geneid | 921 |
---|---|
ensemblid | ENSG00000110448.11 |
hgncid | 1685 |
symbol | CD5 |
name | CD5 molecule |
refseq_nuc | NM_014207.4 |
refseq_prot | NP_055022.2 |
ensembl_nuc | ENST00000347785.8 |
ensembl_prot | ENSP00000342681.3 |
mane_status | MANE Select |
chr | chr11 |
start | 61102489 |
end | 61127852 |
strand | + |
ver | v1.2 |
region | chr11:61102489-61127852 |
region5000 | chr11:61097489-61132852 |
regionname0 | CD5_chr11_61102489_61127852 |
regionname5000 | CD5_chr11_61097489_61132852 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 495 | 105 | 22 | 27 | 32 | 8 | 15 | 24 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002 | 0/0 | 495 | 58 | 30 | 22 | 0 | 4 | 2 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0003 | 0/0 | 495 | 40 | 21 | 5 | 7 | 3 | 4 | 5 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0004 | 1/0 | 495 | 10 | 0 | 3 | 0 | 3 | 3 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0005 | 0/0 | 495 | 9 | 6 | 2 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0006 | 0/0 | 495 | 7 | 2 | 4 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0007 | 0/0 | 495 | 7 | 3 | 1 | 0 | 0 | 3 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0008 | 0/0 | 495 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0009 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0010 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0011 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0012 | 0/0 | 495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0013 | 0/0 | 495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1488 | 105 | 22 | 27 | 32 | 8 | 15 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0002 | 0/0 | 1488 | 40 | 21 | 5 | 7 | 3 | 4 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0003 | 0/0 | 1488 | 32 | 6 | 20 | 0 | 4 | 2 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0004 | 0/0 | 1488 | 19 | 17 | 2 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0005 | 1/0 | 1488 | 10 | 0 | 3 | 0 | 3 | 3 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0006 | 0/0 | 1488 | 9 | 6 | 2 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0007 | 0/0 | 1488 | 7 | 3 | 1 | 0 | 0 | 3 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0008 | 0/0 | 1488 | 7 | 2 | 4 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0009 | 0/0 | 1488 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0010 | 0/0 | 1488 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0011 | 0/0 | 1488 | 3 | 3 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0012 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0013 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0014 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0015 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
c0016 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1648 | 153 | 47 | 32 | 40 | 11 | 22 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0002 | 1/0 | 1640 | 30 | 0 | 21 | 0 | 5 | 3 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0003 | 0/0 | 1641 | 24 | 12 | 7 | 1 | 2 | 2 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0004 | 0/0 | 1640 | 22 | 21 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0005 | 0/0 | 1644 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0006 | 0/0 | 1648 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0007 | 0/0 | 1641 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0008 | 0/0 | 1648 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0009 | 0/0 | 1640 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0010 | 0/0 | 1648 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0011 | 0/0 | 1636 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
t0012 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 19 | 11 | 4 | 1 | 1 | 2 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0002 | 0/0 | 17 | 0 | 5 | 6 | 0 | 6 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0003 | 0/0 | 9 | 0 | 8 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0004 | 0/0 | 8 | 3 | 1 | 0 | 2 | 2 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0006 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0007 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0017 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1488 | 105 | 22 | 27 | 32 | 8 | 15 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0003 | 0/0 | 1488 | 32 | 6 | 20 | 0 | 4 | 2 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0004 | 0/0 | 1488 | 19 | 17 | 2 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0009 | 0/0 | 1488 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0011 | 0/0 | 1488 | 3 | 3 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0003c0002 | 0/0 | 1488 | 40 | 21 | 5 | 7 | 3 | 4 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0004c0005 | 1/0 | 1488 | 10 | 0 | 3 | 0 | 3 | 3 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0005c0006 | 0/0 | 1488 | 9 | 6 | 2 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0006c0008 | 0/0 | 1488 | 7 | 2 | 4 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0007c0007 | 0/0 | 1488 | 7 | 3 | 1 | 0 | 0 | 3 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0008c0010 | 0/0 | 1488 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0009c0013 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0010c0015 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0011c0014 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0012c0016 | 0/0 | 1488 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0013c0012 | 0/0 | 1488 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3135 | 103 | 22 | 26 | 31 | 8 | 15 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0001c0001t0008 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0001c0001t0010 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0003t0002 | 0/0 | 3127 | 20 | 0 | 17 | 0 | 2 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0003t0003 | 0/0 | 3128 | 9 | 4 | 2 | 0 | 2 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0003t0007 | 0/0 | 3128 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0003t0011 | 0/0 | 3123 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0004t0001 | 0/0 | 3135 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0004t0004 | 0/0 | 3127 | 15 | 14 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0009t0004 | 0/0 | 3127 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0002c0011t0004 | 0/0 | 3127 | 3 | 3 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0003c0002t0001 | 0/0 | 3135 | 33 | 15 | 4 | 7 | 3 | 4 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0003c0002t0005 | 0/0 | 3131 | 3 | 3 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0003c0002t0006 | 0/0 | 3135 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0004c0005t0002 | 1/0 | 3127 | 9 | 0 | 3 | 0 | 3 | 2 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0004c0005t0009 | 0/0 | 3127 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0005c0006t0003 | 0/0 | 3128 | 9 | 6 | 2 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0006c0008t0002 | 0/0 | 3127 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0006c0008t0003 | 0/0 | 3128 | 5 | 1 | 3 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0006c0008t0012 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0007c0007t0001 | 0/0 | 3135 | 7 | 3 | 1 | 0 | 0 | 3 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0008c0010t0001 | 0/0 | 3135 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0009c0013t0001 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0010c0015t0005 | 0/0 | 3131 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0011c0014t0001 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0012c0016t0001 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
a0013c0012t0003 | 0/0 | 3128 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | copy fasta | chr11 | 61097489 | 61132852 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 10 | 4 | 0 | 1 | 2 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0002 | 0/0 | 17 | 0 | 5 | 6 | 0 | 6 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0006 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0017 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0001c0001t0010g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0003 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0003g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0003t0011g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0004t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0009t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0009t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0009t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0011t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0002c0011t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0004 | 0/0 | 8 | 3 | 1 | 0 | 2 | 2 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0003c0002t0006g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0004c0005t0002g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0004c0005t0002g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0004c0005t0002g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0004c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0004c0005t0009g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0005c0006t0003g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0005c0006t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0005c0006t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0005c0006t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0005c0006t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0005c0006t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0006c0008t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0006c0008t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0006c0008t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0006c0008t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0006c0008t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0007c0007t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0007c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0007c0007t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0007c0007t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0007c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0007c0007t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0007c0007t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0008c0010t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0008c0010t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0008c0010t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0009c0013t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0010c0015t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0011c0014t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0012c0016t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
a0013c0012t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0002 | t0001 | g0004 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00140 | hp2 | a0002 | c0003 | t0002 | g0003 | EUR | GBR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00280 | hp1 | a0004 | c0005 | t0002 | g0016 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00323 | hp2 | a0002 | c0003 | t0002 | g0060 | EUR | FIN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00609 | hp1 | a0003 | c0002 | t0001 | g0119 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00639 | hp1 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00639 | hp2 | a0003 | c0002 | t0001 | g0123 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00642 | hp1 | a0005 | c0006 | t0003 | g0047 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00642 | hp2 | a0002 | c0003 | t0002 | g0124 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00738 | hp1 | a0002 | c0003 | t0002 | g0059 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00738 | hp2 | a0004 | c0005 | t0002 | g0010 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00741 | hp1 | a0006 | c0008 | t0003 | g0007 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01069 | hp2 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01071 | hp1 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01074 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01109 | hp1 | a0002 | c0004 | t0001 | g0019 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01109 | hp2 | a0003 | c0002 | t0001 | g0133 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01167 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01169 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01243 | hp1 | a0003 | c0002 | t0006 | g0008 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01255 | hp2 | a0002 | c0003 | t0003 | g0007 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01256 | hp1 | a0002 | c0003 | t0002 | g0050 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0125 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01257 | hp1 | a0006 | c0008 | t0003 | g0031 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01257 | hp2 | a0007 | c0007 | t0001 | g0113 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01258 | hp1 | a0006 | c0008 | t0003 | g0031 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01258 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01261 | hp1 | a0005 | c0006 | t0003 | g0013 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01261 | hp2 | a0002 | c0003 | t0011 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01346 | hp1 | a0003 | c0002 | t0001 | g0032 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01346 | hp2 | a0004 | c0005 | t0002 | g0010 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01358 | hp1 | a0006 | c0008 | t0002 | g0108 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01358 | hp2 | a0004 | c0005 | t0002 | g0010 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01433 | hp1 | a0002 | c0003 | t0002 | g0055 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01433 | hp2 | a0003 | c0002 | t0001 | g0004 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01496 | hp1 | a0002 | c0004 | t0004 | g0005 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01496 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01515 | hp1 | a0002 | c0003 | t0003 | g0107 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01516 | hp2 | a0004 | c0005 | t0002 | g0016 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01517 | hp2 | a0002 | c0003 | t0003 | g0007 | EUR | IBS | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01884 | hp1 | a0008 | c0010 | t0001 | g0082 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01884 | hp2 | a0002 | c0003 | t0003 | g0072 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01891 | hp1 | a0003 | c0002 | t0006 | g0008 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01891 | hp2 | a0003 | c0002 | t0001 | g0004 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01943 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01943 | hp2 | a0002 | c0003 | t0003 | g0007 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01978 | hp2 | a0002 | c0003 | t0002 | g0049 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01993 | hp1 | a0002 | c0003 | t0002 | g0054 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02055 | hp2 | a0002 | c0004 | t0004 | g0036 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02071 | hp2 | a0008 | c0010 | t0001 | g0110 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02132 | hp2 | a0003 | c0002 | t0001 | g0011 | EAS | KHV | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02145 | hp1 | a0010 | c0015 | t0005 | g0048 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02165 | hp2 | a0005 | c0006 | t0003 | g0042 | EAS | CDX | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02257 | hp1 | a0003 | c0002 | t0001 | g0103 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02257 | hp2 | a0003 | c0002 | t0001 | g0004 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02258 | hp1 | a0002 | c0004 | t0004 | g0005 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02258 | hp2 | a0003 | c0002 | t0005 | g0127 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02280 | hp1 | a0002 | c0004 | t0001 | g0019 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02300 | hp2 | a0002 | c0003 | t0002 | g0058 | AMR | PEL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02451 | hp1 | a0005 | c0006 | t0003 | g0020 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02451 | hp2 | a0003 | c0002 | t0001 | g0009 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02572 | hp2 | a0002 | c0003 | t0007 | g0022 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02602 | hp1 | a0004 | c0005 | t0002 | g0016 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02615 | hp1 | a0002 | c0009 | t0004 | g0021 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02615 | hp2 | a0002 | c0011 | t0004 | g0030 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02622 | hp1 | a0002 | c0004 | t0004 | g0087 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02622 | hp2 | a0011 | c0014 | t0001 | g0025 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02630 | hp1 | a0002 | c0004 | t0001 | g0019 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02630 | hp2 | a0002 | c0009 | t0004 | g0021 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02647 | hp1 | a0013 | c0012 | t0003 | g0109 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02647 | hp2 | a0005 | c0006 | t0003 | g0118 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02717 | hp2 | a0002 | c0003 | t0007 | g0022 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02723 | hp2 | a0005 | c0006 | t0003 | g0013 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02735 | hp1 | a0002 | c0003 | t0003 | g0106 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02735 | hp2 | a0002 | c0003 | t0002 | g0056 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02809 | hp1 | a0002 | c0009 | t0004 | g0045 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02809 | hp2 | a0003 | c0002 | t0006 | g0008 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02818 | hp1 | a0002 | c0004 | t0004 | g0132 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02818 | hp2 | a0005 | c0006 | t0003 | g0041 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02886 | hp2 | a0003 | c0002 | t0001 | g0009 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02897 | hp1 | a0002 | c0009 | t0004 | g0077 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02897 | hp2 | a0007 | c0007 | t0001 | g0117 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02922 | hp1 | a0003 | c0002 | t0001 | g0134 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02965 | hp1 | a0002 | c0011 | t0004 | g0030 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02965 | hp2 | a0005 | c0006 | t0003 | g0020 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02976 | hp1 | a0002 | c0004 | t0004 | g0005 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02976 | hp2 | a0005 | c0006 | t0003 | g0013 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03130 | hp1 | a0007 | c0007 | t0001 | g0115 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03139 | hp1 | a0003 | c0002 | t0001 | g0009 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03139 | hp2 | a0002 | c0004 | t0004 | g0034 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03209 | hp1 | a0003 | c0002 | t0001 | g0097 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03209 | hp2 | a0002 | c0003 | t0003 | g0071 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03225 | hp2 | a0003 | c0002 | t0001 | g0004 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03239 | hp1 | a0006 | c0008 | t0003 | g0007 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03239 | hp2 | a0004 | c0005 | t0009 | g0051 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03453 | hp2 | a0002 | c0011 | t0004 | g0098 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03486 | hp1 | a0002 | c0003 | t0003 | g0043 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03486 | hp2 | a0009 | c0013 | t0001 | g0137 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03492 | hp2 | a0004 | c0005 | t0002 | g0010 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03540 | hp1 | a0003 | c0002 | t0001 | g0135 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03540 | hp2 | a0006 | c0008 | t0012 | g0104 | AFR | GWD | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03579 | hp1 | a0003 | c0002 | t0001 | g0009 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03579 | hp2 | a0003 | c0002 | t0005 | g0122 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03654 | hp1 | a0003 | c0002 | t0001 | g0129 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03669 | hp1 | a0003 | c0002 | t0001 | g0004 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03669 | hp2 | a0007 | c0007 | t0001 | g0114 | SAS | PJL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03688 | hp2 | a0007 | c0007 | t0001 | g0111 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03927 | hp2 | a0007 | c0007 | t0001 | g0112 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG04204 | hp1 | a0003 | c0002 | t0001 | g0004 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18522 | hp1 | a0003 | c0002 | t0001 | g0040 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18522 | hp2 | a0002 | c0004 | t0004 | g0038 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18941 | hp2 | a0003 | c0002 | t0001 | g0126 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18947 | hp1 | a0003 | c0002 | t0001 | g0120 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18949 | hp1 | a0003 | c0002 | t0001 | g0011 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18951 | hp2 | a0012 | c0016 | t0001 | g0073 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18980 | hp2 | a0003 | c0002 | t0001 | g0011 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18998 | hp1 | a0003 | c0002 | t0001 | g0011 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19030 | hp2 | a0003 | c0002 | t0001 | g0131 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19043 | hp2 | a0002 | c0004 | t0004 | g0005 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19240 | hp1 | a0008 | c0010 | t0001 | g0001 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA19240 | hp2 | a0002 | c0004 | t0004 | g0005 | AFR | YRI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20129 | hp2 | a0002 | c0004 | t0004 | g0035 | AFR | ASW | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20752 | hp2 | a0003 | c0002 | t0001 | g0032 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20805 | hp1 | a0004 | c0005 | t0002 | g0057 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20805 | hp2 | a0003 | c0002 | t0001 | g0004 | EUR | TSI | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20905 | hp1 | a0003 | c0002 | t0001 | g0088 | SAS | GIH | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG01123 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02486 | hp1 | a0007 | c0007 | t0001 | g0116 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02486 | hp2 | a0003 | c0002 | t0005 | g0121 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02559 | hp1 | a0003 | c0002 | t0001 | g0136 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG02559 | hp2 | a0003 | c0002 | t0001 | g0128 | AFR | ACB | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03471 | hp1 | a0002 | c0004 | t0004 | g0037 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG03471 | hp2 | a0002 | c0004 | t0001 | g0102 | AFR | MSL | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG06807 | hp1 | a0002 | c0004 | t0004 | g0005 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
HG06807 | hp2 | a0002 | c0003 | t0003 | g0044 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20300 | hp1 | a0003 | c0002 | t0006 | g0008 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA20300 | hp2 | a0002 | c0004 | t0004 | g0005 | AFR | USA | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA21309 | hp1 | a0002 | c0004 | t0004 | g0101 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
NA21309 | hp2 | a0006 | c0008 | t0003 | g0105 | AFR | LWK | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0067 | REF | REF | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
homoSapiens_grch38 | hp1 | a0004 | c0005 | t0002 | g0053 | REF | REF | CD5_chr11_61097489_61132852 | CD5 | chr11 | 61097489 | 61132852 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61102594
|
T | G | 3 | a0007a0008a0013 | 11 | HG01257.hp2 HG01884.hp1 HG02071.hp2 others(8): Show |
missense_variant | MODERATE | c.34T>G | p.Leu12Val | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/11 | 106/3127 | 34/1488 | 12/495 | chr11 | 61102594 | ||
chr11:61115074
|
G | A | 1 | a0009 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.74G>A | p.Arg25Gln | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/11 | 146/3127 | 74/1488 | 25/495 | chr11 | 61115074 | ||
chr11:61119378
|
A | G | 1 | a0012 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.608A>G | p.Asn203Ser | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/11 | 680/3127 | 608/1488 | 203/495 | chr11 | 61119378 | ||
chr11:61119441
|
C | T | 6 | a0003a0006a0007others(3): Show | 57 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
missense_variant | MODERATE | c.671C>T | p.Pro224Leu | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/11 | 743/3127 | 671/1488 | 224/495 | chr11 | 61119441 | ||
chr11:61123886
|
C | T | 1 | a0010 | 1 | HG02145.hp1 | missense_variant&splice_region_variant | MODERATE | c.1228C>T | p.Arg410Cys | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/11 | 1300/3127 | 1228/1488 | 410/495 | chr11 | 61123886 | ||
chr11:61123901
|
C | T | 1 | a0011 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1243C>T | p.Arg415Cys | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/11 | 1315/3127 | 1243/1488 | 415/495 | chr11 | 61123901 | ||
chr11:61125133
|
C | T | 1 | a0005 | 9 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(6): Show |
missense_variant | MODERATE | c.1381C>T | p.His461Tyr | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/11 | 1453/3127 | 1381/1488 | 461/495 | chr11 | 61125133 | ||
chr11:61125134
|
A | G | 12 | a0001a0002a0003others(9): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
missense_variant | MODERATE | c.1382A>G | p.His461Arg | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/11 | 1454/3127 | 1382/1488 | 461/495 | chr11 | 61125134 | ||
chr11:61125763
|
C | T | 8 | a0001a0003a0007others(5): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
missense_variant | MODERATE | c.1412C>T | p.Ala471Val | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/11 | 1484/3127 | 1412/1488 | 471/495 | chr11 | 61125763 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61121687
|
G | A | 1 | a0002c0004 | 19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
synonymous_variant | LOW | c.882G>A | p.Gly294Gly | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/11 | 954/3127 | 882/1488 | 294/495 | chr11 | 61121687 | ||
chr11:61121774
|
C | T | 1 | a0002c0009 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.969C>T | p.Ser323Ser | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/11 | 1041/3127 | 969/1488 | 323/495 | chr11 | 61121774 | ||
chr11:61122992
|
C | T | 1 | a0002c0011 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.1185C>T | p.Val395Val | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/11 | 1257/3127 | 1185/1488 | 395/495 | chr11 | 61122992 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61126545
|
C | T | 1 | a0002c0003t0007 | 2 | HG02572.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*260C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 706 | chr11 | 61126545 | |||||
chr11:61126592
|
C | T | 1 | a0006c0008t0012 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 753 | chr11 | 61126592 | |||||
chr11:61126732
|
C | T | 1 | a0003c0002t0006 | 4 | HG01243.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*447C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 893 | chr11 | 61126732 | |||||
chr11:61126921
|
CCTCT | C | 3 | a0002c0003t0011a0003c0002t0005a0010c0015t0005 | 5 | HG01261.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*637_*640delCTCT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1083 | chr11 | 61126921 | |||||
chr11:61126957
|
C | A | 1 | a0001c0001t0008 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1118 | chr11 | 61126957 | |||||
chr11:61127020
|
G | T | 22 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(19): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1181 | chr11 | 61127020 | |||||
chr11:61127081
|
A | G | 1 | a0004c0005t0009 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1242 | chr11 | 61127081 | |||||
chr11:61127122
|
C | CT | 6 | a0002c0003t0003a0002c0003t0007a0005c0006t0003others(3): Show | 27 | HG00642.hp1 HG00741.hp1 HG01255.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*839dupT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1286 | INFO_REALIGN_3_PRIME | chr11 | 61127122 | ||||
chr11:61127333
|
CGGCT | C | 13 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(10): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1052delGGCT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1495 | chr11 | 61127333 | |||||
chr11:61127339
|
C | T | 13 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(10): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1054C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1500 | chr11 | 61127339 | |||||
chr11:61127363
|
A | AACACATC others(5): Show |
13 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(10): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1082_*1093dupCATC others(8): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1540 | INFO_REALIGN_3_PRIME | chr11 | 61127363 | ||||
chr11:61127778
|
C | T | 1 | a0001c0001t0010 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1493C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 11/11 | 1939 | chr11 | 61127778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61102641
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0138 | 5 | HG00735.hp1 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+26C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61102641 | ||||||
chr11:61102783
|
C | T | 2 | a0003c0002t0001g0136a0009c0013t0001g0137 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55+168C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61102783 | ||||||
chr11:61102951
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.55+336G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61102951 | ||||||
chr11:61103036
|
C | A | 1 | a0002c0004t0004g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55+421C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103036 | ||||||
chr11:61103039
|
C | T | 1 | a0003c0002t0001g0135 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.55+424C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103039 | ||||||
chr11:61103078
|
G | A | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+463G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103078 | ||||||
chr11:61103108
|
T | C | 6 | a0001c0001t0001g0014a0003c0002t0001g0040a0005c0006t0003g0013others(3): Show | 11 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.55+493T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103108 | ||||||
chr11:61103136
|
C | A | 2 | a0002c0003t0003g0043a0002c0003t0003g0044 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.55+521C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103136 | ||||||
chr11:61103203
|
G | A | 3 | a0003c0002t0001g0009a0003c0002t0001g0135a0003c0002t0006g0008 | 9 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.55+588G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103203 | ||||||
chr11:61103640
|
CTG | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0130a0001c0001t0010g0125others(46): Show | 77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.55+1029_55+1030del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103640 | |||||
chr11:61103642
|
G | GTGTGTGG others(56): Show |
7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+1030_55+1031ins others(63): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103642 | |||||
chr11:61103663
|
C | CTCTGTGT others(62): Show |
1 | a0002c0004t0004g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.55+1099_55+1167dup others(69): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103663 | |||||
chr11:61103663
|
CTCTGTGT others(5): Show |
C | 2 | a0003c0002t0001g0040a0005c0006t0003g0013 | 4 | HG01261.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.55+1064_55+1075del others(12): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61103663 | |||||
chr11:61103805
|
G | T | 2 | a0003c0002t0001g0133a0003c0002t0001g0134 | 2 | HG01109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.55+1190G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103805 | ||||||
chr11:61103841
|
T | G | 2 | a0002c0004t0001g0019a0002c0004t0001g0102 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+1226T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103841 | ||||||
chr11:61103909
|
GT | G | 9 | a0002c0003t0003g0007a0002c0003t0003g0106a0002c0003t0003g0107others(6): Show | 14 | HG00741.hp1 HG01109.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+1295delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103909 | ||||||
chr11:61103910
|
T | G | 1 | a0006c0008t0002g0108 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.55+1295T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103910 | ||||||
chr11:61103911
|
GT | G | 16 | a0001c0001t0001g0014a0001c0001t0001g0039a0002c0003t0007g0022others(13): Show | 29 | HG01261.hp1 HG01496.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.55+1297delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103911 | ||||||
chr11:61103912
|
T | G | 44 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0124others(41): Show | 67 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.55+1297T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103912 | ||||||
chr11:61103918
|
G | A | 9 | a0007c0007t0001g0111a0007c0007t0001g0112a0007c0007t0001g0113others(6): Show | 9 | HG01257.hp2 HG02071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+1303G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61103918 | ||||||
chr11:61104072
|
CTG | C | 48 | a0001c0001t0001g0039a0001c0001t0001g0130a0001c0001t0010g0125others(45): Show | 77 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.55+1464_55+1465del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61104072 | |||||
chr11:61104104
|
ACTGTGTG others(16): Show |
A | 2 | a0002c0003t0003g0043a0002c0003t0003g0044 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.55+1497_55+1519del others(23): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61104104 | |||||
chr11:61104218
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.55+1603G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104218 | ||||||
chr11:61104236
|
T | C | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+1621T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104236 | ||||||
chr11:61104334
|
A | G | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+1719A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104334 | ||||||
chr11:61104430
|
C | T | 1 | a0007c0007t0001g0117 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.55+1815C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104430 | ||||||
chr11:61104601
|
C | A | 42 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0124others(39): Show | 65 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.55+1986C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104601 | ||||||
chr11:61104636
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.55+2021C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104636 | ||||||
chr11:61104750
|
A | G | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+2135A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104750 | ||||||
chr11:61104801
|
C | T | 7 | a0001c0001t0001g0014a0003c0002t0001g0040a0005c0006t0003g0013others(4): Show | 12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.55+2186C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104801 | ||||||
chr11:61104821
|
C | T | 7 | a0001c0001t0001g0014a0003c0002t0001g0040a0005c0006t0003g0013others(4): Show | 12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.55+2206C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61104821 | ||||||
chr11:61105000
|
A | G | 42 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0124others(39): Show | 65 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.55+2385A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105000 | ||||||
chr11:61105079
|
TG | T | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+2468delG | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61105079 | |||||
chr11:61105108
|
C | G | 9 | a0007c0007t0001g0111a0007c0007t0001g0112a0007c0007t0001g0113others(6): Show | 9 | HG01257.hp2 HG02071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+2493C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105108 | ||||||
chr11:61105151
|
C | T | 2 | a0002c0011t0004g0030a0002c0011t0004g0098 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.55+2536C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105151 | ||||||
chr11:61105156
|
G | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(121): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.55+2541G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105156 | ||||||
chr11:61105200
|
C | T | 2 | a0002c0003t0003g0043a0002c0003t0003g0044 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.55+2585C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105200 | ||||||
chr11:61105246
|
G | C | 33 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0124others(30): Show | 56 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.55+2631G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105246 | ||||||
chr11:61105306
|
C | T | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+2691C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105306 | ||||||
chr11:61105372
|
G | C | 5 | a0002c0003t0007g0022a0002c0009t0004g0021a0002c0009t0004g0045others(2): Show | 7 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+2757G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105372 | ||||||
chr11:61105372
|
G | T | 1 | a0003c0002t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.55+2757G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105372 | ||||||
chr11:61105415
|
G | A | 7 | a0001c0001t0001g0014a0003c0002t0001g0040a0005c0006t0003g0013others(4): Show | 12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.55+2800G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105415 | ||||||
chr11:61105631
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.55+3016C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105631 | ||||||
chr11:61105706
|
A | G | 42 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0124others(39): Show | 65 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.55+3091A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61105706 | ||||||
chr11:61106080
|
G | A | 8 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(5): Show | 14 | HG00642.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.55+3465G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61106080 | ||||||
chr11:61106081
|
C | T | 1 | a0003c0002t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.55+3466C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61106081 | ||||||
chr11:61106124
|
C | CA | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(52): Show | 109 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.55+3529dupA | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | |||||
chr11:61106124
|
C | CAA | 19 | a0001c0001t0001g0017a0001c0001t0001g0061a0001c0001t0001g0062others(16): Show | 25 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.55+3528_55+3529dup others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | |||||
chr11:61106124
|
C | CAAA | 28 | a0001c0001t0010g0125a0002c0003t0002g0124a0002c0003t0003g0007others(25): Show | 47 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.55+3527_55+3529dup others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | |||||
chr11:61106124
|
CAAAAA | C | 7 | a0002c0003t0007g0022a0002c0009t0004g0021a0003c0002t0001g0131others(4): Show | 9 | HG01109.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.55+3525_55+3529del others(5): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61106124 | |||||
chr11:61106268
|
G | A | 1 | a0001c0001t0001g0067 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.55+3653G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61106268 | ||||||
chr11:61106650
|
C | T | 1 | a0007c0007t0001g0114 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.55+4035C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61106650 | ||||||
chr11:61107243
|
C | T | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55+4628C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107243 | ||||||
chr11:61107287
|
G | A | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.55+4672G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107287 | ||||||
chr11:61107557
|
T | G | 57 | a0001c0001t0001g0039a0001c0001t0001g0130a0001c0001t0010g0125others(54): Show | 89 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.55+4942T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107557 | ||||||
chr11:61107729
|
C | T | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG00280.hp2 HG01123.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+5114C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107729 | ||||||
chr11:61107748
|
C | T | 2 | a0002c0004t0001g0019a0002c0004t0001g0102 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.55+5133C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107748 | ||||||
chr11:61107816
|
G | A | 9 | a0007c0007t0001g0111a0007c0007t0001g0112a0007c0007t0001g0113others(6): Show | 9 | HG01257.hp2 HG02071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.55+5201G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107816 | ||||||
chr11:61107847
|
C | T | 11 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0124others(8): Show | 25 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.55+5232C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61107847 | ||||||
chr11:61108134
|
G | A | 2 | a0003c0002t0001g0136a0009c0013t0001g0137 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55+5519G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108134 | ||||||
chr11:61108434
|
T | C | 15 | a0002c0003t0003g0007a0002c0003t0003g0106a0002c0003t0003g0107others(12): Show | 24 | HG00609.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+5819T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108434 | ||||||
chr11:61108520
|
C | T | 3 | a0002c0003t0007g0022a0002c0009t0004g0021a0002c0009t0004g0045 | 5 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.55+5905C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108520 | ||||||
chr11:61108690
|
G | A | 2 | a0003c0002t0001g0136a0009c0013t0001g0137 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.55+6075G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108690 | ||||||
chr11:61108700
|
G | C | 14 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0124others(11): Show | 28 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.55+6085G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108700 | ||||||
chr11:61108739
|
T | G | 1 | a0003c0002t0001g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.55+6124T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108739 | ||||||
chr11:61108744
|
G | C | 9 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(6): Show | 15 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.55+6129G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108744 | ||||||
chr11:61108829
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(53): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.55+6214G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108829 | ||||||
chr11:61108927
|
C | T | 1 | a0007c0007t0001g0117 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.56-6129C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61108927 | ||||||
chr11:61109060
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(113): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.56-5996A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109060 | ||||||
chr11:61109089
|
C | G | 8 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(5): Show | 14 | HG00642.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.56-5967C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109089 | ||||||
chr11:61109118
|
C | T | 1 | a0002c0003t0002g0060 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.56-5938C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109118 | ||||||
chr11:61109255
|
G | C | 8 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(5): Show | 14 | HG00642.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.56-5801G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109255 | ||||||
chr11:61109343
|
C | T | 1 | a0003c0002t0001g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.56-5713C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109343 | ||||||
chr11:61109378
|
G | A | 2 | a0003c0002t0001g0136a0009c0013t0001g0137 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.56-5678G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109378 | ||||||
chr11:61109518
|
CT | C | 44 | a0001c0001t0001g0130a0001c0001t0010g0125a0002c0003t0002g0050others(41): Show | 67 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.56-5527delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61109518 | |||||
chr11:61109614
|
C | A | 3 | a0002c0003t0007g0022a0002c0009t0004g0021a0002c0009t0004g0045 | 5 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-5442C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109614 | ||||||
chr11:61109653
|
G | A | 1 | a0002c0004t0004g0035 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.56-5403G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109653 | ||||||
chr11:61109739
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(121): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.56-5317A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109739 | ||||||
chr11:61109935
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.56-5121G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109935 | ||||||
chr11:61109964
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.56-5092G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61109964 | ||||||
chr11:61110112
|
G | A | 7 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(4): Show | 9 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-4944G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110112 | ||||||
chr11:61110152
|
G | T | 5 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(2): Show | 7 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-4904G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110152 | ||||||
chr11:61110300
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.56-4756T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110300 | ||||||
chr11:61110313
|
C | T | 4 | a0003c0002t0001g0009a0003c0002t0001g0131a0003c0002t0001g0135others(1): Show | 10 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-4743C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110313 | ||||||
chr11:61110354
|
T | C | 1 | a0002c0004t0004g0036 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.56-4702T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110354 | ||||||
chr11:61110886
|
T | G | 2 | a0002c0003t0003g0043a0002c0003t0003g0044 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.56-4170T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110886 | ||||||
chr11:61110898
|
T | G | 5 | a0003c0002t0001g0097a0003c0002t0005g0121a0003c0002t0005g0122others(2): Show | 5 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-4158T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110898 | ||||||
chr11:61110941
|
G | A | 1 | a0002c0004t0004g0132 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.56-4115G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61110941 | ||||||
chr11:61111139
|
C | T | 1 | a0002c0003t0002g0059 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56-3917C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111139 | ||||||
chr11:61111190
|
C | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(53): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.56-3866C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111190 | ||||||
chr11:61111393
|
G | A | 1 | a0013c0012t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.56-3663G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111393 | ||||||
chr11:61111423
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0091 | 2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.56-3633A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111423 | ||||||
chr11:61111443
|
C | T | 11 | a0002c0003t0003g0071a0002c0003t0003g0072a0007c0007t0001g0111others(8): Show | 11 | HG01257.hp2 HG01884.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-3613C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111443 | ||||||
chr11:61111517
|
G | A | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-3539G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111517 | ||||||
chr11:61111578
|
T | C | 1 | a0012c0016t0001g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.56-3478T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111578 | ||||||
chr11:61111676
|
C | T | 1 | a0002c0003t0003g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.56-3380C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111676 | ||||||
chr11:61111775
|
G | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0099a0001c0001t0001g0100 | 3 | HG00140.hp1 HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.56-3281G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61111775 | ||||||
chr11:61112059
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.56-2997G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112059 | ||||||
chr11:61112131
|
G | A | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.56-2925G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112131 | ||||||
chr11:61112193
|
G | A | 11 | a0002c0003t0003g0071a0002c0003t0003g0072a0007c0007t0001g0111others(8): Show | 11 | HG01257.hp2 HG01884.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-2863G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112193 | ||||||
chr11:61112306
|
C | CATCT | 6 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0024others(3): Show | 10 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.56-2749_56-2746dup others(4): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61112306 | |||||
chr11:61112503
|
G | A | 2 | a0002c0011t0004g0030a0002c0011t0004g0098 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.56-2553G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112503 | ||||||
chr11:61112536
|
C | T | 2 | a0003c0002t0001g0097a0003c0002t0001g0120 | 2 | HG03209.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.56-2520C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112536 | ||||||
chr11:61112643
|
C | CA | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(53): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.56-2403dupA | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61112643 | |||||
chr11:61112962
|
C | T | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-2094C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61112962 | ||||||
chr11:61113194
|
A | T | 11 | a0002c0003t0003g0007a0002c0003t0003g0106a0002c0003t0003g0107others(8): Show | 18 | HG00741.hp1 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.56-1862A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113194 | ||||||
chr11:61113204
|
G | C | 1 | a0008c0010t0001g0110 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.56-1852G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113204 | ||||||
chr11:61113206
|
T | C | 2 | a0005c0006t0003g0042a0008c0010t0001g0110 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.56-1850T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113206 | ||||||
chr11:61113384
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(113): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.56-1672A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113384 | ||||||
chr11:61113418
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.56-1638G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113418 | ||||||
chr11:61113670
|
CT | C | 3 | a0003c0002t0001g0011a0003c0002t0001g0103a0003c0002t0001g0120 | 6 | HG02132.hp2 HG02257.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.56-1376delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61113670 | |||||
chr11:61113695
|
A | G | 11 | a0002c0003t0003g0071a0002c0003t0003g0072a0007c0007t0001g0111others(8): Show | 11 | HG01257.hp2 HG01884.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-1361A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113695 | ||||||
chr11:61113747
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.56-1309C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113747 | ||||||
chr11:61113960
|
G | A | 3 | a0002c0003t0007g0022a0002c0009t0004g0021a0002c0009t0004g0045 | 5 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-1096G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61113960 | ||||||
chr11:61114289
|
T | TC | 2 | a0001c0001t0001g0029a0001c0001t0001g0069 | 3 | NA18941.hp1 NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.56-765dupC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61114289 | |||||
chr11:61114303
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.56-753A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114303 | ||||||
chr11:61114371
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.56-685C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114371 | ||||||
chr11:61114378
|
C | T | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-678C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114378 | ||||||
chr11:61114454
|
G | GCATACAT others(1): Show |
53 | a0001c0001t0001g0039a0002c0003t0002g0124a0002c0003t0003g0007others(50): Show | 83 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.56-591_56-584dupTA others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61114454 | |||||
chr11:61114454
|
G | GCATACAT others(5): Show |
2 | a0003c0002t0001g0136a0009c0013t0001g0137 | 2 | HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.56-595_56-584dupTA others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 61114454 | |||||
chr11:61114513
|
T | C | 34 | a0002c0003t0002g0124a0002c0003t0003g0007a0002c0003t0003g0106others(31): Show | 57 | HG00099.hp1 HG00609.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.56-543T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114513 | ||||||
chr11:61114570
|
G | A | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.56-486G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114570 | ||||||
chr11:61114753
|
A | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0074 | 3 | NA18977.hp2 NA19010.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.56-303A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114753 | ||||||
chr11:61114812
|
G | A | 5 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(2): Show | 7 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.56-244G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 1/10 | chr11 | 61114812 | ||||||
chr11:61115176
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.94+82G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115176 | ||||||
chr11:61115250
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0076 | 7 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+156T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115250 | ||||||
chr11:61115355
|
T | C | 1 | a0001c0001t0010g0125 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.94+261T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115355 | ||||||
chr11:61115454
|
G | A | 1 | a0013c0012t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+360G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115454 | ||||||
chr11:61115496
|
G | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0095a0003c0002t0001g0040others(5): Show | 13 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+402G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115496 | ||||||
chr11:61115503
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0095a0003c0002t0001g0040others(6): Show | 14 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+409G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115503 | ||||||
chr11:61115622
|
C | G | 36 | a0002c0003t0003g0007a0002c0003t0003g0106a0002c0003t0003g0107others(33): Show | 49 | HG00609.hp1 HG00741.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.94+528C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115622 | ||||||
chr11:61115864
|
A | C | 7 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(4): Show | 13 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+770A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115864 | ||||||
chr11:61115972
|
C | T | 1 | a0002c0003t0003g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+878C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61115972 | ||||||
chr11:61116090
|
G | A | 6 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(3): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+996G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116090 | ||||||
chr11:61116134
|
A | G | 8 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(5): Show | 14 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+1040A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116134 | ||||||
chr11:61116251
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.94+1157G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116251 | ||||||
chr11:61116297
|
C | T | 1 | a0003c0002t0001g0136 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94+1203C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116297 | ||||||
chr11:61116328
|
G | T | 2 | a0002c0003t0003g0071a0002c0003t0003g0072 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.94+1234G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116328 | ||||||
chr11:61116343
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0095a0002c0004t0001g0019others(6): Show | 16 | HG01109.hp1 HG01261.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+1249G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116343 | ||||||
chr11:61116377
|
C | T | 1 | a0002c0004t0004g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.94+1283C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116377 | ||||||
chr11:61116402
|
A | C | 1 | a0002c0003t0003g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1308A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116402 | ||||||
chr11:61116419
|
A | C | 1 | a0002c0003t0003g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1325A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116419 | ||||||
chr11:61116425
|
A | C | 1 | a0002c0003t0003g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1331A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116425 | ||||||
chr11:61116469
|
C | T | 22 | a0002c0003t0003g0007a0002c0003t0003g0106a0002c0003t0003g0107others(19): Show | 29 | HG00609.hp1 HG00741.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+1375C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116469 | ||||||
chr11:61116470
|
G | A | 18 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0095others(15): Show | 31 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.94+1376G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116470 | ||||||
chr11:61116488
|
CCA | C | 6 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(3): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+1402_94+1403del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116488 | |||||
chr11:61116494
|
ACAC | A | 11 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(8): Show | 20 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+1407_94+1409del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116494 | |||||
chr11:61116513
|
ACAC | A | 4 | a0003c0002t0005g0121a0003c0002t0005g0122a0003c0002t0005g0127others(1): Show | 4 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1420_94+1422del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116513 | ||||||
chr11:61116533
|
C | A | 1 | a0002c0003t0003g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+1439C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116533 | ||||||
chr11:61116539
|
C | CCA | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(61): Show | 120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.94+1457_94+1458dup others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116539 | |||||
chr11:61116549
|
AC | A | 6 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(3): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+1456delC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116549 | ||||||
chr11:61116553
|
C | A | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+1459C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116553 | ||||||
chr11:61116554
|
A | C | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+1460A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116554 | ||||||
chr11:61116619
|
ACACACAC others(2): Show |
A | 6 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(3): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-1536_95-1528del others(9): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116619 | |||||
chr11:61116666
|
CCA | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0095others(15): Show | 31 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-1497_95-1496del others(2): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116666 | |||||
chr11:61116691
|
CATACACA others(22): Show |
C | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(52): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.95-1466_95-1438del others(29): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116691 | |||||
chr11:61116705
|
ACAC | A | 1 | a0003c0002t0006g0008 | 4 | HG01243.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1466_95-1464del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116705 | |||||
chr11:61116713
|
T | C | 8 | a0001c0001t0001g0039a0002c0004t0004g0005a0002c0004t0004g0034others(5): Show | 14 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-1462T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116713 | ||||||
chr11:61116772
|
GCAC | G | 18 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0095others(15): Show | 31 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-1396_95-1394del others(3): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 61116772 | |||||
chr11:61116806
|
A | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(52): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.95-1369A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116806 | ||||||
chr11:61116814
|
C | T | 6 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(3): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-1361C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116814 | ||||||
chr11:61116848
|
C | T | 1 | a0006c0008t0003g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-1327C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116848 | ||||||
chr11:61116866
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.95-1309A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61116866 | ||||||
chr11:61117025
|
G | C | 1 | a0002c0004t0004g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.95-1150G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117025 | ||||||
chr11:61117160
|
T | C | 3 | a0007c0007t0001g0111a0007c0007t0001g0112a0007c0007t0001g0114 | 3 | HG03669.hp2 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.95-1015T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117160 | ||||||
chr11:61117551
|
C | T | 1 | a0005c0006t0003g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.95-624C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117551 | ||||||
chr11:61117701
|
G | T | 6 | a0002c0003t0003g0043a0002c0003t0003g0044a0002c0003t0007g0022others(3): Show | 8 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-474G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117701 | ||||||
chr11:61117817
|
A | T | 1 | a0002c0004t0004g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.95-358A>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117817 | ||||||
chr11:61117901
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.95-274G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 2/10 | chr11 | 61117901 | ||||||
chr11:61118502
|
C | A | 1 | a0001c0001t0001g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.400+22C>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 3/10 | chr11 | 61118502 | ||||||
chr11:61118514
|
G | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0095a0005c0006t0003g0013others(4): Show | 12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+34G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 3/10 | chr11 | 61118514 | ||||||
chr11:61118543
|
C | T | 1 | a0003c0002t0001g0097 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.400+63C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 3/10 | chr11 | 61118543 | ||||||
chr11:61119047
|
T | C | 22 | a0002c0003t0003g0007a0002c0003t0003g0106a0002c0003t0003g0107others(19): Show | 29 | HG00609.hp1 HG00741.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.463+70T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 4/10 | chr11 | 61119047 | ||||||
chr11:61119211
|
C | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0095a0005c0006t0003g0013others(4): Show | 12 | HG01261.hp1 HG02165.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.464-23C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 4/10 | chr11 | 61119211 | ||||||
chr11:61119857
|
A | G | 17 | a0001c0001t0001g0014a0001c0001t0001g0095a0002c0003t0003g0071others(14): Show | 28 | HG00642.hp1 HG01261.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.805+282A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61119857 | ||||||
chr11:61119960
|
GC | G | 5 | a0001c0001t0001g0091a0002c0003t0007g0022a0002c0009t0004g0021others(2): Show | 7 | HG02572.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.805+386delC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61119960 | ||||||
chr11:61120241
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.805+666A>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120241 | ||||||
chr11:61120467
|
C | T | 9 | a0002c0004t0004g0005a0002c0004t0004g0034a0002c0004t0004g0035others(6): Show | 15 | HG01496.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.805+892C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120467 | ||||||
chr11:61120529
|
C | T | 42 | a0001c0001t0001g0091a0002c0003t0002g0003a0002c0003t0002g0015others(39): Show | 66 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.805+954C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120529 | ||||||
chr11:61120809
|
G | T | 2 | a0002c0011t0004g0030a0002c0011t0004g0098 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.806-802G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61120809 | ||||||
chr11:61121029
|
G | C | 11 | a0002c0004t0001g0019a0002c0004t0001g0102a0002c0004t0004g0005others(8): Show | 19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.806-582G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121029 | ||||||
chr11:61121047
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(123): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.806-564T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121047 | ||||||
chr11:61121062
|
C | T | 1 | a0006c0008t0012g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.806-549C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121062 | ||||||
chr11:61121116
|
G | A | 1 | a0002c0011t0004g0098 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.806-495G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121116 | ||||||
chr11:61121253
|
AGTGGACC others(3): Show |
A | 2 | a0002c0004t0001g0019a0002c0004t0001g0102 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.806-352_806-343del others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 61121253 | |||||
chr11:61121319
|
C | T | 1 | a0010c0015t0005g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.806-292C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121319 | ||||||
chr11:61121451
|
G | A | 2 | a0002c0011t0004g0030a0002c0011t0004g0098 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.806-160G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121451 | ||||||
chr11:61121570
|
T | G | 11 | a0002c0004t0001g0019a0002c0004t0001g0102a0002c0004t0004g0005others(8): Show | 19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.806-41T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 5/10 | chr11 | 61121570 | ||||||
chr11:61121926
|
G | A | 11 | a0002c0004t0001g0019a0002c0004t0001g0102a0002c0004t0004g0005others(8): Show | 19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1099+22G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61121926 | ||||||
chr11:61122002
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+98T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122002 | ||||||
chr11:61122158
|
TCTC | T | 2 | a0002c0004t0001g0019a0002c0004t0001g0102 | 4 | HG01109.hp1 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099+257_1099+259d others(5): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122158 | |||||
chr11:61122168
|
C | T | 1 | a0002c0003t0002g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1099+264C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122168 | ||||||
chr11:61122263
|
A | AATGG | 6 | a0002c0003t0002g0054a0002c0011t0004g0030a0002c0011t0004g0098others(3): Show | 7 | HG01109.hp2 HG01993.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099+382_1099+385d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122263 | |||||
chr11:61122290
|
T | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+386T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122290 | ||||||
chr11:61122290
|
TGGTG | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 74 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1099+408_1099+411d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122290 | |||||
chr11:61122292
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+388G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122292 | ||||||
chr11:61122294
|
G | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG01975.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1099+390G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122294 | ||||||
chr11:61122308
|
G | GTGGA | 5 | a0001c0001t0001g0027a0001c0001t0001g0083a0001c0001t0001g0099others(2): Show | 6 | HG00323.hp1 HG02055.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+407_1099+408i others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122308 | |||||
chr11:61122308
|
GTGGGTGG others(1): Show |
G | 9 | a0001c0001t0001g0025a0001c0001t0001g0063a0001c0001t0001g0080others(6): Show | 10 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099+408_1099+415d others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122308 | |||||
chr11:61122308
|
GTGGGTGG others(9): Show |
G | 2 | a0002c0011t0004g0030a0002c0011t0004g0098 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1099+408_1099+423d others(18): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122308 | |||||
chr11:61122312
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(58): Show | 104 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.1099+408G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122312 | ||||||
chr11:61122312
|
G | GTGGA | 2 | a0004c0005t0002g0010a0004c0005t0002g0057 | 5 | HG00738.hp2 HG01346.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099+446_1099+449d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122312 | |||||
chr11:61122312
|
G | GTGGATGG others(1): Show |
2 | a0004c0005t0002g0016a0004c0005t0009g0051 | 4 | HG00280.hp1 HG01516.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099+442_1099+449d others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122312 | |||||
chr11:61122312
|
GTGGA | G | 6 | a0002c0003t0002g0055a0002c0003t0002g0060a0002c0004t0001g0019others(3): Show | 8 | HG00323.hp2 HG01109.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099+446_1099+449d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122312 | |||||
chr11:61122354
|
C | G | 4 | a0005c0006t0003g0013a0007c0007t0001g0115a0008c0010t0001g0082others(1): Show | 6 | HG01261.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+450C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122354 | ||||||
chr11:61122354
|
C | T | 12 | a0001c0001t0001g0039a0003c0002t0001g0004a0003c0002t0001g0009others(9): Show | 26 | HG00099.hp1 HG00639.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1099+450C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122354 | ||||||
chr11:61122356
|
G | A | 4 | a0005c0006t0003g0013a0007c0007t0001g0115a0008c0010t0001g0082others(1): Show | 6 | HG01261.hp1 HG01884.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099+452G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122356 | ||||||
chr11:61122358
|
G | C | 3 | a0005c0006t0003g0013a0008c0010t0001g0082a0013c0012t0003g0109 | 5 | HG01261.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099+454G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122358 | ||||||
chr11:61122360
|
G | A | 1 | a0007c0007t0001g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1099+456G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122360 | ||||||
chr11:61122362
|
G | C | 1 | a0007c0007t0001g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1099+458G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122362 | ||||||
chr11:61122368
|
A | G | 2 | a0005c0006t0003g0013a0007c0007t0001g0115 | 4 | HG01261.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+464A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122368 | ||||||
chr11:61122370
|
GGAT | G | 2 | a0005c0006t0003g0013a0007c0007t0001g0115 | 4 | HG01261.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+471_1099+473d others(5): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122370 | |||||
chr11:61122373
|
T | TGATG | 3 | a0002c0003t0002g0056a0002c0004t0004g0038a0002c0004t0004g0132 | 3 | HG02735.hp2 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1100-490_1100-487d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | |||||
chr11:61122373
|
TGATG | T | 5 | a0002c0003t0002g0015a0002c0003t0002g0058a0002c0004t0004g0035others(2): Show | 8 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1100-490_1100-487d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | |||||
chr11:61122373
|
TGATGGAT others(1): Show |
T | 14 | a0001c0001t0001g0039a0001c0001t0001g0066a0001c0001t0001g0081others(11): Show | 20 | HG00642.hp1 HG01109.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1100-494_1100-487d others(10): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | |||||
chr11:61122373
|
TGATGGAT others(5): Show |
T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(89): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1100-498_1100-487d others(14): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | |||||
chr11:61122373
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TGATGGAT others(9): Show |
T | 3 | a0001c0001t0001g0028a0002c0004t0001g0102a0002c0004t0004g0101 | 4 | HG01516.hp1 HG01517.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099+501_1100-487d others(18): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122373 | |||||
chr11:61122375
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A | G | 3 | a0007c0007t0001g0115a0008c0010t0001g0082a0013c0012t0003g0109 | 3 | HG01884.hp1 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1099+471A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122375 | ||||||
chr11:61122380
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TG | T | 1 | a0005c0006t0003g0013 | 3 | HG01261.hp1 HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1099+478delG | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122380 | |||||
chr11:61122384
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TG | T | 3 | a0007c0007t0001g0115a0008c0010t0001g0082a0013c0012t0003g0109 | 3 | HG01884.hp1 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1099+482delG | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122384 | |||||
chr11:61122409
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G | C | 3 | a0002c0009t0004g0021a0002c0009t0004g0045a0002c0009t0004g0077 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-498G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122409 | ||||||
chr11:61122410
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G | A | 3 | a0002c0009t0004g0021a0002c0009t0004g0045a0002c0009t0004g0077 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-497G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122410 | ||||||
chr11:61122411
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A | G | 3 | a0002c0009t0004g0021a0002c0009t0004g0045a0002c0009t0004g0077 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-496A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122411 | ||||||
chr11:61122415
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A | G | 3 | a0002c0009t0004g0021a0002c0009t0004g0045a0002c0009t0004g0077 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-492A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122415 | ||||||
chr11:61122418
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GATCA | G | 3 | a0002c0009t0004g0021a0002c0009t0004g0045a0002c0009t0004g0077 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100-488_1100-485d others(6): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122418 | ||||||
chr11:61122434
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G | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(87): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1100-473G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122434 | ||||||
chr11:61122557
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C | T | 2 | a0002c0003t0003g0043a0002c0003t0003g0044 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1100-350C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122557 | ||||||
chr11:61122586
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AT | A | 12 | a0002c0003t0003g0007a0002c0003t0003g0071a0002c0003t0003g0072others(9): Show | 17 | HG00741.hp1 HG01255.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1100-319delT | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 61122586 | |||||
chr11:61122695
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G | C | 1 | a0001c0001t0001g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1100-212G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 6/10 | chr11 | 61122695 | ||||||
chr11:61123091
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C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(76): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1225+59C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123091 | ||||||
chr11:61123136
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C | T | 11 | a0002c0004t0001g0019a0002c0004t0001g0102a0002c0004t0004g0005others(8): Show | 19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1225+104C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123136 | ||||||
chr11:61123175
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C | G | 1 | a0003c0002t0005g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1225+143C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123175 | ||||||
chr11:61123397
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A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(123): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1225+365A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123397 | ||||||
chr11:61123675
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C | T | 20 | a0002c0003t0003g0007a0002c0003t0003g0043a0002c0003t0003g0044others(17): Show | 28 | HG00642.hp1 HG00741.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1226-209C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123675 | ||||||
chr11:61123676
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G | T | 11 | a0002c0004t0001g0019a0002c0004t0001g0102a0002c0004t0004g0005others(8): Show | 19 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1226-208G>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123676 | ||||||
chr11:61123690
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G | A | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1226-194G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123690 | ||||||
chr11:61123811
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A | G | 34 | a0002c0003t0003g0007a0002c0003t0003g0043a0002c0003t0003g0044others(31): Show | 51 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1226-73A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123811 | ||||||
chr11:61123838
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T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(123): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1226-46T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 7/10 | chr11 | 61123838 | ||||||
chr11:61123949
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C | T | 21 | a0001c0001t0001g0078a0002c0003t0003g0007a0002c0003t0003g0043others(18): Show | 29 | HG00642.hp1 HG00741.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1279+12C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61123949 | ||||||
chr11:61123980
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A | G | 2 | a0002c0003t0003g0043a0002c0003t0003g0044 | 2 | HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1279+43A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61123980 | ||||||
chr11:61124058
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C | T | 3 | a0001c0001t0001g0039a0003c0002t0001g0009a0003c0002t0001g0135 | 6 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+121C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124058 | ||||||
chr11:61124154
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G | A | 1 | a0003c0002t0006g0008 | 4 | HG01243.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+217G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124154 | ||||||
chr11:61124163
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T | G | 1 | a0001c0001t0001g0046 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1279+226T>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124163 | ||||||
chr11:61124513
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GTC | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0085a0011c0014t0001g0025 | 3 | HG02622.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1280-517_1280-516d others(4): Show |
CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 61124513 | |||||
chr11:61124605
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C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0052a0001c0001t0001g0067others(2): Show | 6 | HG01081.hp1 HG01169.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-427C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124605 | ||||||
chr11:61124629
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C | T | 1 | a0001c0001t0001g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1280-403C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124629 | ||||||
chr11:61124685
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T | C | 1 | a0001c0001t0001g0092 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1280-347T>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124685 | ||||||
chr11:61124732
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C | T | 2 | a0002c0004t0004g0087a0002c0004t0004g0101 | 2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1280-300C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 8/10 | chr11 | 61124732 | ||||||
chr11:61125201
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C | T | 2 | a0002c0011t0004g0030a0002c0011t0004g0098 | 3 | HG02615.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1399+50C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125201 | ||||||
chr11:61125202
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G | A | 6 | a0005c0006t0003g0013a0005c0006t0003g0020a0005c0006t0003g0041others(3): Show | 9 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.1399+51G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125202 | ||||||
chr11:61125275
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A | G | 4 | a0002c0004t0001g0019a0002c0004t0001g0102a0002c0004t0004g0087others(1): Show | 6 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1399+124A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125275 | ||||||
chr11:61125639
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C | T | 1 | a0007c0007t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1400-112C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 9/10 | chr11 | 61125639 | ||||||
chr11:61125850
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G | C | 4 | a0004c0005t0002g0010a0004c0005t0002g0016a0004c0005t0002g0057others(1): Show | 9 | HG00280.hp1 HG00738.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.*2+9G>C | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61125850 | ||||||
chr11:61125934
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C | T | 4 | a0002c0004t0001g0019a0002c0004t0001g0102a0002c0004t0004g0087others(1): Show | 6 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.*2+93C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61125934 | ||||||
chr11:61126115
|
G | A | 2 | a0002c0004t0004g0087a0002c0004t0004g0101 | 2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.*3-173G>A | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126115 | ||||||
chr11:61126159
|
C | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(123): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.*3-129C>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126159 | ||||||
chr11:61126162
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A | G | 1 | a0003c0002t0001g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*3-126A>G | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126162 | ||||||
chr11:61126227
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C | T | 6 | a0005c0006t0003g0013a0005c0006t0003g0020a0005c0006t0003g0041others(3): Show | 9 | HG00642.hp1 HG01261.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.*3-61C>T | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | chr11 | 61126227 | ||||||
chr11:61126279
|
AC | A | 3 | a0002c0009t0004g0021a0002c0009t0004g0045a0002c0009t0004g0077 | 4 | HG02615.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.*3-5delC | CD5 | ENSG00000110448.11 | transcript | ENST00000347785.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 61126279 |