t0020 | g0319 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0071 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01167 | hp1 | a0001 | c0001 | t0011 | g0136 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01168 | hp1 | a0001 | c0001 | t0014 | g0014 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01168 | hp2 | a0001 | c0002 | t0015 | g0058 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01169 | hp2 | a0001 | c0002 | t0015 | g0059 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01243 | hp1 | a0001 | c0002 | t0004 | g0144 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01243 | hp2 | a0002 | c0003 | t0009 | g0113 | AMR | PUR | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01255 | hp1 | a0001 | c0001 | t0024 | g0063 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01256 | hp1 | a0001 | c0001 | t0008 | g0262 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01257 | hp1 | a0002 | c0003 | t0002 | g0008 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01257 | hp2 | a0001 | c0002 | t0004 | g0158 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01258 | hp2 | a0002 | c0003 | t0002 | g0008 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01358 | hp2 | a0001 | c0002 | t0004 | g0305 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01361 | hp1 | a0001 | c0002 | t0004 | g0308 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0203 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0070 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01496 | hp2 | a0001 | c0001 | t0052 | g0222 | AMR | CLM | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0207 | EUR | IBS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0048 | EUR | IBS | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01884 | hp1 | a0002 | c0003 | t0002 | g0325 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01884 | hp2 | a0001 | c0001 | t0012 | g0100 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01891 | hp1 | a0002 | c0003 | t0009 | g0068 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01891 | hp2 | a0002 | c0003 | t0002 | g0138 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0315 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01943 | hp1 | a0002 | c0003 | t0002 | g0298 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01952 | hp1 | a0001 | c0001 | t0008 | g0264 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01952 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01975 | hp1 | a0002 | c0003 | t0020 | g0301 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0073 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01978 | hp1 | a0001 | c0001 | t0014 | g0020 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0077 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01981 | hp1 | a0001 | c0002 | t0032 | g0017 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01981 | hp2 | a0001 | c0002 | t0041 | g0066 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01993 | hp1 | a0001 | c0001 | t0007 | g0082 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0080 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0208 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02027 | hp2 | a0002 | c0003 | t0002 | g0188 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02040 | hp2 | a0009 | c0018 | t0004 | g0322 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0137 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02055 | hp2 | a0001 | c0001 | t0026 | g0328 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02071 | hp2 | a0011 | c0012 | t0010 | g0038 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02080 | hp2 | a0001 | c0002 | t0003 | g0267 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02132 | hp1 | a0008 | c0016 | t0003 | g0196 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02132 | hp2 | a0002 | c0003 | t0002 | g0250 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02135 | hp1 | a0001 | c0001 | t0008 | g0190 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02135 | hp2 | a0001 | c0001 | t0021 | g0095 | EAS | KHV | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02145 | hp1 | a0002 | c0003 | t0002 | g0139 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02145 | hp2 | a0001 | c0001 | t0027 | g0132 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0092 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02148 | hp2 | a0001 | c0001 | t0007 | g0075 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02165 | hp1 | a0001 | c0001 | t0023 | g0032 | EAS | CDX | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02257 | hp1 | a0005 | c0006 | t0038 | g0011 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02257 | hp2 | a0002 | c0003 | t0002 | g0279 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02258 | hp1 | a0001 | c0001 | t0057 | g0141 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02258 | hp2 | a0010 | c0011 | t0045 | g0123 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02273 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02280 | hp1 | a0001 | c0001 | t0026 | g0327 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02280 | hp2 | a0001 | c0001 | t0042 | g0097 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02293 | hp1 | a0002 | c0003 | t0018 | g0023 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0201 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0076 | AMR | PEL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0273 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0338 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0118 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02572 | hp2 | a0001 | c0001 | t0019 | g0277 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02602 | hp1 | a0001 | c0002 | t0004 | g0311 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02602 | hp2 | a0001 | c0002 | t0017 | g0069 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02615 | hp1 | a0002 | c0003 | t0025 | g0124 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02615 | hp2 | a0001 | c0002 | t0004 | g0140 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0272 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02622 | hp2 | a0002 | c0003 | t0002 | g0314 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02630 | hp1 | a0002 | c0003 | t0009 | g0115 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02630 | hp2 | a0001 | c0001 | t0047 | g0318 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02647 | hp1 | a0001 | c0001 | t0043 | g0117 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02647 | hp2 | a0002 | c0003 | t0018 | g0018 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02698 | hp1 | a0001 | c0001 | t0007 | g0074 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02698 | hp2 | a0001 | c0002 | t0015 | g0050 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02717 | hp2 | a0013 | c0008 | t0020 | g0280 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02723 | hp1 | a0002 | c0003 | t0009 | g0116 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02723 | hp2 | a0001 | c0001 | t0056 | g0130 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0333 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0306 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02809 | hp1 | a0002 | c0003 | t0011 | g0146 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02809 | hp2 | a0002 | c0003 | t0009 | g0105 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02818 | hp1 | a0002 | c0003 | t0009 | g0119 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02818 | hp2 | a0001 | c0001 | t0016 | g0062 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02886 | hp1 | a0002 | c0003 | t0030 | g0135 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02895 | hp1 | a0001 | c0001 | t0019 | g0276 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02895 | hp2 | a0002 | c0003 | t0002 | g0156 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02896 | hp1 | a0002 | c0003 | t0025 | g0112 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02896 | hp2 | a0002 | c0003 | t0009 | g0107 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02897 | hp1 | a0002 | c0003 | t0009 | g0106 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02897 | hp2 | a0001 | c0001 | t0019 | g0278 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02922 | hp1 | a0001 | c0001 | t0027 | g0157 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02922 | hp2 | a0001 | c0002 | t0050 | g0274 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0108 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02965 | hp2 | a0003 | c0004 | t0022 | g0150 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02970 | hp1 | a0001 | c0001 | t0016 | g0125 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02970 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02976 | hp1 | a0001 | c0001 | t0033 | g0012 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02976 | hp2 | a0001 | c0001 | t0037 | g0057 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03017 | hp2 | a0001 | c0002 | t0004 | g0310 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03041 | hp1 | a0005 | c0006 | t0061 | g0142 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03041 | hp2 | a0002 | c0003 | t0009 | g0122 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03098 | hp1 | a0002 | c0003 | t0002 | g0281 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0110 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03130 | hp1 | a0002 | c0003 | t0002 | g0323 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03130 | hp2 | a0001 | c0001 | t0016 | g0098 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03195 | hp1 | a0002 | c0003 | t0030 | g0147 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0065 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03209 | hp1 | a0001 | c0001 | t0028 | g0321 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03209 | hp2 | a0002 | c0003 | t0002 | g0275 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03239 | hp1 | a0001 | c0002 | t0036 | g0054 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03239 | hp2 | a0001 | c0001 | t0006 | g0044 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03453 | hp1 | a0002 | c0003 | t0002 | g0145 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03453 | hp2 | a0001 | c0002 | t0017 | g0126 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03486 | hp1 | a0001 | c0001 | t0054 | g0269 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03486 | hp2 | a0001 | c0001 | t0019 | g0133 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0263 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0199 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03491 | hp2 | a0001 | c0001 | t0008 | g0154 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03492 | hp1 | a0001 | c0001 | t0008 | g0155 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03492 | hp2 | a0001 | c0002 | t0003 | g0194 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03516 | hp1 | a0002 | c0003 | t0009 | g0127 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0134 | AFR | ESN | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03540 | hp2 | a0002 | c0003 | t0039 | g0055 | AFR | GWD | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03579 | hp1 | a0003 | c0004 | t0022 | g0316 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0149 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03654 | hp1 | a0001 | c0002 | t0003 | g0335 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0051 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0153 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03688 | hp2 | a0001 | c0001 | t0007 | g0078 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03704 | hp2 | a0012 | c0009 | t0014 | g0013 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0304 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03710 | hp2 | a0001 | c0002 | t0049 | g0332 | SAS | PJL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0081 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0159 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0036 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0093 | SAS | BEB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04115 | hp2 | a0001 | c0002 | t0004 | g0282 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04199 | hp1 | a0001 | c0001 | t0007 | g0079 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04204 | hp2 | a0001 | c0002 | t0015 | g0015 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04228 | hp1 | a0001 | c0017 | t0004 | g0162 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | STU | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18522 | hp1 | a0002 | c0003 | t0044 | g0104 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18612 | hp1 | a0001 | c0001 | t0029 | g0165 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0329 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0060 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18939 | hp1 | a0001 | c0001 | t0008 | g0256 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18947 | hp2 | a0001 | c0001 | t0010 | g0026 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18950 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18951 | hp1 | a0006 | c0005 | t0002 | g0009 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18951 | hp2 | a0001 | c0001 | t0010 | g0031 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18952 | hp2 | a0001 | c0001 | t0010 | g0041 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18953 | hp2 | a0001 | c0001 | t0013 | g0255 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18954 | hp2 | a0002 | c0003 | t0002 | g0251 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0084 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18956 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18957 | hp1 | a0001 | c0001 | t0053 | g0293 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0030 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18961 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18963 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18965 | hp2 | a0007 | c0015 | t0001 | g0212 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18969 | hp2 | a0002 | c0003 | t0002 | g0204 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18970 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18977 | hp1 | a0002 | c0003 | t0018 | g0022 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18979 | hp1 | a0001 | c0001 | t0010 | g0039 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18979 | hp2 | a0002 | c0003 | t0002 | g0205 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18990 | hp1 | a0001 | c0001 | t0021 | g0094 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18990 | hp2 | a0002 | c0003 | t0002 | g0186 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18991 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18994 | hp1 | a0002 | c0003 | t0002 | g0206 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18998 | hp2 | a0001 | c0001 | t0013 | g0253 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18999 | hp1 | a0001 | c0001 | t0029 | g0217 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19003 | hp2 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19009 | hp2 | a0004 | c0007 | t0003 | g0334 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19010 | hp1 | a0001 | c0014 | t0001 | g0242 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19010 | hp2 | a0004 | c0007 | t0003 | g0331 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19030 | hp2 | a0001 | c0001 | t0040 | g0067 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19063 | hp1 | a0001 | c0001 | t0058 | g0227 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19066 | hp1 | a0001 | c0001 | t0023 | g0033 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19068 | hp2 | a0001 | c0001 | t0013 | g0254 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19070 | hp2 | a0006 | c0005 | t0002 | g0009 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19077 | hp1 | a0001 | c0001 | t0013 | g0261 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19077 | hp2 | a0001 | c0001 | t0055 | g0164 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19078 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19079 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19087 | hp2 | a0002 | c0003 | t0002 | g0187 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19240 | hp1 | a0001 | c0001 | t0024 | g0102 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | YRI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20129 | hp1 | a0001 | c0002 | t0060 | g0324 | AFR | ASW | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ASW | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20752 | hp1 | a0001 | c0001 | t0014 | g0052 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20752 | hp2 | a0001 | c0002 | t0017 | g0003 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0043 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20905 | hp2 | a0001 | c0002 | t0059 | g0307 | SAS | GIH | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02109 | hp1 | a0001 | c0001 | t0016 | g0099 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02109 | hp2 | a0001 | c0001 | t0031 | g0049 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02486 | hp1 | a0001 | c0001 | t0035 | g0056 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02559 | hp1 | a0003 | c0004 | t0022 | g0131 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG02559 | hp2 | a0002 | c0003 | t0002 | g0312 | AFR | ACB | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03471 | hp1 | a0002 | c0003 | t0020 | g0148 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG03471 | hp2 | a0001 | c0002 | t0004 | g0317 | AFR | MSL | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG06807 | hp1 | a0001 | c0001 | t0046 | g0129 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
HG06807 | hp2 | a0001 | c0001 | t0048 | g0151 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18955 | hp1 | a0001 | c0001 | t0008 | g0211 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20300 | hp1 | a0002 | c0003 | t0009 | g0114 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | USA | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA21309 | hp1 | a0002 | c0003 | t0009 | g0109 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
NA21309 | hp2 | a0001 | c0002 | t0017 | g0096 | AFR | LWK | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0061 | REF | REF | FAM53A_chr4_1634887_1689313 | FAM53A | chr4 | 1634887 | 1689313 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1641397
|
G | A | 1 | a0009 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1093C>T | p.Arg365Cys | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1338/2848 | 1093/1197 | 365/398 | chr4 | 1641397 | ||
chr4:1641477
|
C | T | 1 | a0006 | 2 | NA18951.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.1013G>A | p.Cys338Tyr | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1258/2848 | 1013/1197 | 338/398 | chr4 | 1641477 | ||
chr4:1655033
|
C | T | 1 | a0003 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.827G>A | p.Arg276His | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1072/2848 | 827/1197 | 276/398 | chr4 | 1655033 | ||
chr4:1655049
|
G | C | 1 | a0005 | 2 | HG02257.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.811C>G | p.Arg271Gly | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1056/2848 | 811/1197 | 271/398 | chr4 | 1655049 | ||
chr4:1655109
|
C | T | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.751G>A | p.Gly251Arg | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 996/2848 | 751/1197 | 251/398 | chr4 | 1655109 | ||
chr4:1655129
|
G | A | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.731C>T | p.Thr244Met | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 976/2848 | 731/1197 | 244/398 | chr4 | 1655129 | ||
chr4:1655156
|
G | C | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.704C>G | p.Pro235Arg | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 949/2848 | 704/1197 | 235/398 | chr4 | 1655156 | ||
chr4:1655255
|
G | A | 1 | a0011 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.605C>T | p.Ala202Val | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 850/2848 | 605/1197 | 202/398 | chr4 | 1655255 | ||
chr4:1655400
|
C | T | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.460G>A | p.Asp154Asn | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 705/2848 | 460/1197 | 154/398 | chr4 | 1655400 | ||
chr4:1655423
|
G | C | 1 | a0004 | 2 | NA19009.hp2 NA19010.hp2 |
missense_variant | MODERATE | c.437C>G | p.Thr146Ser | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 682/2848 | 437/1197 | 146/398 | chr4 | 1655423 | ||
chr4:1655459
|
C | G | 1 | a0008 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.401G>C | p.Arg134Pro | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 646/2848 | 401/1197 | 134/398 | chr4 | 1655459 | ||
chr4:1655469
|
C | G | 1 | a0013 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.391G>C | p.Val131Leu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 636/2848 | 391/1197 | 131/398 | chr4 | 1655469 | ||
chr4:1655522
|
G | A | 1 | a0007 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.338C>T | p.Thr113Met | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 583/2848 | 338/1197 | 113/398 | chr4 | 1655522 | ||
chr4:1657435
|
C | T | 3 | a0002a0006a0013 | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
missense_variant | MODERATE | c.109G>A | p.Gly37Ser | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/5 | 354/2848 | 109/1197 | 37/398 | chr4 | 1657435 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1641311
|
C | T | 1 | a0001c0010 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1179G>A | p.Glu393Glu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1424/2848 | 1179/1197 | 393/398 | chr4 | 1641311 | ||
chr4:1655074
|
A | C | 6 | a0001c0002a0001c0017a0004c0007others(3): Show | 59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
synonymous_variant | LOW | c.786T>G | p.Pro262Pro | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1031/2848 | 786/1197 | 262/398 | chr4 | 1655074 | ||
chr4:1655095
|
C | G | 1 | a0005c0006 | 2 | HG02257.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.765G>C | p.Leu255Leu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 1010/2848 | 765/1197 | 255/398 | chr4 | 1655095 | ||
chr4:1655164
|
C | T | 1 | a0001c0017 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.696G>A | p.Ala232Ala | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 941/2848 | 696/1197 | 232/398 | chr4 | 1655164 | ||
chr4:1655230
|
G | A | 1 | a0003c0004 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.630C>T | p.Ser210Ser | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 875/2848 | 630/1197 | 210/398 | chr4 | 1655230 | ||
chr4:1655314
|
G | A | 1 | a0001c0013 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.546C>T | p.Pro182Pro | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 791/2848 | 546/1197 | 182/398 | chr4 | 1655314 | ||
chr4:1655401
|
G | A | 1 | a0001c0014 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.459C>T | p.Cys153Cys | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 704/2848 | 459/1197 | 153/398 | chr4 | 1655401 | ||
chr4:1655476
|
C | T | 1 | a0003c0004 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.384G>A | p.Glu128Glu | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 629/2848 | 384/1197 | 128/398 | chr4 | 1655476 | ||
chr4:1655554
|
G | A | 5 | a0001c0002a0001c0017a0004c0007others(2): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
synonymous_variant | LOW | c.306C>T | p.Thr102Thr | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/5 | 551/2848 | 306/1197 | 102/398 | chr4 | 1655554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1639895
|
T | C | 1 | a0001c0002t0059 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1398A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1398 | chr4 | 1639895 | |||||
chr4:1639968
|
G | T | 9 | a0001c0002t0004a0001c0002t0015a0001c0002t0017others(6): Show | 34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1325C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1325 | chr4 | 1639968 | |||||
chr4:1640002
|
C | T | 1 | a0003c0004t0022 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1291G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1291 | chr4 | 1640002 | |||||
chr4:1640033
|
G | A | 1 | a0001c0002t0049 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1260 | chr4 | 1640033 | |||||
chr4:1640094
|
T | G | 1 | a0001c0001t0029 | 2 | NA18612.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1199A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1199 | chr4 | 1640094 | |||||
chr4:1640182
|
G | A | 2 | a0001c0001t0026a0001c0001t0040 | 3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 1111 | chr4 | 1640182 | |||||
chr4:1640311
|
C | T | 4 | a0002c0003t0020a0002c0003t0039a0002c0003t0044others(1): Show | 6 | HG01109.hp1 HG01975.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*982G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 982 | chr4 | 1640311 | |||||
chr4:1640334
|
C | T | 1 | a0001c0001t0034 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*959G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 959 | chr4 | 1640334 | |||||
chr4:1640339
|
G | C | 1 | a0001c0001t0028 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*954C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 954 | chr4 | 1640339 | |||||
chr4:1640344
|
G | GA | 13 | a0001c0001t0037a0001c0002t0004a0001c0002t0015others(10): Show | 38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*948_*949insT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 948 | chr4 | 1640344 | |||||
chr4:1640437
|
C | T | 5 | a0001c0001t0010a0001c0001t0013a0001c0001t0021others(2): Show | 20 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 856 | chr4 | 1640437 | |||||
chr4:1640612
|
C | T | 1 | a0001c0001t0031 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 681 | chr4 | 1640612 | |||||
chr4:1640619
|
T | C | 1 | a0001c0001t0053 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 674 | chr4 | 1640619 | |||||
chr4:1640623
|
C | T | 2 | a0001c0001t0024a0001c0001t0056 | 3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*670G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 670 | chr4 | 1640623 | |||||
chr4:1640639
|
G | T | 1 | a0001c0001t0046 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*654C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 654 | chr4 | 1640639 | |||||
chr4:1640647
|
A | G | 60 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(57): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*646T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 646 | chr4 | 1640647 | |||||
chr4:1640674
|
T | G | 11 | a0001c0002t0004a0001c0002t0015a0001c0002t0017others(8): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*619A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 619 | chr4 | 1640674 | |||||
chr4:1640683
|
G | C | 11 | a0001c0002t0004a0001c0002t0015a0001c0002t0017others(8): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*610C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 610 | chr4 | 1640683 | |||||
chr4:1640694
|
A | G | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 599 | chr4 | 1640694 | |||||
chr4:1640707
|
C | T | 2 | a0005c0006t0038a0005c0006t0061 | 2 | HG02257.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*586G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 586 | chr4 | 1640707 | |||||
chr4:1640715
|
G | A | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 578 | chr4 | 1640715 | |||||
chr4:1640715
|
GTGGCCCC others(55): Show |
G | 1 | a0002c0003t0030 | 2 | HG02886.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516_*577delTGGCTG others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 516 | chr4 | 1640715 | |||||
chr4:1640728
|
A | G | 35 | a0001c0001t0003a0001c0001t0009a0001c0001t0027others(32): Show | 120 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*565T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 565 | chr4 | 1640728 | |||||
chr4:1640754
|
C | T | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*539G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 539 | chr4 | 1640754 | |||||
chr4:1640755
|
A | G | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*538T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 538 | chr4 | 1640755 | |||||
chr4:1640766
|
C | A | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 527 | chr4 | 1640766 | |||||
chr4:1640769
|
T | C | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 524 | chr4 | 1640769 | |||||
chr4:1640769
|
T | TGGCAGCC others(55): Show |
2 | a0001c0001t0024a0001c0001t0056 | 3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*462_*523dupGCCTGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 523 | chr4 | 1640769 | |||||
chr4:1640769
|
TGGCAGCC others(55): Show |
T | 1 | a0001c0001t0052 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*462_*523delGCCTGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 462 | chr4 | 1640769 | |||||
chr4:1640770
|
G | A | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*523C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 523 | chr4 | 1640770 | |||||
chr4:1640792
|
T | A | 9 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(6): Show | 68 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*501A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 501 | chr4 | 1640792 | |||||
chr4:1640806
|
C | G | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*487G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 487 | chr4 | 1640806 | |||||
chr4:1640817
|
G | A | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 476 | chr4 | 1640817 | |||||
chr4:1640820
|
G | T | 8 | a0001c0001t0003a0001c0001t0027a0001c0002t0003others(5): Show | 27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*473C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 473 | chr4 | 1640820 | |||||
chr4:1640839
|
A | G | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 454 | chr4 | 1640839 | |||||
chr4:1640868
|
CTCTGTGC others(55): Show |
C | 2 | a0001c0001t0046a0001c0001t0047 | 2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*363_*424delCTAGGT others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 363 | chr4 | 1640868 | |||||
chr4:1640878
|
T | C | 18 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(15): Show | 83 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*415A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 415 | chr4 | 1640878 | |||||
chr4:1640879
|
G | A | 2 | a0001c0001t0031a0001c0002t0060 | 2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 414 | chr4 | 1640879 | |||||
chr4:1640890
|
A | C | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 403 | chr4 | 1640890 | |||||
chr4:1640894
|
A | G | 2 | a0001c0001t0031a0001c0002t0060 | 2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*399T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 399 | chr4 | 1640894 | |||||
chr4:1640901
|
A | G | 2 | a0001c0001t0031a0001c0002t0060 | 2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*392T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 392 | chr4 | 1640901 | |||||
chr4:1640920
|
A | T | 1 | a0001c0001t0051 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 373 | chr4 | 1640920 | |||||
chr4:1640930
|
G | C | 2 | a0001c0001t0031a0001c0002t0060 | 2 | HG02109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*363C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 363 | chr4 | 1640930 | |||||
chr4:1640930
|
GTCTGTGC others(54): Show |
G | 1 | a0001c0001t0037 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*302_*362delGTAGGT others(55): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 302 | chr4 | 1640930 | |||||
chr4:1640951
|
A | C | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 342 | chr4 | 1640951 | |||||
chr4:1640954
|
CGGCAGCC others(55): Show |
C | 1 | a0001c0001t0043 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*277_*338delACCGGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 277 | chr4 | 1640954 | |||||
chr4:1640959
|
G | T | 1 | a0001c0001t0019 | 4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*334C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 334 | chr4 | 1640959 | |||||
chr4:1641013
|
C | A | 2 | a0001c0001t0046a0001c0001t0047 | 2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*280G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 280 | chr4 | 1641013 | |||||
chr4:1641016
|
T | A | 20 | a0001c0001t0003a0001c0001t0009a0001c0001t0027others(17): Show | 79 | HG00544.hp1 HG00621.hp1 HG00733.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*277A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 277 | chr4 | 1641016 | |||||
chr4:1641016
|
T | C | 18 | a0001c0001t0037a0001c0001t0042a0001c0001t0046others(15): Show | 45 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*277A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 277 | chr4 | 1641016 | |||||
chr4:1641016
|
T | TGGCAGCC others(55): Show |
2 | a0001c0001t0023a0001c0001t0057 | 3 | HG02165.hp1 HG02258.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*215_*276dupGCCGGC others(56): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 276 | chr4 | 1641016 | |||||
chr4:1641024
|
G | A | 2 | a0001c0001t0026a0001c0001t0040 | 3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*269C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 269 | chr4 | 1641024 | |||||
chr4:1641078
|
C | A | 2 | a0001c0001t0046a0001c0001t0047 | 2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*215G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 215 | chr4 | 1641078 | |||||
chr4:1641086
|
GTGGCCCC others(174): Show |
G | 1 | a0001c0001t0027 | 2 | HG02145.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*26_*206del | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 26 | chr4 | 1641086 | |||||
chr4:1641094
|
G | A | 2 | a0001c0001t0046a0001c0001t0047 | 2 | HG02630.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*199C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 199 | chr4 | 1641094 | |||||
chr4:1641099
|
G | A | 8 | a0001c0001t0003a0001c0002t0003a0001c0002t0032others(5): Show | 28 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 194 | chr4 | 1641099 | |||||
chr4:1641138
|
G | GGGCCGTG others(50): Show |
2 | a0005c0006t0038a0005c0006t0061 | 2 | HG02257.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*154_*155insTGGCAC others(51): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 154 | chr4 | 1641138 | |||||
chr4:1641144
|
AGCCGTGG others(50): Show |
A | 22 | a0001c0001t0003a0001c0001t0009a0001c0001t0031others(19): Show | 82 | HG00544.hp1 HG00621.hp1 HG00733.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*92_*148delCCGGCAC others(50): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 92 | chr4 | 1641144 | |||||
chr4:1641147
|
C | T | 1 | a0001c0002t0060 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 146 | chr4 | 1641147 | |||||
chr4:1641148
|
G | A | 1 | a0001c0002t0036 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 145 | chr4 | 1641148 | |||||
chr4:1641201
|
G | GCGGCA | 7 | a0001c0001t0026a0001c0001t0040a0001c0001t0046others(4): Show | 8 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*91_*92insTGCCG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 91 | chr4 | 1641201 | |||||
chr4:1641201
|
G | GCGGCAGC others(60): Show |
1 | a0001c0002t0050 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*91_*92insTGCCGCCG others(59): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 91 | chr4 | 1641201 | |||||
chr4:1641201
|
G | GCGGCAGC others(122): Show |
7 | a0001c0002t0004a0001c0002t0015a0001c0002t0017others(4): Show | 32 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*91_*92insTGCCGCCG others(121): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 91 | chr4 | 1641201 | |||||
chr4:1641204
|
C | T | 1 | a0001c0002t0050 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 89 | chr4 | 1641204 | |||||
chr4:1641213
|
G | A | 11 | a0001c0001t0009a0002c0003t0002a0002c0003t0009others(8): Show | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*80C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 80 | chr4 | 1641213 | |||||
chr4:1641236
|
C | G | 7 | a0001c0001t0003a0001c0002t0003a0001c0002t0032others(4): Show | 25 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*57G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 5/5 | 57 | chr4 | 1641236 | |||||
chr4:1668765
|
C | T | 1 | a0001c0001t0048 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 24 | chr4 | 1668765 | |||||
chr4:1668781
|
T | C | 1 | a0010c0011t0045 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 40 | chr4 | 1668781 | |||||
chr4:1668790
|
G | A | 1 | a0002c0003t0025 | 2 | HG02615.hp1 HG02896.hp1 |
5_prime_UTR_variant | MODIFIER | c.-49C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 49 | chr4 | 1668790 | |||||
chr4:1668875
|
TC | T | 5 | a0001c0001t0026a0001c0001t0031a0001c0001t0040others(2): Show | 6 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-135delG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/5 | 135 | chr4 | 1668875 | |||||
chr4:1684252
|
T | G | 60 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(57): Show | 274 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
5_prime_UTR_variant | MODIFIER | c.-184A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/5 | 15511 | chr4 | 1684252 | |||||
chr4:1684272
|
G | T | 17 | a0001c0001t0006a0001c0001t0010a0001c0001t0014others(14): Show | 52 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-204C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/5 | 15531 | chr4 | 1684272 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:1641675
|
C | T | 2 | a0002c0003t0030g0135a0002c0003t0030g0147 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.883-68G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641675 | ||||||
chr4:1641731
|
G | A | 4 | a0001c0001t0037g0057a0005c0006t0038g0011a0005c0006t0061g0142others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-124C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641731 | ||||||
chr4:1641850
|
G | A | 3 | a0001c0001t0024g0063a0001c0001t0024g0102a0001c0001t0056g0130 | 3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-243C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641850 | ||||||
chr4:1641863
|
C | T | 2 | a0001c0001t0006g0043a0005c0006t0061g0142 | 2 | HG03041.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.883-256G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641863 | ||||||
chr4:1641984
|
G | A | 36 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318others(33): Show | 37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.883-377C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1641984 | ||||||
chr4:1642135
|
C | T | 1 | a0002c0003t0002g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.883-528G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642135 | ||||||
chr4:1642141
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.883-534G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642141 | ||||||
chr4:1642170
|
C | T | 2 | a0001c0001t0029g0165a0001c0001t0029g0217 | 2 | NA18612.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.883-563G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642170 | ||||||
chr4:1642241
|
C | T | 2 | a0002c0003t0030g0135a0002c0003t0030g0147 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.883-634G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642241 | ||||||
chr4:1642301
|
G | A | 68 | a0001c0001t0006g0024a0001c0001t0006g0025a0001c0001t0006g0027others(65): Show | 72 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.883-694C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642301 | ||||||
chr4:1642403
|
G | A | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.883-796C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642403 | ||||||
chr4:1642404
|
G | A | 1 | a0002c0003t0011g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.883-797C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642404 | ||||||
chr4:1642422
|
C | A | 33 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(30): Show | 34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.883-815G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642422 | ||||||
chr4:1642435
|
C | T | 1 | a0001c0001t0011g0136 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.883-828G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642435 | ||||||
chr4:1642436
|
C | A | 27 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(24): Show | 27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.883-829G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642436 | ||||||
chr4:1642440
|
C | T | 1 | a0001c0002t0004g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.883-833G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642440 | ||||||
chr4:1642441
|
G | A | 42 | a0001c0001t0009g0111a0002c0003t0002g0008a0002c0003t0002g0138others(39): Show | 44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.883-834C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642441 | ||||||
chr4:1642524
|
A | G | 119 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0027g0132others(116): Show | 122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-917T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642524 | ||||||
chr4:1642675
|
C | T | 1 | a0001c0001t0006g0027 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.883-1068G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642675 | ||||||
chr4:1642676
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0005g0083 | 2 | NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.883-1069C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642676 | ||||||
chr4:1642708
|
T | TCTGTGGT others(28): Show |
1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.883-1136_883-1102d others(37): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642708 | ||||||
chr4:1642849
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-1242G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642849 | ||||||
chr4:1642872
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.883-1265A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642872 | ||||||
chr4:1642961
|
C | T | 1 | a0001c0002t0003g0195 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.883-1354G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1642961 | ||||||
chr4:1643023
|
C | G | 1 | a0012c0009t0014g0013 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.883-1416G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643023 | ||||||
chr4:1643233
|
G | A | 2 | a0001c0001t0008g0154a0001c0001t0008g0155 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.883-1626C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643233 | ||||||
chr4:1643241
|
C | T | 35 | a0001c0001t0014g0014a0001c0001t0014g0020a0001c0001t0014g0052others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-1634G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643241 | ||||||
chr4:1643246
|
C | T | 51 | a0001c0001t0006g0025a0001c0001t0006g0036a0001c0001t0006g0040others(48): Show | 55 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.883-1639G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643246 | ||||||
chr4:1643263
|
A | G | 6 | a0001c0001t0001g0240a0001c0001t0005g0080a0001c0001t0011g0329others(3): Show | 6 | HG01168.hp1 HG01928.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1656T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643263 | ||||||
chr4:1643266
|
A | G | 1 | a0001c0002t0003g0330 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.883-1659T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643266 | ||||||
chr4:1643289
|
G | A | 2 | a0001c0001t0001g0171a0002c0003t0002g0251 | 2 | HG02683.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.883-1682C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643289 | ||||||
chr4:1643320
|
A | G | 6 | a0001c0001t0012g0100a0001c0001t0012g0108a0001c0001t0054g0269others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.883-1713T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643320 | ||||||
chr4:1643323
|
A | G | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-1716T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643323 | ||||||
chr4:1643334
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.883-1727G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643334 | ||||||
chr4:1643335
|
G | A | 1 | a0001c0002t0003g0333 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.883-1728C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643335 | ||||||
chr4:1643346
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.883-1739C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643346 | ||||||
chr4:1643464
|
T | C | 2 | a0002c0003t0030g0135a0002c0003t0030g0147 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.883-1857A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643464 | ||||||
chr4:1643567
|
A | AT | 91 | a0001c0001t0001g0214a0001c0001t0001g0237a0001c0001t0001g0245others(88): Show | 93 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.883-1961dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643567 | ||||||
chr4:1643585
|
G | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-1978C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643585 | ||||||
chr4:1643587
|
G | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-1980C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643587 | ||||||
chr4:1643704
|
C | T | 1 | a0006c0005t0002g0009 | 2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.883-2097G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643704 | ||||||
chr4:1643727
|
G | A | 1 | a0001c0001t0029g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.883-2120C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643727 | ||||||
chr4:1643738
|
T | G | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-2131A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643738 | ||||||
chr4:1643752
|
C | T | 33 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(30): Show | 34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.883-2145G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643752 | ||||||
chr4:1643859
|
G | A | 3 | a0001c0001t0014g0014a0001c0001t0014g0020a0001c0001t0014g0052 | 3 | HG01168.hp1 HG01978.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.883-2252C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1643859 | ||||||
chr4:1644031
|
C | A | 35 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-2424G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644031 | ||||||
chr4:1644047
|
T | C | 37 | a0001c0001t0037g0057a0001c0002t0004g0140a0001c0002t0004g0144others(34): Show | 38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-2440A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644047 | ||||||
chr4:1644157
|
A | G | 37 | a0001c0001t0037g0057a0001c0002t0004g0140a0001c0002t0004g0144others(34): Show | 38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-2550T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644157 | ||||||
chr4:1644196
|
G | A | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.883-2589C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644196 | ||||||
chr4:1644290
|
C | G | 119 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0027g0132others(116): Show | 122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-2683G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644290 | ||||||
chr4:1644311
|
C | T | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-2704G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644311 | ||||||
chr4:1644350
|
G | A | 1 | a0001c0001t0053g0293 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.883-2743C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644350 | ||||||
chr4:1644381
|
C | T | 3 | a0001c0001t0024g0063a0001c0001t0024g0102a0001c0001t0056g0130 | 3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.883-2774G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644381 | ||||||
chr4:1644401
|
A | G | 1 | a0001c0001t0010g0030 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.883-2794T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644401 | ||||||
chr4:1644406
|
A | T | 1 | a0001c0001t0012g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.883-2799T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644406 | ||||||
chr4:1644453
|
G | A | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-2846C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644453 | ||||||
chr4:1644487
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.883-2880G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644487 | ||||||
chr4:1644502
|
G | A | 35 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-2895C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644502 | ||||||
chr4:1644516
|
C | A | 1 | a0002c0003t0009g0114 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.883-2909G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644516 | ||||||
chr4:1644556
|
G | A | 1 | a0001c0001t0007g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.883-2949C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644556 | ||||||
chr4:1644560
|
C | T | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-2953G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644560 | ||||||
chr4:1644563
|
G | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-2956C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644563 | ||||||
chr4:1644595
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-2988G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644595 | ||||||
chr4:1644627
|
G | C | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-3020C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644627 | ||||||
chr4:1644630
|
T | C | 40 | a0001c0001t0009g0111a0002c0003t0002g0008a0002c0003t0002g0138others(37): Show | 42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.883-3023A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644630 | ||||||
chr4:1644637
|
T | C | 70 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(67): Show | 71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-3030A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644637 | ||||||
chr4:1644739
|
C | T | 4 | a0002c0003t0002g0312a0002c0003t0009g0106a0002c0003t0009g0107others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-3132G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644739 | ||||||
chr4:1644764
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-3157C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644764 | ||||||
chr4:1644778
|
G | A | 5 | a0001c0001t0016g0062a0001c0001t0016g0098a0001c0001t0016g0110others(2): Show | 5 | HG02809.hp1 HG02818.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-3171C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1644778 | ||||||
chr4:1645100
|
G | A | 27 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(24): Show | 27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.883-3493C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645100 | ||||||
chr4:1645130
|
G | C | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-3523C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645130 | ||||||
chr4:1645193
|
C | T | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-3586G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645193 | ||||||
chr4:1645206
|
G | GCCAGC | 70 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(67): Show | 71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-3600_883-3599i others(7): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645206 | ||||||
chr4:1645209
|
G | A | 27 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(24): Show | 27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.883-3602C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645209 | ||||||
chr4:1645285
|
C | T | 1 | a0001c0001t0008g0211 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.883-3678G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645285 | ||||||
chr4:1645376
|
A | G | 1 | a0001c0002t0004g0309 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.883-3769T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645376 | ||||||
chr4:1645432
|
G | A | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-3825C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645432 | ||||||
chr4:1645625
|
T | C | 35 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-4018A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645625 | ||||||
chr4:1645687
|
G | A | 1 | a0002c0003t0002g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.883-4080C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645687 | ||||||
chr4:1645793
|
G | A | 1 | a0001c0001t0057g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.883-4186C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645793 | ||||||
chr4:1645813
|
G | A | 1 | a0001c0001t0006g0047 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.883-4206C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645813 | ||||||
chr4:1645837
|
A | G | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-4230T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645837 | ||||||
chr4:1645869
|
G | A | 74 | a0001c0001t0006g0024a0001c0001t0006g0025a0001c0001t0006g0027others(71): Show | 78 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.883-4262C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645869 | ||||||
chr4:1645871
|
A | G | 70 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(67): Show | 71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-4264T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645871 | ||||||
chr4:1645873
|
A | C | 119 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0027g0132others(116): Show | 122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-4266T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645873 | ||||||
chr4:1645891
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.883-4284A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645891 | ||||||
chr4:1645917
|
C | T | 22 | a0002c0003t0002g0008a0002c0003t0002g0139a0002c0003t0002g0186others(19): Show | 23 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.883-4310G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1645917 | ||||||
chr4:1646015
|
A | G | 17 | a0001c0001t0010g0001a0001c0001t0010g0026a0001c0001t0010g0029others(14): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.883-4408T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646015 | ||||||
chr4:1646016
|
C | T | 67 | a0001c0001t0006g0024a0001c0001t0006g0025a0001c0001t0006g0027others(64): Show | 71 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.883-4409G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646016 | ||||||
chr4:1646103
|
C | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.883-4496G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646103 | ||||||
chr4:1646122
|
A | G | 3 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0040g0067 | 3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.883-4515T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646122 | ||||||
chr4:1646123
|
C | T | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-4516G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646123 | ||||||
chr4:1646162
|
G | A | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-4555C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646162 | ||||||
chr4:1646238
|
A | C | 37 | a0001c0001t0037g0057a0001c0002t0004g0140a0001c0002t0004g0144others(34): Show | 38 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.883-4631T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646238 | ||||||
chr4:1646331
|
CCTCATGA others(1): Show |
C | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-4732_883-4725d others(10): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646331 | ||||||
chr4:1646348
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-4741G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646348 | ||||||
chr4:1646367
|
G | C | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-4760C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646367 | ||||||
chr4:1646378
|
C | T | 1 | a0002c0003t0020g0319 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.883-4771G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646378 | ||||||
chr4:1646466
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG00642.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.883-4859C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646466 | ||||||
chr4:1646467
|
C | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG00642.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.883-4860G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646467 | ||||||
chr4:1646611
|
C | T | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.883-5004G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646611 | ||||||
chr4:1646625
|
C | T | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.883-5018G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646625 | ||||||
chr4:1646668
|
G | A | 1 | a0001c0001t0047g0318 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883-5061C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646668 | ||||||
chr4:1646744
|
C | A | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.883-5137G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646744 | ||||||
chr4:1646787
|
C | T | 1 | a0001c0001t0006g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.883-5180G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646787 | ||||||
chr4:1646899
|
C | T | 30 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(27): Show | 30 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.883-5292G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1646899 | ||||||
chr4:1647043
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.883-5436G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647043 | ||||||
chr4:1647085
|
A | G | 120 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0016g0062others(117): Show | 123 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.883-5478T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647085 | ||||||
chr4:1647153
|
A | G | 35 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.883-5546T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647153 | ||||||
chr4:1647164
|
CT | C | 29 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(26): Show | 29 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.883-5558delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647164 | ||||||
chr4:1647234
|
A | G | 119 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0027g0132others(116): Show | 122 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.883-5627T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647234 | ||||||
chr4:1647292
|
A | G | 78 | a0001c0001t0006g0024a0001c0001t0006g0025a0001c0001t0006g0027others(75): Show | 82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.883-5685T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647292 | ||||||
chr4:1647313
|
T | C | 67 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.883-5706A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647313 | ||||||
chr4:1647322
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883-5715C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647322 | ||||||
chr4:1647337
|
G | GA | 20 | a0001c0001t0001g0235a0001c0001t0001g0240a0001c0001t0001g0268others(17): Show | 20 | HG00621.hp2 HG00642.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-5731dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647337 | ||||||
chr4:1647582
|
T | C | 329 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(326): Show | 341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.883-5975A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647582 | ||||||
chr4:1647585
|
G | A | 1 | a0001c0002t0041g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.883-5978C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647585 | ||||||
chr4:1647606
|
C | T | 1 | a0002c0003t0002g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.883-5999G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647606 | ||||||
chr4:1647623
|
T | C | 78 | a0001c0001t0001g0236a0001c0001t0003g0338a0001c0001t0016g0062others(75): Show | 79 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.883-6016A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647623 | ||||||
chr4:1647655
|
G | A | 3 | a0001c0001t0007g0071a0001c0001t0007g0120a0001c0001t0007g0121 | 3 | HG01070.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.883-6048C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647655 | ||||||
chr4:1647690
|
C | T | 113 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0027g0132others(110): Show | 116 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.883-6083G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647690 | ||||||
chr4:1647710
|
T | C | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883-6103A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1647710 | ||||||
chr4:1648053
|
G | C | 1 | a0001c0001t0035g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883-6446C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648053 | ||||||
chr4:1648091
|
C | T | 1 | a0001c0010t0001g0243 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.883-6484G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648091 | ||||||
chr4:1648120
|
G | C | 3 | a0001c0001t0005g0004a0001c0001t0005g0087a0001c0001t0005g0090 | 4 | NA18947.hp1 NA18963.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-6513C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648120 | ||||||
chr4:1648190
|
C | G | 20 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0176others(17): Show | 20 | HG00544.hp2 HG00673.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.883-6583G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648190 | ||||||
chr4:1648433
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.882+6545C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648433 | ||||||
chr4:1648464
|
T | G | 1 | a0001c0001t0034g0053 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.882+6514A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648464 | ||||||
chr4:1648513
|
G | A | 2 | a0001c0001t0046g0129a0001c0001t0047g0318 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+6465C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648513 | ||||||
chr4:1648516
|
G | A | 1 | a0001c0001t0007g0079 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.882+6462C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648516 | ||||||
chr4:1648593
|
T | C | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+6385A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648593 | ||||||
chr4:1648603
|
C | T | 3 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0040g0067 | 3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.882+6375G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648603 | ||||||
chr4:1648632
|
G | A | 13 | a0002c0003t0002g0008a0002c0003t0002g0186a0002c0003t0002g0187others(10): Show | 14 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+6346C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648632 | ||||||
chr4:1648728
|
G | T | 1 | a0001c0001t0008g0264 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.882+6250C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648728 | ||||||
chr4:1648771
|
T | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0248 | 2 | NA18991.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.882+6207A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648771 | ||||||
chr4:1648809
|
A | C | 35 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(32): Show | 36 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.882+6169T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648809 | ||||||
chr4:1648819
|
G | A | 49 | a0001c0001t0009g0111a0002c0003t0002g0008a0002c0003t0002g0138others(46): Show | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.882+6159C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648819 | ||||||
chr4:1648830
|
A | T | 1 | a0001c0002t0004g0326 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.882+6148T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648830 | ||||||
chr4:1648835
|
G | A | 1 | a0001c0002t0050g0274 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.882+6143C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648835 | ||||||
chr4:1648867
|
C | A | 1 | a0001c0002t0004g0158 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.882+6111G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648867 | ||||||
chr4:1648890
|
A | G | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+6088T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648890 | ||||||
chr4:1648972
|
G | C | 1 | a0001c0002t0004g0317 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.882+6006C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648972 | ||||||
chr4:1648977
|
G | T | 1 | a0001c0001t0007g0082 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.882+6001C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1648977 | ||||||
chr4:1649072
|
C | T | 8 | a0002c0003t0002g0139a0002c0003t0002g0275a0002c0003t0002g0281others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.882+5906G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649072 | ||||||
chr4:1649134
|
G | GGGGAAGG others(17): Show |
1 | a0001c0001t0008g0190 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.882+5820_882+5843d others(26): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649134 | ||||||
chr4:1649134
|
GGGGAAGG others(5): Show |
G | 1 | a0011c0012t0010g0038 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.882+5832_882+5843d others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649134 | ||||||
chr4:1649140
|
G | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+5838C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649140 | ||||||
chr4:1649152
|
G | A | 8 | a0001c0002t0015g0015a0001c0002t0015g0016a0001c0002t0015g0050others(5): Show | 8 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+5826C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649152 | ||||||
chr4:1649152
|
G | GGGGAAA | 28 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(25): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.882+5820_882+5825d others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649152 | ||||||
chr4:1649158
|
A | G | 8 | a0001c0002t0015g0015a0001c0002t0015g0016a0001c0002t0015g0050others(5): Show | 8 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+5820T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649158 | ||||||
chr4:1649164
|
G | A | 8 | a0001c0002t0015g0015a0001c0002t0015g0016a0001c0002t0015g0050others(5): Show | 8 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+5814C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649164 | ||||||
chr4:1649170
|
A | AGGGAAGG others(41): Show |
2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+5807_882+5808i others(50): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649170 | ||||||
chr4:1649170
|
A | AGGGAAGG others(17): Show |
2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.882+5807_882+5808i others(26): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649170 | ||||||
chr4:1649176
|
A | AGGGAAG | 98 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0016g0062others(95): Show | 101 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.882+5796_882+5801d others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649176 | ||||||
chr4:1649176
|
A | AGGGAAGG others(5): Show |
1 | a0001c0017t0004g0162 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.882+5790_882+5801d others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649176 | ||||||
chr4:1649176
|
A | G | 12 | a0001c0001t0037g0057a0001c0002t0015g0015a0001c0002t0015g0016others(9): Show | 12 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.882+5802T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649176 | ||||||
chr4:1649182
|
G | GGGGAAGG others(17): Show |
1 | a0001c0001t0054g0269 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.882+5772_882+5795d others(26): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649182 | ||||||
chr4:1649183
|
G | A | 3 | a0001c0001t0024g0063a0001c0001t0024g0102a0001c0001t0056g0130 | 3 | HG01255.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.882+5795C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649183 | ||||||
chr4:1649188
|
GGGGAAGG others(5): Show |
G | 1 | a0002c0003t0009g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.882+5778_882+5789d others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649188 | ||||||
chr4:1649200
|
A | G | 48 | a0001c0001t0009g0111a0002c0003t0002g0008a0002c0003t0002g0138others(45): Show | 50 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.882+5778T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649200 | ||||||
chr4:1649227
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+5751C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649227 | ||||||
chr4:1649434
|
C | A | 1 | a0001c0001t0021g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.882+5544G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649434 | ||||||
chr4:1649453
|
T | C | 5 | a0002c0003t0002g0008a0002c0003t0002g0298a0002c0003t0018g0021others(2): Show | 6 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+5525A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649453 | ||||||
chr4:1649473
|
C | T | 1 | a0002c0003t0002g0279 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+5505G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649473 | ||||||
chr4:1649517
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.882+5461C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649517 | ||||||
chr4:1649672
|
T | C | 50 | a0001c0001t0009g0111a0001c0001t0035g0056a0002c0003t0002g0008others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.882+5306A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649672 | ||||||
chr4:1649753
|
G | A | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+5225C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649753 | ||||||
chr4:1649818
|
A | G | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+5160T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649818 | ||||||
chr4:1649842
|
T | C | 36 | a0001c0001t0057g0141a0001c0002t0004g0140a0001c0002t0004g0144others(33): Show | 37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+5136A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649842 | ||||||
chr4:1649855
|
A | T | 120 | a0001c0001t0003g0338a0001c0001t0009g0111a0001c0001t0016g0062others(117): Show | 123 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.882+5123T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649855 | ||||||
chr4:1649870
|
G | A | 27 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(24): Show | 27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.882+5108C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649870 | ||||||
chr4:1649872
|
G | A | 42 | a0001c0001t0009g0111a0002c0003t0002g0008a0002c0003t0002g0138others(39): Show | 44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.882+5106C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649872 | ||||||
chr4:1649876
|
TGTTTGTG others(18): Show |
T | 1 | a0001c0001t0057g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.882+5077_882+5101d others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649876 | ||||||
chr4:1649879
|
T | TTGTGAGG others(51): Show |
1 | a0001c0001t0014g0014 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.882+5041_882+5098d others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649879 | ||||||
chr4:1649879
|
TTGTGAGG others(22): Show |
T | 13 | a0001c0001t0001g0168a0001c0001t0001g0226a0001c0001t0001g0232others(10): Show | 13 | HG00423.hp2 HG02083.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+5070_882+5098d others(31): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649879 | ||||||
chr4:1649879
|
TTGTGAGG others(51): Show |
T | 3 | a0001c0001t0001g0171a0001c0001t0037g0057a0010c0011t0045g0123 | 3 | HG02258.hp2 HG02683.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.882+5041_882+5098d others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649879 | ||||||
chr4:1649897
|
G | A | 1 | a0001c0001t0005g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.882+5081C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649897 | ||||||
chr4:1649908
|
C | CTGTGAGG others(18): Show |
2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.882+5069_882+5070i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649908 | ||||||
chr4:1649930
|
C | G | 24 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(21): Show | 24 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.882+5048G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649930 | ||||||
chr4:1649937
|
C | CTGTGAGG others(18): Show |
1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+5040_882+5041i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649937 | ||||||
chr4:1649959
|
C | T | 26 | a0001c0001t0009g0111a0002c0003t0002g0138a0002c0003t0002g0139others(23): Show | 27 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.882+5019G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649959 | ||||||
chr4:1649962
|
TTGACTGT others(26): Show |
T | 27 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(24): Show | 27 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.882+4983_882+5015d others(35): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649962 | ||||||
chr4:1649962
|
TTGACTGT others(55): Show |
T | 2 | a0001c0001t0046g0129a0001c0001t0047g0318 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+4954_882+5015d others(64): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649962 | ||||||
chr4:1649985
|
TG | T | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | NA18969.hp2 NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.882+4992delC | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649985 | ||||||
chr4:1649995
|
C | CTGTGAGG others(18): Show |
1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+4982_882+4983i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1649995 | ||||||
chr4:1650012
|
C | CGTGGCGT others(22): Show |
32 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(29): Show | 33 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+4965_882+4966i others(31): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650012 | ||||||
chr4:1650020
|
TTGAC | T | 17 | a0001c0001t0009g0111a0002c0003t0002g0138a0002c0003t0002g0156others(14): Show | 18 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.882+4954_882+4957d others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650020 | ||||||
chr4:1650037
|
C | CAGTCATG others(134): Show |
1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+4940_882+4941i others(143): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650037 | ||||||
chr4:1650041
|
C | T | 1 | a0001c0002t0017g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.882+4937G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650041 | ||||||
chr4:1650046
|
C | T | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4932G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650046 | ||||||
chr4:1650046
|
CGTTTGAC others(76): Show |
C | 2 | a0001c0001t0009g0111a0002c0003t0002g0314 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.882+4849_882+4931d others(85): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650046 | ||||||
chr4:1650053
|
C | CTGTGAGG others(18): Show |
1 | a0001c0002t0017g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.882+4924_882+4925i others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650053 | ||||||
chr4:1650075
|
T | C | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4903A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650075 | ||||||
chr4:1650094
|
G | A | 1 | a0001c0002t0036g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.882+4884C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650094 | ||||||
chr4:1650094
|
G | T | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4884C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650094 | ||||||
chr4:1650096
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4882C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650096 | ||||||
chr4:1650100
|
C | T | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4878G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650100 | ||||||
chr4:1650123
|
T | G | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+4855A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650123 | ||||||
chr4:1650125
|
A | G | 3 | a0001c0001t0005g0128a0001c0001t0037g0057a0010c0011t0045g0123 | 3 | HG02258.hp2 HG02976.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.882+4853T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650125 | ||||||
chr4:1650161
|
T | C | 1 | a0002c0003t0002g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.882+4817A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650161 | ||||||
chr4:1650161
|
TTGTGAGG others(51): Show |
T | 1 | a0001c0001t0001g0209 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.882+4759_882+4816d others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650161 | ||||||
chr4:1650178
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+4800G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650178 | ||||||
chr4:1650213
|
A | G | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+4765T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650213 | ||||||
chr4:1650241
|
C | T | 1 | a0002c0003t0002g0279 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.882+4737G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650241 | ||||||
chr4:1650266
|
G | A | 1 | a0002c0003t0018g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.882+4712C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650266 | ||||||
chr4:1650385
|
T | TTGAC | 198 | a0001c0001t0003g0338a0001c0001t0006g0024a0001c0001t0006g0025others(195): Show | 205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.882+4592_882+4593i others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650385 | ||||||
chr4:1650398
|
T | C | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+4580A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650398 | ||||||
chr4:1650557
|
C | T | 13 | a0001c0002t0004g0144a0001c0002t0004g0159a0001c0002t0004g0282others(10): Show | 14 | HG00099.hp2 HG01074.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+4421G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650557 | ||||||
chr4:1650560
|
G | A | 1 | a0001c0001t0016g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.882+4418C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650560 | ||||||
chr4:1650594
|
C | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+4384G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650594 | ||||||
chr4:1650641
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.882+4337C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650641 | ||||||
chr4:1650691
|
T | C | 33 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(30): Show | 34 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.882+4287A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650691 | ||||||
chr4:1650716
|
G | A | 1 | a0001c0001t0040g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.882+4262C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650716 | ||||||
chr4:1650743
|
G | A | 1 | a0001c0001t0006g0037 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.882+4235C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650743 | ||||||
chr4:1650807
|
T | G | 30 | a0001c0001t0003g0338a0001c0001t0027g0132a0001c0001t0027g0157others(27): Show | 30 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.882+4171A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650807 | ||||||
chr4:1650918
|
T | C | 1 | a0002c0003t0002g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882+4060A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1650918 | ||||||
chr4:1651210
|
G | A | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.882+3768C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651210 | ||||||
chr4:1651223
|
G | GA | 41 | a0001c0001t0001g0209a0001c0001t0001g0238a0001c0001t0001g0320others(38): Show | 42 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.882+3754dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651223 | ||||||
chr4:1651223
|
GA | G | 8 | a0001c0001t0001g0189a0001c0001t0001g0214a0001c0001t0006g0043others(5): Show | 8 | HG00544.hp1 HG03490.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+3754delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651223 | ||||||
chr4:1651224
|
A | G | 2 | a0001c0001t0037g0057a0010c0011t0045g0123 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.882+3754T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651224 | ||||||
chr4:1651260
|
G | A | 36 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(33): Show | 37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.882+3718C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651260 | ||||||
chr4:1651271
|
T | C | 202 | a0001c0001t0001g0299a0001c0001t0003g0338a0001c0001t0006g0024others(199): Show | 209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.882+3707A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651271 | ||||||
chr4:1651283
|
G | A | 5 | a0001c0002t0004g0158a0001c0002t0004g0207a0001c0002t0004g0304others(2): Show | 5 | HG01257.hp2 HG01358.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+3695C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651283 | ||||||
chr4:1651298
|
G | A | 1 | a0013c0008t0020g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.882+3680C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651298 | ||||||
chr4:1651479
|
C | T | 1 | a0001c0001t0047g0318 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.882+3499G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651479 | ||||||
chr4:1651519
|
C | T | 4 | a0001c0001t0024g0063a0001c0001t0026g0327a0001c0001t0026g0328others(1): Show | 4 | HG01255.hp1 HG02055.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+3459G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651519 | ||||||
chr4:1651532
|
T | TA | 12 | a0001c0001t0001g0010a0001c0001t0001g0232a0001c0001t0001g0270others(9): Show | 13 | HG01081.hp2 HG01346.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.882+3445dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651532 | ||||||
chr4:1651532
|
TA | T | 70 | a0001c0001t0003g0338a0001c0001t0011g0136a0001c0001t0024g0063others(67): Show | 71 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.882+3445delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651532 | ||||||
chr4:1651532
|
TAA | T | 121 | a0001c0001t0001g0299a0001c0001t0006g0024a0001c0001t0006g0025others(118): Show | 127 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.882+3444_882+3445d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651532 | ||||||
chr4:1651608
|
C | A | 5 | a0001c0001t0012g0101a0001c0001t0012g0108a0001c0001t0043g0117others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+3370G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651608 | ||||||
chr4:1651625
|
T | C | 108 | a0001c0001t0001g0300a0001c0001t0009g0111a0001c0001t0011g0134others(105): Show | 111 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.882+3353A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651625 | ||||||
chr4:1651630
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.882+3348C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651630 | ||||||
chr4:1651675
|
C | T | 1 | a0001c0001t0026g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.882+3303G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651675 | ||||||
chr4:1651681
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.882+3297T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651681 | ||||||
chr4:1651699
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.882+3279G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651699 | ||||||
chr4:1651707
|
T | TGGACAGG others(73): Show |
1 | a0002c0003t0009g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.882+3191_882+3270d others(82): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651707 | ||||||
chr4:1651707
|
T | TGGACAGG others(73): Show |
1 | a0001c0001t0042g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.882+3270_882+3271i others(82): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651707 | ||||||
chr4:1651707
|
TGGACAGG others(33): Show |
T | 13 | a0002c0003t0002g0008a0002c0003t0002g0186a0002c0003t0002g0187others(10): Show | 14 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.882+3231_882+3270d others(42): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651707 | ||||||
chr4:1651720
|
G | GCAGGCTC others(33): Show |
32 | a0001c0001t0026g0328a0001c0002t0004g0140a0001c0002t0004g0144others(29): Show | 33 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.882+3218_882+3257d others(42): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651720 | ||||||
chr4:1651720
|
GCAGGCTC others(33): Show |
G | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+3218_882+3257d others(42): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651720 | ||||||
chr4:1651736
|
A | G | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+3242T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651736 | ||||||
chr4:1651799
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.882+3179G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651799 | ||||||
chr4:1651858
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.882+3120C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651858 | ||||||
chr4:1651890
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.882+3088C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651890 | ||||||
chr4:1651964
|
C | T | 37 | a0001c0001t0011g0329a0001c0001t0033g0012a0002c0003t0002g0008others(34): Show | 39 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.882+3014G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651964 | ||||||
chr4:1651985
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.882+2993C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1651985 | ||||||
chr4:1652011
|
G | A | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.882+2967C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652011 | ||||||
chr4:1652012
|
T | TCACACAC others(13): Show |
4 | a0001c0001t0031g0049a0001c0001t0033g0012a0002c0003t0030g0135others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2946_882+2965d others(22): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652012 | ||||||
chr4:1652012
|
TCACACAC others(13): Show |
T | 63 | a0001c0001t0024g0063a0001c0001t0026g0327a0001c0001t0026g0328others(60): Show | 64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.882+2946_882+2965d others(22): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652012 | ||||||
chr4:1652076
|
T | A | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+2902A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652076 | ||||||
chr4:1652080
|
A | G | 4 | a0001c0001t0027g0132a0001c0001t0027g0157a0002c0003t0009g0122others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2898T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652080 | ||||||
chr4:1652099
|
T | C | 4 | a0001c0001t0009g0111a0001c0001t0016g0062a0001c0001t0016g0098others(1): Show | 4 | HG02818.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+2879A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652099 | ||||||
chr4:1652131
|
T | A | 217 | a0001c0001t0001g0285a0001c0001t0003g0338a0001c0001t0006g0024others(214): Show | 224 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.882+2847A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652131 | ||||||
chr4:1652138
|
CCA | C | 50 | a0001c0001t0011g0136a0001c0001t0011g0272a0002c0003t0002g0008others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.882+2838_882+2839d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652138 | ||||||
chr4:1652172
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.882+2806G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652172 | ||||||
chr4:1652173
|
G | GCCACACA others(358): Show |
1 | a0002c0003t0011g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.882+2804_882+2805i others(367): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652173 | ||||||
chr4:1652190
|
CGCCACAC others(11): Show |
C | 2 | a0002c0003t0030g0135a0002c0003t0030g0147 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.882+2770_882+2787d others(20): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652190 | ||||||
chr4:1652229
|
T | TAC | 59 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.882+2748_882+2749i others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652229 | ||||||
chr4:1652243
|
C | CCACACAC others(66): Show |
2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.882+2662_882+2734d others(75): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652243 | ||||||
chr4:1652316
|
TCA | T | 48 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(45): Show | 50 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.882+2660_882+2661d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652316 | ||||||
chr4:1652346
|
ACAC | A | 8 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.882+2629_882+2631d others(5): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652346 | ||||||
chr4:1652361
|
C | G | 1 | a0001c0001t0012g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.882+2617G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652361 | ||||||
chr4:1652388
|
T | C | 60 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+2590A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652388 | ||||||
chr4:1652389
|
G | GCACACCA | 60 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+2582_882+2588d others(9): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652389 | ||||||
chr4:1652414
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+2564G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652414 | ||||||
chr4:1652416
|
C | T | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | NA18969.hp2 NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.882+2562G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652416 | ||||||
chr4:1652472
|
C | T | 1 | a0013c0008t0020g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.882+2506G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652472 | ||||||
chr4:1652522
|
T | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.882+2456A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652522 | ||||||
chr4:1652620
|
C | G | 1 | a0002c0003t0002g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.882+2358G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652620 | ||||||
chr4:1652667
|
A | G | 15 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(12): Show | 15 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.882+2311T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652667 | ||||||
chr4:1652771
|
C | A | 4 | a0001c0002t0004g0266a0001c0002t0004g0302a0001c0002t0004g0308others(1): Show | 4 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.882+2207G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652771 | ||||||
chr4:1652836
|
C | T | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+2142G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652836 | ||||||
chr4:1652889
|
C | A | 1 | a0001c0002t0004g0282 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.882+2089G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652889 | ||||||
chr4:1652964
|
G | A | 78 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(75): Show | 79 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.882+2014C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1652964 | ||||||
chr4:1653017
|
C | T | 2 | a0001c0002t0003g0161a0001c0002t0003g0208 | 2 | HG00738.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.882+1961G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653017 | ||||||
chr4:1653061
|
T | C | 70 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(67): Show | 72 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.882+1917A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653061 | ||||||
chr4:1653094
|
CCA | C | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+1882_882+1883d others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653094 | ||||||
chr4:1653132
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0313 | 2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.882+1846T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653132 | ||||||
chr4:1653136
|
C | T | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.882+1842G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653136 | ||||||
chr4:1653201
|
A | C | 58 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(55): Show | 59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.882+1777T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653201 | ||||||
chr4:1653225
|
A | G | 2 | a0001c0001t0024g0063a0001c0001t0024g0102 | 2 | HG01255.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.882+1753T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653225 | ||||||
chr4:1653248
|
C | T | 2 | a0002c0003t0030g0135a0002c0003t0030g0147 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.882+1730G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653248 | ||||||
chr4:1653284
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.882+1694C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653284 | ||||||
chr4:1653291
|
C | A | 1 | a0006c0005t0002g0009 | 2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.882+1687G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653291 | ||||||
chr4:1653382
|
C | T | 12 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(9): Show | 12 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.882+1596G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653382 | ||||||
chr4:1653459
|
C | T | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.882+1519G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653459 | ||||||
chr4:1653479
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+1499G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653479 | ||||||
chr4:1653482
|
A | G | 78 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(75): Show | 79 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.882+1496T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653482 | ||||||
chr4:1653485
|
C | T | 18 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(15): Show | 18 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.882+1493G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653485 | ||||||
chr4:1653766
|
G | A | 1 | a0001c0001t0023g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.882+1212C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653766 | ||||||
chr4:1653978
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.882+1000G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1653978 | ||||||
chr4:1654088
|
G | A | 2 | a0001c0002t0050g0274a0001c0002t0060g0324 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.882+890C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654088 | ||||||
chr4:1654197
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.882+781G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654197 | ||||||
chr4:1654209
|
C | T | 11 | a0001c0001t0011g0134a0001c0001t0011g0136a0001c0001t0011g0137others(8): Show | 11 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.882+769G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654209 | ||||||
chr4:1654277
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.882+701G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654277 | ||||||
chr4:1654283
|
C | T | 70 | a0001c0001t0006g0024a0001c0001t0006g0025a0001c0001t0006g0027others(67): Show | 74 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.882+695G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654283 | ||||||
chr4:1654409
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.882+569C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654409 | ||||||
chr4:1654519
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+459G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654519 | ||||||
chr4:1654590
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882+388G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654590 | ||||||
chr4:1654611
|
A | C | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+367T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654611 | ||||||
chr4:1654650
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0286a0001c0001t0001g0292 | 3 | HG01069.hp2 HG01071.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.882+328G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654650 | ||||||
chr4:1654726
|
C | T | 23 | a0002c0003t0002g0008a0002c0003t0002g0139a0002c0003t0002g0186others(20): Show | 24 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.882+252G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654726 | ||||||
chr4:1654740
|
C | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.882+238G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654740 | ||||||
chr4:1654746
|
T | C | 2 | a0001c0001t0007g0072a0001c0001t0007g0078 | 2 | HG01081.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.882+232A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654746 | ||||||
chr4:1654815
|
G | A | 2 | a0001c0001t0006g0048a0001c0001t0008g0263 | 2 | HG01515.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.882+163C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 4/4 | chr4 | 1654815 | ||||||
chr4:1655837
|
C | T | 1 | a0001c0001t0006g0046 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.137-114G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655837 | ||||||
chr4:1655849
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.137-126C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655849 | ||||||
chr4:1655864
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.137-141C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655864 | ||||||
chr4:1655892
|
C | T | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.137-169G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655892 | ||||||
chr4:1655924
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0296 | 2 | NA18953.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.137-201C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655924 | ||||||
chr4:1655931
|
T | C | 2 | a0001c0001t0006g0048a0001c0001t0008g0263 | 2 | HG01515.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.137-208A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1655931 | ||||||
chr4:1656002
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.137-279G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656002 | ||||||
chr4:1656043
|
G | A | 1 | a0001c0002t0004g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.137-320C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656043 | ||||||
chr4:1656048
|
C | T | 49 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(46): Show | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.137-325G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656048 | ||||||
chr4:1656137
|
G | A | 1 | a0001c0001t0057g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137-414C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656137 | ||||||
chr4:1656138
|
C | A | 1 | a0001c0001t0057g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137-415G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656138 | ||||||
chr4:1656155
|
C | T | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.137-432G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656155 | ||||||
chr4:1656186
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.137-463G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656186 | ||||||
chr4:1656218
|
T | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG00673.hp1 NA18965.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-495A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656218 | ||||||
chr4:1656370
|
G | A | 1 | a0001c0001t0008g0211 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.137-647C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656370 | ||||||
chr4:1656394
|
T | TGGCTTGT others(16): Show |
2 | a0001c0002t0003g0194a0001c0002t0003g0199 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.137-694_137-672dup others(23): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656394 | ||||||
chr4:1656409
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.137-686G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656409 | ||||||
chr4:1656484
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.137-761C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656484 | ||||||
chr4:1656609
|
A | C | 25 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(22): Show | 25 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.136+799T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656609 | ||||||
chr4:1656633
|
G | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.136+775C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656633 | ||||||
chr4:1656654
|
G | A | 49 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(46): Show | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.136+754C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656654 | ||||||
chr4:1656736
|
G | A | 1 | a0001c0002t0049g0332 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.136+672C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656736 | ||||||
chr4:1656765
|
C | T | 1 | a0001c0002t0003g0271 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.136+643G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656765 | ||||||
chr4:1656766
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.136+642C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656766 | ||||||
chr4:1656912
|
C | T | 40 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(37): Show | 42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.136+496G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656912 | ||||||
chr4:1656918
|
C | T | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.136+490G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656918 | ||||||
chr4:1656976
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.136+432C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1656976 | ||||||
chr4:1657076
|
C | T | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136+332G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657076 | ||||||
chr4:1657079
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.136+329C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657079 | ||||||
chr4:1657230
|
C | T | 1 | a0001c0002t0004g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.136+178G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657230 | ||||||
chr4:1657270
|
C | T | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136+138G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657270 | ||||||
chr4:1657401
|
T | C | 218 | a0001c0001t0003g0338a0001c0001t0006g0024a0001c0001t0006g0025others(215): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
splice_region_variant&intron_variant | LOW | c.136+7A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 3/4 | chr4 | 1657401 | ||||||
chr4:1657681
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.76-213T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657681 | ||||||
chr4:1657698
|
C | T | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.76-230G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657698 | ||||||
chr4:1657782
|
C | T | 18 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(15): Show | 18 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-314G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657782 | ||||||
chr4:1657799
|
G | A | 15 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(12): Show | 15 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-331C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657799 | ||||||
chr4:1657944
|
C | G | 1 | a0001c0002t0003g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.76-476G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657944 | ||||||
chr4:1657963
|
TA | T | 3 | a0001c0001t0010g0030a0001c0001t0013g0261a0002c0003t0002g0204 | 3 | NA18957.hp2 NA18969.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.76-496delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657963 | ||||||
chr4:1657969
|
A | T | 16 | a0002c0003t0002g0138a0002c0003t0002g0156a0002c0003t0002g0314others(13): Show | 17 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-501T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1657969 | ||||||
chr4:1658004
|
G | A | 128 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(125): Show | 131 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.76-536C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658004 | ||||||
chr4:1658071
|
T | C | 60 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.76-603A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658071 | ||||||
chr4:1658242
|
G | A | 4 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318others(1): Show | 4 | HG02109.hp2 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-774C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658242 | ||||||
chr4:1658247
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.76-779G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658247 | ||||||
chr4:1658299
|
T | C | 63 | a0001c0001t0009g0111a0001c0001t0016g0062a0001c0001t0016g0098others(60): Show | 64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.76-831A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658299 | ||||||
chr4:1658349
|
T | C | 42 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(39): Show | 44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.76-881A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658349 | ||||||
chr4:1658358
|
T | G | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.76-890A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658358 | ||||||
chr4:1658393
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0294 | 2 | HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.76-925C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658393 | ||||||
chr4:1658419
|
C | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-951G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658419 | ||||||
chr4:1658490
|
A | G | 59 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.76-1022T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658490 | ||||||
chr4:1658746
|
C | G | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.76-1278G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658746 | ||||||
chr4:1658755
|
G | A | 12 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(9): Show | 12 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-1287C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658755 | ||||||
chr4:1658803
|
G | A | 15 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(12): Show | 15 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-1335C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658803 | ||||||
chr4:1658889
|
C | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0216 | 2 | NA18965.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.76-1421G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658889 | ||||||
chr4:1658924
|
T | C | 60 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.76-1456A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658924 | ||||||
chr4:1658976
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0005g0088 | 2 | NA18983.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.76-1508G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1658976 | ||||||
chr4:1659019
|
C | T | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-1551G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659019 | ||||||
chr4:1659092
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.76-1624G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659092 | ||||||
chr4:1659143
|
G | A | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.76-1675C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659143 | ||||||
chr4:1659144
|
G | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.76-1676C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659144 | ||||||
chr4:1659261
|
G | A | 4 | a0001c0001t0019g0133a0001c0001t0019g0276a0001c0001t0019g0277others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1793C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659261 | ||||||
chr4:1659332
|
C | T | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-1864G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659332 | ||||||
chr4:1659339
|
C | T | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-1871G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659339 | ||||||
chr4:1659343
|
G | C | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-1875C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659343 | ||||||
chr4:1659401
|
C | A | 60 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.76-1933G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659401 | ||||||
chr4:1659423
|
G | A | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-1955C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659423 | ||||||
chr4:1659551
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.76-2083G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659551 | ||||||
chr4:1659555
|
G | A | 2 | a0001c0001t0029g0165a0001c0001t0029g0217 | 2 | NA18612.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.76-2087C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659555 | ||||||
chr4:1659790
|
C | T | 1 | a0001c0001t0005g0088 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-2322G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659790 | ||||||
chr4:1659966
|
G | A | 19 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(16): Show | 19 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-2498C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1659966 | ||||||
chr4:1660025
|
G | A | 49 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(46): Show | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.76-2557C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660025 | ||||||
chr4:1660090
|
G | A | 4 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0040g0067others(1): Show | 4 | HG02055.hp2 HG02280.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-2622C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660090 | ||||||
chr4:1660198
|
G | A | 1 | a0001c0001t0021g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.76-2730C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660198 | ||||||
chr4:1660358
|
G | GA | 133 | a0001c0001t0003g0338a0001c0001t0011g0134a0001c0001t0011g0136others(130): Show | 136 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.76-2891_76-2890ins others(1): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660358 | ||||||
chr4:1660489
|
T | C | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.76-3021A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660489 | ||||||
chr4:1660629
|
C | T | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-3161G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660629 | ||||||
chr4:1660704
|
C | T | 1 | a0001c0001t0005g0091 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.76-3236G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660704 | ||||||
chr4:1660705
|
G | A | 5 | a0001c0001t0012g0100a0001c0001t0012g0101a0001c0001t0012g0108others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-3237C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660705 | ||||||
chr4:1660832
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3364C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1660832 | ||||||
chr4:1661113
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3645C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661113 | ||||||
chr4:1661116
|
C | T | 2 | a0002c0003t0030g0135a0002c0003t0030g0147 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.76-3648G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661116 | ||||||
chr4:1661238
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.76-3770G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661238 | ||||||
chr4:1661354
|
T | C | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-3886A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661354 | ||||||
chr4:1661383
|
T | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3915A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661383 | ||||||
chr4:1661473
|
C | T | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-4005G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661473 | ||||||
chr4:1661484
|
G | A | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.76-4016C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661484 | ||||||
chr4:1661624
|
T | C | 209 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 218 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.76-4156A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661624 | ||||||
chr4:1661650
|
A | AC | 7 | a0001c0001t0001g0248a0001c0001t0010g0001a0001c0001t0010g0030others(4): Show | 9 | HG00408.hp1 HG00609.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-4183dupG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661650 | ||||||
chr4:1661661
|
C | G | 2 | a0002c0003t0025g0112a0002c0003t0025g0124 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.76-4193G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661661 | ||||||
chr4:1661758
|
C | T | 5 | a0001c0001t0001g0249a0001c0001t0005g0004a0001c0001t0005g0083others(2): Show | 6 | NA18947.hp1 NA18963.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-4290G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661758 | ||||||
chr4:1661835
|
G | A | 40 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(37): Show | 42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.76-4367C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661835 | ||||||
chr4:1661861
|
G | A | 59 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.76-4393C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661861 | ||||||
chr4:1661909
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-4441C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1661909 | ||||||
chr4:1662120
|
A | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-4652T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662120 | ||||||
chr4:1662362
|
C | T | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-4894G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662362 | ||||||
chr4:1662479
|
C | CA | 17 | a0001c0001t0006g0024a0001c0001t0006g0036a0001c0001t0006g0051others(14): Show | 17 | HG00609.hp2 HG02080.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-5012dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | ||||||
chr4:1662479
|
CA | C | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(112): Show | 120 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.76-5012delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | ||||||
chr4:1662479
|
CAA | C | 28 | a0001c0001t0001g0215a0001c0001t0001g0284a0001c0001t0001g0285others(25): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.76-5013_76-5012del others(2): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | ||||||
chr4:1662479
|
CAAA | C | 38 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(35): Show | 38 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.76-5014_76-5012del others(3): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | ||||||
chr4:1662479
|
CAAAAAAA others(6): Show |
C | 42 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(39): Show | 44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.76-5024_76-5012del others(13): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662479 | ||||||
chr4:1662505
|
C | T | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.76-5037G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662505 | ||||||
chr4:1662636
|
C | T | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.76-5168G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662636 | ||||||
chr4:1662649
|
C | CA | 8 | a0001c0001t0051g0192a0002c0003t0002g0145a0002c0003t0002g0323others(5): Show | 8 | HG00438.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-5182dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662649 | ||||||
chr4:1662649
|
CA | C | 287 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(284): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.76-5182delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662649 | ||||||
chr4:1662649
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0248 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.76-5191_76-5182del others(10): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662649 | ||||||
chr4:1662788
|
C | T | 4 | a0001c0001t0019g0133a0001c0001t0019g0276a0001c0001t0019g0277others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5320G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662788 | ||||||
chr4:1662887
|
G | A | 49 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(46): Show | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.76-5419C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662887 | ||||||
chr4:1662946
|
C | A | 1 | a0001c0002t0049g0332 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-5478G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662946 | ||||||
chr4:1662976
|
C | T | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.76-5508G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1662976 | ||||||
chr4:1663011
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.76-5543C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663011 | ||||||
chr4:1663030
|
TA | T | 324 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(321): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.76-5563delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663030 | ||||||
chr4:1663116
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75+5551C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663116 | ||||||
chr4:1663171
|
G | GA | 40 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(37): Show | 42 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.75+5495dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663171 | ||||||
chr4:1663216
|
A | C | 2 | a0001c0001t0008g0154a0001c0001t0008g0155 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.75+5451T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663216 | ||||||
chr4:1663217
|
G | T | 24 | a0001c0002t0004g0144a0001c0002t0004g0158a0001c0002t0004g0159others(21): Show | 25 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.75+5450C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663217 | ||||||
chr4:1663237
|
A | G | 266 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.75+5430T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663237 | ||||||
chr4:1663287
|
A | C | 1 | a0001c0001t0005g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.75+5380T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663287 | ||||||
chr4:1663513
|
C | T | 42 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(39): Show | 44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.75+5154G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663513 | ||||||
chr4:1663550
|
G | A | 1 | a0001c0001t0009g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.75+5117C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663550 | ||||||
chr4:1663590
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 123 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.75+5077G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663590 | ||||||
chr4:1663798
|
G | C | 39 | a0002c0003t0002g0008a0002c0003t0002g0138a0002c0003t0002g0139others(36): Show | 41 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.75+4869C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663798 | ||||||
chr4:1663831
|
C | A | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.75+4836G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663831 | ||||||
chr4:1663840
|
T | TA | 6 | a0001c0001t0001g0234a0001c0001t0001g0295a0001c0001t0012g0065others(3): Show | 6 | HG00423.hp1 HG02145.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4826dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663840 | ||||||
chr4:1663840
|
TA | T | 60 | a0001c0001t0001g0290a0001c0001t0005g0084a0001c0001t0006g0048others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.75+4826delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1663840 | ||||||
chr4:1664127
|
G | C | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+4540C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664127 | ||||||
chr4:1664349
|
G | A | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.75+4318C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664349 | ||||||
chr4:1664354
|
G | A | 1 | a0001c0001t0005g0084 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.75+4313C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664354 | ||||||
chr4:1664371
|
G | A | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.75+4296C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664371 | ||||||
chr4:1664411
|
C | T | 1 | a0001c0002t0017g0003 | 2 | HG00099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.75+4256G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664411 | ||||||
chr4:1664427
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.75+4240G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664427 | ||||||
chr4:1664433
|
G | T | 58 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(55): Show | 59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.75+4234C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664433 | ||||||
chr4:1664612
|
A | C | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.75+4055T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664612 | ||||||
chr4:1664654
|
A | G | 1 | a0001c0001t0058g0227 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.75+4013T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664654 | ||||||
chr4:1664749
|
G | A | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.75+3918C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664749 | ||||||
chr4:1664857
|
A | T | 1 | a0001c0001t0001g0297 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.75+3810T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1664857 | ||||||
chr4:1665179
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+3488C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665179 | ||||||
chr4:1665243
|
G | A | 204 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 213 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.75+3424C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665243 | ||||||
chr4:1665421
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.75+3246C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665421 | ||||||
chr4:1665435
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+3232C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665435 | ||||||
chr4:1665487
|
CA | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0189a0001c0001t0001g0191others(25): Show | 29 | HG00438.hp1 HG00558.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+3179delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665487 | ||||||
chr4:1665580
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0313 | 2 | HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.75+3087C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665580 | ||||||
chr4:1665668
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.75+2999C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665668 | ||||||
chr4:1665963
|
C | CTGTATCT others(27): Show |
3 | a0001c0002t0004g0317a0001c0002t0004g0326a0001c0002t0017g0126 | 3 | HG01106.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.75+2703_75+2704ins others(34): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665963 | ||||||
chr4:1665964
|
A | G | 5 | a0001c0002t0004g0140a0001c0002t0004g0317a0001c0002t0004g0326others(2): Show | 5 | HG01106.hp2 HG02615.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+2703T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665964 | ||||||
chr4:1665997
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2670C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1665997 | ||||||
chr4:1666025
|
C | A | 1 | a0001c0002t0004g0304 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.75+2642G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666025 | ||||||
chr4:1666045
|
T | C | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(314): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.75+2622A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666045 | ||||||
chr4:1666057
|
C | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2610G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666057 | ||||||
chr4:1666063
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.75+2604C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666063 | ||||||
chr4:1666156
|
C | A | 1 | a0001c0001t0010g0041 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2511G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666156 | ||||||
chr4:1666189
|
A | C | 1 | a0001c0001t0010g0041 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2478T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666189 | ||||||
chr4:1666208
|
A | G | 1 | a0001c0001t0010g0041 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2459T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666208 | ||||||
chr4:1666212
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2455C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666212 | ||||||
chr4:1666213
|
C | CACCTGCA others(20): Show |
1 | a0001c0001t0010g0041 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.75+2453_75+2454ins others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666213 | ||||||
chr4:1666241
|
G | A | 2 | a0001c0001t0010g0041a0001c0002t0004g0310 | 2 | HG03017.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.75+2426C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666241 | ||||||
chr4:1666255
|
A | C | 2 | a0001c0001t0010g0041a0012c0009t0014g0013 | 2 | HG03704.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.75+2412T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666255 | ||||||
chr4:1666273
|
A | AACCTGCA others(52): Show |
1 | a0001c0001t0001g0248 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.75+2393_75+2394ins others(59): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | ||||||
chr4:1666273
|
A | AACCTGCA others(59): Show |
1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2328_75+2393dup others(66): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | ||||||
chr4:1666273
|
A | AACGTGCA others(59): Show |
56 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(53): Show | 57 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.75+2393_75+2394ins others(66): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | ||||||
chr4:1666273
|
A | AGCCTGCA others(92): Show |
1 | a0012c0009t0014g0013 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.75+2393_75+2394ins others(99): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666273 | ||||||
chr4:1666276
|
C | G | 1 | a0001c0002t0004g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+2391G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666276 | ||||||
chr4:1666319
|
T | TGTATCTA others(24): Show |
1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+2317_75+2347dup others(31): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666319 | ||||||
chr4:1666319
|
T | TGTATCTA others(57): Show |
258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 269 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.75+2284_75+2347dup others(64): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666319 | ||||||
chr4:1666383
|
C | CCTGTATC others(93): Show |
1 | a0001c0002t0004g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75+2283_75+2284ins others(100): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666383 | ||||||
chr4:1666417
|
C | A | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.75+2250G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666417 | ||||||
chr4:1666451
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+2216C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666451 | ||||||
chr4:1666480
|
T | A | 320 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(317): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.75+2187A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666480 | ||||||
chr4:1666553
|
G | A | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+2114C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666553 | ||||||
chr4:1666577
|
G | C | 326 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(323): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.75+2090C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666577 | ||||||
chr4:1666592
|
C | T | 2 | a0001c0001t0019g0276a0001c0001t0019g0278 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+2075G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666592 | ||||||
chr4:1666598
|
C | G | 1 | a0001c0001t0021g0103 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.75+2069G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666598 | ||||||
chr4:1666609
|
T | C | 1 | a0003c0004t0022g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+2058A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666609 | ||||||
chr4:1666610
|
G | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.75+2057C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666610 | ||||||
chr4:1666648
|
G | A | 1 | a0002c0003t0020g0301 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.75+2019C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666648 | ||||||
chr4:1666682
|
T | A | 1 | a0001c0001t0001g0248 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.75+1985A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666682 | ||||||
chr4:1666740
|
G | A | 3 | a0002c0003t0009g0106a0002c0003t0009g0107a0002c0003t0009g0122 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.75+1927C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666740 | ||||||
chr4:1666777
|
G | A | 1 | a0002c0003t0020g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+1890C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666777 | ||||||
chr4:1666795
|
G | A | 1 | a0001c0002t0004g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.75+1872C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666795 | ||||||
chr4:1666855
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.75+1812A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1666855 | ||||||
chr4:1667058
|
G | T | 1 | a0001c0001t0008g0233 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+1609C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667058 | ||||||
chr4:1667104
|
G | A | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.75+1563C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667104 | ||||||
chr4:1667111
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.75+1556C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667111 | ||||||
chr4:1667127
|
C | CAAA | 53 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(50): Show | 54 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.75+1537_75+1539dup others(3): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667127 | ||||||
chr4:1667169
|
T | A | 1 | a0001c0001t0001g0248 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.75+1498A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667169 | ||||||
chr4:1667267
|
C | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.75+1400G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667267 | ||||||
chr4:1667268
|
C | T | 7 | a0001c0001t0010g0029a0001c0001t0010g0039a0001c0001t0010g0041others(4): Show | 7 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+1399G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667268 | ||||||
chr4:1667326
|
G | A | 9 | a0001c0001t0001g0010a0001c0001t0001g0232a0001c0001t0001g0288others(6): Show | 10 | HG01074.hp1 HG01081.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+1341C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667326 | ||||||
chr4:1667420
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0270 | 2 | HG00558.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.75+1247C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667420 | ||||||
chr4:1667451
|
A | C | 1 | a0001c0001t0005g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+1216T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667451 | ||||||
chr4:1667472
|
C | T | 1 | a0001c0002t0041g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.75+1195G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667472 | ||||||
chr4:1667479
|
C | T | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+1188G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667479 | ||||||
chr4:1667512
|
C | T | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1155G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667512 | ||||||
chr4:1667525
|
C | T | 5 | a0001c0002t0015g0015a0001c0002t0015g0016a0001c0002t0015g0050others(2): Show | 5 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+1142G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667525 | ||||||
chr4:1667526
|
G | A | 4 | a0001c0001t0046g0129a0003c0004t0022g0131a0003c0004t0022g0150others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+1141C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667526 | ||||||
chr4:1667548
|
C | G | 1 | a0001c0002t0004g0311 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.75+1119G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1667548 | ||||||
chr4:1668028
|
G | A | 1 | a0001c0002t0003g0333 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.75+639C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668028 | ||||||
chr4:1668032
|
T | C | 326 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(323): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.75+635A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668032 | ||||||
chr4:1668090
|
C | G | 4 | a0001c0001t0019g0133a0001c0001t0019g0276a0001c0001t0019g0277others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+577G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668090 | ||||||
chr4:1668108
|
T | C | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.75+559A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668108 | ||||||
chr4:1668109
|
T | C | 1 | a0002c0003t0002g0298 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.75+558A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668109 | ||||||
chr4:1668148
|
C | CT | 318 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(315): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.75+518dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668148 | ||||||
chr4:1668203
|
G | C | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+464C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668203 | ||||||
chr4:1668237
|
G | T | 1 | a0001c0001t0007g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+430C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668237 | ||||||
chr4:1668240
|
T | C | 1 | a0001c0001t0007g0074 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+427A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668240 | ||||||
chr4:1668264
|
C | T | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.75+403G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668264 | ||||||
chr4:1668285
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75+382C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668285 | ||||||
chr4:1668391
|
T | C | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.75+276A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668391 | ||||||
chr4:1668470
|
A | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+197T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668470 | ||||||
chr4:1668489
|
G | A | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.75+178C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668489 | ||||||
chr4:1668549
|
A | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+118T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668549 | ||||||
chr4:1668563
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75+104C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 2/4 | chr4 | 1668563 | ||||||
chr4:1668972
|
A | C | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-67T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1668972 | ||||||
chr4:1668975
|
T | C | 1 | a0001c0001t0047g0318 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-164-70A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1668975 | ||||||
chr4:1669092
|
TA | T | 6 | a0002c0003t0020g0148a0002c0003t0020g0301a0002c0003t0020g0319others(3): Show | 6 | HG01109.hp1 HG01975.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-188delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669092 | ||||||
chr4:1669127
|
G | A | 32 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(29): Show | 32 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-164-222C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669127 | ||||||
chr4:1669137
|
A | G | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-232T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669137 | ||||||
chr4:1669228
|
G | A | 1 | a0001c0001t0010g0026 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-164-323C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669228 | ||||||
chr4:1669233
|
T | C | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-164-328A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669233 | ||||||
chr4:1669395
|
G | A | 1 | a0001c0001t0051g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-164-490C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669395 | ||||||
chr4:1669404
|
G | C | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-499C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669404 | ||||||
chr4:1669427
|
C | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-522G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669427 | ||||||
chr4:1669450
|
G | C | 5 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-545C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669450 | ||||||
chr4:1669579
|
C | T | 1 | a0001c0002t0004g0326 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-164-674G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669579 | ||||||
chr4:1669738
|
G | A | 1 | a0001c0001t0012g0118 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-164-833C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669738 | ||||||
chr4:1669803
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-164-898C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669803 | ||||||
chr4:1669896
|
C | T | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-164-991G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669896 | ||||||
chr4:1669984
|
C | T | 1 | a0001c0002t0036g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-1079G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669984 | ||||||
chr4:1669985
|
G | A | 6 | a0001c0002t0003g0153a0001c0002t0003g0194a0001c0002t0003g0199others(3): Show | 6 | HG01070.hp2 HG02300.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.-164-1080C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1669985 | ||||||
chr4:1670001
|
C | A | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-1096G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670001 | ||||||
chr4:1670024
|
C | T | 2 | a0001c0001t0028g0149a0001c0001t0028g0321 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-164-1119G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670024 | ||||||
chr4:1670045
|
G | A | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 195 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.-164-1140C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670045 | ||||||
chr4:1670117
|
GGCCAT | G | 5 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-1217_-164-121 others(9): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670117 | ||||||
chr4:1670320
|
C | T | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-1415G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670320 | ||||||
chr4:1670369
|
G | T | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 126 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.-164-1464C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670369 | ||||||
chr4:1670491
|
C | G | 2 | a0001c0001t0046g0129a0001c0001t0047g0318 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-1586G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670491 | ||||||
chr4:1670649
|
A | G | 4 | a0001c0001t0037g0057a0003c0004t0022g0131a0003c0004t0022g0150others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-1744T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670649 | ||||||
chr4:1670695
|
G | A | 1 | a0001c0001t0008g0233 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-164-1790C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670695 | ||||||
chr4:1670896
|
G | A | 3 | a0001c0001t0005g0089a0002c0003t0030g0135a0002c0003t0030g0147 | 3 | HG02886.hp1 HG03195.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-164-1991C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670896 | ||||||
chr4:1670900
|
G | A | 1 | a0002c0003t0009g0122 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-164-1995C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1670900 | ||||||
chr4:1671032
|
G | A | 1 | a0001c0001t0023g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-164-2127C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671032 | ||||||
chr4:1671047
|
C | G | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-2142G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671047 | ||||||
chr4:1671061
|
A | ACCAGCTC others(49): Show |
7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-2157_-164-215 others(60): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671061 | ||||||
chr4:1671073
|
C | CCACAGCC others(473): Show |
1 | a0002c0003t0002g0281 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-164-2169_-164-216 others(484): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671073 | ||||||
chr4:1671073
|
C | CCACAGCC others(473): Show |
41 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(38): Show | 43 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-164-2169_-164-216 others(484): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671073 | ||||||
chr4:1671095
|
C | T | 1 | a0001c0002t0003g0330 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-164-2190G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671095 | ||||||
chr4:1671117
|
A | C | 2 | a0001c0002t0036g0054a0002c0003t0009g0105 | 2 | HG02809.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-164-2212T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671117 | ||||||
chr4:1671118
|
C | A | 2 | a0001c0001t0046g0129a0001c0001t0047g0318 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-2213G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671118 | ||||||
chr4:1671129
|
C | CCACAGCC others(417): Show |
1 | a0002c0003t0009g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-164-2225_-164-222 others(428): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671129 | ||||||
chr4:1671129
|
C | T | 9 | a0001c0002t0003g0193a0001c0002t0003g0195a0001c0002t0003g0197others(6): Show | 9 | HG00621.hp1 HG01981.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.-164-2224G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671129 | ||||||
chr4:1671138
|
T | C | 44 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(41): Show | 46 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.-164-2233A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671138 | ||||||
chr4:1671173
|
A | C | 42 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(39): Show | 44 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.-164-2268T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671173 | ||||||
chr4:1671189
|
A | G | 1 | a0001c0002t0036g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2284T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671189 | ||||||
chr4:1671212
|
C | G | 2 | a0001c0002t0036g0054a0010c0011t0045g0123 | 2 | HG02258.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-164-2307G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671212 | ||||||
chr4:1671223
|
C | A | 1 | a0001c0002t0036g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2318G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671223 | ||||||
chr4:1671245
|
A | G | 1 | a0001c0002t0036g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2340T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671245 | ||||||
chr4:1671250
|
G | A | 58 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(55): Show | 59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-164-2345C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671250 | ||||||
chr4:1671270
|
G | A | 43 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(40): Show | 45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-2365C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671270 | ||||||
chr4:1671276
|
G | A | 12 | a0001c0002t0004g0159a0001c0002t0004g0282a0001c0002t0004g0310others(9): Show | 13 | HG00099.hp2 HG01074.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-164-2371C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671276 | ||||||
chr4:1671279
|
A | C | 1 | a0002c0003t0009g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-164-2374T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671279 | ||||||
chr4:1671300
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0270 | 2 | HG00558.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-164-2395G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671300 | ||||||
chr4:1671316
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0046g0129a0001c0001t0047g0318 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-2411G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671316 | ||||||
chr4:1671335
|
C | A | 4 | a0001c0001t0001g0176a0001c0001t0007g0076a0001c0002t0036g0054others(1): Show | 4 | HG02015.hp2 HG02258.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-2430G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671335 | ||||||
chr4:1671350
|
C | T | 1 | a0002c0003t0002g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-164-2445G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671350 | ||||||
chr4:1671356
|
G | A | 1 | a0001c0001t0007g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-164-2451C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671356 | ||||||
chr4:1671385
|
A | C | 9 | a0001c0001t0006g0051a0001c0001t0007g0002a0001c0001t0007g0070others(6): Show | 11 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-164-2480T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671385 | ||||||
chr4:1671391
|
T | TCACAGCC others(585): Show |
1 | a0001c0001t0001g0234 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-164-2487_-164-248 others(596): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671391 | ||||||
chr4:1671401
|
G | A | 1 | a0001c0002t0036g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-164-2496C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671401 | ||||||
chr4:1671424
|
G | C | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-2519C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671424 | ||||||
chr4:1671435
|
A | ACCAGCTC others(1333): Show |
7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-2531_-164-253 others(1344): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671435 | ||||||
chr4:1671435
|
A | ACCAGCTC others(155): Show |
43 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(40): Show | 45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-2531_-164-253 others(166): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671435 | ||||||
chr4:1671435
|
A | C | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-2530T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671435 | ||||||
chr4:1671447
|
C | CCACAGCC others(261): Show |
1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(272): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(529): Show |
1 | a0001c0001t0001g0224 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(540): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(529): Show |
3 | a0001c0001t0008g0256a0001c0001t0008g0259a0001c0001t0008g0260 | 3 | NA18939.hp1 NA18956.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(540): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(473): Show |
1 | a0001c0001t0005g0084 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(484): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(579): Show |
181 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 190 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(579): Show |
2 | a0001c0001t0028g0149a0001c0001t0028g0321 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(841): Show |
1 | a0001c0001t0007g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(852): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(579): Show |
2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(579): Show |
5 | a0001c0001t0012g0100a0001c0001t0012g0101a0001c0001t0012g0108others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(579): Show |
6 | a0001c0001t0006g0024a0001c0001t0006g0027a0001c0001t0006g0028others(3): Show | 6 | HG00423.hp2 HG02080.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(261): Show |
4 | a0001c0002t0050g0274a0001c0002t0060g0324a0005c0006t0038g0011others(1): Show | 4 | HG02257.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(272): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(579): Show |
2 | a0001c0001t0001g0225a0010c0011t0045g0123 | 2 | HG02129.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(590): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(417): Show |
1 | a0001c0001t0007g0076 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-164-2543_-164-254 others(428): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(205): Show |
29 | a0001c0002t0004g0140a0001c0002t0004g0144a0001c0002t0004g0158others(26): Show | 29 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(216): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(205): Show |
23 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(20): Show | 23 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(216): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671447
|
C | CCACAGCC others(205): Show |
1 | a0001c0002t0017g0003 | 2 | HG00099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-164-2543_-164-254 others(216): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671447 | ||||||
chr4:1671457
|
A | G | 52 | a0001c0001t0027g0132a0001c0001t0057g0141a0001c0002t0003g0208others(49): Show | 54 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.-164-2552T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671457 | ||||||
chr4:1671461
|
G | C | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(314): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.-164-2556C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671461 | ||||||
chr4:1671480
|
G | C | 265 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(262): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-164-2575C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671480 | ||||||
chr4:1671491
|
C | A | 52 | a0001c0001t0027g0132a0001c0001t0057g0141a0001c0002t0003g0208others(49): Show | 54 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.-164-2586G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671491 | ||||||
chr4:1671491
|
C | CCCAGCTC others(99): Show |
3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-2587_-164-258 others(110): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671491 | ||||||
chr4:1671498
|
C | T | 1 | a0001c0002t0003g0208 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2593G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671498 | ||||||
chr4:1671503
|
C | CCACGGCC others(149): Show |
1 | a0001c0002t0003g0208 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2599_-164-259 others(160): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671503 | ||||||
chr4:1671513
|
G | A | 266 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-164-2608C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671513 | ||||||
chr4:1671513
|
G | GGCCCGGA others(261): Show |
6 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0031g0049others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-164-2609_-164-260 others(272): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671513 | ||||||
chr4:1671518
|
G | A | 2 | a0001c0001t0057g0141a0001c0002t0049g0332 | 2 | HG02258.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-164-2613C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671518 | ||||||
chr4:1671536
|
G | C | 1 | a0001c0002t0003g0208 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2631C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671536 | ||||||
chr4:1671547
|
A | ACCAGCTC others(523): Show |
1 | a0001c0001t0057g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-164-2643_-164-264 others(534): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671547 | ||||||
chr4:1671547
|
A | C | 1 | a0001c0002t0003g0208 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-164-2642T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671547 | ||||||
chr4:1671569
|
A | G | 324 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(321): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.-164-2664T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671569 | ||||||
chr4:1671573
|
G | C | 326 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(323): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-164-2668C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671573 | ||||||
chr4:1671665
|
G | C | 2 | a0002c0003t0009g0113a0002c0003t0009g0114 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-164-2760C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671665 | ||||||
chr4:1671672
|
T | C | 1 | a0001c0002t0003g0333 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-164-2767A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671672 | ||||||
chr4:1671773
|
C | T | 63 | a0001c0001t0037g0057a0001c0002t0003g0153a0001c0002t0003g0160others(60): Show | 64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-2868G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671773 | ||||||
chr4:1671837
|
C | T | 270 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-164-2932G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1671837 | ||||||
chr4:1672004
|
C | T | 2 | a0001c0001t0046g0129a0001c0001t0047g0318 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-3099G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672004 | ||||||
chr4:1672024
|
C | CACCCAGG others(17): Show |
63 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(60): Show | 64 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.-164-3120_-164-311 others(28): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672024 | ||||||
chr4:1672035
|
C | A | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-3130G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672035 | ||||||
chr4:1672043
|
CT | C | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-164-3139delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672043 | ||||||
chr4:1672048
|
A | AT | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-164-3144_-164-314 others(5): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672048 | ||||||
chr4:1672086
|
G | A | 43 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(40): Show | 45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-3181C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672086 | ||||||
chr4:1672093
|
CGAACCCA others(17): Show |
C | 1 | a0001c0001t0023g0033 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-164-3212_-164-318 others(28): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672093 | ||||||
chr4:1672124
|
A | C | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-164-3219T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672124 | ||||||
chr4:1672133
|
G | C | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(204): Show | 216 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-164-3228C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672133 | ||||||
chr4:1672161
|
CCCAGGAA others(48): Show |
C | 59 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-164-3311_-164-325 others(59): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672161 | ||||||
chr4:1672175
|
AACCCACG others(1): Show |
A | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-164-3278_-164-327 others(12): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672175 | ||||||
chr4:1672262
|
GACCCACA others(16): Show |
G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-3380_-164-335 others(27): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672262 | ||||||
chr4:1672285
|
C | T | 59 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-164-3380G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672285 | ||||||
chr4:1672309
|
AACCCATG others(25): Show |
A | 59 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-164-3436_-164-340 others(36): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672309 | ||||||
chr4:1672325
|
AACCCAGG others(17): Show |
A | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-3444_-164-342 others(28): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672325 | ||||||
chr4:1672347
|
T | G | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-164-3442A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672347 | ||||||
chr4:1672349
|
G | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 215 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-164-3444C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672349 | ||||||
chr4:1672363
|
G | C | 2 | a0001c0001t0001g0249a0001c0001t0005g0083 | 2 | NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-164-3458C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672363 | ||||||
chr4:1672363
|
GGAACCCA others(1): Show |
G | 53 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(50): Show | 55 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.-164-3466_-164-345 others(12): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672363 | ||||||
chr4:1672435
|
G | A | 1 | a0002c0003t0025g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-164-3530C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672435 | ||||||
chr4:1672481
|
G | A | 2 | a0001c0001t0010g0026a0001c0001t0010g0034 | 2 | HG00621.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-164-3576C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672481 | ||||||
chr4:1672521
|
A | G | 1 | a0001c0001t0005g0091 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-164-3616T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672521 | ||||||
chr4:1672579
|
C | T | 1 | a0001c0001t0024g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-164-3674G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672579 | ||||||
chr4:1672628
|
G | GCT | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-3725_-164-372 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672628 | ||||||
chr4:1672632
|
G | A | 1 | a0001c0002t0004g0326 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-164-3727C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672632 | ||||||
chr4:1672759
|
CT | C | 9 | a0001c0002t0003g0160a0001c0002t0003g0194a0001c0002t0003g0267others(6): Show | 9 | HG00642.hp1 HG01243.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-164-3855delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | ||||||
chr4:1672759
|
CTT | C | 48 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0031g0049others(45): Show | 49 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.-164-3856_-164-385 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | ||||||
chr4:1672759
|
CTTT | C | 21 | a0001c0001t0001g0240a0001c0001t0001g0248a0001c0001t0001g0283others(18): Show | 21 | HG00438.hp1 HG01109.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-164-3857_-164-385 others(7): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | ||||||
chr4:1672759
|
CTTTT | C | 186 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(183): Show | 195 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.-164-3858_-164-385 others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | ||||||
chr4:1672759
|
CTTTTTTT others(3): Show |
C | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-3864_-164-385 others(14): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | ||||||
chr4:1672759
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0028g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-164-3865_-164-385 others(15): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | ||||||
chr4:1672759
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0006g0040 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-164-3870_-164-385 others(20): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672759 | ||||||
chr4:1672914
|
C | G | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-4009G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1672914 | ||||||
chr4:1673156
|
C | T | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-164-4251G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673156 | ||||||
chr4:1673217
|
T | C | 1 | a0001c0002t0004g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-164-4312A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673217 | ||||||
chr4:1673224
|
C | T | 11 | a0001c0001t0009g0111a0001c0001t0016g0062a0001c0001t0016g0098others(8): Show | 11 | HG02572.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-164-4319G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673224 | ||||||
chr4:1673254
|
G | A | 2 | a0001c0001t0046g0129a0001c0001t0047g0318 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-164-4349C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673254 | ||||||
chr4:1673282
|
G | A | 1 | a0001c0002t0004g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-164-4377C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673282 | ||||||
chr4:1673400
|
G | A | 1 | a0001c0001t0006g0035 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-164-4495C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673400 | ||||||
chr4:1673416
|
C | G | 43 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(40): Show | 45 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.-164-4511G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673416 | ||||||
chr4:1673459
|
C | T | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-4554G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673459 | ||||||
chr4:1673514
|
A | G | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-164-4609T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673514 | ||||||
chr4:1673550
|
T | C | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-164-4645A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673550 | ||||||
chr4:1673615
|
C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-164-4710G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673615 | ||||||
chr4:1673624
|
T | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-4719A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673624 | ||||||
chr4:1673649
|
C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-164-4744G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673649 | ||||||
chr4:1673720
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-164-4815C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673720 | ||||||
chr4:1673728
|
G | A | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-4823C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673728 | ||||||
chr4:1673949
|
G | A | 10 | a0001c0001t0012g0100a0001c0001t0012g0108a0001c0001t0026g0327others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-164-5044C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1673949 | ||||||
chr4:1674013
|
G | A | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-5108C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674013 | ||||||
chr4:1674090
|
C | T | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-164-5185G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674090 | ||||||
chr4:1674261
|
G | A | 1 | a0001c0001t0010g0026 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-164-5356C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674261 | ||||||
chr4:1674272
|
C | T | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-5367G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674272 | ||||||
chr4:1674367
|
A | G | 4 | a0001c0001t0019g0133a0001c0001t0019g0276a0001c0001t0019g0277others(1): Show | 4 | HG02572.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-5462T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674367 | ||||||
chr4:1674407
|
C | T | 2 | a0002c0003t0030g0135a0002c0003t0030g0147 | 2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-164-5502G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674407 | ||||||
chr4:1674466
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-164-5561C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674466 | ||||||
chr4:1674540
|
G | A | 1 | a0001c0001t0005g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-164-5635C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674540 | ||||||
chr4:1674668
|
CA | C | 291 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(288): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.-164-5764delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674668 | ||||||
chr4:1674767
|
T | C | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-5862A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674767 | ||||||
chr4:1674832
|
G | A | 7 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0236others(4): Show | 7 | HG00738.hp2 HG01069.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-164-5927C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674832 | ||||||
chr4:1674871
|
C | A | 5 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0237others(2): Show | 5 | HG02056.hp2 NA18939.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.-164-5966G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674871 | ||||||
chr4:1674961
|
C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-164-6056G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674961 | ||||||
chr4:1674998
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-164-6093C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1674998 | ||||||
chr4:1675028
|
A | AC | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-6124dupG | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675028 | ||||||
chr4:1675062
|
G | A | 16 | a0001c0001t0006g0051a0001c0001t0007g0002a0001c0001t0007g0070others(13): Show | 18 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-164-6157C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675062 | ||||||
chr4:1675291
|
T | C | 326 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(323): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-164-6386A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675291 | ||||||
chr4:1675305
|
C | T | 1 | a0001c0002t0004g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-164-6400G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675305 | ||||||
chr4:1675382
|
T | G | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-164-6477A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675382 | ||||||
chr4:1675593
|
G | C | 316 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-164-6688C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675593 | ||||||
chr4:1675703
|
G | A | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-164-6798C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675703 | ||||||
chr4:1675712
|
G | A | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-164-6807C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675712 | ||||||
chr4:1675757
|
G | C | 203 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 212 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-164-6852C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675757 | ||||||
chr4:1675764
|
G | A | 4 | a0001c0001t0037g0057a0003c0004t0022g0131a0003c0004t0022g0150others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-164-6859C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675764 | ||||||
chr4:1675764
|
G | T | 3 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0040g0067 | 3 | HG02055.hp2 HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-164-6859C>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675764 | ||||||
chr4:1675802
|
C | T | 1 | a0001c0001t0052g0222 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-164-6897G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675802 | ||||||
chr4:1675818
|
C | T | 1 | a0002c0003t0002g0279 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-164-6913G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675818 | ||||||
chr4:1675906
|
G | A | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-164-7001C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675906 | ||||||
chr4:1675936
|
A | T | 1 | a0001c0002t0003g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-164-7031T>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675936 | ||||||
chr4:1675950
|
C | T | 1 | a0001c0001t0008g0262 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-164-7045G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1675950 | ||||||
chr4:1676066
|
G | A | 203 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(200): Show | 212 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-164-7161C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676066 | ||||||
chr4:1676126
|
A | C | 7 | a0001c0001t0012g0100a0001c0001t0012g0108a0001c0001t0031g0049others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-164-7221T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676126 | ||||||
chr4:1676155
|
C | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 123 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-164-7250G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676155 | ||||||
chr4:1676239
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0294 | 2 | HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-164-7334C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676239 | ||||||
chr4:1676259
|
C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-164-7354G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676259 | ||||||
chr4:1676269
|
A | G | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-164-7364T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676269 | ||||||
chr4:1676358
|
G | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0239 | 2 | HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-164-7453C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676358 | ||||||
chr4:1676701
|
G | C | 259 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 270 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.-165+7532C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676701 | ||||||
chr4:1676706
|
G | A | 1 | a0001c0002t0003g0200 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-165+7527C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676706 | ||||||
chr4:1676747
|
C | G | 336 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.-165+7486G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676747 | ||||||
chr4:1676835
|
C | T | 6 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0031g0049others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+7398G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676835 | ||||||
chr4:1676871
|
G | C | 2 | a0001c0001t0046g0129a0001c0001t0047g0318 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-165+7362C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1676871 | ||||||
chr4:1677044
|
G | A | 217 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(214): Show | 226 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-165+7189C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677044 | ||||||
chr4:1677050
|
C | T | 2 | a0005c0006t0038g0011a0005c0006t0061g0142 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-165+7183G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677050 | ||||||
chr4:1677051
|
A | G | 114 | a0001c0001t0027g0132a0001c0001t0037g0057a0001c0002t0003g0153others(111): Show | 117 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-165+7182T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677051 | ||||||
chr4:1677098
|
T | C | 10 | a0001c0001t0012g0100a0001c0001t0012g0108a0001c0001t0026g0327others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+7135A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677098 | ||||||
chr4:1677351
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0029g0165 | 2 | NA18612.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-165+6882G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677351 | ||||||
chr4:1677390
|
G | A | 1 | a0002c0003t0002g0251 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-165+6843C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677390 | ||||||
chr4:1677402
|
C | A | 1 | a0001c0002t0036g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-165+6831G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677402 | ||||||
chr4:1677417
|
G | A | 4 | a0002c0003t0002g0138a0002c0003t0002g0156a0002c0003t0009g0115others(1): Show | 4 | HG01891.hp2 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-165+6816C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677417 | ||||||
chr4:1677524
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+6709C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677524 | ||||||
chr4:1677561
|
T | G | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+6672A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677561 | ||||||
chr4:1677699
|
A | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 211 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-165+6534T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677699 | ||||||
chr4:1677730
|
G | A | 1 | a0001c0001t0026g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-165+6503C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677730 | ||||||
chr4:1677876
|
C | T | 10 | a0002c0003t0009g0113a0002c0003t0009g0114a0002c0003t0020g0148others(7): Show | 10 | HG01109.hp1 HG01243.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-165+6357G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677876 | ||||||
chr4:1677932
|
G | C | 57 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-165+6301C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677932 | ||||||
chr4:1677955
|
T | G | 3 | a0003c0004t0022g0131a0003c0004t0022g0150a0003c0004t0022g0316 | 3 | HG02559.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-165+6278A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1677955 | ||||||
chr4:1678083
|
C | T | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+6150G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678083 | ||||||
chr4:1678134
|
G | A | 9 | a0001c0001t0011g0134a0001c0001t0011g0136a0001c0001t0011g0137others(6): Show | 9 | HG01167.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-165+6099C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678134 | ||||||
chr4:1678157
|
C | A | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+6076G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678157 | ||||||
chr4:1678360
|
T | G | 1 | a0002c0003t0002g0279 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-165+5873A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678360 | ||||||
chr4:1678377
|
C | T | 316 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-165+5856G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678377 | ||||||
chr4:1678407
|
C | T | 326 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(323): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.-165+5826G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678407 | ||||||
chr4:1678550
|
G | A | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+5683C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678550 | ||||||
chr4:1678582
|
G | A | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+5651C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678582 | ||||||
chr4:1678696
|
T | C | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+5537A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678696 | ||||||
chr4:1678725
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG00642.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-165+5508C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678725 | ||||||
chr4:1678746
|
C | T | 58 | a0001c0001t0001g0221a0001c0002t0003g0153a0001c0002t0003g0160others(55): Show | 59 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-165+5487G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678746 | ||||||
chr4:1678835
|
G | A | 10 | a0001c0001t0012g0100a0001c0001t0012g0108a0001c0001t0026g0327others(7): Show | 10 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+5398C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1678835 | ||||||
chr4:1679206
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+5027C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679206 | ||||||
chr4:1679270
|
C | T | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+4963G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679270 | ||||||
chr4:1679309
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-165+4924G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679309 | ||||||
chr4:1679316
|
G | A | 1 | a0001c0001t0028g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-165+4917C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679316 | ||||||
chr4:1679379
|
A | C | 14 | a0001c0001t0006g0025a0001c0001t0006g0036a0001c0001t0006g0043others(11): Show | 14 | HG00280.hp2 HG00733.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-165+4854T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679379 | ||||||
chr4:1679386
|
C | CA | 106 | a0001c0001t0001g0191a0001c0001t0001g0210a0001c0001t0001g0240others(103): Show | 109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-165+4846dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679386 | ||||||
chr4:1679386
|
C | CAA | 8 | a0001c0001t0001g0214a0001c0001t0006g0036a0001c0001t0008g0155others(5): Show | 8 | HG02027.hp2 HG02257.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+4845_-165+484 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679386 | ||||||
chr4:1679484
|
GAGACCAG others(627): Show |
G | 1 | a0001c0001t0046g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-165+4115_-165+474 others(4): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679484 | ||||||
chr4:1679542
|
C | T | 3 | a0001c0001t0008g0256a0001c0001t0008g0259a0001c0001t0008g0260 | 3 | NA18939.hp1 NA18956.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-165+4691G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679542 | ||||||
chr4:1679547
|
G | A | 50 | a0001c0001t0027g0132a0002c0003t0002g0008a0002c0003t0002g0138others(47): Show | 52 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.-165+4686C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679547 | ||||||
chr4:1679680
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-165+4553G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679680 | ||||||
chr4:1679684
|
T | TA | 18 | a0001c0001t0001g0268a0001c0001t0009g0111a0001c0001t0016g0062others(15): Show | 18 | HG02055.hp2 HG02280.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.-165+4548dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679684 | ||||||
chr4:1679684
|
T | TAA | 49 | a0001c0001t0027g0132a0001c0002t0004g0144a0002c0003t0002g0008others(46): Show | 51 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.-165+4547_-165+454 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679684 | ||||||
chr4:1679684
|
TA | T | 56 | a0001c0001t0001g0220a0001c0001t0007g0070a0001c0001t0029g0165others(53): Show | 57 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-165+4548delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679684 | ||||||
chr4:1679815
|
G | A | 4 | a0001c0001t0037g0057a0003c0004t0022g0131a0003c0004t0022g0150others(1): Show | 4 | HG02559.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-165+4418C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679815 | ||||||
chr4:1679847
|
G | A | 2 | a0001c0001t0028g0149a0001c0001t0028g0321 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-165+4386C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679847 | ||||||
chr4:1679875
|
C | T | 1 | a0001c0001t0006g0043 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-165+4358G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679875 | ||||||
chr4:1679987
|
C | T | 1 | a0001c0001t0014g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-165+4246G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1679987 | ||||||
chr4:1680012
|
G | C | 51 | a0001c0001t0027g0132a0001c0002t0004g0144a0002c0003t0002g0008others(48): Show | 53 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+4221C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680012 | ||||||
chr4:1680024
|
G | GA | 304 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.-165+4208dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680024 | ||||||
chr4:1680024
|
G | GAA | 11 | a0001c0001t0001g0249a0001c0001t0005g0093a0001c0001t0006g0025others(8): Show | 11 | HG01099.hp2 HG02027.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-165+4207_-165+420 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680024 | ||||||
chr4:1680135
|
C | T | 1 | a0001c0001t0042g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-165+4098G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680135 | ||||||
chr4:1680166
|
A | C | 1 | a0001c0001t0051g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-165+4067T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680166 | ||||||
chr4:1680235
|
T | C | 322 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(319): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-165+3998A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680235 | ||||||
chr4:1680260
|
G | A | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+3973C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680260 | ||||||
chr4:1680274
|
G | A | 1 | a0001c0002t0032g0017 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-165+3959C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680274 | ||||||
chr4:1680283
|
C | A | 4 | a0001c0001t0026g0327a0001c0001t0026g0328a0001c0001t0031g0049others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+3950G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680283 | ||||||
chr4:1680296
|
G | A | 1 | a0001c0002t0003g0202 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-165+3937C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680296 | ||||||
chr4:1680305
|
G | C | 1 | a0001c0001t0010g0026 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-165+3928C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680305 | ||||||
chr4:1680319
|
C | CA | 9 | a0001c0001t0011g0136a0001c0001t0011g0272a0001c0001t0011g0273others(6): Show | 9 | HG01167.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+3913dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | ||||||
chr4:1680319
|
C | CAA | 60 | a0001c0001t0006g0024a0001c0001t0006g0025a0001c0001t0006g0027others(57): Show | 64 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.-165+3912_-165+391 others(6): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | ||||||
chr4:1680319
|
C | CAAA | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 114 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.-165+3911_-165+391 others(7): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | ||||||
chr4:1680319
|
C | CAAAA | 38 | a0001c0001t0001g0152a0001c0001t0001g0179a0001c0001t0001g0180others(35): Show | 38 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-165+3910_-165+391 others(8): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | ||||||
chr4:1680319
|
CA | C | 93 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(90): Show | 95 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-165+3913delT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680319 | ||||||
chr4:1680330
|
A | C | 1 | a0001c0002t0003g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-165+3903T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680330 | ||||||
chr4:1680331
|
A | C | 54 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0161others(51): Show | 55 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-165+3902T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680331 | ||||||
chr4:1680337
|
A | C | 30 | a0001c0002t0004g0140a0001c0002t0004g0158a0001c0002t0004g0159others(27): Show | 31 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-165+3896T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680337 | ||||||
chr4:1680468
|
T | C | 1 | a0010c0011t0045g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-165+3765A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680468 | ||||||
chr4:1680614
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-165+3619C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680614 | ||||||
chr4:1680632
|
A | G | 51 | a0001c0001t0027g0132a0001c0002t0004g0144a0002c0003t0002g0008others(48): Show | 53 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+3601T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680632 | ||||||
chr4:1680714
|
T | C | 1 | a0001c0002t0004g0144 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-165+3519A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680714 | ||||||
chr4:1680721
|
C | T | 5 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(2): Show | 5 | HG00673.hp1 NA18965.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.-165+3512G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680721 | ||||||
chr4:1680750
|
T | C | 7 | a0002c0003t0002g0145a0002c0003t0002g0323a0002c0003t0002g0325others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-165+3483A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680750 | ||||||
chr4:1680797
|
C | CA | 51 | a0001c0001t0014g0020a0001c0001t0027g0132a0002c0003t0002g0008others(48): Show | 53 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.-165+3435dupT | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680797 | ||||||
chr4:1680847
|
A | AGGGCACA others(7): Show |
1 | a0001c0001t0005g0083 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-165+3372_-165+338 others(18): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680847 | ||||||
chr4:1680864
|
G | C | 1 | a0001c0002t0003g0202 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-165+3369C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680864 | ||||||
chr4:1680890
|
T | C | 10 | a0001c0001t0027g0132a0002c0003t0002g0139a0002c0003t0002g0275others(7): Show | 10 | HG02145.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-165+3343A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680890 | ||||||
chr4:1680955
|
A | C | 114 | a0001c0001t0001g0265a0001c0001t0027g0132a0001c0001t0037g0057others(111): Show | 117 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-165+3278T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1680955 | ||||||
chr4:1681223
|
A | G | 1 | a0007c0015t0001g0212 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-165+3010T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681223 | ||||||
chr4:1681234
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-165+2999A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681234 | ||||||
chr4:1681299
|
T | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 126 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.-165+2934A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681299 | ||||||
chr4:1681342
|
C | T | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+2891G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681342 | ||||||
chr4:1681386
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-165+2847G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681386 | ||||||
chr4:1681439
|
G | A | 258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-165+2794C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681439 | ||||||
chr4:1681448
|
C | T | 1 | a0013c0008t0020g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-165+2785G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681448 | ||||||
chr4:1681489
|
T | C | 51 | a0001c0001t0027g0132a0001c0002t0004g0144a0002c0003t0002g0008others(48): Show | 53 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+2744A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681489 | ||||||
chr4:1681523
|
C | CT | 52 | a0001c0001t0010g0026a0001c0002t0003g0153a0001c0002t0003g0160others(49): Show | 53 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-165+2709dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681523 | ||||||
chr4:1681523
|
CT | C | 54 | a0001c0001t0001g0297a0001c0001t0006g0042a0001c0001t0007g0121others(51): Show | 56 | HG00733.hp1 HG01070.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.-165+2709delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681523 | ||||||
chr4:1681531
|
T | C | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-165+2702A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681531 | ||||||
chr4:1681575
|
C | A | 1 | a0001c0001t0006g0048 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-165+2658G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681575 | ||||||
chr4:1681658
|
A | G | 113 | a0001c0001t0027g0132a0001c0001t0037g0057a0001c0002t0003g0153others(110): Show | 116 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-165+2575T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681658 | ||||||
chr4:1681729
|
C | T | 14 | a0002c0003t0002g0008a0002c0003t0002g0186a0002c0003t0002g0187others(11): Show | 15 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-165+2504G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681729 | ||||||
chr4:1681761
|
C | T | 1 | a0002c0003t0025g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-165+2472G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681761 | ||||||
chr4:1681816
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0320 | 3 | HG00408.hp2 HG02015.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-165+2417G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681816 | ||||||
chr4:1681881
|
T | C | 13 | a0001c0001t0006g0025a0001c0001t0006g0043a0001c0001t0006g0044others(10): Show | 13 | HG00280.hp2 HG00733.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-165+2352A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681881 | ||||||
chr4:1681911
|
C | A | 1 | a0001c0001t0001g0249 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-165+2322G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681911 | ||||||
chr4:1681963
|
G | A | 1 | a0001c0002t0004g0311 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-165+2270C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1681963 | ||||||
chr4:1682239
|
A | G | 64 | a0001c0001t0011g0134a0001c0001t0011g0136a0001c0001t0011g0137others(61): Show | 65 | HG00609.hp1 HG00733.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.-165+1994T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682239 | ||||||
chr4:1682264
|
C | CT | 83 | a0001c0001t0001g0152a0001c0001t0001g0209a0001c0001t0005g0080others(80): Show | 87 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-165+1968dupA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682264 | ||||||
chr4:1682264
|
CT | C | 46 | a0001c0001t0012g0108a0001c0001t0013g0253a0001c0001t0013g0254others(43): Show | 47 | HG00609.hp1 HG00733.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.-165+1968delA | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682264 | ||||||
chr4:1682313
|
C | T | 1 | a0001c0001t0051g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-165+1920G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682313 | ||||||
chr4:1682408
|
A | G | 1 | a0001c0001t0037g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-165+1825T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682408 | ||||||
chr4:1682506
|
C | T | 1 | a0001c0001t0013g0255 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-165+1727G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682506 | ||||||
chr4:1682574
|
T | G | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-165+1659A>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682574 | ||||||
chr4:1682643
|
C | G | 2 | a0003c0004t0022g0150a0003c0004t0022g0316 | 2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-165+1590G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682643 | ||||||
chr4:1682682
|
C | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.-165+1551G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682682 | ||||||
chr4:1682702
|
A | G | 1 | a0001c0001t0031g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-165+1531T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682702 | ||||||
chr4:1682715
|
TGAGCAAC others(30): Show |
T | 1 | a0002c0003t0002g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-165+1481_-165+151 others(41): Show |
FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682715 | ||||||
chr4:1682730
|
A | G | 229 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(226): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.-165+1503T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682730 | ||||||
chr4:1682772
|
T | C | 6 | a0001c0001t0012g0118a0001c0001t0043g0117a0002c0003t0009g0068others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+1461A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682772 | ||||||
chr4:1682869
|
G | C | 190 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0209others(187): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.-165+1364C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682869 | ||||||
chr4:1682883
|
A | G | 1 | a0001c0002t0004g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-165+1350T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682883 | ||||||
chr4:1682900
|
G | C | 118 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0001g0268others(115): Show | 120 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-165+1333C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682900 | ||||||
chr4:1682907
|
G | A | 328 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(325): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.-165+1326C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682907 | ||||||
chr4:1682916
|
C | G | 1 | a0002c0003t0002g0156 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-165+1317G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682916 | ||||||
chr4:1682959
|
A | G | 5 | a0001c0001t0027g0132a0001c0001t0047g0318a0001c0002t0004g0317others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165+1274T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682959 | ||||||
chr4:1682960
|
C | T | 2 | a0001c0001t0008g0154a0001c0001t0008g0155 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-165+1273G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1682960 | ||||||
chr4:1683116
|
T | C | 1 | a0002c0003t0002g0314 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-165+1117A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683116 | ||||||
chr4:1683118
|
C | A | 1 | a0001c0001t0001g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-165+1115G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683118 | ||||||
chr4:1683355
|
T | A | 9 | a0001c0001t0001g0143a0001c0001t0003g0338a0001c0001t0057g0141others(6): Show | 9 | HG01243.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165+878A>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683355 | ||||||
chr4:1683399
|
C | A | 1 | a0001c0001t0008g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-165+834G>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683399 | ||||||
chr4:1683410
|
C | T | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.-165+823G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683410 | ||||||
chr4:1683416
|
C | T | 1 | a0001c0002t0003g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-165+817G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683416 | ||||||
chr4:1683484
|
T | C | 263 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 271 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.-165+749A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683484 | ||||||
chr4:1683512
|
A | C | 9 | a0001c0001t0011g0134a0001c0001t0011g0136a0001c0001t0011g0137others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-165+721T>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683512 | ||||||
chr4:1683586
|
A | G | 8 | a0001c0001t0001g0143a0001c0001t0003g0338a0001c0001t0057g0141others(5): Show | 8 | HG01243.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-165+647T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683586 | ||||||
chr4:1683604
|
T | C | 4 | a0001c0001t0011g0329a0001c0001t0026g0327a0001c0001t0026g0328others(1): Show | 4 | HG01106.hp2 HG02055.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-165+629A>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683604 | ||||||
chr4:1683614
|
G | A | 6 | a0001c0002t0003g0330a0001c0002t0003g0333a0001c0002t0003g0335others(3): Show | 6 | HG00621.hp1 HG02735.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-165+619C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683614 | ||||||
chr4:1683730
|
C | T | 8 | a0001c0001t0011g0134a0001c0001t0011g0136a0001c0001t0011g0137others(5): Show | 8 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+503G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683730 | ||||||
chr4:1683779
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-165+454C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683779 | ||||||
chr4:1683910
|
G | C | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG00642.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-165+323C>G | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683910 | ||||||
chr4:1683976
|
C | G | 8 | a0001c0001t0011g0134a0001c0001t0011g0136a0001c0001t0011g0137others(5): Show | 8 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-165+257G>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683976 | ||||||
chr4:1683980
|
C | T | 2 | a0001c0001t0056g0130a0003c0004t0022g0131 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-165+253G>A | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1683980 | ||||||
chr4:1684031
|
A | G | 1 | a0001c0001t0046g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-165+202T>C | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1684031 | ||||||
chr4:1684092
|
G | A | 1 | a0001c0001t0003g0338 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-165+141C>T | FAM53A | ENSG00000174137.14 | transcript | ENST00000308132.11 | protein_coding | 1/4 | chr4 | 1684092 |