geneid | 10138 |
---|---|
ensemblid | ENSG00000015153.15 |
hgncid | 17363 |
symbol | YAF2 |
name | YY1 associated factor 2 |
refseq_nuc | NM_005748.6 |
refseq_prot | NP_005739.2 |
ensembl_nuc | ENST00000534854.7 |
ensembl_prot | ENSP00000439256.2 |
mane_status | MANE Select |
chr | chr12 |
start | 42157104 |
end | 42238248 |
strand | - |
ver | v1.2 |
region | chr12:42157104-42238248 |
region5000 | chr12:42152104-42243248 |
regionname0 | YAF2_chr12_42157104_42238248 |
regionname5000 | YAF2_chr12_42152104_42243248 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 180 | 374 | 88 | 68 | 168 | 12 | 36 | 132 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 543 | 231 | 57 | 46 | 98 | 8 | 20 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
c0002 | 0/0 | 543 | 136 | 24 | 22 | 70 | 4 | 16 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
c0003 | 0/0 | 543 | 5 | 5 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
c0004 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
c0005 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3554 | 149 | 31 | 33 | 67 | 8 | 8 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0002 | 0/0 | 3554 | 118 | 24 | 11 | 65 | 3 | 15 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0003 | 0/0 | 3556 | 29 | 6 | 6 | 16 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0004 | 0/0 | 3554 | 16 | 0 | 1 | 11 | 0 | 4 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0005 | 0/0 | 3554 | 10 | 0 | 9 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0006 | 0/0 | 3546 | 7 | 0 | 0 | 0 | 0 | 7 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0007 | 0/0 | 3554 | 6 | 0 | 2 | 4 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0008 | 0/0 | 3554 | 5 | 4 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0009 | 0/0 | 3556 | 3 | 2 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0010 | 0/0 | 3554 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0011 | 0/0 | 3554 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0012 | 0/0 | 3556 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0013 | 0/0 | 3556 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0014 | 0/0 | 3554 | 2 | 0 | 2 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0015 | 0/0 | 3554 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0016 | 0/0 | 3554 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0017 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0018 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0019 | 0/0 | 3562 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0020 | 0/0 | 3554 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0021 | 0/0 | 3554 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0022 | 0/0 | 3554 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0023 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0024 | 0/0 | 3554 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0025 | 0/0 | 3554 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0026 | 0/0 | 3554 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0027 | 0/0 | 3556 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0028 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0029 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0030 | 0/0 | 3554 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0031 | 0/0 | 3554 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0032 | 0/0 | 3554 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0033 | 0/0 | 3554 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
t0034 | 0/0 | 3556 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 543 | 231 | 57 | 46 | 98 | 8 | 20 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0002 | 0/0 | 543 | 136 | 24 | 22 | 70 | 4 | 16 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0003 | 0/0 | 543 | 5 | 5 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0004 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0005 | 0/0 | 543 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4096 | 146 | 28 | 33 | 67 | 8 | 8 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0002 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0003 | 0/0 | 4098 | 29 | 6 | 6 | 16 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0004 | 0/0 | 4096 | 16 | 0 | 1 | 11 | 0 | 4 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0006 | 0/0 | 4088 | 7 | 0 | 0 | 0 | 0 | 7 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0008 | 0/0 | 4096 | 5 | 4 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0009 | 0/0 | 4098 | 3 | 2 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0010 | 0/0 | 4096 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0011 | 0/0 | 4096 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0012 | 0/0 | 4098 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0013 | 0/0 | 4098 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0014 | 0/0 | 4096 | 2 | 0 | 2 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0016 | 0/0 | 4096 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0018 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0019 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0020 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0021 | 0/0 | 4096 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0024 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0026 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0027 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0028 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0029 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0030 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0031 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0033 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0001t0034 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0002t0002 | 0/0 | 4096 | 117 | 24 | 11 | 64 | 3 | 15 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0002t0005 | 0/0 | 4096 | 10 | 0 | 9 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0002t0007 | 0/0 | 4096 | 6 | 0 | 2 | 4 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0002t0023 | 0/0 | 4098 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0002t0025 | 0/0 | 4096 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0002t0032 | 0/0 | 4096 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0003t0001 | 0/0 | 4096 | 3 | 3 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0003t0015 | 0/0 | 4096 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0004t0017 | 0/0 | 4104 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
a0001c0005t0022 | 0/0 | 4096 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | copy fasta | chr12 | 42152104 | 42243248 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0008g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0009g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0014g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0014g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0016g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0018g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0019g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0020g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0021g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0024g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0026g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0027g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0028g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0029g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0030g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0031g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0033g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0001t0034g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0023g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0025g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0002t0032g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0015g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0003t0015g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0004t0017g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
a0001c0005t0022g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0296 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0339 | EUR | FIN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | FIN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0309 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00408 | hp2 | a0001 | c0001 | t0024 | g0063 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0338 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0336 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | CHS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0300 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0055 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00642 | hp1 | a0001 | c0002 | t0005 | g0333 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00733 | hp2 | a0001 | c0002 | t0005 | g0331 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00738 | hp2 | a0001 | c0002 | t0005 | g0332 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01069 | hp1 | a0001 | c0001 | t0014 | g0111 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01069 | hp2 | a0001 | c0002 | t0005 | g0330 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01070 | hp2 | a0001 | c0002 | t0005 | g0326 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0327 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01071 | hp2 | a0001 | c0001 | t0014 | g0112 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0260 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0340 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0093 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0269 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01243 | hp2 | a0001 | c0002 | t0005 | g0261 | AMR | PUR | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0262 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0297 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01358 | hp2 | a0001 | c0001 | t0021 | g0188 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0298 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0278 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0279 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0322 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0090 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0299 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01952 | hp2 | a0001 | c0001 | t0016 | g0018 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01975 | hp1 | a0001 | c0002 | t0007 | g0258 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0303 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0304 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0085 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02071 | hp1 | a0001 | c0002 | t0007 | g0281 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0343 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0335 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0305 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | CDX | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0237 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0127 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02280 | hp1 | a0001 | c0002 | t0002 | g0323 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02280 | hp2 | a0001 | c0001 | t0029 | g0091 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02293 | hp2 | a0001 | c0002 | t0007 | g0252 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02300 | hp1 | a0001 | c0002 | t0005 | g0328 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0236 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0271 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0092 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0234 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0308 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02717 | hp1 | a0001 | c0004 | t0017 | g0110 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0348 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0263 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0089 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0315 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0318 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0126 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02809 | hp2 | a0001 | c0001 | t0028 | g0087 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0124 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0321 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02897 | hp1 | a0001 | c0001 | t0031 | g0113 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02922 | hp1 | a0001 | c0001 | t0034 | g0153 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02922 | hp2 | a0001 | c0001 | t0010 | g0118 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0253 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0221 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0347 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0266 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0351 | AFR | ESN | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03209 | hp1 | a0001 | c0001 | t0026 | g0367 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0325 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03225 | hp1 | a0001 | c0003 | t0015 | g0368 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0128 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0223 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03453 | hp1 | a0001 | c0001 | t0018 | g0114 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0121 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0224 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0268 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0235 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03579 | hp2 | a0001 | c0001 | t0033 | g0131 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0225 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0241 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0353 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0312 | SAS | PJL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0099 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0334 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03927 | hp1 | a0001 | c0002 | t0025 | g0232 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0083 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0095 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0317 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0098 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0316 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0226 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0352 | SAS | BEB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0220 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0355 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0354 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0222 | SAS | STU | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0294 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0341 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18948 | hp1 | a0001 | c0002 | t0023 | g0239 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0356 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0344 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18995 | hp2 | a0001 | c0002 | t0007 | g0250 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0350 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19002 | hp2 | a0001 | c0002 | t0032 | g0287 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19003 | hp1 | a0001 | c0001 | t0027 | g0145 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0270 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19030 | hp2 | a0001 | c0001 | t0019 | g0115 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19043 | hp2 | a0001 | c0001 | t0030 | g0088 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19055 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19060 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19066 | hp1 | a0001 | c0002 | t0007 | g0259 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19066 | hp2 | a0001 | c0001 | t0020 | g0191 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19088 | hp2 | a0001 | c0002 | t0007 | g0248 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0122 | AFR | YRI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ASW | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0120 | AFR | ASW | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0307 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20805 | hp1 | a0001 | c0002 | t0005 | g0329 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0123 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02486 | hp1 | a0001 | c0003 | t0015 | g0369 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02486 | hp2 | a0001 | c0005 | t0022 | g0357 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0119 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0346 | AFR | MSL | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0267 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | USA | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0117 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0070 | REF | REF | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0048 | REF | REF | YAF2_chr12_42152104_42243248 | YAF2 | chr12 | 42152104 | 42243248 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42160664
|
A | G | 1 | a0001c0003 | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.468T>C | p.Asp156Asp | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 536/4096 | 468/543 | 156/180 | chr12 | 42160664 | ||
chr12:42160688
|
G | A | 1 | a0001c0004 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.444C>T | p.His148His | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 512/4096 | 444/543 | 148/180 | chr12 | 42160688 | ||
chr12:42160703
|
A | G | 2 | a0001c0002a0001c0005 | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
synonymous_variant | LOW | c.429T>C | p.Ala143Ala | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 497/4096 | 429/543 | 143/180 | chr12 | 42160703 | ||
chr12:42237721
|
C | A | 1 | a0001c0005 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.30G>T | p.Pro10Pro | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/4 | 98/4096 | 30/543 | 10/180 | chr12 | 42237721 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42157219
|
T | C | 2 | a0001c0001t0014a0001c0001t0021 | 3 | HG01069.hp1 HG01071.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3370A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3370 | chr12 | 42157219 | |||||
chr12:42157298
|
T | A | 3 | a0001c0001t0003a0001c0001t0027a0001c0001t0034 | 31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3291A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3291 | chr12 | 42157298 | |||||
chr12:42157455
|
C | G | 1 | a0001c0002t0007 | 6 | HG01975.hp1 HG02071.hp1 HG02293.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3134G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3134 | chr12 | 42157455 | |||||
chr12:42157490
|
G | C | 1 | a0001c0001t0012 | 2 | HG01891.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3099C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3099 | chr12 | 42157490 | |||||
chr12:42157543
|
G | A | 1 | a0001c0001t0010 | 2 | HG02922.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3046C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3046 | chr12 | 42157543 | |||||
chr12:42157571
|
G | A | 1 | a0001c0001t0027 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3018C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 3018 | chr12 | 42157571 | |||||
chr12:42157606
|
A | G | 1 | a0001c0001t0018 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2983T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2983 | chr12 | 42157606 | |||||
chr12:42157621
|
A | C | 1 | a0001c0001t0020 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2968T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2968 | chr12 | 42157621 | |||||
chr12:42157657
|
A | G | 1 | a0001c0002t0025 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2932T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2932 | chr12 | 42157657 | |||||
chr12:42157677
|
G | C | 8 | a0001c0001t0002a0001c0002t0002a0001c0002t0005others(5): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*2912C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2912 | chr12 | 42157677 | |||||
chr12:42157779
|
C | CAT | 9 | a0001c0001t0003a0001c0001t0009a0001c0001t0012others(6): Show | 41 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2808_*2809dupAT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2809 | chr12 | 42157779 | |||||
chr12:42157779
|
C | CATATATA others(1): Show |
3 | a0001c0001t0018a0001c0001t0019a0001c0004t0017 | 3 | HG02717.hp1 HG03453.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2802_*2809dupATAT others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2809 | chr12 | 42157779 | |||||
chr12:42157917
|
G | A | 1 | a0001c0001t0011 | 2 | HG02809.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2672C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2672 | chr12 | 42157917 | |||||
chr12:42158044
|
G | A | 2 | a0001c0002t0005a0001c0005t0022 | 11 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2545C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2545 | chr12 | 42158044 | |||||
chr12:42158096
|
C | G | 1 | a0001c0001t0028 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2493G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2493 | chr12 | 42158096 | |||||
chr12:42158390
|
ATATTTTT others(1): Show |
A | 1 | a0001c0001t0006 | 7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2191_*2198delCAAA others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2191 | chr12 | 42158390 | |||||
chr12:42158392
|
A | C | 1 | a0001c0001t0008 | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2197T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2197 | chr12 | 42158392 | |||||
chr12:42158462
|
A | T | 1 | a0001c0005t0022 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2127T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2127 | chr12 | 42158462 | |||||
chr12:42158489
|
C | T | 5 | a0001c0001t0012a0001c0001t0028a0001c0001t0029others(2): Show | 6 | HG01891.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2100G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2100 | chr12 | 42158489 | |||||
chr12:42158495
|
G | C | 9 | a0001c0001t0002a0001c0001t0024a0001c0002t0002others(6): Show | 139 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2094C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 2094 | chr12 | 42158495 | |||||
chr12:42158620
|
G | A | 1 | a0001c0001t0026 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1969C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1969 | chr12 | 42158620 | |||||
chr12:42158657
|
T | C | 3 | a0001c0001t0003a0001c0001t0027a0001c0001t0034 | 31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1932A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1932 | chr12 | 42158657 | |||||
chr12:42158710
|
G | C | 4 | a0001c0001t0012a0001c0001t0028a0001c0001t0029others(1): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1879C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1879 | chr12 | 42158710 | |||||
chr12:42158787
|
G | C | 1 | a0001c0001t0031 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1802C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1802 | chr12 | 42158787 | |||||
chr12:42158865
|
T | A | 1 | a0001c0001t0031 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1724A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1724 | chr12 | 42158865 | |||||
chr12:42158922
|
T | A | 1 | a0001c0002t0032 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1667A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1667 | chr12 | 42158922 | |||||
chr12:42159005
|
T | G | 1 | a0001c0001t0013 | 2 | HG02258.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1584A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1584 | chr12 | 42159005 | |||||
chr12:42159417
|
T | C | 2 | a0001c0001t0004a0001c0001t0014 | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1172A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 1172 | chr12 | 42159417 | |||||
chr12:42159889
|
T | C | 1 | a0001c0001t0033 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*700A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 700 | chr12 | 42159889 | |||||
chr12:42159928
|
T | A | 1 | a0001c0001t0034 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 661 | chr12 | 42159928 | |||||
chr12:42160245
|
A | C | 1 | a0001c0001t0016 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 4/4 | 344 | chr12 | 42160245 | |||||
chr12:42238185
|
T | C | 1 | a0001c0003t0015 | 2 | HG02486.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-5A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 1/4 | 5 | chr12 | 42238185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:42160870
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.306-44G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42160870 | ||||||
chr12:42160937
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.306-111C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42160937 | ||||||
chr12:42160993
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.306-167T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42160993 | ||||||
chr12:42161041
|
CTG | C | 134 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0004others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.306-217_306-216del others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161041 | ||||||
chr12:42161369
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+244G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161369 | ||||||
chr12:42161415
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0209 | 2 | HG01243.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.305+198G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161415 | ||||||
chr12:42161546
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+67C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 3/3 | chr12 | 42161546 | ||||||
chr12:42161805
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.153-40G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42161805 | ||||||
chr12:42161928
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-163C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42161928 | ||||||
chr12:42162200
|
T | G | 1 | a0001c0002t0002g0353 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153-435A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162200 | ||||||
chr12:42162306
|
G | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-541C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162306 | ||||||
chr12:42162755
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.153-990G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162755 | ||||||
chr12:42162788
|
T | C | 1 | a0001c0002t0002g0324 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.153-1023A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162788 | ||||||
chr12:42162800
|
C | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-1035G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162800 | ||||||
chr12:42162899
|
T | G | 1 | a0001c0001t0004g0099 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.153-1134A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42162899 | ||||||
chr12:42163069
|
G | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-1304C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163069 | ||||||
chr12:42163138
|
T | G | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-1373A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163138 | ||||||
chr12:42163533
|
T | C | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-1768A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163533 | ||||||
chr12:42163656
|
T | C | 1 | a0001c0002t0002g0306 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.153-1891A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163656 | ||||||
chr12:42163779
|
G | C | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-2014C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163779 | ||||||
chr12:42163787
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-2022T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163787 | ||||||
chr12:42163916
|
T | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0116a0001c0001t0001g0125others(4): Show | 7 | HG02630.hp2 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-2151A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42163916 | ||||||
chr12:42164050
|
C | T | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-2285G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164050 | ||||||
chr12:42164120
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.153-2355A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164120 | ||||||
chr12:42164201
|
T | C | 135 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(132): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-2436A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164201 | ||||||
chr12:42164270
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-2505A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164270 | ||||||
chr12:42164384
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.153-2619A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164384 | ||||||
chr12:42164408
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-2643T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164408 | ||||||
chr12:42164538
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-2773C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164538 | ||||||
chr12:42164595
|
T | A | 31 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(28): Show | 31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.153-2830A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164595 | ||||||
chr12:42164721
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-2956T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164721 | ||||||
chr12:42164749
|
C | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG01496.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-2984G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164749 | ||||||
chr12:42164802
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.153-3037C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164802 | ||||||
chr12:42164819
|
C | T | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-3054G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164819 | ||||||
chr12:42164846
|
G | T | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-3081C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164846 | ||||||
chr12:42164859
|
C | G | 16 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(13): Show | 16 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.153-3094G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164859 | ||||||
chr12:42164921
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-3156T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164921 | ||||||
chr12:42164941
|
C | T | 1 | a0001c0001t0029g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-3176G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42164941 | ||||||
chr12:42165061
|
C | CA | 11 | a0001c0001t0001g0061a0001c0001t0001g0116a0001c0001t0001g0192others(8): Show | 11 | HG00408.hp2 HG01433.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-3297dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165061 | ||||||
chr12:42165061
|
CA | C | 7 | a0001c0001t0001g0077a0001c0001t0012g0089a0001c0001t0012g0090others(4): Show | 7 | HG00438.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-3297delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165061 | ||||||
chr12:42165073
|
A | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-3308T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165073 | ||||||
chr12:42165076
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.153-3311T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165076 | ||||||
chr12:42165180
|
C | T | 4 | a0001c0001t0010g0118a0001c0001t0010g0119a0001c0001t0011g0117others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-3415G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165180 | ||||||
chr12:42165187
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.153-3422C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165187 | ||||||
chr12:42165322
|
A | G | 11 | a0001c0002t0002g0086a0001c0002t0002g0162a0001c0002t0002g0169others(8): Show | 11 | HG00621.hp1 HG02129.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-3557T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165322 | ||||||
chr12:42165349
|
G | A | 31 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(28): Show | 31 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.153-3584C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165349 | ||||||
chr12:42165434
|
C | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-3669G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165434 | ||||||
chr12:42165452
|
G | GGTTTTT | 8 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0006g0223others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-3693_153-3688d others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165452 | ||||||
chr12:42165502
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3737G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165502 | ||||||
chr12:42165503
|
G | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0358others(9): Show | 13 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.153-3738C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165503 | ||||||
chr12:42165503
|
G | T | 3 | a0001c0002t0002g0241a0001c0002t0002g0354a0001c0002t0002g0355 | 3 | HG03669.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.153-3738C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165503 | ||||||
chr12:42165624
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3859G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165624 | ||||||
chr12:42165661
|
C | T | 5 | a0001c0002t0002g0264a0001c0002t0002g0265a0001c0002t0002g0266others(2): Show | 5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3896G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165661 | ||||||
chr12:42165723
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-3958T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165723 | ||||||
chr12:42165773
|
G | GT | 40 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0024others(37): Show | 40 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.153-4009dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165773 | ||||||
chr12:42165773
|
GT | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(89): Show | 94 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.153-4009delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165773 | ||||||
chr12:42165773
|
GTTTT | G | 64 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(61): Show | 67 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.153-4012_153-4009d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165773 | ||||||
chr12:42165884
|
A | ATATC | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-4123_153-4120d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165884 | ||||||
chr12:42165902
|
A | ATCTATCT others(25): Show |
3 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088 | 3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-4138_153-4137i others(34): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165902 | ||||||
chr12:42165902
|
A | ATCTATCT others(21): Show |
2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-4138_153-4137i others(30): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165902 | ||||||
chr12:42165957
|
A | G | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-4192T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165957 | ||||||
chr12:42165974
|
G | A | 4 | a0001c0001t0001g0358a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-4209C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42165974 | ||||||
chr12:42166067
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.153-4302A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166067 | ||||||
chr12:42166137
|
G | A | 15 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(12): Show | 15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-4372C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166137 | ||||||
chr12:42166146
|
C | T | 13 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-4381G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166146 | ||||||
chr12:42166166
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.153-4401C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166166 | ||||||
chr12:42166182
|
G | C | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-4417C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166182 | ||||||
chr12:42166205
|
G | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-4440C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166205 | ||||||
chr12:42166207
|
C | T | 15 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(12): Show | 15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-4442G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166207 | ||||||
chr12:42166338
|
T | C | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | NA18747.hp2 NA18956.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-4573A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166338 | ||||||
chr12:42166408
|
C | T | 6 | a0001c0001t0002g0272a0001c0002t0002g0080a0001c0002t0002g0240others(3): Show | 6 | NA18962.hp2 NA18969.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-4643G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166408 | ||||||
chr12:42166441
|
T | C | 5 | a0001c0002t0002g0264a0001c0002t0002g0265a0001c0002t0002g0266others(2): Show | 5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-4676A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166441 | ||||||
chr12:42166447
|
A | G | 1 | a0001c0002t0002g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-4682T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166447 | ||||||
chr12:42166548
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.153-4783A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166548 | ||||||
chr12:42166720
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.153-4955A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166720 | ||||||
chr12:42166829
|
TA | T | 39 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0003g0075others(36): Show | 39 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.153-5065delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166829 | ||||||
chr12:42166894
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-5129C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42166894 | ||||||
chr12:42167156
|
G | T | 1 | a0001c0001t0029g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-5391C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167156 | ||||||
chr12:42167184
|
A | C | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-5419T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167184 | ||||||
chr12:42167331
|
G | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-5566C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167331 | ||||||
chr12:42167360
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.153-5595C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167360 | ||||||
chr12:42167596
|
A | G | 135 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(132): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-5831T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167596 | ||||||
chr12:42167666
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-5901T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167666 | ||||||
chr12:42167712
|
T | C | 1 | a0001c0001t0006g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.153-5947A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167712 | ||||||
chr12:42167750
|
A | G | 2 | a0001c0001t0008g0123a0001c0001t0008g0124 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.153-5985T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167750 | ||||||
chr12:42167754
|
C | T | 4 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0008g0123others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-5989G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167754 | ||||||
chr12:42167913
|
T | C | 3 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0004t0017g0110 | 3 | HG02717.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.153-6148A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42167913 | ||||||
chr12:42168001
|
A | G | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-6236T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168001 | ||||||
chr12:42168175
|
A | AT | 17 | a0001c0001t0001g0070a0001c0001t0001g0136a0001c0001t0001g0195others(14): Show | 17 | HG00544.hp1 HG01978.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-6411dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168175 | ||||||
chr12:42168175
|
AT | A | 14 | a0001c0001t0001g0039a0001c0001t0001g0065a0001c0001t0001g0170others(11): Show | 14 | HG00642.hp2 HG01192.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-6411delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168175 | ||||||
chr12:42168209
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-6444C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168209 | ||||||
chr12:42168242
|
A | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(293): Show | 301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-6477T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168242 | ||||||
chr12:42168286
|
C | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-6521G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168286 | ||||||
chr12:42168305
|
A | G | 135 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(132): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-6540T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168305 | ||||||
chr12:42168458
|
A | C | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-6693T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168458 | ||||||
chr12:42168461
|
T | C | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-6696A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168461 | ||||||
chr12:42168675
|
C | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-6910G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168675 | ||||||
chr12:42168698
|
C | T | 2 | a0001c0001t0028g0087a0001c0001t0029g0091 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.153-6933G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42168698 | ||||||
chr12:42169027
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-7262G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169027 | ||||||
chr12:42169272
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-7507A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169272 | ||||||
chr12:42169337
|
C | A | 2 | a0001c0002t0002g0341a0001c0002t0002g0356 | 2 | NA18947.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.153-7572G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169337 | ||||||
chr12:42169461
|
T | G | 13 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-7696A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169461 | ||||||
chr12:42169527
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-7762A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169527 | ||||||
chr12:42169698
|
C | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-7933G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169698 | ||||||
chr12:42169785
|
T | C | 11 | a0001c0002t0002g0086a0001c0002t0002g0162a0001c0002t0002g0169others(8): Show | 11 | HG00621.hp1 HG02129.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-8020A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169785 | ||||||
chr12:42169872
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0116a0001c0001t0001g0125 | 3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.153-8107A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169872 | ||||||
chr12:42169904
|
A | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(299): Show | 307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.153-8139T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42169904 | ||||||
chr12:42170018
|
G | A | 37 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(34): Show | 37 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.153-8253C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170018 | ||||||
chr12:42170064
|
G | A | 1 | a0001c0001t0012g0090 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.153-8299C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170064 | ||||||
chr12:42170111
|
A | G | 5 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0142others(2): Show | 5 | NA18946.hp2 NA18957.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-8346T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170111 | ||||||
chr12:42170187
|
G | C | 135 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(132): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-8422C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170187 | ||||||
chr12:42170268
|
A | G | 3 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088 | 3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-8503T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170268 | ||||||
chr12:42170289
|
C | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-8524G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170289 | ||||||
chr12:42170312
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-8547A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170312 | ||||||
chr12:42170605
|
T | A | 1 | a0001c0003t0015g0368 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153-8840A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170605 | ||||||
chr12:42170673
|
T | TAC | 3 | a0001c0001t0003g0075a0001c0001t0031g0113a0001c0004t0017g0110 | 3 | HG02717.hp1 HG02897.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.153-8909_153-8908i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170673 | ||||||
chr12:42170675
|
T | C | 37 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(34): Show | 37 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.153-8910A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170675 | ||||||
chr12:42170675
|
T | TAC | 5 | a0001c0001t0001g0031a0001c0001t0001g0360a0001c0001t0001g0362others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-8912_153-8911d others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170675 | ||||||
chr12:42170675
|
T | TACAC | 3 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088 | 3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.153-8914_153-8911d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170675 | ||||||
chr12:42170718
|
C | T | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-8953G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170718 | ||||||
chr12:42170845
|
C | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-9080G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170845 | ||||||
chr12:42170921
|
G | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-9156C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170921 | ||||||
chr12:42170968
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.153-9203C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170968 | ||||||
chr12:42170990
|
G | GT | 6 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0018g0114others(3): Show | 6 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-9226dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170990 | ||||||
chr12:42170991
|
T | G | 58 | a0001c0002t0002g0081a0001c0002t0002g0084a0001c0002t0002g0086others(55): Show | 58 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.153-9226A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42170991 | ||||||
chr12:42171062
|
G | A | 1 | a0001c0002t0025g0232 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.153-9297C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171062 | ||||||
chr12:42171180
|
C | T | 1 | a0001c0001t0031g0113 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.153-9415G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171180 | ||||||
chr12:42171207
|
G | T | 4 | a0001c0002t0002g0251a0001c0002t0002g0254a0001c0002t0002g0255others(1): Show | 4 | NA18957.hp1 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-9442C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171207 | ||||||
chr12:42171230
|
A | T | 1 | a0001c0002t0002g0348 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.153-9465T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171230 | ||||||
chr12:42171233
|
C | T | 1 | a0001c0002t0002g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.153-9468G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171233 | ||||||
chr12:42171247
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.153-9482A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171247 | ||||||
chr12:42171269
|
G | T | 1 | a0001c0001t0011g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153-9504C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171269 | ||||||
chr12:42171495
|
C | A | 9 | a0001c0002t0005g0326a0001c0002t0005g0327a0001c0002t0005g0328others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.153-9730G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171495 | ||||||
chr12:42171509
|
TA | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(121): Show | 126 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.153-9745delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171509 | ||||||
chr12:42171516
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-9751T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171516 | ||||||
chr12:42171522
|
A | C | 1 | a0001c0001t0030g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153-9757T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171522 | ||||||
chr12:42171538
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-9773A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171538 | ||||||
chr12:42171629
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.153-9864T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171629 | ||||||
chr12:42171761
|
C | A | 1 | a0001c0002t0002g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.153-9996G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171761 | ||||||
chr12:42171799
|
C | CA | 16 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(13): Show | 16 | HG02015.hp1 HG02132.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-10035dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171799 | ||||||
chr12:42171799
|
CA | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(255): Show | 263 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.153-10035delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171799 | ||||||
chr12:42171799
|
CAA | C | 6 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(3): Show | 6 | HG01069.hp2 HG01169.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-10036_153-1003 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171799 | ||||||
chr12:42171824
|
T | C | 1 | a0001c0002t0002g0334 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.153-10059A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42171824 | ||||||
chr12:42172006
|
C | A | 1 | a0001c0002t0002g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-10241G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172006 | ||||||
chr12:42172304
|
T | G | 367 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(364): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.153-10539A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172304 | ||||||
chr12:42172305
|
C | T | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.153-10540G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172305 | ||||||
chr12:42172480
|
T | C | 59 | a0001c0002t0002g0081a0001c0002t0002g0084a0001c0002t0002g0086others(56): Show | 59 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.153-10715A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172480 | ||||||
chr12:42172637
|
G | A | 5 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0142others(2): Show | 5 | NA18946.hp2 NA18957.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-10872C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172637 | ||||||
chr12:42172639
|
A | T | 3 | a0001c0002t0002g0344a0001c0002t0002g0345a0001c0002t0002g0349 | 3 | NA18990.hp2 NA18993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.153-10874T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172639 | ||||||
chr12:42172727
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-10962C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172727 | ||||||
chr12:42172778
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-11013C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172778 | ||||||
chr12:42172804
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.153-11039A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172804 | ||||||
chr12:42172858
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-11093G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172858 | ||||||
chr12:42172881
|
A | G | 2 | a0001c0001t0028g0087a0001c0001t0029g0091 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.153-11116T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42172881 | ||||||
chr12:42173066
|
G | C | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.153-11301C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173066 | ||||||
chr12:42173082
|
G | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-11317C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173082 | ||||||
chr12:42173161
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-11396A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173161 | ||||||
chr12:42173163
|
G | A | 1 | a0001c0002t0002g0299 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.153-11398C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173163 | ||||||
chr12:42173202
|
C | G | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-11437G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173202 | ||||||
chr12:42173253
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-11488C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173253 | ||||||
chr12:42173400
|
T | C | 1 | a0001c0002t0002g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.153-11635A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173400 | ||||||
chr12:42173905
|
A | G | 16 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(13): Show | 16 | HG00639.hp2 HG00738.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.153-12140T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173905 | ||||||
chr12:42173917
|
A | G | 5 | a0001c0002t0002g0264a0001c0002t0002g0265a0001c0002t0002g0266others(2): Show | 5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-12152T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173917 | ||||||
chr12:42173998
|
C | T | 135 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(132): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.153-12233G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42173998 | ||||||
chr12:42174100
|
GA | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(122): Show | 127 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.153-12336delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174100 | ||||||
chr12:42174127
|
A | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-12362T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174127 | ||||||
chr12:42174205
|
T | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-12440A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174205 | ||||||
chr12:42174209
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.153-12444G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174209 | ||||||
chr12:42174262
|
C | T | 1 | a0001c0002t0002g0315 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153-12497G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174262 | ||||||
chr12:42174445
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.153-12680G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174445 | ||||||
chr12:42174642
|
G | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-12877C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174642 | ||||||
chr12:42174829
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.153-13064T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174829 | ||||||
chr12:42174891
|
A | AT | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-13127dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174891 | ||||||
chr12:42174963
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(84): Show | 89 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.153-13198G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42174963 | ||||||
chr12:42175018
|
C | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(291): Show | 299 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.153-13253G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175018 | ||||||
chr12:42175112
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-13347A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175112 | ||||||
chr12:42175235
|
G | A | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0362others(5): Show | 8 | HG02055.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-13470C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175235 | ||||||
chr12:42175292
|
T | C | 4 | a0001c0002t0002g0085a0001c0002t0002g0346a0001c0002t0002g0347others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-13527A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175292 | ||||||
chr12:42175332
|
T | C | 1 | a0001c0002t0002g0316 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.153-13567A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175332 | ||||||
chr12:42175350
|
C | A | 2 | a0001c0002t0002g0257a0001c0002t0002g0262 | 2 | HG01257.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.153-13585G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175350 | ||||||
chr12:42175365
|
GGGTAGGT others(6): Show |
G | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-13613_153-1360 others(17): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175365 | ||||||
chr12:42175404
|
G | C | 1 | a0001c0002t0002g0316 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.153-13639C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175404 | ||||||
chr12:42175534
|
CA | C | 366 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(363): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.153-13770delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175534 | ||||||
chr12:42175740
|
C | CA | 39 | a0001c0001t0009g0121a0001c0002t0002g0084a0001c0002t0002g0086others(36): Show | 39 | HG00323.hp1 HG00544.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.153-13976dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAA | 65 | a0001c0001t0013g0127a0001c0001t0013g0128a0001c0002t0002g0002others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.153-13977_153-1397 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAA | 29 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0002g0272others(26): Show | 30 | HG00621.hp2 HG01070.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.153-13978_153-1397 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAA | 11 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0044others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-13979_153-1397 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAA | 15 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG01433.hp1 HG01975.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.153-13980_153-1397 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAA | 18 | a0001c0001t0001g0024a0001c0001t0001g0050a0001c0001t0001g0067others(15): Show | 18 | HG00597.hp1 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-13981_153-1397 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA | 17 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0046others(14): Show | 17 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-13982_153-1397 others(11): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(1): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0069others(8): Show | 11 | HG00408.hp2 HG02071.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-13983_153-1397 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.153-13985_153-1397 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0074 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.153-13986_153-1397 others(15): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0125 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.153-13989_153-1397 others(18): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.153-13992_153-1397 others(21): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0057 | 3 | HG01515.hp2 HG03710.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.153-13994_153-1397 others(23): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(13): Show |
5 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0040others(2): Show | 5 | HG00639.hp2 HG01358.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-13995_153-1397 others(24): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(14): Show |
7 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-13996_153-1397 others(25): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0054others(2): Show | 5 | HG00423.hp2 HG01106.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-13997_153-1397 others(26): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(18): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0031others(1): Show | 4 | NA18977.hp1 NA18982.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-14000_153-1397 others(29): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(19): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0053 | 3 | HG01993.hp2 HG02015.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.153-14001_153-1397 others(30): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(20): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0036a0001c0001t0001g0056others(1): Show | 4 | HG01192.hp2 HG02683.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-14002_153-1397 others(31): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0037 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.153-13976_153-1397 others(35): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0035 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.153-13976_153-1397 others(36): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.153-13976_153-1397 others(40): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
CAAAA | C | 14 | a0001c0001t0001g0009a0001c0001t0003g0139a0001c0001t0003g0140others(11): Show | 14 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-13979_153-1397 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
CAAAAAA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(3): Show | 7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-13981_153-1397 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0116a0001c0001t0008g0092a0001c0001t0008g0093others(3): Show | 6 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-13983_153-1397 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0192a0001c0001t0001g0198a0001c0001t0001g0213others(3): Show | 6 | HG00642.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-13984_153-1397 others(13): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
CAAAAAAA others(3): Show |
C | 71 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(68): Show | 72 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.153-13985_153-1397 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175740
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153-13986_153-1397 others(15): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175740 | ||||||
chr12:42175818
|
C | G | 6 | a0001c0002t0002g0083a0001c0002t0002g0296a0001c0002t0002g0297others(3): Show | 6 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-14053G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175818 | ||||||
chr12:42175998
|
G | C | 1 | a0001c0002t0002g0346 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.153-14233C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42175998 | ||||||
chr12:42176068
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.153-14303C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176068 | ||||||
chr12:42176211
|
C | CA | 13 | a0001c0001t0001g0192a0001c0001t0001g0366a0001c0001t0002g0272others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-14447dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176211 | ||||||
chr12:42176211
|
CA | C | 7 | a0001c0001t0003g0166a0001c0001t0010g0118a0001c0001t0010g0119others(4): Show | 7 | HG00597.hp1 HG02258.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-14447delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176211 | ||||||
chr12:42176366
|
C | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-14601G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176366 | ||||||
chr12:42176367
|
T | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-14602A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176367 | ||||||
chr12:42176538
|
T | C | 1 | a0001c0002t0002g0325 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153-14773A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176538 | ||||||
chr12:42176548
|
G | A | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-14783C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176548 | ||||||
chr12:42176563
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.153-14798G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176563 | ||||||
chr12:42176681
|
G | T | 1 | a0001c0001t0028g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153-14916C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176681 | ||||||
chr12:42176727
|
T | A | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.153-14962A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176727 | ||||||
chr12:42176779
|
T | C | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-15014A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176779 | ||||||
chr12:42176783
|
G | A | 1 | a0001c0002t0002g0169 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153-15018C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176783 | ||||||
chr12:42176790
|
C | T | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-15025G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176790 | ||||||
chr12:42176840
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.153-15075C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176840 | ||||||
chr12:42176882
|
G | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132others(7): Show | 10 | HG00741.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.153-15117C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42176882 | ||||||
chr12:42177208
|
T | C | 1 | a0001c0001t0003g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.153-15443A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177208 | ||||||
chr12:42177275
|
A | G | 1 | a0001c0002t0002g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-15510T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177275 | ||||||
chr12:42177279
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.153-15514G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177279 | ||||||
chr12:42177417
|
T | C | 1 | a0001c0001t0004g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.153-15652A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177417 | ||||||
chr12:42177444
|
C | A | 5 | a0001c0002t0002g0264a0001c0002t0002g0265a0001c0002t0002g0266others(2): Show | 5 | HG01884.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-15679G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177444 | ||||||
chr12:42177484
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0116a0001c0001t0001g0125 | 3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.153-15719G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177484 | ||||||
chr12:42177524
|
C | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-15759G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177524 | ||||||
chr12:42177576
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.153-15811G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177576 | ||||||
chr12:42177588
|
C | G | 1 | a0001c0002t0002g0306 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.153-15823G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177588 | ||||||
chr12:42177593
|
A | G | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-15828T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177593 | ||||||
chr12:42177775
|
T | C | 10 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(7): Show | 10 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.153-16010A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177775 | ||||||
chr12:42177825
|
A | G | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-16060T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177825 | ||||||
chr12:42177929
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-16164G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177929 | ||||||
chr12:42177977
|
T | C | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-16212A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42177977 | ||||||
chr12:42178113
|
T | C | 39 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(36): Show | 39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-16348A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178113 | ||||||
chr12:42178277
|
A | T | 33 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(30): Show | 33 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.153-16512T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178277 | ||||||
chr12:42178302
|
G | A | 4 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0008g0123others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-16537C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178302 | ||||||
chr12:42178370
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0208 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.153-16605C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178370 | ||||||
chr12:42178382
|
G | A | 3 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-16617C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178382 | ||||||
chr12:42178420
|
A | G | 2 | a0001c0001t0001g0360a0001c0001t0001g0362 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.153-16655T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178420 | ||||||
chr12:42178428
|
A | G | 1 | a0001c0002t0002g0335 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.153-16663T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178428 | ||||||
chr12:42178505
|
C | T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-16740G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178505 | ||||||
chr12:42178611
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-16846A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178611 | ||||||
chr12:42178687
|
T | C | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-16922A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178687 | ||||||
chr12:42178811
|
A | T | 1 | a0001c0001t0004g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.153-17046T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42178811 | ||||||
chr12:42179103
|
T | C | 1 | a0001c0001t0004g0109 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.153-17338A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179103 | ||||||
chr12:42179267
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-17502G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179267 | ||||||
chr12:42179315
|
C | G | 1 | a0001c0001t0004g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153-17550G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179315 | ||||||
chr12:42179573
|
T | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-17808A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179573 | ||||||
chr12:42179789
|
C | CA | 116 | a0001c0001t0001g0009a0001c0001t0001g0073a0001c0001t0001g0116others(113): Show | 119 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.153-18025dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179789 | ||||||
chr12:42179789
|
C | CAA | 17 | a0001c0002t0002g0086a0001c0002t0002g0242a0001c0002t0002g0243others(14): Show | 17 | HG00621.hp1 HG01884.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-18026_153-1802 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179789 | ||||||
chr12:42179789
|
CA | C | 69 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(66): Show | 69 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.153-18025delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179789 | ||||||
chr12:42179820
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.153-18055C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179820 | ||||||
chr12:42179909
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.153-18144G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42179909 | ||||||
chr12:42180020
|
T | C | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-18255A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180020 | ||||||
chr12:42180066
|
G | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(274): Show | 282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.153-18301C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180066 | ||||||
chr12:42180195
|
C | T | 12 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(9): Show | 12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-18430G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180195 | ||||||
chr12:42180221
|
G | A | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-18456C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180221 | ||||||
chr12:42180317
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-18552A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180317 | ||||||
chr12:42180390
|
A | G | 13 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-18625T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180390 | ||||||
chr12:42180457
|
G | A | 1 | a0001c0001t0028g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.153-18692C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180457 | ||||||
chr12:42180457
|
G | C | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.153-18692C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180457 | ||||||
chr12:42180580
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-18815G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180580 | ||||||
chr12:42180581
|
G | A | 4 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0008g0123others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-18816C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180581 | ||||||
chr12:42180650
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.153-18885T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180650 | ||||||
chr12:42180736
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0024g0063 | 3 | HG00408.hp2 NA18961.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.153-18971C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42180736 | ||||||
chr12:42181151
|
G | C | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-19386C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181151 | ||||||
chr12:42181379
|
A | T | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-19614T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181379 | ||||||
chr12:42181414
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-19649A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181414 | ||||||
chr12:42181450
|
TCTTGCGT others(10): Show |
T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-19702_153-1968 others(21): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181450 | ||||||
chr12:42181472
|
T | C | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-19707A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181472 | ||||||
chr12:42181740
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153-19975G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42181740 | ||||||
chr12:42182125
|
AAAG | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-20363_153-2036 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182125 | ||||||
chr12:42182244
|
G | T | 12 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(9): Show | 12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-20479C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182244 | ||||||
chr12:42182247
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-20482A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182247 | ||||||
chr12:42182264
|
A | G | 3 | a0001c0002t0002g0266a0001c0002t0002g0267a0001c0002t0002g0278 | 3 | HG01884.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.153-20499T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182264 | ||||||
chr12:42182374
|
GA | G | 7 | a0001c0001t0003g0139a0001c0001t0003g0147a0001c0001t0003g0148others(4): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-20610delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182374 | ||||||
chr12:42182654
|
C | G | 1 | a0001c0001t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153-20889G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182654 | ||||||
chr12:42182661
|
C | T | 1 | a0001c0002t0002g0249 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.153-20896G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182661 | ||||||
chr12:42182694
|
T | C | 1 | a0001c0002t0002g0320 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.153-20929A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182694 | ||||||
chr12:42182735
|
A | G | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-20970T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182735 | ||||||
chr12:42182806
|
C | A | 2 | a0001c0002t0005g0260a0001c0002t0005g0261 | 2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.153-21041G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182806 | ||||||
chr12:42182889
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(1): Show | 4 | NA18986.hp2 NA19007.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-21124G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182889 | ||||||
chr12:42182929
|
A | C | 2 | a0001c0002t0002g0347a0001c0002t0002g0348 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.153-21164T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182929 | ||||||
chr12:42182974
|
G | A | 1 | a0001c0002t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.153-21209C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42182974 | ||||||
chr12:42183025
|
T | C | 1 | a0001c0001t0029g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-21260A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183025 | ||||||
chr12:42183114
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-21349G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183114 | ||||||
chr12:42183218
|
C | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-21453G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183218 | ||||||
chr12:42183427
|
A | G | 1 | a0001c0001t0003g0075 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.153-21662T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183427 | ||||||
chr12:42183442
|
C | G | 2 | a0001c0001t0011g0117a0001c0001t0011g0126 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153-21677G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183442 | ||||||
chr12:42183733
|
T | G | 1 | a0001c0002t0002g0302 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.153-21968A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183733 | ||||||
chr12:42183837
|
A | C | 3 | a0001c0002t0002g0344a0001c0002t0002g0345a0001c0002t0002g0349 | 3 | NA18990.hp2 NA18993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.153-22072T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42183837 | ||||||
chr12:42184275
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(299): Show | 307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.153-22510T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184275 | ||||||
chr12:42184303
|
A | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-22538T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184303 | ||||||
chr12:42184413
|
G | A | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.153-22648C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184413 | ||||||
chr12:42184726
|
C | A | 2 | a0001c0001t0010g0118a0001c0001t0010g0119 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.153-22961G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184726 | ||||||
chr12:42184997
|
C | T | 1 | a0001c0002t0002g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153-23232G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42184997 | ||||||
chr12:42185046
|
C | T | 2 | a0001c0001t0011g0117a0001c0001t0011g0126 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153-23281G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185046 | ||||||
chr12:42185050
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-23285A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185050 | ||||||
chr12:42185134
|
C | T | 1 | a0001c0001t0004g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.153-23369G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185134 | ||||||
chr12:42185135
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-23370C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185135 | ||||||
chr12:42185171
|
T | C | 1 | a0001c0002t0002g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.153-23406A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185171 | ||||||
chr12:42185176
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(72): Show | 76 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.153-23411C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185176 | ||||||
chr12:42185176
|
G | GCAAA | 12 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0001t0004g0095others(9): Show | 12 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.153-23415_153-2341 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185176 | ||||||
chr12:42185176
|
GCAAA | G | 35 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(32): Show | 35 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.153-23415_153-2341 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185176 | ||||||
chr12:42185423
|
G | A | 2 | a0001c0001t0028g0087a0001c0001t0029g0091 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.153-23658C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185423 | ||||||
chr12:42185429
|
G | A | 1 | a0001c0002t0002g0240 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.153-23664C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185429 | ||||||
chr12:42185584
|
C | T | 14 | a0001c0001t0001g0077a0001c0001t0001g0171a0001c0001t0001g0178others(11): Show | 14 | HG00438.hp1 HG00609.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-23819G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185584 | ||||||
chr12:42185722
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0361 | 4 | HG02559.hp2 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-23957G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185722 | ||||||
chr12:42185921
|
C | T | 38 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(35): Show | 38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.153-24156G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185921 | ||||||
chr12:42185938
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0227 | 2 | NA19007.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.153-24173C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42185938 | ||||||
chr12:42186010
|
G | A | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-24245C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186010 | ||||||
chr12:42186017
|
G | A | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.153-24252C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186017 | ||||||
chr12:42186065
|
C | T | 1 | a0001c0001t0011g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-24300G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186065 | ||||||
chr12:42186117
|
G | A | 7 | a0001c0001t0003g0139a0001c0001t0003g0147a0001c0001t0003g0148others(4): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-24352C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186117 | ||||||
chr12:42186121
|
G | A | 6 | a0001c0002t0002g0233a0001c0002t0002g0237a0001c0002t0002g0249others(3): Show | 6 | HG02258.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.153-24356C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186121 | ||||||
chr12:42186170
|
C | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-24405G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186170 | ||||||
chr12:42186189
|
C | CA | 76 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0030others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.153-24425dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186189 | ||||||
chr12:42186189
|
C | CAA | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(182): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.153-24426_153-2442 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186189 | ||||||
chr12:42186189
|
C | CAAA | 46 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0137others(43): Show | 46 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.153-24427_153-2442 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186189 | ||||||
chr12:42186246
|
A | G | 3 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0142 | 3 | NA18946.hp2 NA18957.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.153-24481T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186246 | ||||||
chr12:42186337
|
G | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-24572C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186337 | ||||||
chr12:42186340
|
CA | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-24576delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186340 | ||||||
chr12:42186410
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.153-24645C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186410 | ||||||
chr12:42186600
|
C | T | 38 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(35): Show | 38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.153-24835G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186600 | ||||||
chr12:42186731
|
G | C | 2 | a0001c0001t0014g0111a0001c0001t0014g0112 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.153-24966C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186731 | ||||||
chr12:42186943
|
A | G | 1 | a0001c0002t0025g0232 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.153-25178T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42186943 | ||||||
chr12:42187234
|
G | A | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-25469C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187234 | ||||||
chr12:42187308
|
T | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-25543A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187308 | ||||||
chr12:42187348
|
T | C | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-25583A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187348 | ||||||
chr12:42187553
|
G | C | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-25788C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187553 | ||||||
chr12:42187615
|
C | T | 1 | a0001c0003t0001g0235 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.153-25850G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187615 | ||||||
chr12:42187769
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-26004A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187769 | ||||||
chr12:42187792
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-26027G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187792 | ||||||
chr12:42187801
|
G | T | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-26036C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187801 | ||||||
chr12:42187871
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(293): Show | 301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-26106A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187871 | ||||||
chr12:42187937
|
G | C | 3 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153-26172C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187937 | ||||||
chr12:42187962
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.153-26197C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42187962 | ||||||
chr12:42188155
|
T | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26390A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188155 | ||||||
chr12:42188163
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26398G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188163 | ||||||
chr12:42188198
|
G | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-26433C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188198 | ||||||
chr12:42188336
|
C | G | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-26571G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188336 | ||||||
chr12:42188383
|
C | CT | 51 | a0001c0001t0001g0050a0001c0001t0001g0079a0001c0001t0001g0137others(48): Show | 51 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.153-26619dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188383 | ||||||
chr12:42188383
|
C | CTT | 6 | a0001c0001t0003g0152a0001c0001t0003g0168a0001c0001t0018g0114others(3): Show | 6 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-26620_153-2661 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188383 | ||||||
chr12:42188383
|
CT | C | 9 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(6): Show | 9 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.153-26619delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188383 | ||||||
chr12:42188512
|
A | G | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-26747T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188512 | ||||||
chr12:42188729
|
T | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26964A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188729 | ||||||
chr12:42188730
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-26965C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188730 | ||||||
chr12:42188999
|
T | C | 33 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(30): Show | 33 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.153-27234A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42188999 | ||||||
chr12:42189073
|
T | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(306): Show | 314 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.153-27308A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189073 | ||||||
chr12:42189082
|
G | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-27317C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189082 | ||||||
chr12:42189139
|
T | G | 1 | a0001c0001t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.153-27374A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189139 | ||||||
chr12:42189271
|
G | A | 1 | a0001c0002t0002g0352 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.153-27506C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189271 | ||||||
chr12:42189326
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.153-27561C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189326 | ||||||
chr12:42189387
|
C | T | 2 | a0001c0001t0008g0123a0001c0001t0008g0124 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.153-27622G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189387 | ||||||
chr12:42189467
|
T | C | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-27702A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189467 | ||||||
chr12:42189503
|
A | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0173a0001c0001t0001g0174others(8): Show | 11 | HG00597.hp2 NA18948.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.153-27738T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189503 | ||||||
chr12:42189660
|
A | G | 1 | a0001c0002t0002g0274 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.153-27895T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189660 | ||||||
chr12:42189697
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153-27932G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189697 | ||||||
chr12:42189847
|
A | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-28082T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189847 | ||||||
chr12:42189906
|
G | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-28141C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189906 | ||||||
chr12:42189944
|
A | C | 1 | a0001c0001t0004g0094 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.153-28179T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42189944 | ||||||
chr12:42190014
|
T | C | 1 | a0001c0002t0002g0325 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153-28249A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190014 | ||||||
chr12:42190261
|
T | C | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-28496A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190261 | ||||||
chr12:42190359
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.153-28594T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190359 | ||||||
chr12:42190457
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-28692G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190457 | ||||||
chr12:42190696
|
A | G | 1 | a0001c0001t0002g0272 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.153-28931T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190696 | ||||||
chr12:42190726
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.153-28961A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42190726 | ||||||
chr12:42191020
|
C | T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-29255G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191020 | ||||||
chr12:42191153
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-29388G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191153 | ||||||
chr12:42191294
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.153-29529G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191294 | ||||||
chr12:42191359
|
A | G | 1 | a0001c0002t0025g0232 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.153-29594T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191359 | ||||||
chr12:42191539
|
C | A | 1 | a0001c0001t0003g0165 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.153-29774G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191539 | ||||||
chr12:42191596
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-29831G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191596 | ||||||
chr12:42191597
|
C | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-29832G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191597 | ||||||
chr12:42191740
|
C | T | 1 | a0001c0001t0031g0113 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.153-29975G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42191740 | ||||||
chr12:42192083
|
A | G | 1 | a0001c0002t0023g0239 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.153-30318T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192083 | ||||||
chr12:42192137
|
T | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-30372A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192137 | ||||||
chr12:42192237
|
G | A | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-30472C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192237 | ||||||
chr12:42192258
|
A | G | 1 | a0001c0001t0003g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153-30493T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192258 | ||||||
chr12:42192295
|
C | T | 1 | a0001c0001t0011g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153-30530G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192295 | ||||||
chr12:42192314
|
C | T | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.153-30549G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192314 | ||||||
chr12:42192668
|
G | A | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-30903C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192668 | ||||||
chr12:42192673
|
G | T | 1 | a0001c0001t0011g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.153-30908C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192673 | ||||||
chr12:42192687
|
G | C | 4 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0008g0123others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-30922C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192687 | ||||||
chr12:42192733
|
T | C | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-30968A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192733 | ||||||
chr12:42192798
|
A | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-31033T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192798 | ||||||
chr12:42192839
|
C | T | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31074G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192839 | ||||||
chr12:42192842
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153-31077G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42192842 | ||||||
chr12:42193032
|
G | A | 15 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(12): Show | 15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.153-31267C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193032 | ||||||
chr12:42193080
|
G | A | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-31315C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193080 | ||||||
chr12:42193084
|
G | T | 2 | a0001c0001t0030g0088a0001c0002t0002g0085 | 2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153-31319C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193084 | ||||||
chr12:42193108
|
A | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31343T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193108 | ||||||
chr12:42193207
|
C | T | 60 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(57): Show | 63 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.153-31442G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193207 | ||||||
chr12:42193213
|
G | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31448C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193213 | ||||||
chr12:42193250
|
G | A | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.153-31485C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193250 | ||||||
chr12:42193271
|
C | T | 1 | a0001c0002t0002g0318 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.153-31506G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193271 | ||||||
chr12:42193318
|
CA | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(14): Show | 18 | HG02055.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.153-31554delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193318 | ||||||
chr12:42193687
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(293): Show | 301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-31922C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193687 | ||||||
chr12:42193732
|
G | A | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-31967C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193732 | ||||||
chr12:42193889
|
C | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-32124G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193889 | ||||||
chr12:42193962
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.153-32197C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42193962 | ||||||
chr12:42194107
|
A | G | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-32342T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194107 | ||||||
chr12:42194376
|
G | T | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-32611C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194376 | ||||||
chr12:42194397
|
A | G | 39 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(36): Show | 39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-32632T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194397 | ||||||
chr12:42194438
|
G | A | 2 | a0001c0002t0007g0250a0001c0002t0007g0259 | 2 | NA18995.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.153-32673C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194438 | ||||||
chr12:42194462
|
G | A | 3 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0002t0002g0335 | 3 | HG01169.hp2 HG02132.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.153-32697C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194462 | ||||||
chr12:42194482
|
A | G | 1 | a0001c0002t0002g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-32717T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194482 | ||||||
chr12:42194539
|
G | A | 2 | a0001c0003t0015g0368a0001c0003t0015g0369 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.153-32774C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194539 | ||||||
chr12:42194874
|
T | C | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-33109A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194874 | ||||||
chr12:42194893
|
A | T | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-33128T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42194893 | ||||||
chr12:42195019
|
A | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-33254T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195019 | ||||||
chr12:42195120
|
G | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-33355C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195120 | ||||||
chr12:42195137
|
G | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-33372C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195137 | ||||||
chr12:42195202
|
T | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153-33437A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195202 | ||||||
chr12:42195309
|
G | T | 1 | a0001c0001t0018g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.153-33544C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195309 | ||||||
chr12:42195438
|
A | G | 1 | a0001c0001t0029g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-33673T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195438 | ||||||
chr12:42195440
|
G | A | 1 | a0001c0002t0002g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.153-33675C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195440 | ||||||
chr12:42195693
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-33928A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195693 | ||||||
chr12:42195819
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-34054C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195819 | ||||||
chr12:42195894
|
G | A | 1 | a0001c0002t0002g0346 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.153-34129C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42195894 | ||||||
chr12:42196027
|
G | C | 2 | a0001c0001t0011g0117a0001c0001t0011g0126 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.153-34262C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196027 | ||||||
chr12:42196032
|
G | C | 1 | a0001c0001t0030g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153-34267C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196032 | ||||||
chr12:42196080
|
G | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.153-34315C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196080 | ||||||
chr12:42196082
|
T | C | 14 | a0001c0001t0001g0077a0001c0001t0001g0171a0001c0001t0001g0178others(11): Show | 14 | HG00438.hp1 HG00609.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.153-34317A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196082 | ||||||
chr12:42196183
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.153-34418G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196183 | ||||||
chr12:42196223
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.153-34458A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196223 | ||||||
chr12:42196227
|
G | GA | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.153-34463dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | ||||||
chr12:42196227
|
G | GAA | 18 | a0001c0001t0003g0156a0001c0001t0004g0094a0001c0001t0004g0095others(15): Show | 18 | HG00423.hp1 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-34464_153-3446 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | ||||||
chr12:42196227
|
GA | G | 63 | a0001c0001t0001g0358a0001c0001t0001g0362a0001c0001t0001g0363others(60): Show | 63 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.153-34463delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | ||||||
chr12:42196227
|
GAA | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0361others(2): Show | 6 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-34464_153-3446 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196227 | ||||||
chr12:42196256
|
G | A | 1 | a0001c0001t0003g0075 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.153-34491C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196256 | ||||||
chr12:42196270
|
AACAGCAT others(8): Show |
A | 1 | a0001c0001t0001g0015 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.153-34520_153-3450 others(19): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196270 | ||||||
chr12:42196340
|
C | A | 1 | a0001c0001t0004g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.153-34575G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196340 | ||||||
chr12:42196365
|
TACAGGTT others(4): Show |
T | 1 | a0001c0001t0001g0069 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.153-34611_153-3460 others(15): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196365 | ||||||
chr12:42196422
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-34657G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196422 | ||||||
chr12:42196426
|
T | G | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-34661A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196426 | ||||||
chr12:42196538
|
T | A | 1 | a0001c0001t0004g0094 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.153-34773A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196538 | ||||||
chr12:42196949
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.153-35184A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196949 | ||||||
chr12:42196986
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0360others(3): Show | 7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-35221G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42196986 | ||||||
chr12:42197001
|
C | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-35236G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197001 | ||||||
chr12:42197013
|
C | A | 2 | a0001c0001t0010g0118a0001c0001t0010g0119 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.153-35248G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197013 | ||||||
chr12:42197058
|
A | G | 1 | a0001c0004t0017g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.153-35293T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197058 | ||||||
chr12:42197093
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.153-35328A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197093 | ||||||
chr12:42197098
|
T | A | 1 | a0001c0001t0029g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.153-35333A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197098 | ||||||
chr12:42197112
|
A | G | 1 | a0001c0001t0004g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.153-35347T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197112 | ||||||
chr12:42197127
|
G | A | 39 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(36): Show | 39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-35362C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197127 | ||||||
chr12:42197216
|
A | G | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-35451T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197216 | ||||||
chr12:42197277
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-35512G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197277 | ||||||
chr12:42197540
|
A | C | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.153-35775T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197540 | ||||||
chr12:42197591
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-35826C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197591 | ||||||
chr12:42197600
|
C | T | 1 | a0001c0001t0031g0113 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.153-35835G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197600 | ||||||
chr12:42197739
|
G | C | 39 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(36): Show | 39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.153-35974C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197739 | ||||||
chr12:42197747
|
A | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-35982T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197747 | ||||||
chr12:42197831
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-36066G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197831 | ||||||
chr12:42197854
|
A | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-36089T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197854 | ||||||
chr12:42197942
|
C | A | 1 | a0001c0002t0002g0325 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153-36177G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197942 | ||||||
chr12:42197993
|
A | T | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-36228T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42197993 | ||||||
chr12:42198030
|
C | A | 1 | a0001c0002t0002g0315 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.153-36265G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198030 | ||||||
chr12:42198047
|
T | G | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-36282A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198047 | ||||||
chr12:42198105
|
C | G | 1 | a0001c0002t0002g0307 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.153-36340G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198105 | ||||||
chr12:42198569
|
C | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-36804G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198569 | ||||||
chr12:42198726
|
AATTG | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-36965_153-3696 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198726 | ||||||
chr12:42198746
|
A | G | 4 | a0001c0001t0010g0118a0001c0001t0010g0119a0001c0001t0011g0117others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-36981T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198746 | ||||||
chr12:42198788
|
T | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(293): Show | 301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-37023A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198788 | ||||||
chr12:42198796
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(293): Show | 301 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.153-37031C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198796 | ||||||
chr12:42198822
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153-37057A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198822 | ||||||
chr12:42198961
|
T | A | 1 | a0001c0002t0002g0334 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.153-37196A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42198961 | ||||||
chr12:42199008
|
T | C | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153-37243A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199008 | ||||||
chr12:42199311
|
A | G | 4 | a0001c0001t0030g0088a0001c0002t0002g0346a0001c0002t0002g0347others(1): Show | 4 | HG02717.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-37546T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199311 | ||||||
chr12:42199498
|
A | G | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153-37733T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199498 | ||||||
chr12:42199634
|
A | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.153-37869T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199634 | ||||||
chr12:42199727
|
A | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+37872T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199727 | ||||||
chr12:42199772
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.152+37827A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199772 | ||||||
chr12:42199891
|
T | C | 8 | a0001c0001t0003g0139a0001c0001t0003g0146a0001c0001t0003g0147others(5): Show | 8 | HG00738.hp1 HG01192.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+37708A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42199891 | ||||||
chr12:42200087
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+37512G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200087 | ||||||
chr12:42200217
|
G | A | 1 | a0001c0002t0002g0286 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.152+37382C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200217 | ||||||
chr12:42200321
|
A | G | 1 | a0001c0001t0004g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.152+37278T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200321 | ||||||
chr12:42200377
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+37222C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200377 | ||||||
chr12:42200391
|
C | T | 1 | a0001c0002t0002g0268 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.152+37208G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200391 | ||||||
chr12:42200405
|
T | A | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+37194A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200405 | ||||||
chr12:42200422
|
C | A | 1 | a0001c0002t0002g0336 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.152+37177G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200422 | ||||||
chr12:42200684
|
G | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+36915C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200684 | ||||||
chr12:42200699
|
A | G | 1 | a0001c0001t0003g0164 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.152+36900T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200699 | ||||||
chr12:42200707
|
G | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG01099.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152+36892C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200707 | ||||||
chr12:42200946
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+36653A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42200946 | ||||||
chr12:42201018
|
C | G | 1 | a0001c0001t0006g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.152+36581G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201018 | ||||||
chr12:42201128
|
T | G | 4 | a0001c0002t0002g0251a0001c0002t0002g0254a0001c0002t0002g0255others(1): Show | 4 | NA18957.hp1 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+36471A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201128 | ||||||
chr12:42201522
|
A | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+36077T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201522 | ||||||
chr12:42201523
|
T | TTG | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+36074_152+3607 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201523 | ||||||
chr12:42201595
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(274): Show | 282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+36004G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201595 | ||||||
chr12:42201819
|
G | T | 2 | a0001c0001t0008g0123a0001c0001t0008g0124 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.152+35780C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201819 | ||||||
chr12:42201820
|
C | G | 2 | a0001c0001t0008g0123a0001c0001t0008g0124 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.152+35779G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42201820 | ||||||
chr12:42202105
|
C | T | 6 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+35494G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202105 | ||||||
chr12:42202112
|
C | A | 1 | a0001c0004t0017g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.152+35487G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202112 | ||||||
chr12:42202130
|
G | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+35469C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202130 | ||||||
chr12:42202177
|
C | T | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+35422G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202177 | ||||||
chr12:42202218
|
C | T | 7 | a0001c0001t0003g0139a0001c0001t0003g0147a0001c0001t0003g0148others(4): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+35381G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202218 | ||||||
chr12:42202249
|
T | C | 1 | a0001c0001t0002g0272 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.152+35350A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202249 | ||||||
chr12:42202332
|
A | T | 1 | a0001c0002t0002g0317 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152+35267T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202332 | ||||||
chr12:42202412
|
C | T | 7 | a0001c0001t0006g0220a0001c0001t0006g0221a0001c0001t0006g0222others(4): Show | 7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+35187G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202412 | ||||||
chr12:42202447
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0031others(2): Show | 5 | NA18747.hp1 NA18954.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+35152T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202447 | ||||||
chr12:42202496
|
C | T | 4 | a0001c0001t0001g0358a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+35103G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202496 | ||||||
chr12:42202660
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(274): Show | 282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+34939A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202660 | ||||||
chr12:42202875
|
G | A | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+34724C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42202875 | ||||||
chr12:42203021
|
G | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+34578C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203021 | ||||||
chr12:42203045
|
G | T | 1 | a0001c0002t0002g0347 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152+34554C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203045 | ||||||
chr12:42203066
|
C | CA | 11 | a0001c0001t0001g0050a0001c0001t0001g0077a0001c0001t0001g0190others(8): Show | 11 | HG00438.hp1 HG01169.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+34532dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203066 | ||||||
chr12:42203344
|
C | A | 4 | a0001c0002t0002g0251a0001c0002t0002g0254a0001c0002t0002g0255others(1): Show | 4 | NA18957.hp1 NA18959.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+34255G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203344 | ||||||
chr12:42203366
|
T | C | 3 | a0001c0002t0002g0274a0001c0002t0002g0275a0001c0002t0002g0276 | 3 | HG00621.hp2 HG02155.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.152+34233A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203366 | ||||||
chr12:42203453
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+34146A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203453 | ||||||
chr12:42203490
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+34109T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203490 | ||||||
chr12:42203529
|
G | A | 1 | a0001c0002t0002g0291 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.152+34070C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203529 | ||||||
chr12:42203643
|
AT | A | 12 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0358others(9): Show | 13 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.152+33955delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203643 | ||||||
chr12:42203733
|
G | A | 7 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | HG00733.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+33866C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203733 | ||||||
chr12:42203740
|
A | C | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+33859T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203740 | ||||||
chr12:42203840
|
T | C | 1 | a0001c0002t0002g0319 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.152+33759A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203840 | ||||||
chr12:42203886
|
C | T | 2 | a0001c0003t0015g0368a0001c0003t0015g0369 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+33713G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203886 | ||||||
chr12:42203887
|
G | A | 1 | a0001c0001t0004g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.152+33712C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42203887 | ||||||
chr12:42204020
|
C | T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+33579G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204020 | ||||||
chr12:42204146
|
G | T | 8 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(5): Show | 8 | HG00741.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+33453C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204146 | ||||||
chr12:42204161
|
T | C | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+33438A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204161 | ||||||
chr12:42204176
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+33423T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204176 | ||||||
chr12:42204279
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+33320G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204279 | ||||||
chr12:42204374
|
G | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+33225C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204374 | ||||||
chr12:42204440
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.152+33159A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204440 | ||||||
chr12:42204447
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+33152A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204447 | ||||||
chr12:42204533
|
G | A | 1 | a0001c0002t0002g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+33066C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204533 | ||||||
chr12:42204767
|
C | G | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+32832G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204767 | ||||||
chr12:42204775
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0227 | 2 | NA19007.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.152+32824G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204775 | ||||||
chr12:42204834
|
G | A | 3 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0004t0017g0110 | 3 | HG02717.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.152+32765C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204834 | ||||||
chr12:42204836
|
A | G | 3 | a0001c0002t0002g0237a0001c0002t0002g0249a0001c0002t0002g0321 | 3 | HG02258.hp1 HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.152+32763T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42204836 | ||||||
chr12:42205055
|
T | TA | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 96 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.152+32543dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205055 | ||||||
chr12:42205055
|
TA | T | 24 | a0001c0001t0003g0139a0001c0001t0003g0146a0001c0001t0003g0147others(21): Show | 24 | HG00423.hp1 HG00738.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.152+32543delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205055 | ||||||
chr12:42205162
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.152+32437A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205162 | ||||||
chr12:42205237
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+32362A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205237 | ||||||
chr12:42205320
|
C | T | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+32279G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205320 | ||||||
chr12:42205371
|
TTCTTC | T | 9 | a0001c0001t0003g0076a0001c0001t0003g0154a0001c0001t0003g0155others(6): Show | 9 | HG01891.hp2 HG01975.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+32223_152+3222 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205371 | ||||||
chr12:42205372
|
T | G | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.152+32227A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205372 | ||||||
chr12:42205378
|
C | CT | 6 | a0001c0001t0001g0360a0001c0001t0008g0092a0001c0001t0008g0093others(3): Show | 6 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+32220dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205378 | ||||||
chr12:42205585
|
G | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+32014C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205585 | ||||||
chr12:42205892
|
A | C | 4 | a0001c0001t0010g0118a0001c0001t0010g0119a0001c0001t0011g0117others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+31707T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205892 | ||||||
chr12:42205894
|
T | A | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+31705A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205894 | ||||||
chr12:42205917
|
T | TTTTG | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+31681_152+3168 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42205917 | ||||||
chr12:42206105
|
A | T | 3 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+31494T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206105 | ||||||
chr12:42206131
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+31468G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206131 | ||||||
chr12:42206297
|
T | TA | 11 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0039others(8): Show | 11 | HG00408.hp2 HG01081.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+31301dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206297 | ||||||
chr12:42206297
|
TA | T | 182 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0211others(179): Show | 186 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.152+31301delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206297 | ||||||
chr12:42206297
|
TAA | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(82): Show | 86 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.152+31300_152+3130 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206297 | ||||||
chr12:42206323
|
G | A | 1 | a0001c0001t0011g0126 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.152+31276C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206323 | ||||||
chr12:42206335
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+31264C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206335 | ||||||
chr12:42206471
|
C | T | 2 | a0001c0003t0015g0368a0001c0003t0015g0369 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+31128G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206471 | ||||||
chr12:42206577
|
C | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+31022G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206577 | ||||||
chr12:42206602
|
C | T | 1 | a0001c0002t0002g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+30997G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206602 | ||||||
chr12:42206704
|
C | CA | 11 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0360others(8): Show | 12 | HG01891.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+30894dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206704 | ||||||
chr12:42206856
|
T | C | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+30743A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206856 | ||||||
chr12:42206858
|
TCTC | T | 13 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+30738_152+3074 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42206858 | ||||||
chr12:42207108
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.152+30491A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207108 | ||||||
chr12:42207112
|
A | G | 16 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(13): Show | 16 | HG00639.hp2 HG00738.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.152+30487T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207112 | ||||||
chr12:42207194
|
A | G | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152+30405T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207194 | ||||||
chr12:42207349
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.152+30250G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207349 | ||||||
chr12:42207469
|
TTAA | T | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+30127_152+3012 others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207469 | ||||||
chr12:42207531
|
T | C | 1 | a0001c0001t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152+30068A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207531 | ||||||
chr12:42207630
|
T | C | 1 | a0001c0002t0002g0338 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.152+29969A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207630 | ||||||
chr12:42207668
|
A | G | 6 | a0001c0001t0001g0021a0001c0001t0012g0089a0001c0001t0012g0090others(3): Show | 6 | HG01891.hp2 HG02165.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+29931T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207668 | ||||||
chr12:42207683
|
G | A | 2 | a0001c0001t0010g0118a0001c0002t0002g0085 | 2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.152+29916C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207683 | ||||||
chr12:42207684
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+29915G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207684 | ||||||
chr12:42207685
|
G | C | 4 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0189others(1): Show | 4 | HG00323.hp2 HG01106.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+29914C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207685 | ||||||
chr12:42207708
|
C | T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+29891G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207708 | ||||||
chr12:42207709
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.152+29890C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207709 | ||||||
chr12:42207720
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0030others(280): Show | 288 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.152+29879C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207720 | ||||||
chr12:42207754
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+29845G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207754 | ||||||
chr12:42207754
|
C | G | 5 | a0001c0001t0001g0116a0001c0001t0001g0125a0001c0002t0002g0344others(2): Show | 5 | HG03098.hp2 HG03453.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+29845G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207754 | ||||||
chr12:42207794
|
G | GGCAGGAG others(12): Show |
90 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0070others(87): Show | 92 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.152+29786_152+2980 others(23): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207794 | ||||||
chr12:42207846
|
G | A | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+29753C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207846 | ||||||
chr12:42207846
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152+29753C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207846 | ||||||
chr12:42207847
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152+29752A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207847 | ||||||
chr12:42207857
|
C | T | 1 | a0001c0002t0002g0350 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.152+29742G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207857 | ||||||
chr12:42207862
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152+29737C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207862 | ||||||
chr12:42207869
|
C | T | 1 | a0001c0001t0030g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+29730G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207869 | ||||||
chr12:42207870
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.152+29729C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42207870 | ||||||
chr12:42208111
|
A | T | 1 | a0001c0001t0003g0157 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.152+29488T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208111 | ||||||
chr12:42208154
|
G | A | 3 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088 | 3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+29445C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208154 | ||||||
chr12:42208210
|
T | C | 7 | a0001c0001t0006g0220a0001c0001t0006g0221a0001c0001t0006g0222others(4): Show | 7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+29389A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208210 | ||||||
chr12:42208267
|
T | A | 3 | a0001c0002t0002g0084a0001c0002t0002g0342a0001c0002t0002g0350 | 3 | NA18944.hp1 NA19000.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.152+29332A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208267 | ||||||
chr12:42208377
|
T | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+29222A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208377 | ||||||
chr12:42208511
|
A | T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+29088T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208511 | ||||||
chr12:42208581
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152+29018A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208581 | ||||||
chr12:42208679
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0173 | 2 | NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.152+28920T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208679 | ||||||
chr12:42208930
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+28669T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208930 | ||||||
chr12:42208931
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02148.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+28668C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42208931 | ||||||
chr12:42209126
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+28473T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209126 | ||||||
chr12:42209133
|
A | G | 1 | a0001c0002t0002g0300 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.152+28466T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209133 | ||||||
chr12:42209257
|
G | GA | 17 | a0001c0001t0001g0005a0001c0001t0001g0171a0001c0001t0001g0358others(14): Show | 18 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+28341dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209257 | ||||||
chr12:42209257
|
GA | G | 8 | a0001c0001t0001g0178a0001c0001t0001g0227a0001c0001t0002g0272others(5): Show | 8 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+28341delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209257 | ||||||
chr12:42209304
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+28295G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209304 | ||||||
chr12:42209421
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+28178T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209421 | ||||||
chr12:42209490
|
G | A | 6 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0018g0114others(3): Show | 6 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+28109C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209490 | ||||||
chr12:42209563
|
C | CA | 82 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0030others(79): Show | 82 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.152+28035dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209563 | ||||||
chr12:42209563
|
C | CAA | 7 | a0001c0001t0001g0010a0001c0001t0001g0182a0001c0001t0004g0097others(4): Show | 7 | HG01175.hp2 HG01952.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+28034_152+2803 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209563 | ||||||
chr12:42209563
|
CA | C | 35 | a0001c0001t0001g0031a0001c0001t0001g0129a0001c0001t0001g0190others(32): Show | 35 | HG00544.hp1 HG00597.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.152+28035delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209563 | ||||||
chr12:42209591
|
T | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+28008A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209591 | ||||||
chr12:42209684
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+27915T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209684 | ||||||
chr12:42209726
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+27873G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209726 | ||||||
chr12:42209762
|
T | C | 1 | a0001c0002t0002g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.152+27837A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209762 | ||||||
chr12:42209828
|
C | T | 2 | a0001c0001t0014g0111a0001c0001t0014g0112 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.152+27771G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209828 | ||||||
chr12:42209960
|
G | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132others(7): Show | 10 | HG00741.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+27639C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209960 | ||||||
chr12:42209979
|
G | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+27620C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42209979 | ||||||
chr12:42210236
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+27363A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210236 | ||||||
chr12:42210330
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+27269C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210330 | ||||||
chr12:42210385
|
T | A | 1 | a0001c0002t0005g0260 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.152+27214A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210385 | ||||||
chr12:42210537
|
C | T | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+27062G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210537 | ||||||
chr12:42210889
|
C | T | 2 | a0001c0003t0015g0368a0001c0003t0015g0369 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+26710G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210889 | ||||||
chr12:42210975
|
T | C | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+26624A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42210975 | ||||||
chr12:42211225
|
G | A | 1 | a0001c0002t0002g0320 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.152+26374C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211225 | ||||||
chr12:42211414
|
G | A | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+26185C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211414 | ||||||
chr12:42211427
|
C | CA | 83 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(80): Show | 84 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.152+26171dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | ||||||
chr12:42211427
|
C | CAA | 10 | a0001c0001t0001g0079a0001c0001t0001g0135a0001c0001t0001g0175others(7): Show | 10 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+26170_152+2617 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | ||||||
chr12:42211427
|
CA | C | 118 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0116others(115): Show | 121 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.152+26171delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | ||||||
chr12:42211427
|
CAA | C | 10 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0144others(7): Show | 10 | HG01891.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+26170_152+2617 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211427 | ||||||
chr12:42211469
|
G | A | 2 | a0001c0002t0002g0257a0001c0002t0002g0262 | 2 | HG01257.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.152+26130C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211469 | ||||||
chr12:42211495
|
T | C | 1 | a0001c0001t0031g0113 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.152+26104A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211495 | ||||||
chr12:42211511
|
T | C | 8 | a0001c0002t0002g0169a0001c0002t0002g0242a0001c0002t0002g0243others(5): Show | 8 | HG00621.hp1 HG02135.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+26088A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211511 | ||||||
chr12:42211521
|
G | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+26078C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211521 | ||||||
chr12:42211527
|
G | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+26072C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211527 | ||||||
chr12:42211597
|
T | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+26002A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211597 | ||||||
chr12:42211617
|
C | T | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+25982G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211617 | ||||||
chr12:42211742
|
C | CA | 17 | a0001c0001t0001g0054a0001c0001t0001g0172a0001c0001t0001g0203others(14): Show | 17 | HG00423.hp2 HG01891.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+25856dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211742 | ||||||
chr12:42211742
|
CA | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0073others(13): Show | 16 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.152+25856delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211742 | ||||||
chr12:42211776
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.152+25823G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211776 | ||||||
chr12:42211781
|
G | T | 2 | a0001c0001t0028g0087a0001c0001t0029g0091 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.152+25818C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211781 | ||||||
chr12:42211806
|
T | G | 1 | a0001c0001t0001g0046 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.152+25793A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211806 | ||||||
chr12:42211876
|
C | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+25723G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211876 | ||||||
chr12:42211878
|
G | A | 19 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(16): Show | 19 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.152+25721C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42211878 | ||||||
chr12:42212034
|
CA | C | 12 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0142others(9): Show | 12 | HG01169.hp2 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+25564delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212034 | ||||||
chr12:42212148
|
CAAAA | C | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+25447_152+2545 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212148 | ||||||
chr12:42212261
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.152+25338G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212261 | ||||||
chr12:42212280
|
T | C | 1 | a0001c0001t0018g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152+25319A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212280 | ||||||
chr12:42212333
|
C | T | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+25266G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212333 | ||||||
chr12:42212427
|
T | C | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+25172A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212427 | ||||||
chr12:42212564
|
A | T | 1 | a0001c0002t0002g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.152+25035T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212564 | ||||||
chr12:42212694
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG01243.hp1 HG01255.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.152+24905C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212694 | ||||||
chr12:42212738
|
TCTTA | T | 5 | a0001c0001t0004g0095a0001c0001t0004g0096a0001c0001t0004g0097others(2): Show | 5 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+24857_152+2486 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212738 | ||||||
chr12:42212894
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(294): Show | 302 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.152+24705G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212894 | ||||||
chr12:42212946
|
G | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+24653C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42212946 | ||||||
chr12:42213062
|
A | AG | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.152+24536dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213062 | ||||||
chr12:42213230
|
C | T | 1 | a0001c0002t0002g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152+24369G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213230 | ||||||
chr12:42213281
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+24318A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213281 | ||||||
chr12:42213784
|
T | C | 1 | a0001c0002t0002g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.152+23815A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213784 | ||||||
chr12:42213946
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+23653G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213946 | ||||||
chr12:42213985
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+23614C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42213985 | ||||||
chr12:42214199
|
T | C | 135 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(132): Show | 138 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.152+23400A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214199 | ||||||
chr12:42214236
|
T | G | 1 | a0001c0001t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.152+23363A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214236 | ||||||
chr12:42214482
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0208 | 2 | HG00323.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.152+23117C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214482 | ||||||
chr12:42214559
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0197a0001c0001t0001g0198others(1): Show | 4 | NA18952.hp1 NA18990.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+23040C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214559 | ||||||
chr12:42214604
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+22995G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214604 | ||||||
chr12:42214685
|
G | T | 1 | a0001c0001t0030g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+22914C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214685 | ||||||
chr12:42214687
|
A | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+22912T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214687 | ||||||
chr12:42214775
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+22824C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214775 | ||||||
chr12:42214824
|
C | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+22775G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214824 | ||||||
chr12:42214883
|
G | A | 1 | a0001c0002t0002g0314 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.152+22716C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214883 | ||||||
chr12:42214934
|
G | T | 15 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(12): Show | 15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+22665C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42214934 | ||||||
chr12:42215156
|
C | T | 1 | a0001c0001t0018g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152+22443G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215156 | ||||||
chr12:42215302
|
G | T | 2 | a0001c0001t0003g0141a0001c0001t0003g0142 | 2 | NA18946.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.152+22297C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215302 | ||||||
chr12:42215345
|
T | A | 1 | a0001c0001t0001g0031 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152+22254A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215345 | ||||||
chr12:42215346
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152+22253G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215346 | ||||||
chr12:42215367
|
G | T | 1 | a0001c0001t0004g0100 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.152+22232C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215367 | ||||||
chr12:42215405
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(274): Show | 282 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.152+22194G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215405 | ||||||
chr12:42215642
|
G | T | 7 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(4): Show | 7 | HG02129.hp1 HG02523.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+21957C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215642 | ||||||
chr12:42215742
|
C | T | 2 | a0001c0002t0002g0288a0001c0002t0002g0311 | 2 | NA18960.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.152+21857G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215742 | ||||||
chr12:42215775
|
C | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+21824G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215775 | ||||||
chr12:42215921
|
G | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+21678C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215921 | ||||||
chr12:42215927
|
A | AAAAT | 3 | a0001c0001t0001g0013a0001c0001t0003g0154a0001c0001t0009g0055 | 3 | HG00639.hp2 HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.152+21668_152+2167 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | ||||||
chr12:42215927
|
AAAAT | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(50): Show | 53 | HG00423.hp2 HG00738.hp1 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.152+21668_152+2167 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | ||||||
chr12:42215927
|
AAAATAAA others(1): Show |
A | 44 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0001g0359others(41): Show | 45 | HG00099.hp1 HG00423.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.152+21664_152+2167 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | ||||||
chr12:42215927
|
AAAATAAA others(5): Show |
A | 128 | a0001c0001t0001g0045a0001c0001t0001g0196a0001c0001t0002g0272others(125): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.152+21660_152+2167 others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | ||||||
chr12:42215927
|
AAAATAAA others(9): Show |
A | 79 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(76): Show | 80 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.152+21656_152+2167 others(20): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | ||||||
chr12:42215927
|
AAAATAAA others(13): Show |
A | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+21652_152+2167 others(24): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215927 | ||||||
chr12:42215982
|
A | G | 1 | a0001c0001t0004g0094 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.152+21617T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42215982 | ||||||
chr12:42216042
|
T | G | 38 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(35): Show | 38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.152+21557A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216042 | ||||||
chr12:42216091
|
G | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+21508C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216091 | ||||||
chr12:42216146
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.152+21453G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216146 | ||||||
chr12:42216212
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0173a0001c0001t0001g0174others(8): Show | 11 | HG00597.hp2 NA18948.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+21387A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216212 | ||||||
chr12:42216266
|
C | T | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+21333G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216266 | ||||||
chr12:42216594
|
T | A | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+21005A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216594 | ||||||
chr12:42216680
|
T | G | 1 | a0001c0001t0001g0218 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.152+20919A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216680 | ||||||
chr12:42216706
|
T | C | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+20893A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216706 | ||||||
chr12:42216815
|
C | T | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+20784G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216815 | ||||||
chr12:42216975
|
C | T | 2 | a0001c0001t0010g0118a0001c0001t0010g0119 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.152+20624G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216975 | ||||||
chr12:42216991
|
A | G | 1 | a0001c0001t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152+20608T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216991 | ||||||
chr12:42216992
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+20607A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42216992 | ||||||
chr12:42217111
|
A | G | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+20488T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217111 | ||||||
chr12:42217114
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.152+20485G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217114 | ||||||
chr12:42217132
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+20467C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217132 | ||||||
chr12:42217676
|
T | C | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+19923A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217676 | ||||||
chr12:42217697
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.152+19902A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217697 | ||||||
chr12:42217758
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+19841T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42217758 | ||||||
chr12:42218020
|
C | T | 4 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0008g0123others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+19579G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218020 | ||||||
chr12:42218029
|
T | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG01099.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152+19570A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218029 | ||||||
chr12:42218120
|
T | C | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+19479A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218120 | ||||||
chr12:42218170
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+19429T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218170 | ||||||
chr12:42218182
|
G | GGA | 8 | a0001c0002t0002g0344a0001c0002t0002g0345a0001c0002t0002g0349others(5): Show | 8 | HG00642.hp1 HG02486.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218182 | ||||||
chr12:42218183
|
G | GAGAA | 13 | a0001c0002t0002g0081a0001c0002t0002g0084a0001c0002t0002g0169others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218183 | ||||||
chr12:42218183
|
G | GAGAAAC | 28 | a0001c0002t0002g0233a0001c0002t0002g0242a0001c0002t0002g0243others(25): Show | 28 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218183 | ||||||
chr12:42218183
|
G | GAGAAACA others(1): Show |
8 | a0001c0002t0002g0086a0001c0002t0002g0237a0001c0002t0002g0251others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+19415_152+1941 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218183 | ||||||
chr12:42218185
|
A | AAC | 65 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(62): Show | 68 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.152+19412_152+1941 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
A | AACAC | 14 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0046others(11): Show | 14 | HG01515.hp2 HG01943.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.152+19410_152+1941 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
A | AACACAC | 36 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0021others(33): Show | 36 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.152+19408_152+1941 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
A | AACACACA others(1): Show |
26 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(23): Show | 26 | HG01175.hp2 HG01255.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.152+19406_152+1941 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
A | C | 49 | a0001c0002t0002g0081a0001c0002t0002g0084a0001c0002t0002g0086others(46): Show | 49 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.152+19414T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
A | G | 1 | a0001c0002t0025g0232 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152+19414T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AAC | A | 4 | a0001c0001t0003g0146a0001c0001t0008g0092a0001c0001t0010g0119others(1): Show | 4 | HG01192.hp1 HG02615.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+19412_152+1941 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AACAC | A | 31 | a0001c0001t0001g0177a0001c0001t0001g0196a0001c0001t0001g0197others(28): Show | 31 | HG00738.hp1 HG02083.hp1 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.152+19410_152+1941 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AACACAC | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.152+19408_152+1941 others(10): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AACACACA others(1): Show |
A | 41 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0074others(38): Show | 42 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.152+19406_152+1941 others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AACACACA others(3): Show |
A | 5 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0003t0001g0234others(2): Show | 5 | HG02451.hp1 HG02647.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+19404_152+1941 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AACACACA others(5): Show |
A | 2 | a0001c0003t0015g0368a0001c0003t0015g0369 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+19402_152+1941 others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0029g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152+19400_152+1941 others(18): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218185
|
AACACACA others(9): Show |
A | 2 | a0001c0001t0028g0087a0001c0001t0030g0088 | 2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+19398_152+1941 others(20): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218185 | ||||||
chr12:42218187
|
C | A | 1 | a0001c0002t0025g0232 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152+19412G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218187 | ||||||
chr12:42218375
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+19224C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218375 | ||||||
chr12:42218440
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152+19159A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218440 | ||||||
chr12:42218530
|
A | C | 13 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+19069T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218530 | ||||||
chr12:42218660
|
A | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+18939T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218660 | ||||||
chr12:42218691
|
A | G | 1 | a0001c0002t0002g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.152+18908T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218691 | ||||||
chr12:42218870
|
A | G | 7 | a0001c0001t0003g0139a0001c0001t0003g0147a0001c0001t0003g0148others(4): Show | 7 | HG00738.hp1 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+18729T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218870 | ||||||
chr12:42218901
|
G | C | 7 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0176others(4): Show | 7 | HG01099.hp2 HG01515.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+18698C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42218901 | ||||||
chr12:42219115
|
T | C | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+18484A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219115 | ||||||
chr12:42219122
|
T | C | 5 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0205others(2): Show | 5 | HG01099.hp2 HG01515.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+18477A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219122 | ||||||
chr12:42219138
|
A | T | 1 | a0001c0002t0002g0354 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.152+18461T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219138 | ||||||
chr12:42219142
|
G | A | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+18457C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219142 | ||||||
chr12:42219450
|
G | A | 1 | a0001c0001t0004g0107 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.152+18149C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219450 | ||||||
chr12:42219468
|
T | C | 1 | a0001c0001t0004g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.152+18131A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219468 | ||||||
chr12:42219488
|
T | G | 132 | a0001c0001t0001g0190a0001c0001t0001g0209a0001c0001t0001g0210others(129): Show | 135 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.152+18111A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219488 | ||||||
chr12:42219509
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+18090A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219509 | ||||||
chr12:42219510
|
T | C | 4 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+18089A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219510 | ||||||
chr12:42219564
|
T | C | 4 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+18035A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219564 | ||||||
chr12:42219667
|
G | A | 2 | a0001c0002t0002g0322a0001c0002t0002g0323 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.152+17932C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219667 | ||||||
chr12:42219712
|
C | A | 1 | a0001c0002t0002g0337 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.152+17887G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219712 | ||||||
chr12:42219754
|
C | A | 1 | a0001c0001t0011g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+17845G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42219754 | ||||||
chr12:42220074
|
G | A | 3 | a0001c0002t0002g0346a0001c0002t0002g0347a0001c0002t0002g0348 | 3 | HG02717.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.152+17525C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220074 | ||||||
chr12:42220324
|
ATTATC | A | 3 | a0001c0001t0001g0207a0001c0001t0013g0127a0001c0001t0013g0128 | 3 | HG01928.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+17270_152+1727 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220324 | ||||||
chr12:42220347
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.152+17252G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220347 | ||||||
chr12:42220421
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.152+17178T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220421 | ||||||
chr12:42220521
|
T | C | 1 | a0001c0001t0004g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.152+17078A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220521 | ||||||
chr12:42220653
|
A | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+16946T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220653 | ||||||
chr12:42220695
|
T | C | 13 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+16904A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220695 | ||||||
chr12:42220722
|
T | C | 4 | a0001c0001t0001g0358a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+16877A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220722 | ||||||
chr12:42220844
|
C | T | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+16755G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220844 | ||||||
chr12:42220904
|
A | G | 1 | a0001c0002t0002g0249 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.152+16695T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42220904 | ||||||
chr12:42221199
|
T | C | 1 | a0001c0001t0029g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152+16400A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42221199 | ||||||
chr12:42221473
|
A | AG | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.152+16125dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42221473 | ||||||
chr12:42221570
|
T | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(56): Show | 60 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.152+16029A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42221570 | ||||||
chr12:42222055
|
C | T | 4 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0008g0123others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+15544G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222055 | ||||||
chr12:42222120
|
A | T | 1 | a0001c0001t0034g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+15479T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222120 | ||||||
chr12:42222238
|
A | T | 129 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(126): Show | 132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.152+15361T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222238 | ||||||
chr12:42222520
|
G | T | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+15079C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222520 | ||||||
chr12:42222721
|
T | C | 1 | a0001c0001t0001g0366 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.152+14878A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222721 | ||||||
chr12:42222754
|
A | AT | 18 | a0001c0001t0001g0079a0001c0001t0001g0173a0001c0001t0001g0174others(15): Show | 18 | HG00597.hp2 HG00733.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.152+14844dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222754 | ||||||
chr12:42222893
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+14706A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222893 | ||||||
chr12:42222927
|
C | T | 1 | a0001c0002t0002g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.152+14672G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222927 | ||||||
chr12:42222937
|
C | CT | 81 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(78): Show | 82 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.152+14661dupA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42222937 | ||||||
chr12:42223100
|
G | A | 1 | a0001c0001t0027g0145 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.152+14499C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223100 | ||||||
chr12:42223186
|
T | G | 1 | a0001c0001t0001g0001 | 2 | HG00099.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.152+14413A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223186 | ||||||
chr12:42223249
|
T | C | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+14350A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223249 | ||||||
chr12:42223300
|
A | C | 4 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0008g0123others(1): Show | 4 | HG01169.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+14299T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223300 | ||||||
chr12:42223327
|
T | TACACACA others(3): Show |
1 | a0001c0001t0012g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.152+14271_152+1427 others(14): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223327 | ||||||
chr12:42223327
|
T | TACACACA others(5): Show |
2 | a0001c0001t0012g0090a0001c0001t0028g0087 | 2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.152+14271_152+1427 others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223327 | ||||||
chr12:42223331
|
T | C | 4 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(1): Show | 4 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+14268A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | ||||||
chr12:42223331
|
T | TAC | 142 | a0001c0001t0001g0049a0001c0001t0001g0138a0001c0001t0001g0182others(139): Show | 145 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.152+14266_152+1426 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | ||||||
chr12:42223331
|
TAC | T | 6 | a0001c0001t0001g0060a0001c0001t0004g0109a0001c0001t0018g0114others(3): Show | 6 | HG00140.hp2 HG02717.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+14266_152+1426 others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | ||||||
chr12:42223331
|
TACAC | T | 34 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(31): Show | 34 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.152+14264_152+1426 others(8): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223331 | ||||||
chr12:42223401
|
G | T | 1 | a0001c0001t0001g0217 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.152+14198C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223401 | ||||||
chr12:42223806
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.152+13793T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223806 | ||||||
chr12:42223807
|
T | G | 129 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(126): Show | 132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.152+13792A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223807 | ||||||
chr12:42223883
|
G | A | 1 | a0001c0001t0034g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+13716C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42223883 | ||||||
chr12:42224066
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0031others(2): Show | 5 | NA18747.hp1 NA18954.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+13533C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224066 | ||||||
chr12:42224099
|
C | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(272): Show | 280 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.152+13500G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224099 | ||||||
chr12:42224313
|
G | A | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+13286C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224313 | ||||||
chr12:42224372
|
CAATAT | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0361 | 4 | HG02559.hp2 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+13222_152+1322 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224372 | ||||||
chr12:42224512
|
T | C | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+13087A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224512 | ||||||
chr12:42224540
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0192 | 2 | NA18954.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.152+13059C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224540 | ||||||
chr12:42224548
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0031others(2): Show | 5 | NA18747.hp1 NA18954.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+13051G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224548 | ||||||
chr12:42224579
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.152+13020G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224579 | ||||||
chr12:42224628
|
T | G | 1 | a0001c0002t0002g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152+12971A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224628 | ||||||
chr12:42224643
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(3): Show | 6 | HG01106.hp1 HG01175.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+12956G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224643 | ||||||
chr12:42224728
|
A | G | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+12871T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224728 | ||||||
chr12:42224745
|
A | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+12854T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224745 | ||||||
chr12:42224915
|
T | C | 1 | a0001c0001t0004g0097 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.152+12684A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42224915 | ||||||
chr12:42225005
|
C | T | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+12594G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225005 | ||||||
chr12:42225214
|
TG | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+12384delC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225214 | ||||||
chr12:42225215
|
G | T | 1 | a0001c0001t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152+12384C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225215 | ||||||
chr12:42225439
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0212 | 2 | HG00597.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.152+12160C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225439 | ||||||
chr12:42225468
|
T | C | 1 | a0001c0002t0002g0348 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.152+12131A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225468 | ||||||
chr12:42225629
|
T | C | 3 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088 | 3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+11970A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225629 | ||||||
chr12:42225632
|
G | C | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+11967C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225632 | ||||||
chr12:42225671
|
G | A | 1 | a0001c0002t0005g0261 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.152+11928C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225671 | ||||||
chr12:42225693
|
C | A | 2 | a0001c0001t0001g0360a0001c0001t0001g0362 | 2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.152+11906G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225693 | ||||||
chr12:42225722
|
G | A | 60 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(57): Show | 63 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.152+11877C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225722 | ||||||
chr12:42225730
|
G | A | 1 | a0001c0002t0002g0325 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.152+11869C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225730 | ||||||
chr12:42225885
|
TTTAAA | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+11709_152+1171 others(9): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42225885 | ||||||
chr12:42226047
|
T | C | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+11552A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226047 | ||||||
chr12:42226126
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0361 | 4 | HG02559.hp2 NA18522.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+11473A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226126 | ||||||
chr12:42226173
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+11426G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226173 | ||||||
chr12:42226233
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(124): Show | 129 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.152+11366A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226233 | ||||||
chr12:42226287
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.152+11312C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226287 | ||||||
chr12:42226575
|
G | A | 139 | a0001c0001t0002g0272a0001c0001t0008g0092a0001c0001t0008g0093others(136): Show | 142 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.152+11024C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226575 | ||||||
chr12:42226603
|
G | T | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10996C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226603 | ||||||
chr12:42226686
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(273): Show | 281 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.152+10913C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226686 | ||||||
chr12:42226693
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10906G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226693 | ||||||
chr12:42226694
|
G | A | 6 | a0001c0001t0001g0171a0001c0001t0001g0178a0001c0001t0001g0193others(3): Show | 6 | HG02040.hp2 NA18941.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+10905C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226694 | ||||||
chr12:42226760
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.152+10839A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226760 | ||||||
chr12:42226776
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(299): Show | 307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+10823G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226776 | ||||||
chr12:42226840
|
C | T | 1 | a0001c0002t0002g0265 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.152+10759G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226840 | ||||||
chr12:42226861
|
C | T | 3 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+10738G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226861 | ||||||
chr12:42226862
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10737C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226862 | ||||||
chr12:42226884
|
G | A | 1 | a0001c0001t0004g0102 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.152+10715C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226884 | ||||||
chr12:42226889
|
G | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(92): Show | 97 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.152+10710C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226889 | ||||||
chr12:42226959
|
C | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+10640G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226959 | ||||||
chr12:42226997
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152+10602C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226997 | ||||||
chr12:42226997
|
G | C | 4 | a0001c0002t0002g0004a0001c0002t0002g0293a0001c0002t0002g0294others(1): Show | 5 | HG02015.hp2 NA18941.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10602C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226997 | ||||||
chr12:42226997
|
G | T | 130 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(127): Show | 132 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.152+10602C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42226997 | ||||||
chr12:42227006
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+10593C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227006 | ||||||
chr12:42227036
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0360others(3): Show | 7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+10563C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227036 | ||||||
chr12:42227041
|
C | T | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+10558G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227041 | ||||||
chr12:42227047
|
C | T | 4 | a0001c0002t0002g0085a0001c0002t0002g0346a0001c0002t0002g0347others(1): Show | 4 | HG02055.hp1 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+10552G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227047 | ||||||
chr12:42227049
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0116a0001c0001t0001g0125 | 3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152+10550G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227049 | ||||||
chr12:42227050
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+10549C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227050 | ||||||
chr12:42227053
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+10546G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227053 | ||||||
chr12:42227054
|
G | A | 1 | a0001c0002t0002g0308 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.152+10545C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227054 | ||||||
chr12:42227064
|
G | A | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+10535C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227064 | ||||||
chr12:42227074
|
G | A | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+10525C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227074 | ||||||
chr12:42227078
|
G | GCAGCCGC others(13): Show |
5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10520_152+1052 others(24): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227078 | ||||||
chr12:42227099
|
G | A | 1 | a0001c0002t0002g0081 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.152+10500C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227099 | ||||||
chr12:42227113
|
T | G | 1 | a0001c0001t0010g0118 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152+10486A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227113 | ||||||
chr12:42227129
|
C | T | 1 | a0001c0002t0002g0299 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.152+10470G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227129 | ||||||
chr12:42227130
|
G | A | 6 | a0001c0002t0002g0083a0001c0002t0002g0296a0001c0002t0002g0297others(3): Show | 6 | HG00140.hp1 HG01346.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+10469C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227130 | ||||||
chr12:42227144
|
C | A | 1 | a0001c0002t0002g0299 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.152+10455G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227144 | ||||||
chr12:42227148
|
C | A | 1 | a0001c0001t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152+10451G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227148 | ||||||
chr12:42227149
|
G | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+10450C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227149 | ||||||
chr12:42227175
|
G | A | 1 | a0001c0002t0002g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152+10424C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227175 | ||||||
chr12:42227187
|
GC | G | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+10411delG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227187 | ||||||
chr12:42227190
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.152+10409G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227190 | ||||||
chr12:42227191
|
G | A | 18 | a0001c0001t0001g0079a0001c0001t0001g0173a0001c0001t0001g0174others(15): Show | 18 | HG00597.hp2 HG00733.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.152+10408C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227191 | ||||||
chr12:42227226
|
A | G | 3 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088 | 3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+10373T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227226 | ||||||
chr12:42227252
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10347C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227252 | ||||||
chr12:42227296
|
G | A | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.152+10303C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227296 | ||||||
chr12:42227308
|
C | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+10291G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227308 | ||||||
chr12:42227311
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(299): Show | 307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+10288G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227311 | ||||||
chr12:42227325
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+10274G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227325 | ||||||
chr12:42227353
|
G | C | 6 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0018g0114others(3): Show | 6 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+10246C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227353 | ||||||
chr12:42227359
|
T | A | 1 | a0001c0001t0004g0099 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.152+10240A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227359 | ||||||
chr12:42227368
|
G | A | 2 | a0001c0002t0002g0347a0001c0002t0002g0348 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.152+10231C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227368 | ||||||
chr12:42227411
|
C | T | 1 | a0001c0002t0002g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152+10188G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227411 | ||||||
chr12:42227451
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10148G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227451 | ||||||
chr12:42227490
|
C | T | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+10109G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227490 | ||||||
chr12:42227528
|
G | A | 6 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+10071C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227528 | ||||||
chr12:42227564
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0116a0001c0001t0001g0125 | 3 | HG02630.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152+10035C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227564 | ||||||
chr12:42227572
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+10027A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227572 | ||||||
chr12:42227615
|
C | T | 1 | a0001c0001t0027g0145 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.152+9984G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227615 | ||||||
chr12:42227652
|
C | T | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+9947G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227652 | ||||||
chr12:42227677
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.152+9922C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227677 | ||||||
chr12:42227680
|
C | T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9919G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227680 | ||||||
chr12:42227681
|
G | A | 1 | a0001c0001t0010g0119 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.152+9918C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227681 | ||||||
chr12:42227686
|
C | G | 1 | a0001c0002t0002g0300 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.152+9913G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227686 | ||||||
chr12:42227706
|
G | A | 2 | a0001c0001t0011g0117a0001c0001t0011g0126 | 2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.152+9893C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227706 | ||||||
chr12:42227716
|
C | A | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.152+9883G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227716 | ||||||
chr12:42227732
|
CGTCCGGG others(41): Show |
C | 13 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+9819_152+9866d others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227732 | ||||||
chr12:42227733
|
G | GTCCGGGA others(44): Show |
2 | a0001c0001t0028g0087a0001c0001t0029g0091 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.152+9865_152+9866i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227733 | ||||||
chr12:42227733
|
G | GTCCGGGA others(43): Show |
3 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0030g0088 | 3 | HG01891.hp2 HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+9865_152+9866i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227733 | ||||||
chr12:42227736
|
C | T | 1 | a0001c0002t0002g0353 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.152+9863G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227736 | ||||||
chr12:42227737
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+9862C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227737 | ||||||
chr12:42227764
|
C | T | 3 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+9835G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227764 | ||||||
chr12:42227780
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+9819A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227780 | ||||||
chr12:42227803
|
T | C | 9 | a0001c0002t0005g0326a0001c0002t0005g0327a0001c0002t0005g0328others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+9796A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227803 | ||||||
chr12:42227808
|
C | T | 1 | a0001c0002t0002g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.152+9791G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227808 | ||||||
chr12:42227830
|
G | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.152+9769C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227830 | ||||||
chr12:42227834
|
G | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9765C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227834 | ||||||
chr12:42227862
|
G | A | 12 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(9): Show | 12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+9737C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227862 | ||||||
chr12:42227866
|
C | CGCCAGCC others(447): Show |
1 | a0001c0001t0001g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.152+9279_152+9732d others(456): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227866 | ||||||
chr12:42227867
|
G | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+9732C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227867 | ||||||
chr12:42227869
|
C | G | 1 | a0001c0001t0013g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+9730G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227869 | ||||||
chr12:42227880
|
T | C | 1 | a0001c0002t0002g0262 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.152+9719A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227880 | ||||||
chr12:42227882
|
C | T | 1 | a0001c0001t0026g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.152+9717G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227882 | ||||||
chr12:42227883
|
G | A | 5 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9716C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227883 | ||||||
chr12:42227896
|
CGCCTCTG others(629): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.152+9067_152+9702d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227896 | ||||||
chr12:42227897
|
G | A | 39 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(36): Show | 39 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.152+9702C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227897 | ||||||
chr12:42227911
|
G | A | 17 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0154others(14): Show | 17 | HG00544.hp1 HG00597.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.152+9688C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227911 | ||||||
chr12:42227944
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+9655T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227944 | ||||||
chr12:42227964
|
A | C | 4 | a0001c0001t0003g0140a0001c0001t0003g0141a0001c0001t0003g0142others(1): Show | 4 | NA18946.hp2 NA18957.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9635T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227964 | ||||||
chr12:42227977
|
G | A | 1 | a0001c0001t0004g0108 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.152+9622C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227977 | ||||||
chr12:42227988
|
C | T | 15 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(12): Show | 15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+9611G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42227988 | ||||||
chr12:42228007
|
T | C | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9592A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228007 | ||||||
chr12:42228010
|
A | G | 7 | a0001c0001t0008g0093a0001c0001t0008g0122a0001c0001t0012g0089others(4): Show | 7 | HG01169.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+9589T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228010 | ||||||
chr12:42228020
|
T | TG | 10 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0359others(7): Show | 11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.152+9578dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228020 | ||||||
chr12:42228020
|
TGGGGGGT others(449): Show |
T | 2 | a0001c0001t0008g0093a0001c0001t0008g0122 | 2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.152+9123_152+9578d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228020 | ||||||
chr12:42228020
|
TGGGGGGT others(453): Show |
T | 57 | a0001c0002t0002g0084a0001c0002t0002g0086a0001c0002t0002g0169others(54): Show | 57 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.152+9119_152+9578d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228020 | ||||||
chr12:42228126
|
C | T | 1 | a0001c0001t0004g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.152+9473G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228126 | ||||||
chr12:42228132
|
G | A | 4 | a0001c0001t0011g0126a0001c0001t0028g0087a0001c0001t0029g0091others(1): Show | 4 | HG02280.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9467C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228132 | ||||||
chr12:42228135
|
C | T | 80 | a0001c0001t0002g0272a0001c0001t0008g0092a0001c0001t0008g0123others(77): Show | 83 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.152+9464G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228135 | ||||||
chr12:42228144
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.152+9455C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228144 | ||||||
chr12:42228146
|
TG | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(212): Show | 220 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.152+9452delC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228146 | ||||||
chr12:42228153
|
G | T | 21 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(18): Show | 21 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.152+9446C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228153 | ||||||
chr12:42228154
|
G | T | 19 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(16): Show | 19 | HG00597.hp2 HG00733.hp1 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+9445C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228154 | ||||||
chr12:42228158
|
G | GC | 9 | a0001c0001t0001g0026a0001c0001t0001g0072a0001c0001t0001g0211others(6): Show | 9 | HG00597.hp2 HG01192.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+9440dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228158 | ||||||
chr12:42228169
|
G | GC | 4 | a0001c0002t0002g0302a0001c0002t0002g0303a0001c0002t0002g0304others(1): Show | 4 | HG01993.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9429_152+9430i others(3): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228169 | ||||||
chr12:42228182
|
G | A | 10 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0177others(7): Show | 10 | HG00597.hp2 NA18948.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+9417C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228182 | ||||||
chr12:42228186
|
G | A | 12 | a0001c0001t0004g0094a0001c0001t0004g0100a0001c0001t0004g0101others(9): Show | 12 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.152+9413C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228186 | ||||||
chr12:42228186
|
G | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(208): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.152+9413C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228186 | ||||||
chr12:42228196
|
T | TG | 24 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0001g0136others(21): Show | 24 | HG00544.hp1 HG00597.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.152+9402dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228196 | ||||||
chr12:42228202
|
G | T | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9397C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228202 | ||||||
chr12:42228207
|
G | GC | 12 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0217others(9): Show | 12 | HG00597.hp1 HG02109.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+9391dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228207 | ||||||
chr12:42228214
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0051others(1): Show | 4 | HG01175.hp2 HG01346.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9385C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228214 | ||||||
chr12:42228218
|
G | A | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+9381C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228218 | ||||||
chr12:42228231
|
G | A | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9368C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228231 | ||||||
chr12:42228235
|
T | G | 6 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0002t0002g0302others(3): Show | 6 | HG01891.hp2 HG01993.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+9364A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228235 | ||||||
chr12:42228246
|
GGGGGTGT others(42): Show |
G | 4 | a0001c0002t0002g0302a0001c0002t0002g0303a0001c0002t0002g0304others(1): Show | 4 | HG01993.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9304_152+9352d others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228246 | ||||||
chr12:42228251
|
T | G | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+9348A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228251 | ||||||
chr12:42228256
|
G | GC | 11 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0203others(8): Show | 11 | HG00597.hp1 HG00597.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+9342dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228256 | ||||||
chr12:42228264
|
C | A | 4 | a0001c0001t0001g0358a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9335G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228264 | ||||||
chr12:42228267
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0359a0001c0001t0001g0360others(3): Show | 7 | HG02055.hp2 HG02559.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+9332C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228267 | ||||||
chr12:42228268
|
C | CGCCAGCC others(42): Show |
1 | a0001c0001t0028g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.152+9330_152+9331i others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228268 | ||||||
chr12:42228268
|
C | CGCCAGCC others(42): Show |
3 | a0001c0001t0001g0177a0001c0001t0009g0120a0001c0001t0009g0121 | 3 | HG03486.hp2 NA18952.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.152+9330_152+9331i others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228268 | ||||||
chr12:42228268
|
CGCCAGCC others(123): Show |
C | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9201_152+9330d others(2): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228268 | ||||||
chr12:42228281
|
G | A | 2 | a0001c0001t0029g0091a0001c0001t0030g0088 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+9318C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228281 | ||||||
chr12:42228295
|
T | TGGGGGGG others(45): Show |
1 | a0001c0002t0002g0319 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(46): Show |
2 | a0001c0002t0002g0317a0001c0002t0002g0325 | 2 | HG03209.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.152+9303_152+9304i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(44): Show |
57 | a0001c0001t0001g0204a0001c0001t0002g0272a0001c0002t0002g0003others(54): Show | 59 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(45): Show |
14 | a0001c0001t0003g0146a0001c0002t0002g0002a0001c0002t0002g0083others(11): Show | 15 | HG01192.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(46): Show |
3 | a0001c0001t0003g0165a0001c0001t0003g0168a0001c0002t0002g0309 | 3 | HG00408.hp1 HG03831.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.152+9303_152+9304i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(47): Show |
1 | a0001c0001t0004g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.152+9303_152+9304i others(56): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(45): Show |
1 | a0001c0001t0003g0159 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(43): Show |
84 | a0001c0001t0001g0001a0001c0001t0001g0073a0001c0001t0001g0077others(81): Show | 85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(44): Show |
36 | a0001c0001t0001g0005a0001c0001t0001g0078a0001c0001t0001g0175others(33): Show | 37 | HG00738.hp1 HG01099.hp2 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(45): Show |
16 | a0001c0001t0001g0212a0001c0001t0001g0360a0001c0001t0001g0362others(13): Show | 16 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.152+9303_152+9304i others(54): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228295
|
T | TGGGGGGG others(46): Show |
3 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0034g0153 | 3 | HG02922.hp1 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.152+9303_152+9304i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228295 | ||||||
chr12:42228296
|
G | GGGGGGGT others(43): Show |
2 | a0001c0001t0029g0091a0001c0001t0030g0088 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+9302_152+9303i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228296 | ||||||
chr12:42228309
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG01099.hp2 HG01515.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152+9290G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228309 | ||||||
chr12:42228320
|
G | A | 1 | a0001c0001t0003g0144 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.152+9279C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228320 | ||||||
chr12:42228328
|
A | G | 4 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088others(1): Show | 4 | HG02280.hp2 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+9271T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228328 | ||||||
chr12:42228333
|
A | G | 6 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+9266T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228333 | ||||||
chr12:42228360
|
C | T | 18 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0096others(15): Show | 18 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.152+9239G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228360 | ||||||
chr12:42228385
|
A | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(84): Show | 89 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.152+9214T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228385 | ||||||
chr12:42228389
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+9210A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228389 | ||||||
chr12:42228393
|
T | TGCCCGGC others(43): Show |
1 | a0001c0001t0006g0226 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.152+9205_152+9206i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228393 | ||||||
chr12:42228393
|
T | TGCCCGGC others(42): Show |
19 | a0001c0001t0001g0078a0001c0001t0001g0130a0001c0001t0001g0170others(16): Show | 19 | HG00597.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.152+9157_152+9205d others(51): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228393 | ||||||
chr12:42228426
|
G | GGGGGGGT others(41): Show |
4 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(1): Show | 4 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+9172_152+9173i others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228426 | ||||||
chr12:42228435
|
A | G | 6 | a0001c0001t0030g0088a0001c0003t0001g0234a0001c0003t0001g0235others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+9164T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228435 | ||||||
chr12:42228441
|
C | T | 1 | a0001c0004t0017g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.152+9158G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228441 | ||||||
chr12:42228446
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(212): Show | 220 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.152+9153A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228446 | ||||||
chr12:42228474
|
T | TG | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0022others(18): Show | 21 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.152+9124dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | ||||||
chr12:42228474
|
T | TGGGGGGG others(44): Show |
2 | a0001c0001t0004g0104a0001c0001t0004g0105 | 2 | HG01081.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.152+9124_152+9125i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | ||||||
chr12:42228474
|
T | TGGGGGGG others(43): Show |
7 | a0001c0001t0001g0213a0001c0001t0004g0095a0001c0001t0004g0100others(4): Show | 7 | HG00423.hp1 HG00642.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+9124_152+9125i others(52): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | ||||||
chr12:42228474
|
T | TGGGGGGG others(44): Show |
7 | a0001c0001t0004g0094a0001c0001t0004g0096a0001c0001t0004g0097others(4): Show | 7 | HG02071.hp2 HG03704.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.152+9124_152+9125i others(53): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | ||||||
chr12:42228474
|
T | TGGGGGGG others(46): Show |
1 | a0001c0001t0004g0099 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.152+9124_152+9125i others(55): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228474 | ||||||
chr12:42228475
|
G | GGGGGGGT others(41): Show |
73 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0129others(70): Show | 74 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.152+9123_152+9124i others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228475 | ||||||
chr12:42228475
|
G | GGGGGGGT others(40): Show |
1 | a0001c0001t0001g0175 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.152+9123_152+9124i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228475 | ||||||
chr12:42228476
|
G | GGGGGGGT others(41): Show |
1 | a0001c0001t0003g0160 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.152+9122_152+9123i others(50): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | ||||||
chr12:42228476
|
G | GGGGGGTC others(40): Show |
1 | a0001c0001t0008g0124 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.152+9122_152+9123i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | ||||||
chr12:42228476
|
G | GGGGGGTC others(40): Show |
28 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0171others(25): Show | 29 | HG01192.hp1 HG01975.hp2 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.152+9122_152+9123i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | ||||||
chr12:42228476
|
G | GGGGGTCA others(39): Show |
1 | a0001c0001t0030g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+9122_152+9123i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228476 | ||||||
chr12:42228477
|
G | GGGGGGTC others(40): Show |
2 | a0001c0001t0027g0145a0001c0002t0002g0318 | 2 | HG02738.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.152+9121_152+9122i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228477 | ||||||
chr12:42228477
|
G | GGGGGTCA others(39): Show |
1 | a0001c0001t0008g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.152+9121_152+9122i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228477 | ||||||
chr12:42228477
|
G | GGGGGTCA others(39): Show |
80 | a0001c0001t0002g0272a0001c0001t0003g0139a0001c0001t0003g0140others(77): Show | 83 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.152+9121_152+9122i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228477 | ||||||
chr12:42228479
|
G | GGGTCAGC others(40): Show |
2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+9119_152+9120i others(49): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228479 | ||||||
chr12:42228479
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.152+9120C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228479 | ||||||
chr12:42228480
|
G | GGTCAGCC others(39): Show |
2 | a0001c0002t0002g0313a0001c0002t0002g0320 | 2 | HG00609.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.152+9118_152+9119i others(48): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228480 | ||||||
chr12:42228497
|
C | T | 6 | a0001c0001t0034g0153a0001c0003t0001g0234a0001c0003t0001g0235others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.152+9102G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228497 | ||||||
chr12:42228501
|
T | C | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9098A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228501 | ||||||
chr12:42228510
|
G | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9089C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228510 | ||||||
chr12:42228515
|
G | A | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9084C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228515 | ||||||
chr12:42228519
|
G | A | 1 | a0001c0003t0015g0369 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.152+9080C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228519 | ||||||
chr12:42228531
|
G | A | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+9068C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228531 | ||||||
chr12:42228532
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(278): Show | 286 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.152+9067A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228532 | ||||||
chr12:42228543
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.152+9056C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228543 | ||||||
chr12:42228571
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+9028G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228571 | ||||||
chr12:42228580
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.152+9019C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228580 | ||||||
chr12:42228596
|
A | C | 10 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(7): Show | 10 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.152+9003T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228596 | ||||||
chr12:42228612
|
G | T | 1 | a0001c0002t0002g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.152+8987C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228612 | ||||||
chr12:42228613
|
T | G | 8 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088others(5): Show | 8 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+8986A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228613 | ||||||
chr12:42228623
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.152+8976G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228623 | ||||||
chr12:42228628
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8971G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228628 | ||||||
chr12:42228636
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8963G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228636 | ||||||
chr12:42228645
|
C | T | 10 | a0001c0002t0002g0086a0001c0002t0002g0169a0001c0002t0002g0242others(7): Show | 10 | HG00621.hp1 HG02135.hp2 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+8954G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228645 | ||||||
chr12:42228656
|
T | TG | 83 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0025others(80): Show | 85 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.152+8942dupC | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228656 | ||||||
chr12:42228656
|
T | TGG | 19 | a0001c0001t0001g0005a0001c0001t0001g0361a0001c0001t0001g0362others(16): Show | 20 | HG00609.hp2 HG02132.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.152+8941_152+8942d others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228656 | ||||||
chr12:42228671
|
C | A | 4 | a0001c0001t0010g0118a0001c0001t0010g0119a0001c0001t0011g0117others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+8928G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228671 | ||||||
chr12:42228689
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.152+8910G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228689 | ||||||
chr12:42228695
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | NA18962.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.152+8904C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228695 | ||||||
chr12:42228705
|
T | G | 1 | a0001c0001t0003g0075 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.152+8894A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228705 | ||||||
chr12:42228710
|
G | A | 7 | a0001c0001t0006g0220a0001c0001t0006g0221a0001c0001t0006g0222others(4): Show | 7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+8889C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228710 | ||||||
chr12:42228727
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152+8872C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228727 | ||||||
chr12:42228772
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8827G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228772 | ||||||
chr12:42228805
|
G | T | 4 | a0001c0001t0003g0076a0001c0001t0003g0154a0001c0001t0003g0155others(1): Show | 4 | HG01975.hp2 HG01978.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+8794C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228805 | ||||||
chr12:42228809
|
G | A | 1 | a0001c0001t0011g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+8790C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228809 | ||||||
chr12:42228816
|
C | T | 1 | a0001c0001t0006g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.152+8783G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228816 | ||||||
chr12:42228834
|
A | G | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+8765T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228834 | ||||||
chr12:42228840
|
G | A | 9 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0003g0167others(6): Show | 9 | HG00544.hp1 HG00597.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+8759C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228840 | ||||||
chr12:42228849
|
C | T | 1 | a0001c0002t0002g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.152+8750G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228849 | ||||||
chr12:42228850
|
G | A | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+8749C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228850 | ||||||
chr12:42228854
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(299): Show | 307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+8745T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228854 | ||||||
chr12:42228891
|
A | AGCCGCCC others(117): Show |
1 | a0001c0001t0010g0118 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.152+8707_152+8708i others(126): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228891 | ||||||
chr12:42228901
|
C | T | 1 | a0001c0002t0002g0337 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.152+8698G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42228901 | ||||||
chr12:42229013
|
G | A | 3 | a0001c0001t0028g0087a0001c0001t0029g0091a0001c0001t0030g0088 | 3 | HG02280.hp2 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+8586C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229013 | ||||||
chr12:42229015
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.152+8584C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229015 | ||||||
chr12:42229032
|
T | C | 1 | a0001c0001t0030g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+8567A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229032 | ||||||
chr12:42229034
|
G | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(84): Show | 89 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.152+8565C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229034 | ||||||
chr12:42229038
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+8561A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229038 | ||||||
chr12:42229204
|
T | C | 134 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(131): Show | 137 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.152+8395A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229204 | ||||||
chr12:42229221
|
G | C | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+8378C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229221 | ||||||
chr12:42229227
|
A | C | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+8372T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229227 | ||||||
chr12:42229243
|
T | C | 38 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(35): Show | 38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.152+8356A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229243 | ||||||
chr12:42229275
|
G | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+8324C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229275 | ||||||
chr12:42229415
|
AT | A | 8 | a0001c0002t0002g0237a0001c0002t0002g0240a0001c0002t0002g0321others(5): Show | 8 | HG00544.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+8183delA | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229415 | ||||||
chr12:42229416
|
T | A | 127 | a0001c0001t0001g0027a0001c0001t0002g0272a0001c0002t0002g0002others(124): Show | 130 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.152+8183A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229416 | ||||||
chr12:42229419
|
A | T | 126 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(123): Show | 129 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.152+8180T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229419 | ||||||
chr12:42229421
|
T | A | 126 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(123): Show | 129 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.152+8178A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | ||||||
chr12:42229421
|
T | TA | 91 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(88): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.152+8177dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | ||||||
chr12:42229421
|
T | TAA | 11 | a0001c0001t0001g0219a0001c0001t0004g0099a0001c0001t0012g0089others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+8176_152+8177d others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | ||||||
chr12:42229421
|
TA | T | 34 | a0001c0001t0003g0076a0001c0001t0003g0139a0001c0001t0003g0140others(31): Show | 34 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.152+8177delT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229421 | ||||||
chr12:42229549
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+8050T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229549 | ||||||
chr12:42229975
|
A | G | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+7624T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42229975 | ||||||
chr12:42230054
|
G | A | 1 | a0001c0002t0002g0324 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.152+7545C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230054 | ||||||
chr12:42230057
|
G | C | 38 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(35): Show | 38 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.152+7542C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230057 | ||||||
chr12:42230084
|
C | T | 1 | a0001c0001t0011g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+7515G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230084 | ||||||
chr12:42230188
|
C | T | 1 | a0001c0001t0008g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.152+7411G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230188 | ||||||
chr12:42230212
|
G | A | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+7387C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230212 | ||||||
chr12:42230235
|
G | A | 7 | a0001c0001t0006g0220a0001c0001t0006g0221a0001c0001t0006g0222others(4): Show | 7 | HG03017.hp2 HG03239.hp1 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.152+7364C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230235 | ||||||
chr12:42230261
|
AAAAG | A | 4 | a0001c0001t0001g0358a0001c0001t0001g0364a0001c0001t0001g0365others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+7334_152+7337d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230261 | ||||||
chr12:42230262
|
AAAGAAAG others(2): Show |
A | 10 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0006g0220others(7): Show | 10 | HG02155.hp2 HG03017.hp2 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+7328_152+7336d others(11): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230262 | ||||||
chr12:42230266
|
A | AAAGAGAA others(7): Show |
5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+7319_152+7332d others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230266 | ||||||
chr12:42230289
|
G | GAAGA | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+7306_152+7309d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230289 | ||||||
chr12:42230315
|
A | G | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+7284T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230315 | ||||||
chr12:42230391
|
G | A | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+7208C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230391 | ||||||
chr12:42230428
|
A | G | 1 | a0001c0002t0002g0238 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.152+7171T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230428 | ||||||
chr12:42230541
|
C | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(291): Show | 299 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.152+7058G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230541 | ||||||
chr12:42230544
|
G | A | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152+7055C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230544 | ||||||
chr12:42230737
|
G | A | 1 | a0001c0001t0033g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.152+6862C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230737 | ||||||
chr12:42230779
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+6820T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230779 | ||||||
chr12:42230883
|
G | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+6716C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230883 | ||||||
chr12:42230986
|
T | TA | 9 | a0001c0002t0005g0326a0001c0002t0005g0327a0001c0002t0005g0328others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+6612dupT | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42230986 | ||||||
chr12:42231255
|
A | C | 1 | a0001c0002t0002g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152+6344T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231255 | ||||||
chr12:42231278
|
G | A | 4 | a0001c0001t0018g0114a0001c0001t0019g0115a0001c0001t0031g0113others(1): Show | 4 | HG02717.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+6321C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231278 | ||||||
chr12:42231477
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.152+6122C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231477 | ||||||
chr12:42231499
|
T | A | 5 | a0001c0001t0008g0092a0001c0001t0008g0093a0001c0001t0008g0122others(2): Show | 5 | HG01169.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+6100A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231499 | ||||||
chr12:42231674
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+5925G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231674 | ||||||
chr12:42231726
|
C | A | 1 | a0001c0001t0003g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.152+5873G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231726 | ||||||
chr12:42231889
|
T | C | 2 | a0001c0001t0012g0089a0001c0001t0012g0090 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+5710A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42231889 | ||||||
chr12:42232328
|
T | C | 3 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236 | 3 | HG02451.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.152+5271A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232328 | ||||||
chr12:42232412
|
C | T | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+5187G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232412 | ||||||
chr12:42232672
|
C | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.152+4927G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232672 | ||||||
chr12:42232771
|
TAAGC | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0235a0001c0003t0001g0236others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+4824_152+4827d others(6): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232771 | ||||||
chr12:42232990
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0125 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.152+4609C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42232990 | ||||||
chr12:42233027
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.152+4572A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233027 | ||||||
chr12:42233050
|
G | A | 1 | a0001c0001t0034g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+4549C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233050 | ||||||
chr12:42233176
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.152+4423G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233176 | ||||||
chr12:42233202
|
T | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+4397A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233202 | ||||||
chr12:42233317
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152+4282T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233317 | ||||||
chr12:42233356
|
C | G | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.152+4243G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233356 | ||||||
chr12:42233484
|
T | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(73): Show | 77 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.152+4115A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233484 | ||||||
chr12:42233613
|
G | C | 1 | a0001c0001t0013g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.152+3986C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233613 | ||||||
chr12:42233712
|
T | C | 2 | a0001c0002t0002g0334a0001c0002t0002g0335 | 2 | HG02132.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.152+3887A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233712 | ||||||
chr12:42233988
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+3611A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42233988 | ||||||
chr12:42234188
|
AAAAGAGA others(4): Show |
A | 3 | a0001c0001t0008g0093a0001c0001t0012g0089a0001c0001t0012g0090 | 3 | HG01169.hp2 HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.152+3400_152+3410d others(13): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234188 | ||||||
chr12:42234189
|
AAAGAGAA others(3): Show |
A | 2 | a0001c0001t0029g0091a0001c0001t0030g0088 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.152+3400_152+3409d others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234189 | ||||||
chr12:42234190
|
AAGAGAAA others(7): Show |
A | 25 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(22): Show | 25 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.152+3395_152+3408d others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234190 | ||||||
chr12:42234192
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01192.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.152+3407C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | ||||||
chr12:42234192
|
G | GAGAAA | 19 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0116others(16): Show | 19 | HG00738.hp1 HG02109.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.152+3402_152+3406d others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | ||||||
chr12:42234192
|
G | GAGAAAAG others(3): Show |
2 | a0001c0001t0003g0152a0001c0001t0011g0126 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.152+3397_152+3406d others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | ||||||
chr12:42234192
|
GAGAAA | G | 46 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.152+3402_152+3406d others(7): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | ||||||
chr12:42234192
|
GAGAAAAG others(3): Show |
G | 11 | a0001c0001t0001g0011a0001c0001t0001g0228a0001c0001t0001g0229others(8): Show | 11 | HG03704.hp1 HG03831.hp2 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.152+3397_152+3406d others(12): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | ||||||
chr12:42234192
|
GAGAAAAG others(8): Show |
G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(195): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.152+3392_152+3406d others(17): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234192 | ||||||
chr12:42234202
|
A | G | 1 | a0001c0001t0008g0093 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.152+3397T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234202 | ||||||
chr12:42234204
|
G | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+3395C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234204 | ||||||
chr12:42234207
|
A | G | 25 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(22): Show | 25 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.152+3392T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234207 | ||||||
chr12:42234434
|
A | C | 1 | a0001c0001t0003g0075 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.152+3165T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234434 | ||||||
chr12:42234478
|
C | A | 1 | a0001c0001t0034g0153 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.152+3121G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234478 | ||||||
chr12:42234711
|
C | T | 1 | a0001c0001t0030g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152+2888G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234711 | ||||||
chr12:42234805
|
T | A | 2 | a0001c0001t0013g0127a0001c0001t0013g0128 | 2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.152+2794A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234805 | ||||||
chr12:42234921
|
G | A | 2 | a0001c0003t0015g0368a0001c0003t0015g0369 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+2678C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234921 | ||||||
chr12:42234935
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.152+2664G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42234935 | ||||||
chr12:42235387
|
T | TATTAATA others(7): Show |
1 | a0001c0002t0002g0350 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.152+2198_152+2211d others(16): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235387 | ||||||
chr12:42235489
|
T | C | 1 | a0001c0002t0002g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.152+2110A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235489 | ||||||
chr12:42235536
|
T | C | 6 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(3): Show | 6 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+2063A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235536 | ||||||
chr12:42235560
|
G | GAC | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+2038_152+2039i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235560 | ||||||
chr12:42235566
|
A | C | 1 | a0001c0002t0002g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.152+2033T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235566 | ||||||
chr12:42235748
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(299): Show | 307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.152+1851A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235748 | ||||||
chr12:42235757
|
T | C | 2 | a0001c0002t0002g0086a0001c0002t0002g0352 | 2 | HG04184.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.152+1842A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235757 | ||||||
chr12:42235783
|
C | T | 1 | a0001c0001t0008g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.152+1816G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235783 | ||||||
chr12:42235799
|
A | T | 15 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(12): Show | 15 | HG00738.hp1 HG01192.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.152+1800T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235799 | ||||||
chr12:42235871
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.152+1728T>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42235871 | ||||||
chr12:42236238
|
C | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1361G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236238 | ||||||
chr12:42236281
|
A | C | 1 | a0001c0002t0025g0232 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.152+1318T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236281 | ||||||
chr12:42236330
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(74): Show | 78 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.152+1269A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236330 | ||||||
chr12:42236425
|
A | C | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1174T>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236425 | ||||||
chr12:42236474
|
T | C | 3 | a0001c0002t0002g0353a0001c0002t0002g0354a0001c0002t0002g0355 | 3 | HG03669.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.152+1125A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236474 | ||||||
chr12:42236567
|
A | AAC | 295 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(292): Show | 300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.152+1031_152+1032i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236567 | ||||||
chr12:42236568
|
A | ACG | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+1030_152+1031i others(4): Show |
YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236568 | ||||||
chr12:42236569
|
G | C | 1 | a0001c0002t0002g0356 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152+1030C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236569 | ||||||
chr12:42236570
|
T | A | 1 | a0001c0002t0002g0356 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.152+1029A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236570 | ||||||
chr12:42236612
|
G | A | 32 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0001t0003g0139others(29): Show | 32 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.152+987C>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236612 | ||||||
chr12:42236615
|
T | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(64): Show | 68 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.152+984A>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236615 | ||||||
chr12:42236664
|
C | A | 138 | a0001c0001t0002g0272a0001c0002t0002g0002a0001c0002t0002g0003others(135): Show | 141 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.152+935G>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236664 | ||||||
chr12:42236817
|
A | G | 2 | a0001c0003t0015g0368a0001c0003t0015g0369 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.152+782T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236817 | ||||||
chr12:42236950
|
T | A | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+649A>T | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42236950 | ||||||
chr12:42237101
|
C | G | 1 | a0001c0001t0028g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.152+498G>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237101 | ||||||
chr12:42237302
|
A | G | 5 | a0001c0001t0012g0089a0001c0001t0012g0090a0001c0001t0028g0087others(2): Show | 5 | HG01891.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+297T>C | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237302 | ||||||
chr12:42237532
|
G | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.152+67C>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237532 | ||||||
chr12:42237557
|
A | AC | 17 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(14): Show | 17 | HG00438.hp1 HG01978.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.152+41dupG | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237557 | ||||||
chr12:42237587
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152+12G>A | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 2/3 | chr12 | 42237587 | ||||||
chr12:42237851
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0073others(299): Show | 307 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.27-127A>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 1/3 | chr12 | 42237851 | ||||||
chr12:42237905
|
G | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0358a0001c0001t0001g0359others(8): Show | 12 | HG02055.hp2 HG02559.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.27-181C>G | YAF2 | ENSG00000015153.15 | transcript | ENST00000534854.7 | protein_coding | 1/3 | chr12 | 42237905 |