geneid | 26751 |
---|---|
ensemblid | ENSG00000035115.22 |
hgncid | 29546 |
symbol | SH3YL1 |
name | SH3 and SYLF domain containing 1 |
refseq_nuc | NM_015677.4 |
refseq_prot | NP_056492.2 |
ensembl_nuc | ENST00000356150.10 |
ensembl_prot | ENSP00000348471.5 |
mane_status | MANE Select |
chr | chr2 |
start | 218144 |
end | 264032 |
strand | - |
ver | v1.2 |
region | chr2:218144-264032 |
region5000 | chr2:213144-269032 |
regionname0 | SH3YL1_chr2_218144_264032 |
regionname5000 | SH3YL1_chr2_213144_269032 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 10 | 360 | 90 | 74 | 138 | 14 | 42 | 102 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1028 | 263 | 74 | 55 | 98 | 6 | 28 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
c0002 | 0/0 | 1028 | 91 | 14 | 19 | 38 | 7 | 13 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
c0003 | 0/0 | 1028 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
c0004 | 0/0 | 1028 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
c0005 | 0/0 | 1028 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
c0006 | 0/0 | 1028 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
c0007 | 0/0 | 1028 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
c0008 | 0/0 | 1028 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 716 | 250 | 64 | 51 | 99 | 7 | 28 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
t0002 | 0/0 | 716 | 97 | 19 | 19 | 39 | 7 | 13 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
t0003 | 0/1 | 716 | 4 | 0 | 2 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
t0004 | 0/0 | 716 | 3 | 1 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
t0005 | 0/0 | 716 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
t0006 | 0/0 | 716 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
t0007 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
t0008 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 0 | 5 | 10 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0002 | 0/0 | 14 | 1 | 1 | 12 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0003 | 0/0 | 14 | 0 | 0 | 11 | 1 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0004 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0028 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1028 | 263 | 74 | 55 | 98 | 6 | 28 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0002 | 0/0 | 1028 | 91 | 14 | 19 | 38 | 7 | 13 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0003 | 0/0 | 1028 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0004 | 0/0 | 1028 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0005 | 0/0 | 1028 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0006 | 0/0 | 1028 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0007 | 0/0 | 1028 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0008 | 0/0 | 1028 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1743 | 246 | 63 | 51 | 98 | 6 | 27 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0001t0002 | 0/0 | 1743 | 4 | 4 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0001t0003 | 0/1 | 1743 | 4 | 0 | 2 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0001t0004 | 0/0 | 1743 | 3 | 1 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0001t0005 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0001t0006 | 0/0 | 1743 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0001t0007 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0001t0008 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0002t0002 | 0/0 | 1743 | 91 | 14 | 19 | 38 | 7 | 13 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0003t0001 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0004t0001 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0005t0002 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0006t0002 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0007t0001 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
a0001c0008t0001 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | copy fasta | chr2 | 213144 | 269032 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 16 | 0 | 5 | 10 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0002 | 0/0 | 14 | 1 | 1 | 12 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0003g0028 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0003 | 0/0 | 14 | 0 | 0 | 11 | 1 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0004 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0005t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0006t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0007t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
a0001c0008t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0002 | g0244 | EUR | GBR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0215 | EUR | GBR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0241 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | FIN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0240 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0045 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01516 | hp2 | a0001 | c0007 | t0001 | g0106 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0045 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01884 | hp2 | a0001 | c0008 | t0001 | g0193 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0227 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0250 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02976 | hp1 | a0001 | c0005 | t0002 | g0243 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0253 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0208 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0198 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0196 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0223 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0181 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0238 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0235 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0247 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18939 | hp2 | a0001 | c0006 | t0002 | g0218 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | YRI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0213 | AFR | ASW | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ASW | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0016 | EUR | TSI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0091 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0194 | AFR | ACB | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18955 | hp1 | a0001 | c0004 | t0001 | g0141 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0236 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | USA | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0028 | REF | REF | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0067 | REF | REF | SH3YL1_chr2_213144_269032 | SH3YL1 | chr2 | 213144 | 269032 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218858
|
G | A | 1 | a0001 | 1 | HG01516.hp2 | stop_gained | HIGH | c.982C>T | p.Arg328* | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 1030/1744 | 982/1029 | 328/342 | chr2 | 218858 | ||
chr2:224885
|
A | G | 1 | a0001 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.817T>C | p.Ser273Pro | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/10 | 865/1744 | 817/1029 | 273/342 | chr2 | 224885 | ||
chr2:231153
|
A | G | 1 | a0001 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.572T>C | p.Phe191Ser | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/10 | 620/1744 | 572/1029 | 191/342 | chr2 | 231153 | ||
chr2:231171
|
C | G | 1 | a0001 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.554G>C | p.Arg185Pro | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/10 | 602/1744 | 554/1029 | 185/342 | chr2 | 231171 | ||
chr2:233172
|
C | G | 1 | a0001 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.462G>C | p.Lys154Asn | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/10 | 510/1744 | 462/1029 | 154/342 | chr2 | 233172 | ||
chr2:233195
|
C | T | 1 | a0001 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.439G>A | p.Ala147Thr | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/10 | 487/1744 | 439/1029 | 147/342 | chr2 | 233195 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:224919
|
A | G | 3 | a0001c0002a0001c0005a0001c0006 | 93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
splice_region_variant&synonymous_variant | LOW | c.783T>C | p.Ser261Ser | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/10 | 831/1744 | 783/1029 | 261/342 | chr2 | 224919 | ||
chr2:249792
|
G | A | 1 | a0001c0008 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.165C>T | p.Ala55Ala | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/10 | 213/1744 | 165/1029 | 55/342 | chr2 | 249792 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218165
|
A | T | 1 | a0001c0001t0005 | 2 | HG02109.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*646T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 646 | chr2 | 218165 | |||||
chr2:218386
|
G | A | 7 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(4): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*425C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 425 | chr2 | 218386 | |||||
chr2:218476
|
C | G | 1 | a0001c0001t0003 | 4 | HG01106.hp1 HG01167.hp2 HG03017.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*335G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 335 | chr2 | 218476 | |||||
chr2:218542
|
G | A | 1 | a0001c0001t0008 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 10/10 | 269 | chr2 | 218542 | |||||
chr2:263995
|
C | T | 1 | a0001c0001t0006 | 2 | HG02559.hp1 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-11G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/10 | 11 | chr2 | 263995 | |||||
chr2:264014
|
C | A | 1 | a0001c0001t0007 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/10 | chr2 | 264014 | ||||||
chr2:264019
|
C | A | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(3): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/10 | 35 | chr2 | 264019 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219018
|
G | A | 1 | a0001c0001t0001g0012 | 3 | HG02257.hp2 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-17C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219018 | ||||||
chr2:219051
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.839-50C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219051 | ||||||
chr2:219082
|
C | A | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.839-81G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219082 | ||||||
chr2:219140
|
T | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0007g0194 | 3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.839-139A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219140 | ||||||
chr2:219346
|
G | T | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.839-345C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219346 | ||||||
chr2:219461
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.839-460G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219461 | ||||||
chr2:219482
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0072 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.839-481A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219482 | ||||||
chr2:219622
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0007g0194 | 3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.839-621G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219622 | ||||||
chr2:219641
|
A | C | 2 | a0001c0001t0001g0035a0001c0003t0001g0181 | 3 | HG03704.hp1 HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.839-640T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219641 | ||||||
chr2:219932
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.839-931C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 219932 | ||||||
chr2:220084
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0072 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.839-1083A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220084 | ||||||
chr2:220188
|
C | CAAT | 110 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(107): Show | 153 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.839-1190_839-1188d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220188 | ||||||
chr2:220188
|
C | CAATAAT | 30 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(27): Show | 39 | HG00642.hp1 HG01069.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.839-1193_839-1188d others(8): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220188 | ||||||
chr2:220188
|
C | CAATAATA others(2): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0103others(7): Show | 14 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-1196_839-1188d others(11): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220188 | ||||||
chr2:220542
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.839-1541A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220542 | ||||||
chr2:220548
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(7): Show | 14 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.839-1547C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220548 | ||||||
chr2:220615
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.839-1614C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220615 | ||||||
chr2:220638
|
C | T | 1 | a0001c0002t0002g0225 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.839-1637G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220638 | ||||||
chr2:220647
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.839-1646C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220647 | ||||||
chr2:220889
|
G | A | 60 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(57): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.839-1888C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 220889 | ||||||
chr2:221032
|
T | TCAGGCAC others(4): Show |
155 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(152): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.839-2032_839-2031i others(13): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221032 | ||||||
chr2:221069
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.839-2068C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221069 | ||||||
chr2:221384
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.839-2383T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221384 | ||||||
chr2:221391
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.839-2390A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221391 | ||||||
chr2:221451
|
C | T | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.839-2450G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221451 | ||||||
chr2:221456
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.839-2455A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221456 | ||||||
chr2:221492
|
G | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.839-2491C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221492 | ||||||
chr2:221560
|
G | A | 61 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(58): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.839-2559C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221560 | ||||||
chr2:221799
|
AGAGT | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0029others(15): Show | 26 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.839-2802_839-2799d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221799 | ||||||
chr2:221943
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.838+2921A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221943 | ||||||
chr2:221981
|
C | T | 74 | a0001c0001t0001g0131a0001c0001t0002g0200a0001c0001t0002g0202others(71): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.838+2883G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 221981 | ||||||
chr2:222050
|
C | T | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.838+2814G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222050 | ||||||
chr2:222145
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0030 | 6 | HG01069.hp2 HG01261.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+2719C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222145 | ||||||
chr2:222164
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.838+2700A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222164 | ||||||
chr2:222213
|
T | C | 6 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+2651A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222213 | ||||||
chr2:222307
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 8 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.838+2557G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222307 | ||||||
chr2:222336
|
T | C | 64 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(61): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.838+2528A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222336 | ||||||
chr2:222483
|
A | T | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.838+2381T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222483 | ||||||
chr2:222501
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.838+2363A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222501 | ||||||
chr2:222553
|
G | T | 1 | a0001c0001t0004g0127 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.838+2311C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222553 | ||||||
chr2:222561
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.838+2303T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222561 | ||||||
chr2:222690
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.838+2174C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222690 | ||||||
chr2:222854
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0191others(1): Show | 4 | HG02258.hp1 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+2010A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222854 | ||||||
chr2:222903
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.838+1961C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222903 | ||||||
chr2:222958
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.838+1906G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 222958 | ||||||
chr2:223088
|
A | G | 4 | a0001c0001t0001g0169a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | NA18984.hp1 NA19060.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+1776T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223088 | ||||||
chr2:223135
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.838+1729G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223135 | ||||||
chr2:223180
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.838+1684C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223180 | ||||||
chr2:223375
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.838+1489C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223375 | ||||||
chr2:223549
|
T | C | 1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.838+1315A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223549 | ||||||
chr2:223724
|
T | A | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.838+1140A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223724 | ||||||
chr2:223783
|
A | C | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.838+1081T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223783 | ||||||
chr2:223818
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.838+1046G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223818 | ||||||
chr2:223823
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.838+1041G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223823 | ||||||
chr2:223892
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(250): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.838+972T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223892 | ||||||
chr2:223897
|
G | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.838+967C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 223897 | ||||||
chr2:224086
|
T | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(153): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.838+778A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224086 | ||||||
chr2:224123
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0154a0001c0001t0001g0161 | 4 | HG00408.hp2 HG00609.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+741G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224123 | ||||||
chr2:224160
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.838+704A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224160 | ||||||
chr2:224192
|
A | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(82): Show | 118 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.838+672T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224192 | ||||||
chr2:224266
|
G | A | 1 | a0001c0002t0002g0219 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.838+598C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224266 | ||||||
chr2:224317
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.838+547G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224317 | ||||||
chr2:224517
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0153 | 2 | HG00673.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.838+347T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224517 | ||||||
chr2:224607
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.838+257C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224607 | ||||||
chr2:224625
|
T | C | 1 | a0001c0002t0002g0224 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.838+239A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224625 | ||||||
chr2:224829
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.838+35A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 9/9 | chr2 | 224829 | ||||||
chr2:224970
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(151): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.782-50G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 224970 | ||||||
chr2:225059
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.782-139G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225059 | ||||||
chr2:225140
|
A | G | 1 | a0001c0001t0004g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.782-220T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225140 | ||||||
chr2:225258
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.782-338G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225258 | ||||||
chr2:225437
|
T | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(10): Show | 17 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.782-517A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225437 | ||||||
chr2:225515
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.782-595G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225515 | ||||||
chr2:225578
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0073 | 6 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-658T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225578 | ||||||
chr2:225708
|
A | G | 1 | a0001c0002t0002g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.782-788T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225708 | ||||||
chr2:225753
|
T | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | NA18980.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.782-833A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225753 | ||||||
chr2:225886
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.782-966A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225886 | ||||||
chr2:225951
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(153): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.782-1031T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 225951 | ||||||
chr2:226231
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.782-1311C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226231 | ||||||
chr2:226243
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0166 | 3 | HG01168.hp2 HG01255.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.782-1323A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226243 | ||||||
chr2:226330
|
T | C | 1 | a0001c0002t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.782-1410A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226330 | ||||||
chr2:226528
|
C | T | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.782-1608G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226528 | ||||||
chr2:226529
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0166 | 3 | HG01168.hp2 HG01255.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.782-1609C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226529 | ||||||
chr2:226568
|
C | T | 1 | a0001c0002t0002g0223 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.782-1648G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226568 | ||||||
chr2:226594
|
C | T | 3 | a0001c0002t0002g0015a0001c0002t0002g0215a0001c0002t0002g0223 | 5 | HG00140.hp2 HG00738.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1674G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226594 | ||||||
chr2:226749
|
TTGGGGAG others(11): Show |
T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.782-1847_782-1830d others(20): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226749 | ||||||
chr2:226753
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.782-1833C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226753 | ||||||
chr2:226781
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.782-1861A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226781 | ||||||
chr2:226855
|
C | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.782-1935G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226855 | ||||||
chr2:226856
|
G | A | 2 | a0001c0002t0002g0047a0001c0002t0002g0220 | 3 | NA18962.hp1 NA19003.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.782-1936C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226856 | ||||||
chr2:226867
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.782-1947G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226867 | ||||||
chr2:226933
|
A | G | 73 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0200others(70): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.782-2013T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226933 | ||||||
chr2:226999
|
A | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(10): Show | 17 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.782-2079T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 226999 | ||||||
chr2:227066
|
G | A | 73 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0200others(70): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.782-2146C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227066 | ||||||
chr2:227081
|
T | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.782-2161A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227081 | ||||||
chr2:227121
|
A | G | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.782-2201T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227121 | ||||||
chr2:227201
|
C | T | 70 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(67): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.782-2281G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227201 | ||||||
chr2:227505
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.781+2461G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227505 | ||||||
chr2:227553
|
A | C | 1 | a0001c0001t0004g0127 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.781+2413T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227553 | ||||||
chr2:227684
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.781+2282C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227684 | ||||||
chr2:227722
|
TAATTTAT others(7): Show |
T | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.781+2230_781+2243d others(16): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227722 | ||||||
chr2:227806
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+2160C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227806 | ||||||
chr2:227889
|
A | ATG | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.781+2075_781+2076d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227889 | ||||||
chr2:227889
|
ATG | A | 70 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0002g0200others(67): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.781+2075_781+2076d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227889 | ||||||
chr2:227978
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.781+1988T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 227978 | ||||||
chr2:228088
|
G | A | 65 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(62): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.781+1878C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228088 | ||||||
chr2:228268
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781+1698T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228268 | ||||||
chr2:228450
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0007g0194 | 3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.781+1516G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228450 | ||||||
chr2:228505
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.781+1461G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228505 | ||||||
chr2:228670
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781+1296G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 228670 | ||||||
chr2:229000
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.781+966G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229000 | ||||||
chr2:229112
|
A | G | 1 | a0001c0001t0004g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.781+854T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229112 | ||||||
chr2:229456
|
A | G | 79 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0155others(76): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.781+510T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229456 | ||||||
chr2:229536
|
C | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(10): Show | 17 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.781+430G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229536 | ||||||
chr2:229590
|
G | A | 2 | a0001c0001t0001g0129a0001c0003t0001g0181 | 2 | HG02809.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.781+376C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229590 | ||||||
chr2:229597
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.781+369G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229597 | ||||||
chr2:229644
|
G | A | 6 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 6 | HG00597.hp1 HG02074.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+322C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229644 | ||||||
chr2:229646
|
G | C | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.781+320C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229646 | ||||||
chr2:229686
|
G | A | 1 | a0001c0002t0002g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.781+280C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229686 | ||||||
chr2:229716
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.781+250C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229716 | ||||||
chr2:229723
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.781+243G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229723 | ||||||
chr2:229728
|
C | CA | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(72): Show | 107 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.781+237dupT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229728 | ||||||
chr2:229728
|
CA | C | 71 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0059others(68): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.781+237delT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229728 | ||||||
chr2:229728
|
CAA | C | 6 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0002g0204others(3): Show | 6 | HG01496.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+236_781+237del others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 8/9 | chr2 | 229728 | ||||||
chr2:230055
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.703-11G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230055 | ||||||
chr2:230141
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703-97A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230141 | ||||||
chr2:230233
|
T | A | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.703-189A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230233 | ||||||
chr2:230440
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.703-396G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230440 | ||||||
chr2:230442
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(126): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.703-398A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230442 | ||||||
chr2:230658
|
C | T | 1 | a0001c0002t0002g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+365G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230658 | ||||||
chr2:230716
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+307G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230716 | ||||||
chr2:230721
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.702+302G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230721 | ||||||
chr2:230912
|
A | C | 71 | a0001c0001t0001g0131a0001c0001t0002g0200a0001c0001t0002g0202others(68): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.702+111T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 7/9 | chr2 | 230912 | ||||||
chr2:231260
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.534-69C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231260 | ||||||
chr2:231532
|
A | G | 2 | a0001c0002t0002g0221a0001c0002t0002g0245 | 2 | NA18969.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.534-341T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231532 | ||||||
chr2:231571
|
A | T | 1 | a0001c0002t0002g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.534-380T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231571 | ||||||
chr2:231583
|
C | G | 14 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(11): Show | 18 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.534-392G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231583 | ||||||
chr2:231741
|
C | T | 59 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(56): Show | 89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.534-550G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231741 | ||||||
chr2:231742
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.534-551C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231742 | ||||||
chr2:231905
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.534-714G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231905 | ||||||
chr2:231995
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.534-804G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 231995 | ||||||
chr2:232238
|
CT | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0088a0001c0001t0001g0089others(3): Show | 6 | HG00639.hp2 HG02723.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+862delA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232238 | ||||||
chr2:232276
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.533+825A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232276 | ||||||
chr2:232343
|
G | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(56): Show | 87 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.533+758C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232343 | ||||||
chr2:232445
|
C | CT | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.533+655dupA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232445 | ||||||
chr2:232550
|
G | A | 2 | a0001c0002t0002g0227a0001c0002t0002g0234 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.533+551C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232550 | ||||||
chr2:232701
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.533+400A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 232701 | ||||||
chr2:233077
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.533+24T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 6/9 | chr2 | 233077 | ||||||
chr2:233355
|
T | C | 1 | a0001c0008t0001g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.405-126A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233355 | ||||||
chr2:233382
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.405-153C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233382 | ||||||
chr2:233416
|
G | A | 53 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(50): Show | 75 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.405-187C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233416 | ||||||
chr2:233570
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0007g0194 | 3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.405-341T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233570 | ||||||
chr2:233693
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.405-464G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233693 | ||||||
chr2:233713
|
A | C | 1 | a0001c0001t0001g0032 | 2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.404+447T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233713 | ||||||
chr2:233752
|
G | T | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.404+408C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233752 | ||||||
chr2:233848
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.404+312T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 233848 | ||||||
chr2:234130
|
T | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.404+30A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 5/9 | chr2 | 234130 | ||||||
chr2:234454
|
C | T | 1 | a0001c0001t0001g0038 | 2 | NA18943.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.292-182G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234454 | ||||||
chr2:234668
|
A | AAC | 78 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0191others(75): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.292-398_292-397dup others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234668 | ||||||
chr2:234716
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-444C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234716 | ||||||
chr2:234737
|
T | C | 5 | a0001c0002t0002g0007a0001c0002t0002g0213a0001c0002t0002g0228others(2): Show | 8 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-465A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234737 | ||||||
chr2:234801
|
A | C | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-529T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 234801 | ||||||
chr2:235158
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.292-886C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235158 | ||||||
chr2:235278
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.292-1006G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235278 | ||||||
chr2:235332
|
AGAGGCAG others(12): Show |
A | 1 | a0001c0002t0002g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.292-1079_292-1061d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235332 | ||||||
chr2:235346
|
T | TCAGGGGA others(12): Show |
1 | a0001c0001t0001g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292-1093_292-1075d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235346 | ||||||
chr2:235376
|
A | AGCAGCAT others(12): Show |
69 | a0001c0001t0001g0131a0001c0001t0001g0191a0001c0001t0001g0192others(66): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.292-1123_292-1105d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235376 | ||||||
chr2:235376
|
AGCAGCAT others(12): Show |
A | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.292-1123_292-1105d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235376 | ||||||
chr2:235425
|
T | C | 5 | a0001c0001t0006g0195a0001c0001t0006g0196a0001c0002t0002g0049others(2): Show | 6 | HG02559.hp1 HG03209.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1153A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235425 | ||||||
chr2:235444
|
C | T | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1172G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235444 | ||||||
chr2:235478
|
G | A | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1206C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235478 | ||||||
chr2:235484
|
C | CGGGCCAG others(12): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 8 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.292-1231_292-1213d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235484 | ||||||
chr2:235484
|
C | T | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1212G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235484 | ||||||
chr2:235503
|
T | C | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1231A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235503 | ||||||
chr2:235507
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.292-1235G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235507 | ||||||
chr2:235526
|
T | C | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1254A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235526 | ||||||
chr2:235545
|
C | T | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1273G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235545 | ||||||
chr2:235557
|
A | G | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1285T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235557 | ||||||
chr2:235585
|
C | CGGGCCAG others(34): Show |
1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1314_292-1313i others(43): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235585 | ||||||
chr2:235585
|
C | T | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1313G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235585 | ||||||
chr2:235586
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0072 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.292-1314C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235586 | ||||||
chr2:235604
|
T | C | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1332A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235604 | ||||||
chr2:235608
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1336G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235608 | ||||||
chr2:235627
|
T | C | 2 | a0001c0001t0001g0131a0001c0002t0002g0049 | 3 | HG02055.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1355A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235627 | ||||||
chr2:235627
|
T | TCAGGGGA others(15): Show |
52 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(49): Show | 68 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.292-1377_292-1356d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235627 | ||||||
chr2:235627
|
T | TCAGGGGA others(116): Show |
2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.292-1356_292-1355i others(125): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235627 | ||||||
chr2:235635
|
GGCA | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG02258.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-1366_292-1364d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235635 | ||||||
chr2:235638
|
A | AGCAGCAT others(56): Show |
1 | a0001c0002t0002g0047 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1367_292-1366i others(65): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235638 | ||||||
chr2:235639
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1367C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235639 | ||||||
chr2:235639
|
G | GCATGGGC others(12): Show |
5 | a0001c0001t0001g0130a0001c0001t0004g0126a0001c0001t0004g0127others(2): Show | 5 | HG00642.hp1 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1368_292-1367i others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235639 | ||||||
chr2:235645
|
T | C | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1373A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235645 | ||||||
chr2:235649
|
C | T | 1 | a0001c0002t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.292-1377G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235649 | ||||||
chr2:235660
|
AGCAGCAC others(12): Show |
A | 1 | a0001c0002t0002g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1407_292-1389d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235660 | ||||||
chr2:235661
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG02258.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-1389C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235661 | ||||||
chr2:235667
|
C | T | 26 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192others(23): Show | 33 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.292-1395G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235667 | ||||||
chr2:235671
|
C | T | 1 | a0001c0002t0002g0047 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1399G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235671 | ||||||
chr2:235673
|
A | G | 1 | a0001c0002t0002g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.292-1401T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235673 | ||||||
chr2:235679
|
G | GGCA | 22 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192others(19): Show | 28 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.292-1410_292-1408d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235679 | ||||||
chr2:235686
|
T | C | 20 | a0001c0001t0001g0129a0001c0001t0008g0253a0001c0002t0002g0003others(17): Show | 26 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.292-1414A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235686 | ||||||
chr2:235698
|
GGCA | G | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(6): Show | 9 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-1429_292-1427d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235698 | ||||||
chr2:235701
|
A | AGCATGGG others(31): Show |
19 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(16): Show | 25 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.292-1430_292-1429i others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235701 | ||||||
chr2:235702
|
G | A | 1 | a0001c0002t0002g0047 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1430C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235702 | ||||||
chr2:235708
|
T | C | 56 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(53): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.292-1436A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235708 | ||||||
chr2:235712
|
C | T | 60 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0200others(57): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1440G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235712 | ||||||
chr2:235720
|
GGCAGCAT others(15): Show |
G | 1 | a0001c0001t0001g0058 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.292-1470_292-1449d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235720 | ||||||
chr2:235721
|
G | GCAA | 19 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(16): Show | 25 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.292-1450_292-1449i others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235721 | ||||||
chr2:235727
|
T | C | 1 | a0001c0002t0002g0047 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1455A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235727 | ||||||
chr2:235731
|
T | C | 76 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0200others(73): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.292-1459A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235731 | ||||||
chr2:235742
|
A | AGCAGCAC others(31): Show |
19 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(16): Show | 25 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.292-1471_292-1470i others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235742 | ||||||
chr2:235742
|
A | AGCATGGG others(9): Show |
1 | a0001c0002t0002g0047 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.292-1471_292-1470i others(18): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235742 | ||||||
chr2:235743
|
G | A | 60 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0200others(57): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1471C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235743 | ||||||
chr2:235749
|
T | C | 1 | a0001c0002t0002g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1477A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235749 | ||||||
chr2:235753
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(137): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.292-1481A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235753 | ||||||
chr2:235753
|
TCAGGGGA others(53): Show |
T | 1 | a0001c0002t0002g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1541_292-1482d others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235753 | ||||||
chr2:235764
|
AGCAGCAT others(31): Show |
A | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.292-1530_292-1493d others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235764 | ||||||
chr2:235771
|
T | C | 63 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(60): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.292-1499A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235771 | ||||||
chr2:235775
|
T | C | 79 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(76): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.292-1503A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235775 | ||||||
chr2:235775
|
TCAGGGGA others(12): Show |
T | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292-1522_292-1504d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235775 | ||||||
chr2:235783
|
G | GGCA | 21 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(18): Show | 29 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.292-1514_292-1512d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235783 | ||||||
chr2:235790
|
TGGGCCAG others(53): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.292-1578_292-1519d others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235790 | ||||||
chr2:235802
|
G | GGCA | 21 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(18): Show | 29 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.292-1533_292-1531d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235802 | ||||||
chr2:235805
|
A | G | 1 | a0001c0001t0001g0042 | 2 | HG02074.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.292-1533T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235805 | ||||||
chr2:235805
|
AGCATGGG others(9): Show |
A | 3 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG02258.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-1549_292-1534d others(18): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235805 | ||||||
chr2:235809
|
T | C | 21 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(18): Show | 29 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.292-1537A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235809 | ||||||
chr2:235813
|
C | T | 60 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0200others(57): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1541G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235813 | ||||||
chr2:235821
|
G | GGCA | 57 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0002g0200others(54): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.292-1552_292-1550d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235821 | ||||||
chr2:235840
|
GGCA | G | 24 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.292-1571_292-1569d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235840 | ||||||
chr2:235844
|
G | A | 4 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128others(1): Show | 4 | HG00642.hp1 HG01109.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1572C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235844 | ||||||
chr2:235850
|
C | T | 76 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192others(73): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.292-1578G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235850 | ||||||
chr2:235851
|
G | A | 1 | a0001c0001t0001g0041 | 2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.292-1579C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235851 | ||||||
chr2:235854
|
C | CCAGGGGA others(53): Show |
54 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(51): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.292-1583_292-1582i others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235854 | ||||||
chr2:235854
|
C | CCAGGGGA others(53): Show |
2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1583_292-1582i others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235854 | ||||||
chr2:235854
|
C | T | 24 | a0001c0001t0001g0129a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 32 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.292-1582G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235854 | ||||||
chr2:235872
|
T | C | 5 | a0001c0001t0001g0168a0001c0001t0004g0126a0001c0001t0004g0127others(2): Show | 5 | HG00642.hp1 HG01109.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1600A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235872 | ||||||
chr2:235876
|
T | C | 80 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(77): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.292-1604A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235876 | ||||||
chr2:235887
|
A | AGCATGGG others(9): Show |
3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1616_292-1615i others(18): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235887 | ||||||
chr2:235898
|
T | C | 76 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(73): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.292-1626A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235898 | ||||||
chr2:235906
|
G | GGCA | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1637_292-1635d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235906 | ||||||
chr2:235913
|
TGGGCCAG others(15): Show |
T | 57 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 77 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.292-1663_292-1642d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235913 | ||||||
chr2:235917
|
C | T | 2 | a0001c0001t0001g0131a0001c0002t0002g0234 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.292-1645G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235917 | ||||||
chr2:235922
|
G | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | NA18984.hp1 NA19060.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1650C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235922 | ||||||
chr2:235935
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(28): Show | 35 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.292-1663G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235935 | ||||||
chr2:235939
|
C | CCAGGGGA others(15): Show |
2 | a0001c0001t0001g0094a0001c0001t0003g0093 | 2 | HG02109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.292-1689_292-1668d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235939 | ||||||
chr2:235939
|
C | CCAGGGGA others(53): Show |
3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1668_292-1667i others(62): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235939 | ||||||
chr2:235961
|
T | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 82 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.292-1689A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235961 | ||||||
chr2:235972
|
AGCAGCAT others(31): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.292-1738_292-1701d others(40): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235972 | ||||||
chr2:235979
|
T | C | 1 | a0001c0002t0002g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1707A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235979 | ||||||
chr2:235983
|
T | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(30): Show | 37 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.292-1711A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235983 | ||||||
chr2:235983
|
TCAGGGGA others(12): Show |
T | 3 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0073 | 6 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1730_292-1712d others(21): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235983 | ||||||
chr2:235994
|
AGCATGGG others(28): Show |
A | 56 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(53): Show | 76 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.292-1757_292-1723d others(37): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235994 | ||||||
chr2:235998
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1726A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 235998 | ||||||
chr2:236010
|
G | GGCA | 4 | a0001c0001t0001g0131a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-1741_292-1739d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236010 | ||||||
chr2:236017
|
T | C | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1745A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236017 | ||||||
chr2:236021
|
C | T | 2 | a0001c0001t0001g0131a0001c0002t0002g0234 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.292-1749G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236021 | ||||||
chr2:236029
|
G | GGCA | 5 | a0001c0001t0001g0131a0001c0001t0004g0126a0001c0001t0004g0127others(2): Show | 5 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-1760_292-1758d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236029 | ||||||
chr2:236029
|
GGCAGCAT others(15): Show |
G | 1 | a0001c0001t0001g0168 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.292-1779_292-1758d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236029 | ||||||
chr2:236029
|
GGCAGCAT others(97): Show |
G | 1 | a0001c0001t0001g0161 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.292-1861_292-1758d others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236029 | ||||||
chr2:236040
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 77 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.292-1768A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236040 | ||||||
chr2:236048
|
GGCA | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 77 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.292-1779_292-1777d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236048 | ||||||
chr2:236058
|
TGGGCCAG others(116): Show |
T | 31 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(28): Show | 35 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.292-1909_292-1787d others(2): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236058 | ||||||
chr2:236062
|
C | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1790G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236062 | ||||||
chr2:236070
|
G | GGCAGCAG others(37): Show |
68 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(65): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.292-1799_292-1798i others(46): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236070 | ||||||
chr2:236070
|
G | GGCAGCAG others(37): Show |
1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292-1799_292-1798i others(46): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236070 | ||||||
chr2:236096
|
T | C | 1 | a0001c0002t0002g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1824A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236096 | ||||||
chr2:236100
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0007g0194a0001c0002t0002g0234 | 3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1828A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236100 | ||||||
chr2:236104
|
G | A | 1 | a0001c0002t0002g0242 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.292-1832C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236104 | ||||||
chr2:236108
|
GGCA | G | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.292-1839_292-1837d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236108 | ||||||
chr2:236122
|
C | T | 1 | a0001c0002t0002g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.292-1850G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236122 | ||||||
chr2:236130
|
GGCA | G | 5 | a0001c0001t0001g0130a0001c0001t0004g0126a0001c0001t0004g0127others(2): Show | 5 | HG00642.hp1 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1861_292-1859d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236130 | ||||||
chr2:236140
|
T | C | 1 | a0001c0002t0002g0233 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.292-1868A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236140 | ||||||
chr2:236144
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0007g0194a0001c0002t0002g0234 | 3 | HG02559.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1872G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236144 | ||||||
chr2:236152
|
GGCAGCAT others(59): Show |
G | 57 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(54): Show | 77 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.292-1946_292-1881d others(68): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236152 | ||||||
chr2:236159
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1887A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236159 | ||||||
chr2:236163
|
C | T | 4 | a0001c0001t0001g0161a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1891G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236163 | ||||||
chr2:236181
|
C | T | 8 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0161others(5): Show | 8 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-1909G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236181 | ||||||
chr2:236185
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1913G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236185 | ||||||
chr2:236185
|
CCAGGGGA others(15): Show |
C | 1 | a0001c0001t0001g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.292-1935_292-1914d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236185 | ||||||
chr2:236193
|
GGCAGCAG others(18): Show |
G | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-1946_292-1922d others(27): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236193 | ||||||
chr2:236196
|
A | AGCAGCAT others(72): Show |
59 | a0001c0001t0008g0253a0001c0002t0002g0003a0001c0002t0002g0004others(56): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.292-1925_292-1924i others(81): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236196 | ||||||
chr2:236196
|
A | AGCAGCAT others(72): Show |
3 | a0001c0002t0002g0016a0001c0002t0002g0216a0001c0002t0002g0247 | 5 | HG01192.hp1 HG01346.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1925_292-1924i others(81): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236196 | ||||||
chr2:236207
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(32): Show | 39 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.292-1935A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236207 | ||||||
chr2:236207
|
T | TCAGGGGA others(15): Show |
1 | a0001c0001t0001g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292-1957_292-1936d others(24): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236207 | ||||||
chr2:236207
|
T | TCAGGGGA others(72): Show |
1 | a0001c0002t0002g0238 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292-1936_292-1935i others(81): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236207 | ||||||
chr2:236215
|
GGCA | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(32): Show | 39 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.292-1946_292-1944d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236215 | ||||||
chr2:236218
|
A | AGCAGCAT others(113): Show |
6 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.292-1947_292-1946i others(122): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236218 | ||||||
chr2:236218
|
A | AGCATGGG others(50): Show |
2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1947_292-1946i others(59): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236218 | ||||||
chr2:236559
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-2287G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236559 | ||||||
chr2:236838
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292-2566A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236838 | ||||||
chr2:236950
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-2678G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 236950 | ||||||
chr2:237137
|
AT | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.292-2866delA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237137 | ||||||
chr2:237140
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.292-2868A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237140 | ||||||
chr2:237142
|
C | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.292-2870G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237142 | ||||||
chr2:237208
|
G | A | 1 | a0001c0002t0002g0235 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.292-2936C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237208 | ||||||
chr2:237346
|
GGTGACAC others(5): Show |
G | 70 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(67): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.292-3086_292-3075d others(14): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237346 | ||||||
chr2:237471
|
G | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.292-3199C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237471 | ||||||
chr2:237506
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-3234G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237506 | ||||||
chr2:237826
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0081a0001c0001t0001g0083 | 4 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-3554T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237826 | ||||||
chr2:237867
|
T | C | 1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292-3595A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 237867 | ||||||
chr2:238259
|
T | TTG | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0051others(13): Show | 18 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.292-3989_292-3988d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | ||||||
chr2:238259
|
TTG | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(53): Show | 79 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.292-3989_292-3988d others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | ||||||
chr2:238259
|
TTGTG | T | 60 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(57): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.292-3991_292-3988d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | ||||||
chr2:238259
|
TTGTGTG | T | 6 | a0001c0001t0001g0098a0001c0001t0006g0195a0001c0002t0002g0046others(3): Show | 7 | HG01192.hp2 HG01358.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.292-3993_292-3988d others(8): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | ||||||
chr2:238259
|
TTGTGTGT others(3): Show |
T | 12 | a0001c0001t0001g0043a0001c0001t0001g0133a0001c0001t0001g0147others(9): Show | 13 | HG00558.hp2 HG00597.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.292-3997_292-3988d others(12): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | ||||||
chr2:238259
|
TTGTGTGT others(5): Show |
T | 65 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 97 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.292-3999_292-3988d others(14): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238259 | ||||||
chr2:238308
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-4036C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238308 | ||||||
chr2:238328
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292-4056G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238328 | ||||||
chr2:238600
|
G | C | 1 | a0001c0002t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.292-4328C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238600 | ||||||
chr2:238975
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-4703T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238975 | ||||||
chr2:238989
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0145others(1): Show | 4 | HG03491.hp1 HG03710.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-4717C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 238989 | ||||||
chr2:239111
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.292-4839T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239111 | ||||||
chr2:239144
|
G | T | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0008t0001g0193 | 3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.292-4872C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239144 | ||||||
chr2:239263
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.292-4991A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239263 | ||||||
chr2:239416
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.292-5144G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239416 | ||||||
chr2:239515
|
A | G | 1 | a0001c0001t0001g0025 | 2 | HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.292-5243T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239515 | ||||||
chr2:239597
|
C | G | 70 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(67): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.292-5325G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239597 | ||||||
chr2:239612
|
C | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 4 | HG02647.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-5340G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239612 | ||||||
chr2:239655
|
TAAC | T | 13 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0032others(10): Show | 17 | HG00597.hp1 HG02074.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.292-5386_292-5384d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239655 | ||||||
chr2:239736
|
C | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(56): Show | 87 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.292-5464G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239736 | ||||||
chr2:239898
|
A | G | 1 | a0001c0001t0007g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292-5626T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239898 | ||||||
chr2:239964
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.292-5692C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239964 | ||||||
chr2:239969
|
C | T | 78 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0191others(75): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.292-5697G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 239969 | ||||||
chr2:240053
|
C | T | 1 | a0001c0001t0004g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.292-5781G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240053 | ||||||
chr2:240054
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(153): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.292-5782T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240054 | ||||||
chr2:240085
|
C | G | 4 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-5813G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240085 | ||||||
chr2:240210
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.292-5938C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240210 | ||||||
chr2:240255
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.292-5983T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240255 | ||||||
chr2:240326
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.292-6054G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240326 | ||||||
chr2:240342
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0065others(1): Show | 5 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.292-6070C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240342 | ||||||
chr2:240567
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292-6295T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240567 | ||||||
chr2:240575
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.292-6303G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240575 | ||||||
chr2:240630
|
T | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.292-6358A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240630 | ||||||
chr2:240696
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0159 | 2 | HG00423.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.292-6424G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240696 | ||||||
chr2:240785
|
G | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(68): Show | 97 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.292-6513C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240785 | ||||||
chr2:240800
|
C | T | 1 | a0001c0002t0002g0217 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.292-6528G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240800 | ||||||
chr2:240824
|
T | C | 1 | a0001c0001t0001g0014 | 3 | HG00438.hp1 HG02040.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.292-6552A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240824 | ||||||
chr2:240923
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.291+6615T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240923 | ||||||
chr2:240926
|
T | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(10): Show | 17 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.291+6612A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240926 | ||||||
chr2:240976
|
A | T | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.291+6562T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 240976 | ||||||
chr2:241049
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.291+6489G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241049 | ||||||
chr2:241167
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 4 | HG02698.hp1 HG02738.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+6371G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241167 | ||||||
chr2:241263
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.291+6275A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241263 | ||||||
chr2:241669
|
A | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.291+5869T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241669 | ||||||
chr2:241692
|
T | C | 1 | a0001c0001t0001g0024 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.291+5846A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241692 | ||||||
chr2:241719
|
G | A | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+5819C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241719 | ||||||
chr2:241842
|
T | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01361.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.291+5696A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241842 | ||||||
chr2:241852
|
A | G | 2 | a0001c0002t0002g0207a0001c0002t0002g0208 | 2 | HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.291+5686T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 241852 | ||||||
chr2:242132
|
G | A | 70 | a0001c0001t0001g0131a0001c0001t0002g0200a0001c0001t0002g0202others(67): Show | 100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.291+5406C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242132 | ||||||
chr2:242177
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0007g0194 | 3 | HG02559.hp2 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.291+5361G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242177 | ||||||
chr2:242202
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.291+5336C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242202 | ||||||
chr2:242426
|
A | G | 62 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(59): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.291+5112T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242426 | ||||||
chr2:242458
|
A | G | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0008t0001g0193 | 3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291+5080T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242458 | ||||||
chr2:242605
|
C | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(62): Show | 90 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.291+4933G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242605 | ||||||
chr2:242732
|
T | TAAC | 156 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(153): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.291+4803_291+4805d others(5): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242732 | ||||||
chr2:242778
|
C | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0004g0126others(1): Show | 4 | HG00642.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+4760G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242778 | ||||||
chr2:242793
|
G | C | 54 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(51): Show | 81 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.291+4745C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242793 | ||||||
chr2:242800
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 114 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.291+4738A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242800 | ||||||
chr2:242860
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.291+4678A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242860 | ||||||
chr2:242879
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291+4659A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 242879 | ||||||
chr2:243056
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.291+4482A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243056 | ||||||
chr2:243107
|
T | G | 1 | a0001c0001t0001g0107 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.291+4431A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243107 | ||||||
chr2:243504
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.291+4034G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243504 | ||||||
chr2:243567
|
T | TA | 156 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(153): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.291+3970dupT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243567 | ||||||
chr2:243806
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.291+3732C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243806 | ||||||
chr2:243929
|
G | A | 77 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0191others(74): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.291+3609C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243929 | ||||||
chr2:243987
|
G | T | 1 | a0001c0002t0002g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.291+3551C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 243987 | ||||||
chr2:244003
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.291+3535G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244003 | ||||||
chr2:244133
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.291+3405A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244133 | ||||||
chr2:244139
|
C | T | 2 | a0001c0001t0001g0104a0001c0002t0002g0199 | 2 | HG01175.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.291+3399G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244139 | ||||||
chr2:244188
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG01993.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.291+3350A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244188 | ||||||
chr2:244201
|
T | TA | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.291+3336dupT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244201 | ||||||
chr2:244209
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.291+3329T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244209 | ||||||
chr2:244239
|
T | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.291+3299A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244239 | ||||||
chr2:244262
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078 | 3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.291+3276G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244262 | ||||||
chr2:244292
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.291+3246G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244292 | ||||||
chr2:244474
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0190 | 2 | HG00621.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.291+3064G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244474 | ||||||
chr2:244496
|
A | AAAAG | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(3): Show | 9 | HG01168.hp2 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.291+3038_291+3041d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244496 | ||||||
chr2:244568
|
A | AAAAG | 155 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(152): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.291+2966_291+2969d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244568 | ||||||
chr2:244568
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291+2970T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244568 | ||||||
chr2:244568
|
AAAAG | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 38 | HG00323.hp1 HG00639.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.291+2966_291+2969d others(6): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244568 | ||||||
chr2:244736
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.291+2802A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244736 | ||||||
chr2:244805
|
C | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0157 | 3 | NA18964.hp1 NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.291+2733G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244805 | ||||||
chr2:244847
|
A | G | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291+2691T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244847 | ||||||
chr2:244877
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.291+2661A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244877 | ||||||
chr2:244894
|
G | A | 1 | a0001c0002t0002g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.291+2644C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244894 | ||||||
chr2:244994
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.291+2544A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 244994 | ||||||
chr2:245184
|
A | C | 19 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0191others(16): Show | 19 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.291+2354T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245184 | ||||||
chr2:245257
|
A | G | 19 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0191others(16): Show | 19 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.291+2281T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245257 | ||||||
chr2:245286
|
TTCTTA | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0143 | 3 | HG02647.hp1 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.291+2247_291+2251d others(7): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245286 | ||||||
chr2:245311
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.291+2227A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245311 | ||||||
chr2:245350
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.291+2188A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245350 | ||||||
chr2:245507
|
A | C | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.291+2031T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245507 | ||||||
chr2:245511
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.291+2027T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245511 | ||||||
chr2:245613
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.291+1925C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245613 | ||||||
chr2:245661
|
T | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0090 | 3 | HG00609.hp1 NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.291+1877A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245661 | ||||||
chr2:245672
|
T | A | 72 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(69): Show | 98 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.291+1866A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245672 | ||||||
chr2:245689
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0077others(4): Show | 10 | HG00280.hp1 HG00609.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.291+1849A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245689 | ||||||
chr2:245778
|
T | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(11): Show | 18 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.291+1760A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245778 | ||||||
chr2:245806
|
G | A | 1 | a0001c0002t0002g0242 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.291+1732C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 245806 | ||||||
chr2:246077
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.291+1461G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246077 | ||||||
chr2:246156
|
T | C | 1 | a0001c0004t0001g0141 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.291+1382A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246156 | ||||||
chr2:246211
|
A | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0107a0001c0001t0001g0108 | 4 | HG01074.hp2 HG01099.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1327T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246211 | ||||||
chr2:246301
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.291+1237A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246301 | ||||||
chr2:246435
|
C | A | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+1103G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246435 | ||||||
chr2:246592
|
GGAAAGGG others(3): Show |
G | 1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.291+936_291+945del others(10): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246592 | ||||||
chr2:246651
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.291+887T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246651 | ||||||
chr2:246800
|
GAATA | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(13): Show | 32 | HG00673.hp1 HG01346.hp1 HG01952.hp1 others(29): Show |
intron_variant | MODIFIER | c.291+734_291+737del others(4): Show |
SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246800 | ||||||
chr2:246875
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.291+663G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246875 | ||||||
chr2:246974
|
G | A | 1 | a0001c0004t0001g0141 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.291+564C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 246974 | ||||||
chr2:247138
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291+400T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247138 | ||||||
chr2:247303
|
A | T | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.291+235T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247303 | ||||||
chr2:247319
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0004g0128 | 3 | HG00642.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.291+219C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247319 | ||||||
chr2:247466
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.291+72T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 4/9 | chr2 | 247466 | ||||||
chr2:247620
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.227-18C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 247620 | ||||||
chr2:247635
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.227-33T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 247635 | ||||||
chr2:248037
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(130): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.227-435T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248037 | ||||||
chr2:248340
|
A | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0155a0001c0003t0001g0181 | 4 | HG03704.hp1 HG03942.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-738T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248340 | ||||||
chr2:248375
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.227-773A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248375 | ||||||
chr2:248428
|
G | A | 1 | a0001c0002t0002g0244 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.227-826C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248428 | ||||||
chr2:248644
|
T | G | 1 | a0001c0002t0002g0245 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.227-1042A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248644 | ||||||
chr2:248754
|
T | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18984.hp1 NA19080.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.226+977A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248754 | ||||||
chr2:248759
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.226+972G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248759 | ||||||
chr2:248822
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.226+909T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248822 | ||||||
chr2:248910
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.226+821G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 248910 | ||||||
chr2:249092
|
A | C | 72 | a0001c0001t0001g0034a0001c0001t0001g0125a0001c0001t0002g0200others(69): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.226+639T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249092 | ||||||
chr2:249337
|
T | A | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.226+394A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249337 | ||||||
chr2:249463
|
C | T | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.226+268G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249463 | ||||||
chr2:249586
|
G | A | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.226+145C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249586 | ||||||
chr2:249598
|
G | A | 1 | a0001c0001t0001g0042 | 2 | HG02074.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.226+133C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 3/9 | chr2 | 249598 | ||||||
chr2:249919
|
G | C | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0004g0126others(2): Show | 5 | HG00642.hp1 HG01109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-75C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 249919 | ||||||
chr2:250008
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078 | 3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.113-164G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250008 | ||||||
chr2:250195
|
TA | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 6 | HG01891.hp1 HG02647.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-352delT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250195 | ||||||
chr2:250219
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.113-375A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250219 | ||||||
chr2:250332
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.113-488A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250332 | ||||||
chr2:250412
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.113-568A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250412 | ||||||
chr2:250541
|
C | T | 1 | a0001c0002t0002g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-697G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250541 | ||||||
chr2:250562
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.113-718G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250562 | ||||||
chr2:250584
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.113-740T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250584 | ||||||
chr2:250751
|
C | A | 1 | a0001c0002t0002g0246 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.113-907G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250751 | ||||||
chr2:250806
|
T | C | 1 | a0001c0002t0002g0247 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113-962A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250806 | ||||||
chr2:250902
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.113-1058A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250902 | ||||||
chr2:250936
|
T | C | 2 | a0001c0002t0002g0205a0001c0002t0002g0206 | 2 | NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.113-1092A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250936 | ||||||
chr2:250958
|
A | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 14 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.113-1114T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250958 | ||||||
chr2:250982
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.113-1138G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 250982 | ||||||
chr2:251104
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.113-1260T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251104 | ||||||
chr2:251369
|
T | C | 1 | a0001c0002t0002g0247 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113-1525A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251369 | ||||||
chr2:251379
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.113-1535T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251379 | ||||||
chr2:251388
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.113-1544G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251388 | ||||||
chr2:251449
|
G | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18984.hp1 NA19080.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.112+1556C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251449 | ||||||
chr2:251514
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.112+1491G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251514 | ||||||
chr2:251534
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.112+1471G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251534 | ||||||
chr2:251535
|
G | A | 1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.112+1470C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251535 | ||||||
chr2:251606
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0008t0001g0193 | 3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.112+1399C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251606 | ||||||
chr2:251673
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.112+1332C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251673 | ||||||
chr2:251774
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.112+1231C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251774 | ||||||
chr2:251839
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.112+1166T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251839 | ||||||
chr2:251877
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.112+1128T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 251877 | ||||||
chr2:252197
|
C | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.112+808G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252197 | ||||||
chr2:252309
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.112+696T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252309 | ||||||
chr2:252340
|
C | A | 1 | a0001c0001t0005g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.112+665G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252340 | ||||||
chr2:252418
|
A | G | 1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.112+587T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252418 | ||||||
chr2:252471
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.112+534T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252471 | ||||||
chr2:252692
|
C | T | 3 | a0001c0002t0002g0210a0001c0002t0002g0211a0001c0002t0002g0212 | 3 | HG02809.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.112+313G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 2/9 | chr2 | 252692 | ||||||
chr2:253227
|
G | A | 4 | a0001c0001t0002g0200a0001c0001t0002g0202a0001c0001t0002g0203others(1): Show | 4 | HG02572.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2-112C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253227 | ||||||
chr2:253291
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(66): Show | 94 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.2-176T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253291 | ||||||
chr2:253348
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG03540.hp2 NA18964.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2-233G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253348 | ||||||
chr2:253411
|
A | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(155): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2-296T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253411 | ||||||
chr2:253468
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2-353G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253468 | ||||||
chr2:253469
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2-354C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253469 | ||||||
chr2:253533
|
G | C | 1 | a0001c0002t0002g0250 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2-418C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253533 | ||||||
chr2:253566
|
C | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(155): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.2-451G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253566 | ||||||
chr2:253604
|
A | G | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2-489T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253604 | ||||||
chr2:253636
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2-521T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253636 | ||||||
chr2:253760
|
C | G | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2-645G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253760 | ||||||
chr2:253833
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2-718T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253833 | ||||||
chr2:253953
|
C | T | 1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2-838G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 253953 | ||||||
chr2:254215
|
G | A | 71 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0001g0130others(68): Show | 102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.2-1100C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254215 | ||||||
chr2:254393
|
G | A | 1 | a0001c0002t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2-1278C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254393 | ||||||
chr2:254488
|
G | C | 1 | a0001c0001t0007g0194 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2-1373C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254488 | ||||||
chr2:254510
|
G | A | 2 | a0001c0002t0002g0249a0001c0002t0002g0254 | 2 | NA18968.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2-1395C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254510 | ||||||
chr2:254791
|
T | C | 1 | a0001c0002t0002g0250 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2-1676A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254791 | ||||||
chr2:254882
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2-1767T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254882 | ||||||
chr2:254972
|
G | C | 2 | a0001c0001t0004g0126a0001c0001t0004g0127 | 2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2-1857C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 254972 | ||||||
chr2:255062
|
C | G | 1 | a0001c0001t0002g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2-1947G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255062 | ||||||
chr2:255073
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2-1958G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255073 | ||||||
chr2:255154
|
T | C | 1 | a0001c0001t0001g0033 | 2 | HG02647.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2-2039A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255154 | ||||||
chr2:255262
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2-2147T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255262 | ||||||
chr2:255446
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2-2331T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255446 | ||||||
chr2:255497
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0007g0194 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2-2382C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255497 | ||||||
chr2:255580
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2-2465C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255580 | ||||||
chr2:255581
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2-2466C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255581 | ||||||
chr2:255674
|
G | A | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2-2559C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255674 | ||||||
chr2:255729
|
GA | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0103others(9): Show | 16 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2-2615delT | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 255729 | ||||||
chr2:256116
|
G | T | 78 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0001g0125others(75): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.2-3001C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256116 | ||||||
chr2:256278
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0034others(55): Show | 86 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2-3163A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256278 | ||||||
chr2:256278
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2-3163A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256278 | ||||||
chr2:256295
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2-3180T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256295 | ||||||
chr2:256414
|
G | A | 1 | a0001c0001t0001g0043 | 2 | HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.2-3299C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256414 | ||||||
chr2:256440
|
C | G | 12 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 16 | HG00597.hp1 HG02074.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.2-3325G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256440 | ||||||
chr2:256529
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2-3414A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256529 | ||||||
chr2:256839
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2-3724G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256839 | ||||||
chr2:256841
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2-3726T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256841 | ||||||
chr2:256897
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2-3782G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 256897 | ||||||
chr2:257206
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2-4091G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257206 | ||||||
chr2:257341
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2-4226G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257341 | ||||||
chr2:257432
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2-4317A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257432 | ||||||
chr2:257434
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2-4319A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257434 | ||||||
chr2:257635
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078 | 3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2-4520C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257635 | ||||||
chr2:257725
|
C | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2-4610G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257725 | ||||||
chr2:257733
|
A | G | 3 | a0001c0001t0001g0105a0001c0001t0001g0187a0001c0007t0001g0106 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2-4618T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257733 | ||||||
chr2:257763
|
A | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0078 | 3 | HG02622.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2-4648T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257763 | ||||||
chr2:257820
|
G | GT | 5 | a0001c0001t0001g0077a0001c0001t0001g0132a0001c0001t0001g0182others(2): Show | 5 | HG00544.hp1 HG00741.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2-4706dupA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257820 | ||||||
chr2:257900
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2-4785A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257900 | ||||||
chr2:257907
|
T | C | 1 | a0001c0001t0004g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2-4792A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257907 | ||||||
chr2:257991
|
C | T | 2 | a0001c0002t0002g0205a0001c0002t0002g0206 | 2 | NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2-4876G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257991 | ||||||
chr2:257992
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(7): Show | 14 | HG01106.hp1 HG01167.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2-4877C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 257992 | ||||||
chr2:258210
|
T | C | 65 | a0001c0001t0001g0125a0001c0001t0008g0253a0001c0002t0002g0003others(62): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.2-5095A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258210 | ||||||
chr2:258463
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2-5348G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258463 | ||||||
chr2:258546
|
A | C | 1 | a0001c0001t0001g0050 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2-5431T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258546 | ||||||
chr2:258763
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1+5221C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258763 | ||||||
chr2:258767
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0104 | 4 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1+5217G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258767 | ||||||
chr2:258790
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1+5194C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258790 | ||||||
chr2:258938
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1+5046C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 258938 | ||||||
chr2:259015
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1+4969A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259015 | ||||||
chr2:259221
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1+4763C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259221 | ||||||
chr2:259296
|
C | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1+4688G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259296 | ||||||
chr2:259588
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1+4396C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259588 | ||||||
chr2:259772
|
C | T | 1 | a0001c0002t0002g0201 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1+4212G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259772 | ||||||
chr2:259774
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1+4210A>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 259774 | ||||||
chr2:260049
|
T | C | 1 | a0001c0001t0008g0253 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1+3935A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260049 | ||||||
chr2:260107
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1+3877T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260107 | ||||||
chr2:260303
|
T | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0008t0001g0193 | 3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1+3681A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260303 | ||||||
chr2:260378
|
T | C | 2 | a0001c0001t0006g0195a0001c0001t0006g0196 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1+3606A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260378 | ||||||
chr2:260391
|
T | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1+3593A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260391 | ||||||
chr2:260402
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1+3582C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260402 | ||||||
chr2:260594
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(250): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1+3390T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260594 | ||||||
chr2:260661
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1+3323G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260661 | ||||||
chr2:260677
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(73): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1+3307C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 260677 | ||||||
chr2:261432
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1+2552G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261432 | ||||||
chr2:261433
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1+2551G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261433 | ||||||
chr2:261478
|
A | G | 1 | a0001c0002t0002g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1+2506T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261478 | ||||||
chr2:261513
|
AT | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0097a0001c0001t0001g0098others(4): Show | 9 | HG01243.hp1 HG01256.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1+2470delA | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261513 | ||||||
chr2:261524
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1+2460T>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261524 | ||||||
chr2:261800
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1+2184G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261800 | ||||||
chr2:261839
|
T | C | 1 | a0001c0003t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1+2145A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 261839 | ||||||
chr2:262119
|
T | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(26): Show | 39 | HG00738.hp2 HG01069.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1+1865A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262119 | ||||||
chr2:262189
|
G | C | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0008t0001g0193 | 3 | HG01884.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1+1795C>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262189 | ||||||
chr2:262250
|
C | T | 3 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128 | 3 | HG00642.hp1 HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1+1734G>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262250 | ||||||
chr2:262297
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1+1687T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262297 | ||||||
chr2:262335
|
A | G | 71 | a0001c0001t0001g0125a0001c0001t0002g0200a0001c0001t0002g0202others(68): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1+1649T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262335 | ||||||
chr2:262408
|
C | G | 1 | a0001c0002t0002g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1+1576G>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262408 | ||||||
chr2:262490
|
G | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | HG00408.hp1 HG00438.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1+1494C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262490 | ||||||
chr2:262553
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(156): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1+1431A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262553 | ||||||
chr2:262886
|
A | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0068others(5): Show | 11 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1+1098T>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 262886 | ||||||
chr2:263270
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1+714A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263270 | ||||||
chr2:263392
|
A | G | 1 | a0001c0002t0002g0197 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1+592T>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263392 | ||||||
chr2:263435
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1+549G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263435 | ||||||
chr2:263540
|
G | T | 1 | a0001c0002t0002g0254 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1+444C>A | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263540 | ||||||
chr2:263541
|
T | C | 1 | a0001c0008t0001g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1+443A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263541 | ||||||
chr2:263542
|
T | G | 1 | a0001c0002t0002g0254 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1+442A>C | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263542 | ||||||
chr2:263666
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 5 | HG00621.hp2 NA18968.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.1+318C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263666 | ||||||
chr2:263709
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1+275C>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263709 | ||||||
chr2:263938
|
T | C | 1 | a0001c0008t0001g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1+46A>G | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263938 | ||||||
chr2:263972
|
C | A | 1 | a0001c0002t0002g0254 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1+12G>T | SH3YL1 | ENSG00000035115.22 | transcript | ENST00000356150.10 | protein_coding | 1/9 | chr2 | 263972 |