Item | Value |
---|---|
geneid | 29106 |
ensemblid | ENSG00000104112.9 |
hgncid | 13707 |
symbol | SCG3 |
name | secretogranin III |
refseq_nuc | NM_013243.4 |
refseq_prot | NP_037375.2 |
ensembl_nuc | ENST00000220478.8 |
ensembl_prot | ENSP00000220478.3 |
mane_status | MANE Select |
chr | chr15 |
start | 51681503 |
end | 51721026 |
strand | + |
ver | v1.2 |
region | chr15:51681503-51721026 |
region5000 | chr15:51676503-51726026 |
regionname0 | SCG3_chr15_51681503_51721026 |
regionname5000 | SCG3_chr15_51676503_51726026 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 468 | 352 | 62 | 72 | 164 | 12 | 40 | 137 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0002 | 0/0 | 468 | 31 | 30 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0003 | 0/0 | 468 | 14 | 0 | 5 | 7 | 0 | 2 | 6 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0004 | 0/0 | 468 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0005 | 0/0 | 468 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0006 | 0/0 | 468 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1407 | 312 | 54 | 69 | 137 | 11 | 39 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0002 | 0/0 | 1407 | 34 | 6 | 1 | 27 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0003 | 0/0 | 1407 | 30 | 29 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0004 | 0/0 | 1407 | 14 | 0 | 5 | 7 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0005 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0006 | 0/0 | 1407 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0007 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0008 | 0/0 | 1407 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0009 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0010 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0011 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
c0012 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1754 | 128 | 22 | 33 | 53 | 8 | 11 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0002 | 1/0 | 1754 | 109 | 17 | 10 | 68 | 0 | 13 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0003 | 0/0 | 1754 | 79 | 32 | 29 | 0 | 3 | 15 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0004 | 0/0 | 1754 | 25 | 2 | 1 | 21 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0005 | 0/0 | 1754 | 17 | 5 | 0 | 10 | 1 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0006 | 0/0 | 1754 | 17 | 0 | 0 | 16 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0007 | 0/0 | 1754 | 7 | 7 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0008 | 0/0 | 1754 | 5 | 3 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0009 | 0/0 | 1754 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0010 | 0/0 | 1754 | 3 | 3 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0011 | 0/0 | 1754 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0012 | 0/0 | 1754 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0013 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0014 | 0/0 | 1754 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0015 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
t0016 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1407 | 312 | 54 | 69 | 137 | 11 | 39 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0001c0002 | 0/0 | 1407 | 34 | 6 | 1 | 27 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0001c0005 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0001c0006 | 0/0 | 1407 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0001c0010 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0001c0011 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0002c0003 | 0/0 | 1407 | 30 | 29 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0002c0009 | 0/0 | 1407 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0003c0004 | 0/0 | 1407 | 14 | 0 | 5 | 7 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0004c0008 | 0/0 | 1407 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0005c0007 | 0/0 | 1407 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 | |
a0006c0012 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3160 | 111 | 19 | 29 | 45 | 7 | 10 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0002 | 1/0 | 3160 | 104 | 17 | 10 | 65 | 0 | 11 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0003 | 0/0 | 3160 | 52 | 7 | 27 | 0 | 3 | 15 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0004 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0005 | 0/0 | 3160 | 13 | 2 | 0 | 9 | 1 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0006 | 0/0 | 3160 | 13 | 0 | 0 | 12 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0007 | 0/0 | 3160 | 5 | 5 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0008 | 0/0 | 3160 | 5 | 3 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0009 | 0/0 | 3160 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0013 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0014 | 0/0 | 3160 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0015 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0001t0016 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0002t0001 | 0/0 | 3160 | 5 | 1 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0002t0002 | 0/0 | 3160 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0002t0004 | 0/0 | 3160 | 24 | 2 | 1 | 21 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0002t0010 | 0/0 | 3160 | 3 | 3 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0005t0005 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0006t0011 | 0/0 | 3160 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0010t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0001c0011t0001 | 0/0 | 3160 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0002c0003t0001 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0002c0003t0003 | 0/0 | 3160 | 25 | 24 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0002c0003t0005 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0002c0003t0012 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0002c0009t0003 | 0/0 | 3160 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0003c0004t0001 | 0/0 | 3160 | 6 | 0 | 4 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0003c0004t0002 | 0/0 | 3160 | 3 | 0 | 0 | 1 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0003c0004t0003 | 0/0 | 3160 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0003c0004t0006 | 0/0 | 3160 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0004c0008t0001 | 0/0 | 3160 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0005c0007t0007 | 0/0 | 3160 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
a0006c0012t0005 | 0/0 | 3160 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | copy fasta | chr15 | 51676503 | 51726026 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0002g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0008g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0013g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0014g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0001t0016g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0004g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0010g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0010g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0002t0010g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0005t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0005t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0006t0011g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0010t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0001c0011t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0003g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0005g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0012g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0003t0012g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0002c0009t0003g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0003c0004t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0004c0008t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0004c0008t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0005c0007t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0005c0007t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
a0006c0012t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0334 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0283 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | GBR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0027 | EUR | FIN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00423 | hp1 | a0001 | c0002 | t0004 | g0358 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG00741 | hp2 | a0001 | c0001 | t0014 | g0159 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01167 | hp2 | a0001 | c0006 | t0011 | g0010 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0286 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01169 | hp2 | a0001 | c0006 | t0011 | g0010 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01255 | hp1 | a0002 | c0003 | t0003 | g0368 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01257 | hp2 | a0001 | c0002 | t0004 | g0350 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01258 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01433 | hp2 | a0003 | c0004 | t0003 | g0253 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0039 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01517 | hp1 | a0001 | c0010 | t0001 | g0321 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0050 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0343 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01891 | hp2 | a0002 | c0003 | t0003 | g0382 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01975 | hp2 | a0003 | c0004 | t0001 | g0263 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01981 | hp2 | a0003 | c0004 | t0001 | g0264 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01993 | hp2 | a0003 | c0004 | t0001 | g0272 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02055 | hp1 | a0002 | c0003 | t0003 | g0059 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02055 | hp2 | a0002 | c0003 | t0003 | g0373 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02056 | hp2 | a0001 | c0002 | t0004 | g0345 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02155 | hp2 | a0003 | c0004 | t0001 | g0022 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CDX | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02257 | hp1 | a0002 | c0003 | t0003 | g0379 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02280 | hp2 | a0002 | c0003 | t0003 | g0364 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02293 | hp1 | a0003 | c0004 | t0001 | g0247 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02572 | hp2 | a0002 | c0003 | t0012 | g0362 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02602 | hp2 | a0003 | c0004 | t0002 | g0273 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02615 | hp2 | a0001 | c0002 | t0010 | g0340 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02622 | hp1 | a0005 | c0007 | t0007 | g0062 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02622 | hp2 | a0002 | c0003 | t0003 | g0375 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02630 | hp1 | a0002 | c0003 | t0003 | g0365 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0290 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0323 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0389 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02717 | hp2 | a0005 | c0007 | t0007 | g0061 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0363 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02809 | hp2 | a0002 | c0009 | t0003 | g0378 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02818 | hp1 | a0002 | c0003 | t0003 | g0060 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02895 | hp2 | a0002 | c0003 | t0003 | g0366 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02896 | hp1 | a0002 | c0003 | t0003 | g0380 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02922 | hp1 | a0001 | c0005 | t0005 | g0089 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02965 | hp2 | a0002 | c0003 | t0003 | g0371 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03098 | hp1 | a0002 | c0003 | t0003 | g0057 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03130 | hp1 | a0002 | c0003 | t0003 | g0367 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03130 | hp2 | a0001 | c0001 | t0016 | g0088 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03139 | hp1 | a0002 | c0003 | t0003 | g0383 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03139 | hp2 | a0002 | c0003 | t0003 | g0303 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03195 | hp1 | a0002 | c0003 | t0003 | g0360 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03225 | hp2 | a0002 | c0003 | t0001 | g0056 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0325 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03453 | hp1 | a0002 | c0003 | t0003 | g0377 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03486 | hp1 | a0002 | c0003 | t0005 | g0381 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03516 | hp1 | a0001 | c0002 | t0010 | g0342 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03516 | hp2 | a0002 | c0003 | t0003 | g0372 | AFR | ESN | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03540 | hp2 | a0002 | c0003 | t0003 | g0384 | AFR | GWD | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03579 | hp2 | a0001 | c0005 | t0005 | g0090 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0324 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03834 | hp1 | a0001 | c0011 | t0001 | g0187 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0231 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04184 | hp1 | a0003 | c0004 | t0002 | g0268 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0086 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | STU | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0226 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18906 | hp1 | a0002 | c0003 | t0003 | g0374 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18906 | hp2 | a0001 | c0002 | t0004 | g0359 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18939 | hp2 | a0001 | c0002 | t0004 | g0012 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18942 | hp2 | a0001 | c0002 | t0004 | g0351 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18943 | hp2 | a0001 | c0002 | t0004 | g0354 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18946 | hp2 | a0001 | c0002 | t0004 | g0355 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18951 | hp1 | a0001 | c0002 | t0004 | g0346 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18953 | hp1 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18954 | hp2 | a0001 | c0002 | t0004 | g0387 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18964 | hp1 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18964 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18965 | hp2 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18966 | hp2 | a0001 | c0002 | t0004 | g0386 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18972 | hp2 | a0001 | c0001 | t0009 | g0185 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18973 | hp2 | a0004 | c0008 | t0001 | g0251 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18977 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18977 | hp2 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18978 | hp1 | a0006 | c0012 | t0005 | g0079 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18979 | hp2 | a0001 | c0002 | t0004 | g0344 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18981 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18983 | hp2 | a0003 | c0004 | t0001 | g0266 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18987 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18987 | hp2 | a0003 | c0004 | t0006 | g0262 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18992 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18993 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19003 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19004 | hp2 | a0001 | c0001 | t0009 | g0172 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19005 | hp1 | a0001 | c0001 | t0013 | g0221 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19006 | hp2 | a0003 | c0004 | t0006 | g0271 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19007 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19009 | hp1 | a0001 | c0002 | t0004 | g0356 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19030 | hp2 | a0002 | c0003 | t0003 | g0376 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0058 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19057 | hp2 | a0003 | c0004 | t0002 | g0265 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19062 | hp1 | a0001 | c0001 | t0009 | g0186 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19062 | hp2 | a0003 | c0004 | t0006 | g0261 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19072 | hp2 | a0001 | c0002 | t0004 | g0388 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19076 | hp2 | a0001 | c0002 | t0004 | g0385 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19077 | hp2 | a0001 | c0002 | t0004 | g0352 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19081 | hp2 | a0001 | c0002 | t0004 | g0015 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19083 | hp1 | a0004 | c0008 | t0001 | g0252 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19086 | hp1 | a0001 | c0002 | t0004 | g0348 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0220 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19090 | hp2 | a0003 | c0004 | t0006 | g0270 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0066 | AFR | YRI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20129 | hp1 | a0001 | c0002 | t0010 | g0341 | AFR | ASW | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ASW | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0318 | EUR | TSI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0326 | EUR | TSI | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | GIH | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0072 | SAS | GIH | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02486 | hp2 | a0002 | c0003 | t0003 | g0055 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02559 | hp1 | a0001 | c0002 | t0004 | g0347 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03471 | hp1 | a0002 | c0003 | t0003 | g0369 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG03471 | hp2 | a0002 | c0003 | t0012 | g0370 | AFR | MSL | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0048 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | USA | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | LWK | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0335 | REF | REF | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0046 | REF | REF | SCG3_chr15_51676503_51726026 | SCG3 | chr15 | 51676503 | 51726026 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51683411 | G | A | 1 | a0003 | 14 | HG01433.hp2 HG01975.hp2 HG01981.hp2 others(11): Show |
missense_variant | MODERATE | c.374G>A | p.Ser125Asn | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/12 | 627/3160 | 374/1407 | 125/468 | chr15 | 51683411 | ||
chr15:51688293 | C | T | 1 | a0006 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.431C>T | p.Thr144Ile | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/12 | 684/3160 | 431/1407 | 144/468 | chr15 | 51688293 | ||
chr15:51692165 | A | G | 1 | a0002 | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
missense_variant | MODERATE | c.697A>G | p.Met233Val | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/12 | 950/3160 | 697/1407 | 233/468 | chr15 | 51692165 | ||
chr15:51701121 | A | G | 1 | a0004 | 2 | NA18973.hp2 NA19083.hp1 |
missense_variant | MODERATE | c.1084A>G | p.Ser362Gly | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/12 | 1337/3160 | 1084/1407 | 362/468 | chr15 | 51701121 | ||
chr15:51719507 | G | A | 1 | a0005 | 2 | HG02622.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.1388G>A | p.Arg463His | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1641/3160 | 1388/1407 | 463/468 | chr15 | 51719507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51683349 | T | C | 2 | a0001c0005a0002c0009 | 3 | HG02809.hp2 HG02922.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.312T>C | p.Asn104Asn | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/12 | 565/3160 | 312/1407 | 104/468 | chr15 | 51683349 | ||
chr15:51683388 | C | A | 1 | a0001c0002 | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
synonymous_variant | LOW | c.351C>A | p.Ile117Ile | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/12 | 604/3160 | 351/1407 | 117/468 | chr15 | 51683388 | ||
chr15:51688378 | T | G | 1 | a0001c0006 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.516T>G | p.Val172Val | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/12 | 769/3160 | 516/1407 | 172/468 | chr15 | 51688378 | ||
chr15:51692317 | A | G | 1 | a0001c0006 | 2 | HG01167.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.849A>G | p.Leu283Leu | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/12 | 1102/3160 | 849/1407 | 283/468 | chr15 | 51692317 | ||
chr15:51695954 | T | C | 1 | a0001c0010 | 1 | HG01517.hp1 | synonymous_variant | LOW | c.948T>C | p.Tyr316Tyr | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/12 | 1201/3160 | 948/1407 | 316/468 | chr15 | 51695954 | ||
chr15:51719472 | C | T | 1 | a0001c0011 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1353C>T | p.Gly451Gly | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1606/3160 | 1353/1407 | 451/468 | chr15 | 51719472 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51681633 | C | A | 1 | a0001c0006t0011 | 2 | HG01167.hp2 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/12 | 123 | chr15 | 51681633 | |||||
chr15:51681688 | C | G | 1 | a0001c0001t0016 | 1 | HG03130.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/12 | chr15 | 51681688 | ||||||
chr15:51719528 | A | G | 2 | a0001c0001t0007a0005c0007t0007 | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 2 | chr15 | 51719528 | |||||
chr15:51719575 | A | G | 1 | a0001c0001t0015 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 49 | chr15 | 51719575 | |||||
chr15:51719610 | T | G | 2 | a0001c0001t0007a0005c0007t0007 | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*84T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 84 | chr15 | 51719610 | |||||
chr15:51719779 | C | G | 1 | a0001c0001t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*253C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 253 | chr15 | 51719779 | |||||
chr15:51719806 | T | C | 1 | a0001c0001t0008 | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*280T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 280 | chr15 | 51719806 | |||||
chr15:51719866 | G | A | 1 | a0001c0001t0008 | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 340 | chr15 | 51719866 | |||||
chr15:51720188 | G | C | 1 | a0001c0001t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 662 | chr15 | 51720188 | |||||
chr15:51720255 | A | G | 1 | a0001c0001t0013 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*729A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 729 | chr15 | 51720255 | |||||
chr15:51720433 | C | G | 2 | a0001c0001t0007a0005c0007t0007 | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*907C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 907 | chr15 | 51720433 | |||||
chr15:51720453 | G | A | 1 | a0001c0001t0009 | 4 | NA18972.hp2 NA18977.hp1 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*927G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 927 | chr15 | 51720453 | |||||
chr15:51720603 | T | C | 1 | a0001c0002t0010 | 3 | HG02615.hp2 HG03516.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1077 | chr15 | 51720603 | |||||
chr15:51720703 | A | C | 1 | a0002c0003t0012 | 2 | HG02572.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1177A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1177 | chr15 | 51720703 | |||||
chr15:51720814 | A | G | 2 | a0001c0001t0006a0003c0004t0006 | 17 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1288A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1288 | chr15 | 51720814 | |||||
chr15:51720826 | T | G | 4 | a0001c0001t0005a0001c0005t0005a0002c0003t0005others(1): Show | 17 | HG00140.hp1 HG02145.hp1 HG02922.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1300T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1300 | chr15 | 51720826 | |||||
chr15:51720904 | G | A | 5 | a0001c0001t0003a0002c0003t0003a0002c0003t0012others(2): Show | 81 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1378G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1378 | chr15 | 51720904 | |||||
chr15:51720950 | C | T | 1 | a0001c0006t0011 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1424C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1424 | chr15 | 51720950 | |||||
chr15:51720951 | A | G | 21 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(18): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*1425A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1425 | chr15 | 51720951 | |||||
chr15:51720968 | G | A | 2 | a0001c0001t0007a0005c0007t0007 | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1442G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1442 | chr15 | 51720968 | |||||
chr15:51720974 | C | T | 10 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(7): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1448C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1448 | chr15 | 51720974 | |||||
chr15:51721023 | T | C | 2 | a0001c0001t0007a0005c0007t0007 | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1497T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 12/12 | 1497 | chr15 | 51721023 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:51681906 | T | C | 1 | a0001c0001t0002g0011 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.82+69T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51681906 | ||||||
chr15:51681916 | G | A | 10 | a0001c0002t0001g0021a0001c0002t0002g0016a0001c0002t0002g0019others(7): Show | 10 | NA18939.hp2 NA18964.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.82+79G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51681916 | ||||||
chr15:51681999 | C | T | 1 | a0001c0001t0002g0389 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.82+162C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51681999 | ||||||
chr15:51682027 | A | G | 59 | a0001c0001t0001g0361a0001c0002t0001g0021a0001c0002t0001g0343others(56): Show | 59 | HG00423.hp1 HG01255.hp1 HG01257.hp2 others(56): Show |
intron_variant | MODIFIER | c.82+190A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682027 | ||||||
chr15:51682053 | A | G | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.82+216A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682053 | ||||||
chr15:51682232 | G | A | 1 | a0003c0004t0001g0022 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.83-285G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682232 | ||||||
chr15:51682236 | A | G | 354 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(351): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.83-281A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682236 | ||||||
chr15:51682256 | A | G | 4 | a0001c0002t0004g0385a0001c0002t0004g0386a0001c0002t0004g0387others(1): Show | 4 | NA18954.hp2 NA18966.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-261A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682256 | ||||||
chr15:51682276 | G | GAA | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.83-230_83-229dupAA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 51682276 | |||||
chr15:51682315 | C | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.83-202C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682315 | ||||||
chr15:51682321 | GATAATAA others(8): Show |
G | 1 | a0001c0001t0001g0339 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.83-192_83-178delAT others(13): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr15 | 51682321 | |||||
chr15:51682442 | A | C | 30 | a0001c0002t0001g0021a0001c0002t0001g0349a0001c0002t0001g0353others(27): Show | 30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.83-75A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 1/11 | chr15 | 51682442 | ||||||
chr15:51682713 | A | T | 111 | a0001c0001t0001g0007a0001c0001t0001g0232a0001c0001t0001g0233others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.135+144A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682713 | ||||||
chr15:51682753 | C | T | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.135+184C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682753 | ||||||
chr15:51682788 | A | G | 128 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(125): Show | 131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.135+219A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682788 | ||||||
chr15:51682914 | A | T | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.136-165A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 2/11 | chr15 | 51682914 | ||||||
chr15:51683135 | A | ATCATATT others(39): Show |
1 | a0001c0001t0005g0093 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.181+13_182-37dupCA others(44): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr15 | 51683135 | |||||
chr15:51683543 | G | A | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.397+109G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683543 | ||||||
chr15:51683561 | A | G | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+127A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683561 | ||||||
chr15:51683714 | ATTTAT | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+285_397+289del others(5): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51683714 | |||||
chr15:51683770 | G | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+336G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683770 | ||||||
chr15:51683919 | G | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+485G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683919 | ||||||
chr15:51683938 | A | C | 1 | a0001c0001t0002g0092 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.397+504A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683938 | ||||||
chr15:51683949 | T | C | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.397+515T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683949 | ||||||
chr15:51683965 | C | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+531C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51683965 | ||||||
chr15:51684011 | C | A | 31 | a0001c0001t0001g0361a0002c0003t0001g0056a0002c0003t0001g0363others(28): Show | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.397+577C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684011 | ||||||
chr15:51684033 | G | T | 354 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(351): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.397+599G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684033 | ||||||
chr15:51684155 | A | C | 1 | a0001c0001t0002g0218 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.397+721A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684155 | ||||||
chr15:51684218 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.397+784T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684218 | ||||||
chr15:51684241 | G | A | 25 | a0001c0001t0001g0361a0002c0003t0001g0363a0002c0003t0003g0360others(22): Show | 25 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.397+807G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684241 | ||||||
chr15:51684422 | C | T | 299 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(296): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.397+988C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684422 | ||||||
chr15:51684509 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.397+1075A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684509 | ||||||
chr15:51684533 | C | T | 30 | a0001c0002t0001g0021a0001c0002t0001g0349a0001c0002t0001g0353others(27): Show | 30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.397+1099C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684533 | ||||||
chr15:51684555 | C | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1121C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684555 | ||||||
chr15:51684592 | A | G | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1158A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684592 | ||||||
chr15:51684880 | A | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1446A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684880 | ||||||
chr15:51684882 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.397+1448A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684882 | ||||||
chr15:51684962 | C | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1528C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684962 | ||||||
chr15:51684974 | G | A | 24 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0002g0006others(21): Show | 25 | HG01496.hp2 HG03098.hp2 HG04204.hp1 others(22): Show |
intron_variant | MODIFIER | c.397+1540G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51684974 | ||||||
chr15:51685014 | A | G | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1580A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685014 | ||||||
chr15:51685115 | C | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+1681C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685115 | ||||||
chr15:51685200 | T | A | 31 | a0001c0001t0001g0361a0002c0003t0001g0056a0002c0003t0001g0363others(28): Show | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.397+1766T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685200 | ||||||
chr15:51685353 | C | G | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+1919C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685353 | ||||||
chr15:51685396 | G | A | 10 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 11 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+1962G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685396 | ||||||
chr15:51685397 | A | G | 1 | a0001c0005t0005g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.397+1963A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685397 | ||||||
chr15:51685466 | T | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+2032T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685466 | ||||||
chr15:51685469 | A | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.397+2035A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51685469 | ||||||
chr15:51686104 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.398-2156T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686104 | ||||||
chr15:51686111 | G | C | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.398-2149G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686111 | ||||||
chr15:51686524 | C | A | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.398-1736C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686524 | ||||||
chr15:51686565 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.398-1695G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686565 | ||||||
chr15:51686585 | G | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1675G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686585 | ||||||
chr15:51686588 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.398-1672A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686588 | ||||||
chr15:51686628 | G | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1632G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686628 | ||||||
chr15:51686641 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.398-1619C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686641 | ||||||
chr15:51686681 | A | ATGTT | 35 | a0001c0001t0001g0091a0001c0001t0001g0228a0001c0001t0002g0006others(32): Show | 36 | HG00597.hp2 HG02145.hp1 HG02922.hp1 others(33): Show |
intron_variant | MODIFIER | c.398-1559_398-1556d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | |||||
chr15:51686681 | A | ATGTTTGT others(1): Show |
155 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(152): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.398-1563_398-1556d others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | |||||
chr15:51686681 | A | ATGTTTGT others(5): Show |
120 | a0001c0001t0001g0068a0001c0001t0001g0115a0001c0001t0001g0120others(117): Show | 123 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.398-1567_398-1556d others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | |||||
chr15:51686681 | A | ATGTTTGT others(9): Show |
5 | a0001c0001t0001g0212a0001c0001t0002g0210a0001c0001t0002g0211others(2): Show | 5 | HG01261.hp1 HG02572.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-1571_398-1556d others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686681 | |||||
chr15:51686705 | A | T | 59 | a0001c0001t0001g0091a0001c0001t0002g0006a0001c0001t0002g0071others(56): Show | 60 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(57): Show |
intron_variant | MODIFIER | c.398-1555A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686705 | ||||||
chr15:51686709 | T | A | 4 | a0001c0002t0001g0343a0001c0002t0010g0340a0001c0002t0010g0341others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-1551T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686709 | ||||||
chr15:51686713 | T | A | 30 | a0001c0002t0001g0021a0001c0002t0001g0349a0001c0002t0001g0353others(27): Show | 30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.398-1547T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686713 | ||||||
chr15:51686721 | T | TTG | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1538_398-1537i others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr15 | 51686721 | |||||
chr15:51686725 | C | G | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1535C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686725 | ||||||
chr15:51686728 | A | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1532A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686728 | ||||||
chr15:51686729 | G | GTTTCTCA others(115): Show |
7 | a0001c0002t0001g0343a0001c0002t0004g0344a0001c0002t0004g0345others(4): Show | 7 | HG01891.hp1 HG02056.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-1531_398-1530i others(124): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686729 | ||||||
chr15:51686729 | G | GTTTGTTT others(119): Show |
26 | a0001c0002t0001g0349a0001c0002t0001g0353a0001c0002t0001g0357others(23): Show | 26 | HG00423.hp1 HG01257.hp2 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.398-1531_398-1530i others(128): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686729 | ||||||
chr15:51686729 | G | GTTTGTTT others(119): Show |
1 | a0001c0002t0001g0021 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.398-1531_398-1530i others(128): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686729 | ||||||
chr15:51686730 | G | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1530G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686730 | ||||||
chr15:51686731 | G | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1529G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686731 | ||||||
chr15:51686880 | A | G | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-1380A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686880 | ||||||
chr15:51686950 | G | A | 3 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0013g0221 | 3 | NA18953.hp1 NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.398-1310G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51686950 | ||||||
chr15:51687031 | T | C | 4 | a0001c0001t0002g0097a0001c0001t0002g0109a0001c0001t0002g0110others(1): Show | 4 | HG00544.hp2 HG01934.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-1229T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687031 | ||||||
chr15:51687099 | G | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-1161G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687099 | ||||||
chr15:51687233 | C | A | 1 | a0002c0003t0003g0360 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.398-1027C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687233 | ||||||
chr15:51687458 | C | T | 333 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(330): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.398-802C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687458 | ||||||
chr15:51687477 | G | A | 299 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(296): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.398-783G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687477 | ||||||
chr15:51687616 | G | A | 354 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(351): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.398-644G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687616 | ||||||
chr15:51687621 | C | T | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.398-639C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687621 | ||||||
chr15:51687755 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.398-505G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687755 | ||||||
chr15:51687791 | C | T | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.398-469C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687791 | ||||||
chr15:51687797 | C | T | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.398-463C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687797 | ||||||
chr15:51687912 | A | G | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-348A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687912 | ||||||
chr15:51687940 | A | G | 128 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(125): Show | 131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.398-320A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51687940 | ||||||
chr15:51688002 | T | G | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.398-258T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688002 | ||||||
chr15:51688114 | G | A | 354 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(351): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.398-146G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688114 | ||||||
chr15:51688135 | A | G | 1 | a0001c0001t0001g0330 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.398-125A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688135 | ||||||
chr15:51688249 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.398-11G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 4/11 | chr15 | 51688249 | ||||||
chr15:51688412 | T | G | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+10T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688412 | ||||||
chr15:51688415 | G | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+13G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688415 | ||||||
chr15:51688416 | T | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+14T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688416 | ||||||
chr15:51688417 | A | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.540+15A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688417 | ||||||
chr15:51688503 | T | C | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.540+101T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688503 | ||||||
chr15:51688508 | C | T | 2 | a0001c0001t0003g0053a0001c0001t0003g0054 | 2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.540+106C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688508 | ||||||
chr15:51688522 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540+120C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688522 | ||||||
chr15:51688553 | C | G | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.540+151C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688553 | ||||||
chr15:51688563 | TAGG | T | 120 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(117): Show | 123 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.540+164_540+166del others(3): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr15 | 51688563 | |||||
chr15:51688624 | C | T | 119 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.540+222C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688624 | ||||||
chr15:51688698 | A | G | 1 | a0001c0001t0007g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540+296A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688698 | ||||||
chr15:51688737 | A | C | 1 | a0002c0003t0003g0383 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.540+335A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688737 | ||||||
chr15:51688908 | G | A | 1 | a0001c0001t0003g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.541-311G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51688908 | ||||||
chr15:51689079 | G | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.541-140G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689079 | ||||||
chr15:51689094 | C | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(118): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.541-125C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689094 | ||||||
chr15:51689102 | T | C | 2 | a0001c0005t0005g0089a0001c0005t0005g0090 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.541-117T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689102 | ||||||
chr15:51689145 | G | A | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 5 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-74G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689145 | ||||||
chr15:51689151 | T | TCCACATT others(348): Show |
1 | a0001c0001t0001g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.541-54_541-53insTT others(353): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr15 | 51689151 | |||||
chr15:51689215 | A | G | 11 | a0001c0001t0002g0006a0001c0001t0002g0071a0001c0001t0002g0080others(8): Show | 12 | NA18939.hp1 NA18945.hp2 NA18947.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.541-4A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 5/11 | chr15 | 51689215 | ||||||
chr15:51689398 | G | GGT | 43 | a0001c0001t0001g0091a0001c0001t0001g0207a0001c0001t0001g0304others(40): Show | 44 | HG00408.hp2 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.690+31_690+32insTG | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | |||||
chr15:51689398 | G | GGTGT | 25 | a0001c0001t0001g0068a0001c0001t0001g0315a0001c0001t0001g0316others(22): Show | 25 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.690+31_690+32insTG others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | |||||
chr15:51689398 | G | GGTGTGT | 17 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.690+31_690+32insTG others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | |||||
chr15:51689398 | G | T | 3 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0337 | 3 | HG00140.hp2 HG03492.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.690+30G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689398 | ||||||
chr15:51689398 | GGGGT | G | 113 | a0001c0001t0001g0107a0001c0001t0001g0120a0001c0001t0001g0124others(110): Show | 116 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.690+32_690+35delGG others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | |||||
chr15:51689398 | GGGGTGT | G | 15 | a0001c0001t0001g0115a0001c0001t0001g0228a0001c0001t0001g0339others(12): Show | 15 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.690+32_690+37delGG others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689398 | |||||
chr15:51689400 | G | T | 223 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0068others(220): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.690+32G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689400 | ||||||
chr15:51689433 | A | G | 2 | a0001c0001t0005g0077a0001c0001t0005g0078 | 2 | NA18982.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.690+65A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689433 | ||||||
chr15:51689480 | G | C | 1 | a0001c0001t0001g0361 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.690+112G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689480 | ||||||
chr15:51689602 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.690+234C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689602 | ||||||
chr15:51689643 | G | A | 2 | a0001c0001t0001g0068a0001c0001t0002g0069 | 2 | HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.690+275G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689643 | ||||||
chr15:51689655 | G | A | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.690+287G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689655 | ||||||
chr15:51689702 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.690+334G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689702 | ||||||
chr15:51689790 | AAATT | A | 3 | a0001c0001t0003g0323a0001c0001t0003g0324a0001c0001t0003g0325 | 3 | HG02683.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.690+439_690+442del others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51689790 | |||||
chr15:51689819 | T | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(117): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.690+451T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689819 | ||||||
chr15:51689868 | T | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(105): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.690+500T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689868 | ||||||
chr15:51689905 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.690+537T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689905 | ||||||
chr15:51689940 | A | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.690+572A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689940 | ||||||
chr15:51689990 | T | C | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG02451.hp2 HG03453.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+622T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51689990 | ||||||
chr15:51690272 | G | A | 1 | a0001c0001t0006g0222 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.690+904G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690272 | ||||||
chr15:51690410 | C | T | 31 | a0002c0003t0001g0056a0002c0003t0001g0363a0002c0003t0003g0055others(28): Show | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.690+1042C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690410 | ||||||
chr15:51690431 | A | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.690+1063A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690431 | ||||||
chr15:51690652 | CA | C | 355 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(352): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.690+1295delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51690652 | |||||
chr15:51690663 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.690+1295A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690663 | ||||||
chr15:51690765 | A | G | 4 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0003g0100others(1): Show | 4 | HG00738.hp1 HG01081.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1394A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51690765 | ||||||
chr15:51691401 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.691-758C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691401 | ||||||
chr15:51691401 | C | T | 2 | a0001c0005t0005g0089a0001c0005t0005g0090 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.691-758C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691401 | ||||||
chr15:51691484 | G | A | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 3 | NA18948.hp2 NA19001.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.691-675G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691484 | ||||||
chr15:51691911 | CCCCTGAG others(47): Show |
C | 4 | a0001c0001t0008g0005a0001c0001t0008g0048a0001c0001t0008g0049others(1): Show | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.691-239_691-186del others(54): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr15 | 51691911 | |||||
chr15:51691941 | G | T | 26 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0002g0006others(23): Show | 27 | HG01496.hp2 HG02145.hp1 HG03098.hp2 others(24): Show |
intron_variant | MODIFIER | c.691-218G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51691941 | ||||||
chr15:51692034 | G | C | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.691-125G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692034 | ||||||
chr15:51692045 | C | T | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.691-114C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692045 | ||||||
chr15:51692095 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.691-64T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692095 | ||||||
chr15:51692096 | C | G | 5 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 5 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-63C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 6/11 | chr15 | 51692096 | ||||||
chr15:51692428 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.868+92A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692428 | ||||||
chr15:51692480 | C | T | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.868+144C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692480 | ||||||
chr15:51692544 | T | C | 1 | a0001c0001t0002g0119 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.868+208T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692544 | ||||||
chr15:51692864 | CT | C | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.868+536delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51692864 | |||||
chr15:51692879 | TTC | T | 13 | a0001c0001t0001g0233a0001c0001t0001g0309a0001c0001t0001g0315others(10): Show | 14 | HG01074.hp2 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.868+545_868+546del others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51692879 | |||||
chr15:51692898 | G | A | 1 | a0001c0002t0004g0348 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.868+562G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692898 | ||||||
chr15:51692911 | A | T | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.868+575A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692911 | ||||||
chr15:51692950 | T | C | 306 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(303): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.868+614T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692950 | ||||||
chr15:51692987 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.868+651A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51692987 | ||||||
chr15:51693078 | A | G | 306 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(303): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.868+742A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693078 | ||||||
chr15:51693163 | T | C | 4 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+827T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693163 | ||||||
chr15:51693277 | A | G | 1 | a0002c0003t0003g0382 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.868+941A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693277 | ||||||
chr15:51693367 | T | C | 299 | a0001c0001t0001g0007a0001c0001t0001g0068a0001c0001t0001g0091others(296): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.868+1031T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693367 | ||||||
chr15:51693400 | G | A | 8 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.868+1064G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693400 | ||||||
chr15:51693403 | C | T | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.868+1067C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693403 | ||||||
chr15:51693425 | ATTTGTT | A | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.868+1105_868+1110d others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51693425 | |||||
chr15:51693441 | G | T | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.868+1105G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693441 | ||||||
chr15:51693638 | C | T | 271 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.868+1302C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693638 | ||||||
chr15:51693693 | G | A | 4 | a0001c0001t0008g0005a0001c0001t0008g0048a0001c0001t0008g0049others(1): Show | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.868+1357G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51693693 | ||||||
chr15:51694013 | C | A | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.868+1677C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694013 | ||||||
chr15:51694248 | A | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | NA18945.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.869-1627A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694248 | ||||||
chr15:51694307 | G | A | 1 | a0003c0004t0001g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.869-1568G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694307 | ||||||
chr15:51694310 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.869-1565C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694310 | ||||||
chr15:51694756 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.869-1119C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694756 | ||||||
chr15:51694768 | C | T | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.869-1107C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694768 | ||||||
chr15:51694800 | G | A | 1 | a0001c0001t0006g0223 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.869-1075G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694800 | ||||||
chr15:51694811 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.869-1064G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694811 | ||||||
chr15:51694956 | A | G | 4 | a0001c0002t0001g0343a0001c0002t0010g0340a0001c0002t0010g0341others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-919A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51694956 | ||||||
chr15:51695030 | C | CA | 17 | a0001c0001t0001g0228a0001c0001t0001g0249a0001c0001t0002g0230others(14): Show | 17 | HG00597.hp2 HG01167.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.869-830dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695030 | |||||
chr15:51695046 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.869-829G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695046 | ||||||
chr15:51695078 | G | A | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.869-797G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695078 | ||||||
chr15:51695231 | A | G | 128 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(125): Show | 131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.869-644A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695231 | ||||||
chr15:51695254 | GTTC | G | 31 | a0002c0003t0001g0056a0002c0003t0001g0363a0002c0003t0003g0055others(28): Show | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.869-618_869-616del others(3): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695254 | |||||
chr15:51695475 | C | T | 1 | a0001c0001t0003g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.869-400C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695475 | ||||||
chr15:51695524 | A | G | 3 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0013g0221 | 3 | NA18953.hp1 NA19005.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.869-351A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695524 | ||||||
chr15:51695625 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.869-250G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695625 | ||||||
chr15:51695710 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.869-165G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695710 | ||||||
chr15:51695762 | G | GA | 6 | a0001c0001t0002g0121a0001c0001t0002g0206a0001c0001t0003g0234others(3): Show | 6 | HG01175.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-99dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695762 | |||||
chr15:51695762 | G | GAA | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.869-100_869-99dupA others(1): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695762 | |||||
chr15:51695762 | GA | G | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.869-99delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr15 | 51695762 | |||||
chr15:51695778 | C | G | 1 | a0001c0001t0002g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.869-97C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 7/11 | chr15 | 51695778 | ||||||
chr15:51696016 | T | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.985+25T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696016 | ||||||
chr15:51696135 | A | G | 14 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(11): Show | 14 | HG00597.hp2 HG03130.hp2 HG04115.hp2 others(11): Show |
intron_variant | MODIFIER | c.985+144A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696135 | ||||||
chr15:51696142 | T | C | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.985+151T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696142 | ||||||
chr15:51696181 | T | C | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.985+190T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696181 | ||||||
chr15:51696277 | C | T | 1 | a0001c0001t0007g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.985+286C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696277 | ||||||
chr15:51696543 | C | T | 22 | a0001c0001t0001g0091a0001c0001t0002g0006a0001c0001t0002g0071others(19): Show | 23 | HG04204.hp1 NA18939.hp1 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.985+552C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696543 | ||||||
chr15:51696871 | A | C | 4 | a0001c0001t0001g0068a0001c0001t0002g0069a0001c0005t0005g0089others(1): Show | 4 | HG01496.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.985+880A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696871 | ||||||
chr15:51696885 | T | C | 90 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(87): Show | 95 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.985+894T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696885 | ||||||
chr15:51696935 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.985+944G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51696935 | ||||||
chr15:51697002 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.985+1011C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697002 | ||||||
chr15:51697132 | C | CTG | 30 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0236others(27): Show | 33 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.985+1173_985+1174d others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | |||||
chr15:51697132 | C | CTGTG | 34 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(31): Show | 35 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.985+1171_985+1174d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | |||||
chr15:51697132 | C | CTGTGTG | 119 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(116): Show | 122 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.985+1169_985+1174d others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | |||||
chr15:51697132 | C | CTGTGTGT others(1): Show |
24 | a0001c0001t0001g0188a0001c0001t0001g0191a0001c0001t0001g0192others(21): Show | 24 | HG00621.hp1 HG01069.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.985+1167_985+1174d others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | |||||
chr15:51697132 | C | CTGTGTGT others(3): Show |
41 | a0001c0001t0001g0068a0001c0001t0001g0228a0001c0001t0002g0069others(38): Show | 41 | HG00597.hp2 HG01496.hp2 HG02056.hp2 others(38): Show |
intron_variant | MODIFIER | c.985+1165_985+1174d others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | |||||
chr15:51697132 | C | CTGTGTGT others(5): Show |
10 | a0001c0001t0002g0216a0001c0001t0005g0077a0001c0001t0006g0231others(7): Show | 11 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.985+1163_985+1174d others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | |||||
chr15:51697132 | C | CTGTGTGT others(7): Show |
23 | a0001c0001t0001g0091a0001c0001t0002g0006a0001c0001t0002g0071others(20): Show | 24 | HG02559.hp1 HG04204.hp1 NA18906.hp2 others(21): Show |
intron_variant | MODIFIER | c.985+1161_985+1174d others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697132 | |||||
chr15:51697177 | TTCTTTCT others(106): Show |
T | 24 | a0002c0003t0001g0363a0002c0003t0003g0303a0002c0003t0003g0360others(21): Show | 24 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.985+1189_985+1301d others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51697177 | |||||
chr15:51697283 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.985+1292C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697283 | ||||||
chr15:51697337 | T | C | 1 | a0001c0001t0002g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.985+1346T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697337 | ||||||
chr15:51697440 | C | T | 1 | a0001c0011t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.985+1449C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697440 | ||||||
chr15:51697769 | A | G | 4 | a0001c0001t0001g0068a0001c0001t0002g0069a0001c0005t0005g0089others(1): Show | 4 | HG01496.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.986-1550A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697769 | ||||||
chr15:51697776 | C | T | 2 | a0001c0001t0001g0068a0001c0001t0002g0069 | 2 | HG01496.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.986-1543C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697776 | ||||||
chr15:51697860 | G | T | 30 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 33 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.986-1459G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697860 | ||||||
chr15:51697861 | A | T | 30 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 33 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.986-1458A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51697861 | ||||||
chr15:51698050 | C | T | 86 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(83): Show | 90 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.986-1269C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698050 | ||||||
chr15:51698171 | G | A | 1 | a0001c0001t0006g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.986-1148G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698171 | ||||||
chr15:51698268 | G | A | 30 | a0001c0002t0001g0021a0001c0002t0001g0349a0001c0002t0001g0353others(27): Show | 30 | HG00423.hp1 HG01257.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.986-1051G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698268 | ||||||
chr15:51698309 | A | C | 1 | a0001c0001t0006g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.986-1010A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698309 | ||||||
chr15:51698329 | G | A | 1 | a0002c0003t0003g0372 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.986-990G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698329 | ||||||
chr15:51698366 | A | G | 24 | a0001c0001t0001g0091a0001c0001t0002g0006a0001c0001t0002g0071others(21): Show | 25 | HG02145.hp1 HG03195.hp2 HG04204.hp1 others(22): Show |
intron_variant | MODIFIER | c.986-953A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698366 | ||||||
chr15:51698452 | T | C | 1 | a0001c0001t0001g0339 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.986-867T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698452 | ||||||
chr15:51698504 | C | T | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.986-815C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698504 | ||||||
chr15:51698590 | T | C | 86 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(83): Show | 90 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.986-729T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698590 | ||||||
chr15:51698596 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.986-723G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51698596 | ||||||
chr15:51698793 | A | AAAGAGAG others(318): Show |
3 | a0001c0001t0006g0222a0001c0001t0006g0225a0001c0001t0006g0226 | 3 | NA18747.hp1 NA18971.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.986-510_986-509ins others(325): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698793 | |||||
chr15:51698793 | A | AAAGAGAG others(319): Show |
6 | a0001c0001t0001g0228a0001c0001t0006g0220a0001c0001t0006g0227others(3): Show | 6 | HG04115.hp2 NA18977.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.986-510_986-509ins others(326): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698793 | |||||
chr15:51698793 | A | AAAGAGAG others(320): Show |
4 | a0001c0001t0002g0230a0001c0001t0006g0219a0001c0001t0006g0223others(1): Show | 4 | HG00597.hp2 NA18952.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-510_986-509ins others(327): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698793 | |||||
chr15:51698794 | AAG | A | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-520_986-519del others(2): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | 51698794 | |||||
chr15:51699062 | T | C | 6 | a0001c0001t0001g0250a0001c0001t0001g0297a0001c0001t0001g0298others(3): Show | 6 | HG02129.hp2 NA18944.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.986-257T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51699062 | ||||||
chr15:51699099 | T | C | 22 | a0001c0001t0001g0091a0001c0001t0002g0006a0001c0001t0002g0071others(19): Show | 23 | HG04204.hp1 NA18939.hp1 NA18945.hp2 others(20): Show |
intron_variant | MODIFIER | c.986-220T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51699099 | ||||||
chr15:51699257 | C | T | 151 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(148): Show | 154 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.986-62C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 8/11 | chr15 | 51699257 | ||||||
chr15:51699454 | T | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+52T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699454 | ||||||
chr15:51699551 | C | A | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1069+149C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699551 | ||||||
chr15:51699687 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1069+285C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699687 | ||||||
chr15:51699767 | A | G | 1 | a0001c0001t0008g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1069+365A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699767 | ||||||
chr15:51699802 | C | T | 2 | a0001c0001t0006g0196a0001c0001t0006g0200 | 2 | HG02165.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1069+400C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699802 | ||||||
chr15:51699864 | C | T | 120 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(117): Show | 123 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1069+462C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699864 | ||||||
chr15:51699903 | C | T | 1 | a0001c0001t0003g0319 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1069+501C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51699903 | ||||||
chr15:51700016 | T | C | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1069+614T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700016 | ||||||
chr15:51700099 | T | C | 34 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(31): Show | 34 | HG00423.hp1 HG01257.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+697T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700099 | ||||||
chr15:51700162 | A | C | 1 | a0001c0001t0001g0296 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1069+760A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700162 | ||||||
chr15:51700229 | T | C | 114 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(111): Show | 120 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1069+827T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700229 | ||||||
chr15:51700394 | T | C | 37 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(34): Show | 37 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.1070-713T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700394 | ||||||
chr15:51700555 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1070-552T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700555 | ||||||
chr15:51700628 | T | C | 241 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(238): Show | 249 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1070-479T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700628 | ||||||
chr15:51700807 | C | G | 3 | a0001c0002t0010g0340a0001c0002t0010g0341a0001c0002t0010g0342 | 3 | HG02615.hp2 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1070-300C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700807 | ||||||
chr15:51700928 | A | G | 2 | a0001c0001t0003g0099a0001c0001t0003g0100 | 2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1070-179A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700928 | ||||||
chr15:51700962 | G | T | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1070-145G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 9/11 | chr15 | 51700962 | ||||||
chr15:51701331 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1207+87C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701331 | ||||||
chr15:51701387 | A | G | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+143A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701387 | ||||||
chr15:51701469 | G | C | 4 | a0001c0001t0008g0005a0001c0001t0008g0048a0001c0001t0008g0049others(1): Show | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+225G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701469 | ||||||
chr15:51701521 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1207+277T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701521 | ||||||
chr15:51701712 | C | G | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+468C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701712 | ||||||
chr15:51701934 | G | A | 1 | a0001c0002t0004g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1207+690G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701934 | ||||||
chr15:51701990 | G | A | 4 | a0001c0002t0001g0343a0001c0002t0010g0340a0001c0002t0010g0341others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+746G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51701990 | ||||||
chr15:51702046 | C | T | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+802C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702046 | ||||||
chr15:51702048 | C | A | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0314 | 3 | HG01243.hp2 HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1207+804C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702048 | ||||||
chr15:51702319 | C | T | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+1075C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702319 | ||||||
chr15:51702508 | A | C | 96 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(93): Show | 101 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.1207+1264A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702508 | ||||||
chr15:51702831 | T | G | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+1587T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51702831 | ||||||
chr15:51703184 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1207+1940G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703184 | ||||||
chr15:51703246 | C | T | 43 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(40): Show | 43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+2002C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703246 | ||||||
chr15:51703293 | C | T | 48 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(45): Show | 51 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1207+2049C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703293 | ||||||
chr15:51703397 | T | C | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+2153T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703397 | ||||||
chr15:51703493 | T | C | 43 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(40): Show | 43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+2249T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703493 | ||||||
chr15:51703566 | C | T | 151 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(148): Show | 155 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.1207+2322C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703566 | ||||||
chr15:51703583 | C | T | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2339C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703583 | ||||||
chr15:51703611 | T | C | 1 | a0001c0001t0006g0220 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1207+2367T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703611 | ||||||
chr15:51703773 | A | G | 39 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(36): Show | 39 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.1207+2529A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703773 | ||||||
chr15:51703860 | T | C | 2 | a0001c0001t0001g0332a0001c0001t0001g0337 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1207+2616T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703860 | ||||||
chr15:51703953 | T | C | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+2709T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703953 | ||||||
chr15:51703984 | C | T | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+2740C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703984 | ||||||
chr15:51703987 | A | G | 43 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(40): Show | 43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+2743A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51703987 | ||||||
chr15:51704105 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1207+2861G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704105 | ||||||
chr15:51704118 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1207+2874C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704118 | ||||||
chr15:51704147 | G | T | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2903G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704147 | ||||||
chr15:51704236 | C | CATATATA others(3): Show |
1 | a0001c0001t0008g0005 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1207+2995_1207+299 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704236 | |||||
chr15:51704236 | CATACATA others(7): Show |
C | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1207+2996_1207+300 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704236 | |||||
chr15:51704236 | CATACATA others(19): Show |
C | 3 | a0001c0001t0008g0048a0001c0001t0008g0049a0001c0001t0008g0050 | 3 | HG01884.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1207+2996_1207+302 others(30): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704236 | |||||
chr15:51704240 | C | CAT | 7 | a0001c0001t0001g0037a0001c0001t0003g0029a0001c0001t0003g0030others(4): Show | 7 | HG00735.hp2 HG01515.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207+2998_1207+299 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | C | CATAT | 4 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0045others(1): Show | 4 | HG01081.hp2 HG02683.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+2999_1207+300 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | C | CATATATA others(3): Show |
4 | a0001c0001t0003g0004a0001c0001t0003g0042a0001c0001t0003g0043others(1): Show | 5 | HG00639.hp2 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+2999_1207+300 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | C | CATATATA others(5): Show |
1 | a0001c0001t0003g0044 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1207+2999_1207+300 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | C | T | 3 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0008g0005 | 4 | HG01256.hp2 HG01258.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207+2996C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704240 | ||||||
chr15:51704240 | CATACAT | C | 6 | a0001c0001t0001g0051a0001c0001t0005g0074a0001c0001t0005g0075others(3): Show | 6 | NA18946.hp1 NA18981.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | CATACATA others(1): Show |
C | 10 | a0001c0001t0001g0091a0001c0001t0004g0086a0001c0001t0005g0070others(7): Show | 10 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | CATACATA others(3): Show |
C | 3 | a0001c0001t0005g0072a0001c0001t0007g0063a0001c0001t0007g0067 | 3 | HG02965.hp1 NA20905.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | CATACATA others(5): Show |
C | 2 | a0001c0002t0004g0347a0001c0002t0004g0358 | 2 | HG00423.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1207+3000_1207+301 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | CATACATA others(9): Show |
C | 32 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(29): Show | 32 | HG01069.hp2 HG01261.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.1207+3000_1207+301 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | CATACATA others(11): Show |
C | 8 | a0001c0002t0001g0021a0001c0002t0001g0343a0001c0002t0001g0349others(5): Show | 8 | HG01257.hp2 HG01891.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+3000_1207+301 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704240 | CATACATA others(13): Show |
C | 1 | a0001c0002t0010g0342 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207+3000_1207+301 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704240 | |||||
chr15:51704242 | TAC | T | 5 | a0001c0001t0003g0027a0001c0001t0003g0031a0001c0001t0003g0033others(2): Show | 5 | HG00323.hp1 HG00733.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+3000_1207+300 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704242 | |||||
chr15:51704244 | C | CAT | 28 | a0001c0001t0001g0103a0001c0001t0001g0235a0001c0001t0001g0236others(25): Show | 28 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1207+3034_1207+303 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACAT | 10 | a0001c0001t0001g0232a0001c0001t0001g0254a0001c0001t0001g0255others(7): Show | 10 | HG00735.hp1 HG01358.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(7): Show |
1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1207+3003_1207+300 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(1): Show |
17 | a0001c0001t0001g0007a0001c0001t0001g0115a0001c0001t0001g0246others(14): Show | 18 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(3): Show |
14 | a0001c0001t0001g0107a0001c0001t0001g0150a0001c0001t0001g0201others(11): Show | 14 | HG00639.hp1 HG01993.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(5): Show |
19 | a0001c0001t0001g0120a0001c0001t0001g0158a0001c0001t0001g0160others(16): Show | 19 | HG00597.hp1 HG00741.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(7): Show |
24 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0260others(21): Show | 24 | HG00099.hp2 HG01175.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(9): Show |
9 | a0001c0001t0001g0024a0001c0001t0001g0335a0001c0001t0002g0080others(6): Show | 9 | HG01109.hp1 HG02165.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(11): Show |
16 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0191others(13): Show | 16 | HG00423.hp2 HG01515.hp1 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(13): Show |
9 | a0001c0001t0001g0131a0001c0001t0001g0178a0001c0001t0002g0006others(6): Show | 10 | HG01934.hp1 HG02056.hp1 HG04184.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(15): Show |
4 | a0001c0001t0002g0119a0001c0001t0002g0179a0001c0001t0002g0193others(1): Show | 4 | HG00621.hp1 HG03704.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(17): Show |
2 | a0001c0001t0001g0180a0001c0001t0002g0092 | 2 | HG00544.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1207+3003_1207+300 others(28): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATACATA others(21): Show |
1 | a0001c0001t0002g0109 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1207+3003_1207+300 others(32): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATAT | 22 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0307others(19): Show | 22 | HG01255.hp1 HG01517.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1207+3032_1207+303 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATAT | 19 | a0001c0001t0001g0104a0001c0001t0001g0287a0001c0001t0001g0288others(16): Show | 20 | HG01168.hp2 HG01256.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1207+3030_1207+303 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATATA others(1): Show |
9 | a0001c0001t0001g0184a0001c0001t0001g0289a0001c0001t0002g0183others(6): Show | 9 | HG01074.hp2 HG01081.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207+3028_1207+303 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATATA others(3): Show |
9 | a0001c0001t0001g0242a0001c0001t0001g0292a0001c0001t0002g0085others(6): Show | 10 | HG02027.hp1 HG02027.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3026_1207+303 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATATA others(5): Show |
2 | a0001c0001t0001g0293a0002c0003t0003g0367 | 2 | HG03130.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1207+3024_1207+303 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATATA others(7): Show |
1 | a0002c0003t0003g0303 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1207+3022_1207+303 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATATA others(11): Show |
1 | a0002c0003t0003g0380 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1207+3018_1207+303 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATATA others(13): Show |
2 | a0001c0001t0001g0068a0001c0001t0002g0114 | 2 | HG01496.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1207+3016_1207+303 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | CATATATA others(15): Show |
2 | a0001c0001t0002g0069a0001c0001t0003g0294 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1207+3014_1207+303 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | C | T | 25 | a0001c0001t0001g0037a0001c0001t0003g0002a0001c0001t0003g0004others(22): Show | 28 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1207+3000C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704244 | ||||||
chr15:51704244 | CAT | C | 16 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0315others(13): Show | 16 | HG01975.hp2 HG01981.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1207+3034_1207+303 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | CATAT | C | 12 | a0001c0001t0001g0102a0001c0001t0001g0309a0001c0001t0001g0310others(9): Show | 12 | HG00323.hp2 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207+3032_1207+303 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704244 | CATATATA others(1): Show |
C | 6 | a0001c0001t0002g0001a0001c0001t0002g0112a0001c0001t0002g0133others(3): Show | 9 | HG00408.hp1 NA18940.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1207+3028_1207+303 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704244 | |||||
chr15:51704248 | T | C | 3 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0016g0088 | 3 | HG02895.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1207+3004T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704248 | ||||||
chr15:51704248 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0249 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1207+3024_1207+302 others(46): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704248 | |||||
chr15:51704250 | T | TATATATA others(12): Show |
1 | a0001c0001t0001g0195 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1207+3007_1207+302 others(23): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704250 | |||||
chr15:51704252 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1207+3008T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704252 | ||||||
chr15:51704254 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1207+3010T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704254 | ||||||
chr15:51704256 | T | C | 6 | a0001c0001t0002g0001a0001c0001t0002g0112a0001c0001t0002g0133others(3): Show | 9 | HG00408.hp1 NA18940.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1207+3012T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704256 | ||||||
chr15:51704278 | T | A | 9 | a0001c0001t0001g0051a0001c0001t0004g0086a0001c0001t0005g0072others(6): Show | 10 | HG01167.hp2 HG01169.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1207+3034T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704278 | ||||||
chr15:51704280 | A | T | 44 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(41): Show | 44 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.1207+3036A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704280 | ||||||
chr15:51704482 | C | T | 1 | a0001c0001t0006g0223 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1207+3238C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704482 | ||||||
chr15:51704724 | C | T | 1 | a0002c0003t0003g0365 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1207+3480C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704724 | ||||||
chr15:51704738 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1207+3494C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704738 | ||||||
chr15:51704760 | A | AATAC | 18 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0232others(15): Show | 19 | HG00735.hp1 HG00741.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1207+3520_1207+352 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704760 | |||||
chr15:51704764 | C | CAT | 40 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0120others(37): Show | 43 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1207+3550_1207+355 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATACAT | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(2): Show | 5 | HG00140.hp2 HG01109.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+3523_1207+352 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATAT | 19 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0107others(16): Show | 19 | HG00544.hp1 HG01070.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1207+3548_1207+355 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATAT | 19 | a0001c0001t0001g0051a0001c0001t0001g0195a0001c0001t0001g0207others(16): Show | 19 | HG01358.hp1 HG01884.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1207+3546_1207+355 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(1): Show |
14 | a0001c0001t0001g0037a0001c0001t0001g0249a0001c0001t0002g0208others(11): Show | 17 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1207+3544_1207+355 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(3): Show |
8 | a0001c0001t0001g0320a0001c0001t0001g0338a0001c0001t0003g0034others(5): Show | 8 | HG00642.hp2 HG01168.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207+3542_1207+355 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(5): Show |
10 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0304others(7): Show | 10 | HG00408.hp2 HG02109.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+3540_1207+355 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(7): Show |
13 | a0001c0001t0001g0150a0001c0001t0001g0276a0001c0001t0003g0003others(10): Show | 14 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1207+3538_1207+355 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(9): Show |
11 | a0001c0001t0001g0132a0001c0001t0001g0289a0001c0001t0001g0293others(8): Show | 12 | HG01074.hp2 HG01361.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207+3536_1207+355 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(11): Show |
15 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0295others(12): Show | 16 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207+3534_1207+355 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(13): Show |
8 | a0001c0001t0001g0280a0001c0001t0001g0307a0001c0001t0002g0096others(5): Show | 8 | HG02027.hp2 HG02486.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1207+3532_1207+355 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(15): Show |
10 | a0001c0001t0001g0242a0001c0001t0001g0284a0001c0001t0001g0287others(7): Show | 10 | HG02027.hp1 HG02257.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1207+3530_1207+355 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(17): Show |
12 | a0001c0001t0001g0091a0001c0001t0001g0282a0001c0001t0002g0281others(9): Show | 12 | HG00735.hp2 HG01361.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207+3528_1207+355 others(28): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(19): Show |
6 | a0001c0001t0001g0311a0001c0001t0001g0329a0001c0001t0003g0028others(3): Show | 6 | HG00639.hp2 HG01081.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+3526_1207+355 others(30): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(21): Show |
6 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(3): Show | 6 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+3524_1207+355 others(32): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(23): Show |
6 | a0001c0001t0001g0235a0001c0001t0001g0309a0001c0001t0003g0027others(3): Show | 6 | HG00323.hp1 HG01515.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207+3522_1207+355 others(34): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(25): Show |
5 | a0001c0001t0001g0250a0001c0001t0001g0317a0001c0001t0003g0047others(2): Show | 5 | HG01081.hp2 HG01123.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(36): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(27): Show |
3 | a0001c0001t0001g0308a0001c0001t0005g0075a0001c0001t0005g0076 | 3 | NA18946.hp1 NA18981.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(38): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(29): Show |
2 | a0001c0001t0001g0288a0001c0001t0005g0283 | 2 | HG00140.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(40): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(31): Show |
2 | a0001c0001t0001g0243a0001c0001t0001g0245 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1207+3551_1207+355 others(42): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(33): Show |
1 | a0001c0001t0001g0244 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(44): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(35): Show |
1 | a0001c0001t0001g0312 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(46): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(39): Show |
1 | a0001c0001t0001g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(50): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | C | CATATATA others(43): Show |
1 | a0001c0001t0001g0233 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1207+3551_1207+355 others(54): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | CATATAT | C | 3 | a0001c0001t0013g0221a0001c0006t0011g0010a0005c0007t0007g0061 | 4 | HG01167.hp2 HG01169.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207+3546_1207+355 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | CATATATA others(1): Show |
C | 12 | a0001c0001t0003g0052a0001c0001t0006g0223a0001c0001t0016g0088others(9): Show | 12 | HG00423.hp1 HG01243.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1207+3544_1207+355 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | CATATATA others(3): Show |
C | 47 | a0001c0001t0001g0068a0001c0001t0001g0124a0001c0001t0001g0125others(44): Show | 47 | HG00597.hp2 HG01069.hp2 HG01261.hp1 others(44): Show |
intron_variant | MODIFIER | c.1207+3542_1207+355 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704764 | CATATATA others(5): Show |
C | 24 | a0002c0003t0001g0363a0002c0003t0003g0303a0002c0003t0003g0360others(21): Show | 24 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1207+3540_1207+355 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704764 | |||||
chr15:51704779 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0285 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1207+3548_1207+354 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51704779 | |||||
chr15:51704794 | T | C | 2 | a0001c0001t0001g0256a0001c0002t0004g0351 | 2 | HG00735.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1207+3550T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704794 | ||||||
chr15:51704796 | C | T | 2 | a0001c0001t0003g0009a0001c0001t0003g0023 | 3 | HG02486.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1207+3552C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704796 | ||||||
chr15:51704806 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1207+3562T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704806 | ||||||
chr15:51704950 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1207+3706G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51704950 | ||||||
chr15:51705444 | C | G | 2 | a0005c0007t0007g0061a0005c0007t0007g0062 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1207+4200C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705444 | ||||||
chr15:51705523 | T | C | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+4279T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705523 | ||||||
chr15:51705536 | T | C | 43 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(40): Show | 43 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.1207+4292T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705536 | ||||||
chr15:51705540 | G | A | 46 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(43): Show | 49 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.1207+4296G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705540 | ||||||
chr15:51705749 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1207+4505C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705749 | ||||||
chr15:51705938 | C | T | 2 | a0001c0001t0003g0003a0001c0001t0003g0033 | 3 | HG00733.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1207+4694C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51705938 | ||||||
chr15:51706219 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1207+4975C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706219 | ||||||
chr15:51706320 | G | C | 1 | a0002c0003t0003g0303 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1207+5076G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706320 | ||||||
chr15:51706380 | C | T | 3 | a0001c0002t0001g0349a0001c0002t0001g0353a0001c0002t0001g0357 | 3 | HG02074.hp1 NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1207+5136C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706380 | ||||||
chr15:51706444 | G | C | 1 | a0001c0001t0007g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1207+5200G>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706444 | ||||||
chr15:51706592 | C | T | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207+5348C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706592 | ||||||
chr15:51706593 | G | A | 24 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 25 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1207+5349G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51706593 | ||||||
chr15:51707060 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1207+5816G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707060 | ||||||
chr15:51707112 | T | G | 5 | a0002c0003t0001g0056a0002c0003t0003g0055a0002c0003t0003g0057others(2): Show | 5 | HG02055.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207+5868T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707112 | ||||||
chr15:51707296 | A | T | 4 | a0001c0001t0008g0005a0001c0001t0008g0048a0001c0001t0008g0049others(1): Show | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-6037A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707296 | ||||||
chr15:51707330 | C | A | 1 | a0003c0004t0003g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1208-6003C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707330 | ||||||
chr15:51707471 | G | A | 31 | a0002c0003t0001g0056a0002c0003t0001g0363a0002c0003t0003g0055others(28): Show | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1208-5862G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707471 | ||||||
chr15:51707542 | T | A | 1 | a0003c0004t0003g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1208-5791T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707542 | ||||||
chr15:51707682 | C | A | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1208-5651C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707682 | ||||||
chr15:51707773 | C | T | 262 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(259): Show | 271 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.1208-5560C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707773 | ||||||
chr15:51707950 | T | A | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1208-5383T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707950 | ||||||
chr15:51707991 | C | T | 1 | a0001c0001t0003g0325 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1208-5342C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51707991 | ||||||
chr15:51708026 | G | A | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-5307G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708026 | ||||||
chr15:51708257 | A | G | 1 | a0002c0003t0003g0366 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1208-5076A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708257 | ||||||
chr15:51708415 | G | T | 1 | a0001c0001t0001g0338 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1208-4918G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708415 | ||||||
chr15:51708537 | G | T | 4 | a0002c0003t0003g0376a0002c0003t0003g0377a0002c0003t0003g0382others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-4796G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708537 | ||||||
chr15:51708594 | G | A | 3 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0181 | 3 | HG01109.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1208-4739G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708594 | ||||||
chr15:51708623 | A | T | 1 | a0001c0001t0002g0071 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1208-4710A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708623 | ||||||
chr15:51708851 | T | TC | 31 | a0002c0003t0001g0056a0002c0003t0001g0363a0002c0003t0003g0055others(28): Show | 31 | HG01255.hp1 HG01891.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1208-4480dupC | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51708851 | |||||
chr15:51708857 | T | TA | 47 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0003g0002others(44): Show | 51 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1208-4465dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51708857 | |||||
chr15:51708919 | T | A | 81 | a0001c0001t0001g0115a0001c0001t0001g0150a0001c0001t0001g0160others(78): Show | 85 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1208-4414T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708919 | ||||||
chr15:51708936 | T | C | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1208-4397T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51708936 | ||||||
chr15:51709210 | C | G | 4 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG02451.hp2 HG03453.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-4123C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709210 | ||||||
chr15:51709314 | A | G | 1 | a0001c0002t0004g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1208-4019A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709314 | ||||||
chr15:51709401 | C | G | 154 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(151): Show | 158 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1208-3932C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709401 | ||||||
chr15:51709516 | ATATC | A | 47 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(44): Show | 48 | HG00423.hp1 HG01069.hp2 HG01256.hp2 others(45): Show |
intron_variant | MODIFIER | c.1208-3812_1208-380 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709516 | |||||
chr15:51709633 | TA | T | 267 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(264): Show | 277 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1208-3691delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709633 | |||||
chr15:51709662 | C | CAT | 4 | a0001c0001t0001g0320a0001c0001t0002g0240a0001c0002t0001g0353others(1): Show | 4 | HG01433.hp1 HG01884.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-3632_1208-363 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | |||||
chr15:51709662 | C | CATAT | 5 | a0001c0001t0001g0332a0001c0001t0001g0337a0001c0001t0008g0005others(2): Show | 6 | HG01256.hp2 HG01258.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-3634_1208-363 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | |||||
chr15:51709662 | CAT | C | 3 | a0001c0001t0007g0066a0001c0002t0004g0018a0001c0002t0004g0020 | 3 | NA18964.hp1 NA19012.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1208-3632_1208-363 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | |||||
chr15:51709662 | CATATATA others(1): Show |
C | 9 | a0001c0001t0001g0037a0001c0001t0003g0039a0001c0001t0003g0040others(6): Show | 9 | HG00639.hp2 HG01081.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1208-3638_1208-363 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | |||||
chr15:51709662 | CATATATA others(3): Show |
C | 8 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0030others(5): Show | 10 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1208-3640_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | |||||
chr15:51709662 | CATATATA others(5): Show |
C | 3 | a0001c0001t0005g0073a0001c0001t0005g0075a0001c0001t0005g0093 | 3 | NA18981.hp1 NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1208-3642_1208-363 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709662 | |||||
chr15:51709675 | ATATATAT others(21): Show |
A | 2 | a0002c0003t0003g0055a0002c0003t0003g0059 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1208-3656_1208-362 others(32): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | |||||
chr15:51709675 | ATATATAT others(22): Show |
A | 3 | a0002c0003t0001g0056a0002c0003t0003g0057a0002c0003t0003g0058 | 3 | HG03098.hp1 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1208-3656_1208-362 others(33): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | |||||
chr15:51709675 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1208-3656_1208-362 others(35): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | |||||
chr15:51709675 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1208-3656_1208-362 others(36): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709675 | |||||
chr15:51709677 | ATATATAT others(20): Show |
A | 1 | a0003c0004t0001g0264 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1208-3654_1208-362 others(31): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709677 | |||||
chr15:51709679 | ATATATAT others(19): Show |
A | 1 | a0001c0001t0003g0165 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1208-3652_1208-362 others(30): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709679 | |||||
chr15:51709681 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1208-3650_1208-362 others(27): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709681 | |||||
chr15:51709681 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0004g0086 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1208-3650_1208-362 others(29): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709681 | |||||
chr15:51709683 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0002g0106 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1208-3648_1208-362 others(28): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709683 | |||||
chr15:51709683 | ATATATAT others(20): Show |
A | 1 | a0001c0001t0005g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1208-3648_1208-362 others(31): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709683 | |||||
chr15:51709684 | TATATATA others(4): Show |
T | 1 | a0001c0001t0003g0053 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1208-3648_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709684 | ||||||
chr15:51709685 | ATATATAT others(15): Show |
A | 1 | a0003c0004t0003g0253 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1208-3646_1208-362 others(26): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709685 | |||||
chr15:51709685 | ATATATAT others(29): Show |
A | 4 | a0001c0001t0006g0219a0001c0001t0006g0220a0001c0001t0006g0223others(1): Show | 4 | NA18952.hp2 NA18953.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3646_1208-361 others(40): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709685 | |||||
chr15:51709686 | TATATATA others(2): Show |
T | 6 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(3): Show | 6 | HG00733.hp2 HG00735.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-3646_1208-363 others(13): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709686 | ||||||
chr15:51709686 | TATATATA others(4): Show |
T | 4 | a0001c0001t0001g0091a0001c0001t0005g0076a0001c0001t0005g0077others(1): Show | 4 | NA18946.hp1 NA18982.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3646_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709686 | ||||||
chr15:51709687 | ATATATAT others(8): Show |
A | 1 | a0003c0004t0002g0265 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1208-3644_1208-363 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709687 | |||||
chr15:51709687 | ATATATAT others(27): Show |
A | 6 | a0001c0001t0006g0222a0001c0001t0006g0225a0001c0001t0006g0226others(3): Show | 6 | HG04115.hp2 NA18747.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1208-3644_1208-361 others(38): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709687 | |||||
chr15:51709687 | ATATATAT others(29): Show |
A | 1 | a0001c0001t0006g0224 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1208-3644_1208-360 others(40): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709687 | |||||
chr15:51709688 | TATATATA others(2): Show |
T | 7 | a0001c0001t0003g0002a0001c0001t0003g0023a0001c0001t0003g0027others(4): Show | 8 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3644_1208-363 others(13): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709688 | ||||||
chr15:51709688 | TATATATA others(4): Show |
T | 1 | a0001c0001t0005g0070 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-3644_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709688 | ||||||
chr15:51709688 | TATATATA others(6): Show |
T | 1 | a0001c0001t0002g0198 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1208-3644_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709688 | ||||||
chr15:51709689 | ATATATAT others(7): Show |
A | 3 | a0001c0001t0002g0181a0001c0001t0002g0197a0001c0001t0002g0199 | 3 | HG01109.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1208-3642_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709689 | |||||
chr15:51709689 | ATATATAT others(9): Show |
A | 1 | a0001c0011t0001g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1208-3642_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709689 | |||||
chr15:51709689 | ATATATAT others(27): Show |
A | 2 | a0001c0001t0001g0228a0001c0001t0002g0230 | 2 | HG00597.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1208-3642_1208-360 others(38): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709689 | |||||
chr15:51709690 | TATATATA others(4): Show |
T | 2 | a0001c0001t0001g0306a0005c0007t0007g0061 | 2 | HG02717.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1208-3642_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709690 | ||||||
chr15:51709691 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0001g0207a0002c0003t0003g0371 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1208-3640_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | |||||
chr15:51709691 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1208-3640_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | |||||
chr15:51709691 | ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0180a0001c0001t0002g0137 | 2 | HG00544.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1208-3640_1208-362 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | |||||
chr15:51709691 | ATATATAT others(9): Show |
A | 4 | a0001c0001t0001g0120a0001c0001t0001g0201a0001c0001t0002g0136others(1): Show | 4 | HG02074.hp2 HG02895.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3640_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709691 | |||||
chr15:51709693 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0285 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1208-3639_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709693 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0002g0277 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1208-3639_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709693 | A | T | 3 | a0001c0001t0001g0287a0001c0001t0003g0036a0001c0001t0003g0042 | 3 | HG03688.hp2 HG04115.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1208-3640A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709693 | ||||||
chr15:51709693 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0002g0190a0001c0001t0002g0203a0001c0001t0009g0186 | 3 | HG03490.hp1 NA19062.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709693 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0002g0085 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1208-3638_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709693 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0209a0002c0003t0003g0303 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709693 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1208-3638_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709693 | ATATATAT others(8): Show |
A | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709693 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0014g0159a0002c0003t0012g0362 | 2 | HG00741.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1208-3638_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709693 | |||||
chr15:51709695 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0330 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1208-3637_1208-363 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709695 | A | T | 15 | a0001c0001t0001g0037a0001c0001t0001g0280a0001c0001t0001g0284others(12): Show | 15 | HG00639.hp2 HG01515.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.1208-3638A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709695 | ||||||
chr15:51709695 | ATATATAT others(3): Show |
A | 7 | a0001c0001t0001g0103a0001c0001t0002g0155a0001c0001t0002g0157others(4): Show | 7 | HG00423.hp2 HG01099.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709695 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0143a0002c0003t0003g0368 | 2 | HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709695 | ATATATAT others(5): Show |
A | 5 | a0001c0001t0001g0104a0001c0001t0001g0232a0001c0001t0002g0154others(2): Show | 5 | HG01978.hp2 HG03130.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709695 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0001g0160a0003c0004t0001g0022 | 2 | HG02155.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1208-3636_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709695 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1208-3636_1208-362 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709695 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1208-3636_1208-361 others(22): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709695 | ATATATAT others(14): Show |
A | 3 | a0001c0001t0001g0158a0001c0001t0002g0141a0001c0001t0002g0169 | 3 | HG01192.hp2 HG01358.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1208-3636_1208-361 others(25): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709695 | |||||
chr15:51709697 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0275 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1208-3635_1208-363 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0305 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1208-3635_1208-363 others(21): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | A | T | 34 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0131others(31): Show | 37 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1208-3636A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709697 | ||||||
chr15:51709697 | ATATATT | A | 6 | a0001c0001t0001g0279a0001c0001t0001g0338a0001c0001t0002g0135others(3): Show | 6 | HG01517.hp1 HG02109.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT | A | 7 | a0001c0001t0001g0130a0001c0001t0001g0312a0001c0001t0002g0081others(4): Show | 7 | HG00642.hp2 HG01496.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(11): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(3): Show |
A | 12 | a0001c0001t0001g0150a0001c0001t0002g0149a0001c0001t0002g0156others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(4): Show |
A | 2 | a0001c0001t0001g0068a0001c0001t0002g0147 | 2 | HG00639.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0002g0139a0002c0003t0012g0370 | 2 | HG03471.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(6): Show |
A | 3 | a0002c0003t0001g0363a0002c0003t0003g0365a0002c0003t0003g0366 | 3 | HG02630.hp1 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(7): Show |
A | 2 | a0001c0001t0001g0132a0001c0001t0002g0140 | 2 | HG04199.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(8): Show |
A | 3 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0002g0177 | 3 | HG01934.hp2 HG02056.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-362 others(19): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(9): Show |
A | 3 | a0001c0001t0001g0167a0001c0001t0001g0191a0001c0001t0006g0200 | 3 | HG01952.hp2 HG02165.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1208-3634_1208-361 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709697 | ATATATTT others(12): Show |
A | 1 | a0001c0001t0001g0236 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1208-3634_1208-361 others(23): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709697 | |||||
chr15:51709699 | A | AT | 3 | a0001c0001t0001g0288a0001c0002t0002g0019a0001c0002t0004g0013 | 3 | HG02135.hp2 NA18974.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1208-3633dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0308 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1208-3633_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0307 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1208-3633_1208-363 others(21): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | A | T | 65 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(62): Show | 69 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1208-3634A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709699 | ||||||
chr15:51709699 | ATATTTT | A | 6 | a0001c0001t0002g0001a0001c0001t0002g0112a0001c0001t0002g0133others(3): Show | 9 | HG01175.hp1 NA18941.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | ATATTTTT | A | 6 | a0001c0001t0001g0162a0001c0001t0001g0339a0001c0001t0002g0069others(3): Show | 6 | HG03098.hp2 NA18747.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(11): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | ATATTTTT others(3): Show |
A | 7 | a0001c0001t0001g0101a0001c0001t0001g0178a0001c0001t0002g0071others(4): Show | 7 | HG00099.hp1 HG02809.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | ATATTTTT others(4): Show |
A | 4 | a0001c0001t0006g0032a0002c0003t0003g0364a0002c0003t0003g0374others(1): Show | 4 | HG02257.hp1 HG02280.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3632_1208-362 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | ATATTTTT others(7): Show |
A | 4 | a0001c0001t0002g0011a0001c0001t0002g0168a0001c0001t0002g0179others(1): Show | 4 | HG00642.hp1 HG03704.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208-3632_1208-361 others(18): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709699 | ATATTTTT others(9): Show |
A | 1 | a0001c0001t0006g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1208-3632_1208-361 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709699 | |||||
chr15:51709701 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0254 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0246 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0250 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | A | ATATATTT others(3): Show |
1 | a0001c0001t0001g0297 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0331 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | A | ATATATTT others(13): Show |
1 | a0001c0001t0001g0276 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1208-3631_1208-363 others(24): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | A | ATATTTTT others(3): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0333 | 2 | HG01261.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1208-3631_1208-363 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | A | T | 80 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0037others(77): Show | 84 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1208-3632A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709701 | ||||||
chr15:51709701 | AT | A | 7 | a0001c0001t0001g0310a0001c0001t0002g0096a0001c0001t0002g0166others(4): Show | 7 | HG02027.hp2 HG02056.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3595delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATT | A | 9 | a0001c0001t0001g0212a0001c0001t0002g0097a0001c0001t0002g0110others(6): Show | 9 | HG01261.hp1 HG01934.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-3596_1208-359 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATTT | A | 6 | a0001c0001t0001g0124a0001c0001t0001g0304a0001c0001t0002g0114others(3): Show | 6 | HG00408.hp2 NA18941.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1208-3597_1208-359 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATTTTT | A | 8 | a0001c0001t0001g0128a0001c0001t0001g0233a0001c0001t0001g0235others(5): Show | 8 | HG01123.hp2 HG01192.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208-3599_1208-359 others(9): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATTTTTTT | A | 8 | a0001c0001t0001g0127a0001c0001t0001g0188a0001c0001t0002g0122others(5): Show | 8 | HG00621.hp2 HG01069.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3601_1208-359 others(11): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0002g0006a0001c0001t0002g0142a0001c0001t0002g0175others(3): Show | 7 | HG02735.hp1 HG02922.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3602_1208-359 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0001g0361a0001c0001t0002g0204a0001c0001t0002g0215others(2): Show | 5 | HG02258.hp1 HG02818.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-3604_1208-359 others(14): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0193 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1208-3605_1208-359 others(15): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709701 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0145 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1208-3606_1208-359 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709701 | |||||
chr15:51709702 | T | TA | 5 | a0001c0001t0001g0125a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG00099.hp2 HG02451.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-3631_1208-363 others(5): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709702 | ||||||
chr15:51709702 | T | TATA | 8 | a0001c0001t0001g0314a0001c0001t0001g0316a0001c0001t0001g0317others(5): Show | 8 | HG02074.hp1 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3631_1208-363 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709702 | ||||||
chr15:51709703 | T | A | 14 | a0001c0001t0001g0184a0001c0001t0001g0311a0001c0001t0001g0320others(11): Show | 15 | HG00544.hp2 HG01243.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1208-3630T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709703 | ||||||
chr15:51709704 | T | A | 13 | a0001c0001t0001g0125a0001c0001t0001g0310a0001c0001t0001g0314others(10): Show | 13 | HG00099.hp2 HG02027.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1208-3629T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709704 | ||||||
chr15:51709705 | T | A | 15 | a0001c0001t0001g0184a0001c0001t0001g0311a0001c0001t0001g0320others(12): Show | 15 | HG00544.hp2 HG01243.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.1208-3628T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709705 | ||||||
chr15:51709706 | T | A | 10 | a0001c0001t0001g0124a0001c0001t0001g0304a0001c0001t0001g0310others(7): Show | 10 | HG00408.hp2 HG02273.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1208-3627T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709706 | ||||||
chr15:51709707 | T | A | 8 | a0001c0001t0001g0126a0001c0001t0002g0109a0001c0001t0002g0183others(5): Show | 8 | HG00544.hp2 HG02004.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3626T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709707 | ||||||
chr15:51709708 | T | A | 7 | a0001c0001t0001g0124a0001c0001t0002g0114a0001c0001t0002g0182others(4): Show | 7 | HG01192.hp1 HG03195.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-3625T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709708 | ||||||
chr15:51709709 | T | A | 3 | a0001c0001t0001g0126a0001c0001t0002g0151a0002c0003t0003g0377 | 3 | HG00597.hp1 HG02004.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1208-3624T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709709 | ||||||
chr15:51709710 | T | A | 3 | a0001c0001t0002g0144a0001c0001t0002g0170a0001c0001t0002g0182 | 3 | NA18951.hp2 NA19077.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1208-3623T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709710 | ||||||
chr15:51709711 | T | A | 2 | a0001c0001t0002g0142a0001c0001t0002g0151 | 2 | HG00597.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1208-3622T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709711 | ||||||
chr15:51709712 | T | A | 33 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0002g0144others(30): Show | 36 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208-3621T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709712 | ||||||
chr15:51709713 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1208-3620T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709713 | ||||||
chr15:51709715 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1208-3618T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709715 | ||||||
chr15:51709718 | T | A | 1 | a0001c0001t0005g0070 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-3615T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709718 | ||||||
chr15:51709725 | T | A | 48 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(45): Show | 52 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1208-3608T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709725 | ||||||
chr15:51709781 | C | T | 36 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(33): Show | 36 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208-3552C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709781 | ||||||
chr15:51709806 | C | T | 1 | a0001c0001t0005g0087 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1208-3527C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709806 | ||||||
chr15:51709845 | C | T | 1 | a0001c0001t0007g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1208-3488C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709845 | ||||||
chr15:51709878 | G | A | 1 | a0003c0004t0001g0247 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1208-3455G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709878 | ||||||
chr15:51709887 | A | AT | 48 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0051others(45): Show | 53 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1208-3424dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | |||||
chr15:51709887 | A | ATT | 20 | a0001c0001t0001g0232a0001c0001t0003g0008a0001c0001t0003g0023others(17): Show | 21 | HG01123.hp1 HG01243.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1208-3425_1208-342 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | |||||
chr15:51709887 | A | ATTT | 8 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0005g0095others(5): Show | 8 | HG00597.hp2 HG02145.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3426_1208-342 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | |||||
chr15:51709887 | AT | A | 140 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(137): Show | 144 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.1208-3424delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51709887 | |||||
chr15:51709926 | C | T | 1 | a0001c0001t0005g0070 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-3407C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51709926 | ||||||
chr15:51710035 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1208-3298C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710035 | ||||||
chr15:51710038 | C | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG03704.hp1 HG03831.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1208-3295C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710038 | ||||||
chr15:51710073 | G | A | 7 | a0001c0001t0003g0002a0001c0001t0003g0023a0001c0001t0003g0027others(4): Show | 8 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-3260G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710073 | ||||||
chr15:51710341 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1208-2992T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710341 | ||||||
chr15:51710355 | G | A | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1208-2978G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710355 | ||||||
chr15:51710593 | T | C | 39 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(36): Show | 39 | HG00423.hp1 HG01069.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.1208-2740T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710593 | ||||||
chr15:51710655 | T | C | 50 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(47): Show | 54 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1208-2678T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51710655 | ||||||
chr15:51710752 | A | AT | 102 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0001t0001g0125others(99): Show | 103 | HG00423.hp1 HG01069.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.1208-2558dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | |||||
chr15:51710752 | A | ATT | 133 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0026others(130): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1208-2559_1208-255 others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | |||||
chr15:51710752 | A | ATTT | 12 | a0001c0001t0001g0091a0001c0001t0001g0297a0001c0001t0001g0300others(9): Show | 12 | HG00639.hp2 HG01358.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1208-2560_1208-255 others(7): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | |||||
chr15:51710752 | ATTTTTT | A | 118 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(115): Show | 122 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1208-2563_1208-255 others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr15 | 51710752 | |||||
chr15:51711042 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1208-2291A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711042 | ||||||
chr15:51711079 | C | T | 1 | a0001c0001t0004g0086 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1208-2254C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711079 | ||||||
chr15:51711353 | A | G | 1 | a0002c0003t0003g0373 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1208-1980A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711353 | ||||||
chr15:51711568 | A | T | 3 | a0001c0001t0003g0299a0001c0001t0003g0318a0001c0001t0003g0322 | 3 | HG01074.hp2 HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1208-1765A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711568 | ||||||
chr15:51711650 | A | G | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1208-1683A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711650 | ||||||
chr15:51711726 | C | G | 2 | a0001c0001t0001g0288a0001c0001t0001g0308 | 2 | HG02135.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1208-1607C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711726 | ||||||
chr15:51711814 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1208-1519C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711814 | ||||||
chr15:51711846 | T | C | 1 | a0001c0001t0014g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1208-1487T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51711846 | ||||||
chr15:51712053 | G | A | 264 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(261): Show | 274 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.1208-1280G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712053 | ||||||
chr15:51712209 | C | A | 1 | a0001c0001t0002g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1208-1124C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712209 | ||||||
chr15:51712363 | G | T | 39 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0003g0002others(36): Show | 43 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1208-970G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712363 | ||||||
chr15:51712420 | C | T | 3 | a0001c0001t0002g0197a0001c0001t0002g0198a0001c0001t0002g0199 | 3 | HG02970.hp1 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1208-913C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712420 | ||||||
chr15:51712452 | T | C | 1 | a0001c0001t0005g0070 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1208-881T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712452 | ||||||
chr15:51712587 | G | A | 4 | a0003c0004t0006g0261a0003c0004t0006g0262a0003c0004t0006g0270others(1): Show | 4 | NA18987.hp2 NA19006.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-746G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712587 | ||||||
chr15:51712700 | T | G | 8 | a0001c0001t0001g0280a0001c0001t0001g0284a0001c0001t0001g0285others(5): Show | 8 | HG02135.hp2 NA18956.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208-633T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712700 | ||||||
chr15:51712709 | A | T | 1 | a0001c0002t0004g0013 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1208-624A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712709 | ||||||
chr15:51712953 | T | C | 1 | a0002c0003t0003g0060 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1208-380T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51712953 | ||||||
chr15:51713085 | C | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 25 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1208-248C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51713085 | ||||||
chr15:51713089 | T | A | 1 | a0002c0003t0003g0057 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1208-244T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51713089 | ||||||
chr15:51713130 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1208-203C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 10/11 | chr15 | 51713130 | ||||||
chr15:51713511 | C | T | 4 | a0001c0002t0001g0343a0001c0002t0010g0340a0001c0002t0010g0341others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+98C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713511 | ||||||
chr15:51713516 | C | T | 48 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0091others(45): Show | 52 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.1288+103C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713516 | ||||||
chr15:51713517 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1288+104G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713517 | ||||||
chr15:51713639 | G | T | 46 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(43): Show | 47 | HG00423.hp1 HG01069.hp2 HG01256.hp2 others(44): Show |
intron_variant | MODIFIER | c.1288+226G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713639 | ||||||
chr15:51713701 | T | A | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1288+288T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713701 | ||||||
chr15:51713762 | T | G | 4 | a0001c0001t0001g0274a0001c0001t0001g0278a0001c0001t0001g0279others(1): Show | 4 | NA18612.hp2 NA18972.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+349T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713762 | ||||||
chr15:51713872 | G | T | 13 | a0001c0001t0001g0228a0001c0001t0002g0230a0001c0001t0006g0219others(10): Show | 13 | HG00597.hp2 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1288+459G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51713872 | ||||||
chr15:51714150 | C | T | 39 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0003g0002others(36): Show | 43 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1288+737C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714150 | ||||||
chr15:51714419 | G | A | 1 | a0002c0003t0012g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1288+1006G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714419 | ||||||
chr15:51714467 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1288+1054G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714467 | ||||||
chr15:51714472 | AG | A | 22 | a0001c0001t0001g0207a0001c0005t0005g0089a0002c0003t0003g0303others(19): Show | 22 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1288+1061delG | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51714472 | |||||
chr15:51714554 | C | T | 4 | a0001c0001t0008g0005a0001c0001t0008g0048a0001c0001t0008g0049others(1): Show | 5 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288+1141C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714554 | ||||||
chr15:51714581 | T | C | 2 | a0001c0005t0005g0089a0001c0005t0005g0090 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1288+1168T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714581 | ||||||
chr15:51714613 | C | T | 264 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0068others(261): Show | 274 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(271): Show |
intron_variant | MODIFIER | c.1288+1200C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51714613 | ||||||
chr15:51715020 | G | A | 214 | a0001c0001t0001g0051a0001c0001t0001g0091a0001c0001t0001g0107others(211): Show | 223 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1288+1607G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715020 | ||||||
chr15:51715325 | G | A | 193 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(190): Show | 201 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.1288+1912G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715325 | ||||||
chr15:51715381 | T | C | 18 | a0001c0001t0001g0091a0001c0001t0003g0042a0001c0001t0003g0044others(15): Show | 19 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1288+1968T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715381 | ||||||
chr15:51715426 | T | C | 236 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(233): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1288+2013T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715426 | ||||||
chr15:51715498 | C | T | 13 | a0001c0001t0006g0196a0001c0001t0006g0200a0001c0001t0006g0219others(10): Show | 13 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.1288+2085C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715498 | ||||||
chr15:51715529 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1288+2116T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715529 | ||||||
chr15:51715609 | C | G | 20 | a0001c0001t0001g0091a0001c0001t0005g0070a0001c0001t0005g0072others(17): Show | 21 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1288+2196C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715609 | ||||||
chr15:51715671 | C | G | 14 | a0001c0001t0001g0091a0001c0001t0005g0070a0001c0001t0005g0072others(11): Show | 15 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1288+2258C>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715671 | ||||||
chr15:51715861 | C | CT | 8 | a0001c0001t0008g0005a0001c0001t0008g0048a0001c0001t0008g0049others(5): Show | 9 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1288+2462dupT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51715861 | |||||
chr15:51715861 | CT | C | 15 | a0001c0001t0001g0091a0001c0001t0005g0070a0001c0001t0005g0072others(12): Show | 16 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1288+2462delT | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51715861 | |||||
chr15:51715889 | G | A | 14 | a0001c0001t0001g0091a0001c0001t0005g0070a0001c0001t0005g0072others(11): Show | 15 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1288+2476G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715889 | ||||||
chr15:51715911 | G | A | 1 | a0001c0002t0002g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1288+2498G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51715911 | ||||||
chr15:51716014 | T | A | 1 | a0001c0001t0014g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1288+2601T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716014 | ||||||
chr15:51716065 | G | T | 14 | a0001c0001t0001g0228a0001c0001t0006g0196a0001c0001t0006g0200others(11): Show | 14 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1288+2652G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716065 | ||||||
chr15:51716147 | G | A | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1288+2734G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716147 | ||||||
chr15:51716176 | T | C | 4 | a0001c0001t0001g0132a0001c0001t0001g0309a0001c0001t0001g0320others(1): Show | 4 | HG01433.hp1 HG02109.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+2763T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716176 | ||||||
chr15:51716270 | A | G | 2 | a0002c0003t0003g0060a0002c0003t0003g0384 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1288+2857A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716270 | ||||||
chr15:51716363 | G | A | 1 | a0001c0001t0016g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1288+2950G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716363 | ||||||
chr15:51716368 | G | A | 38 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(35): Show | 42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1288+2955G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716368 | ||||||
chr15:51716544 | A | G | 39 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(36): Show | 43 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1289-2864A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716544 | ||||||
chr15:51716745 | T | G | 38 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(35): Show | 42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1289-2663T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716745 | ||||||
chr15:51716838 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1289-2570T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716838 | ||||||
chr15:51716955 | G | A | 38 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(35): Show | 42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1289-2453G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51716955 | ||||||
chr15:51716959 | C | CTCACACC others(281): Show |
1 | a0001c0001t0002g0389 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1289-2273_1289-227 others(292): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51716959 | |||||
chr15:51717046 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1289-2362C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717046 | ||||||
chr15:51717050 | A | AC | 14 | a0001c0001t0001g0228a0001c0001t0006g0196a0001c0001t0006g0200others(11): Show | 14 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1289-2354dupC | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717050 | |||||
chr15:51717165 | C | T | 38 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(35): Show | 42 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1289-2243C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717165 | ||||||
chr15:51717281 | T | C | 39 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(36): Show | 43 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1289-2127T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717281 | ||||||
chr15:51717367 | C | CA | 22 | a0001c0001t0001g0295a0001c0001t0002g0215a0001c0001t0005g0070others(19): Show | 23 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1289-2025dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717367 | |||||
chr15:51717384 | T | A | 1 | a0001c0001t0007g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1289-2024T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717384 | ||||||
chr15:51717388 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1289-2020C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717388 | ||||||
chr15:51717441 | G | A | 12 | a0001c0001t0005g0070a0001c0001t0005g0072a0001c0001t0005g0073others(9): Show | 13 | HG01167.hp2 HG01169.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.1289-1967G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717441 | ||||||
chr15:51717548 | G | GA | 368 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(365): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1289-1851dupA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717548 | |||||
chr15:51717570 | T | TTCAGAGA others(6): Show |
1 | a0001c0001t0001g0162 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-1836_1289-182 others(17): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51717570 | |||||
chr15:51717689 | C | A | 1 | a0001c0001t0002g0170 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1289-1719C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717689 | ||||||
chr15:51717761 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1289-1647C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717761 | ||||||
chr15:51717762 | G | A | 1 | a0001c0001t0003g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1289-1646G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717762 | ||||||
chr15:51717859 | T | C | 1 | a0003c0004t0002g0265 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1289-1549T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51717859 | ||||||
chr15:51718183 | T | A | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1289-1225T>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718183 | ||||||
chr15:51718184 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1289-1224G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718184 | ||||||
chr15:51718187 | T | C | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-1221T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718187 | ||||||
chr15:51718195 | T | C | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1289-1213T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718195 | ||||||
chr15:51718195 | TAGATAGA others(9): Show |
T | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-1209_1289-119 others(20): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718195 | |||||
chr15:51718199 | T | C | 2 | a0001c0001t0002g0148a0001c0001t0006g0226 | 2 | NA18747.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1289-1209T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718199 | ||||||
chr15:51718199 | T | TAGAC | 47 | a0001c0001t0002g0189a0001c0001t0002g0230a0001c0001t0002g0241others(44): Show | 51 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1289-1173_1289-117 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | |||||
chr15:51718199 | T | TAGACAGA others(1): Show |
19 | a0001c0001t0003g0045a0001c0001t0003g0323a0002c0003t0003g0360others(16): Show | 19 | HG01255.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1289-1177_1289-117 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | |||||
chr15:51718199 | T | TAGACAGA others(5): Show |
3 | a0002c0003t0003g0364a0002c0003t0003g0366a0002c0003t0003g0367 | 3 | HG02280.hp2 HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1289-1181_1289-117 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | |||||
chr15:51718199 | TAGAC | T | 60 | a0001c0001t0001g0091a0001c0001t0001g0274a0001c0001t0001g0278others(57): Show | 61 | HG00140.hp1 HG00423.hp1 HG01123.hp1 others(58): Show |
intron_variant | MODIFIER | c.1289-1173_1289-117 others(8): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | |||||
chr15:51718199 | TAGACAGA others(1): Show |
T | 118 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1289-1177_1289-117 others(12): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | |||||
chr15:51718199 | TAGACAGA others(5): Show |
T | 2 | a0001c0001t0001g0150a0001c0001t0001g0201 | 2 | HG02074.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1289-1181_1289-117 others(16): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718199 | |||||
chr15:51718203 | C | T | 1 | a0001c0006t0011g0010 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1289-1205C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718203 | ||||||
chr15:51718207 | C | T | 5 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0005t0005g0089others(2): Show | 5 | HG02145.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-1201C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718207 | ||||||
chr15:51718239 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-1169T>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718239 | ||||||
chr15:51718296 | A | G | 2 | a0001c0002t0004g0347a0001c0002t0004g0359 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1289-1112A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718296 | ||||||
chr15:51718443 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-965T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718443 | ||||||
chr15:51718561 | CAACT | C | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-843_1289-840d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718561 | |||||
chr15:51718602 | G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0011others(77): Show | 84 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.1289-806G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718602 | ||||||
chr15:51718610 | C | T | 207 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1289-798C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718610 | ||||||
chr15:51718641 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1289-767G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718641 | ||||||
chr15:51718646 | TA | T | 189 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1289-758delA | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718646 | |||||
chr15:51718730 | T | TTTTG | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-662_1289-659d others(6): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718730 | |||||
chr15:51718753 | G | T | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-655G>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718753 | ||||||
chr15:51718802 | C | A | 1 | a0001c0001t0002g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1289-606C>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718802 | ||||||
chr15:51718807 | A | G | 132 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1289-601A>G | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718807 | ||||||
chr15:51718835 | CTT | C | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-572_1289-571d others(4): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51718835 | ||||||
chr15:51718890 | TAAGTCAG others(1): Show |
T | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-502_1289-495d others(10): Show |
SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr15 | 51718890 | |||||
chr15:51719011 | C | T | 17 | a0001c0001t0006g0032a0001c0001t0006g0196a0001c0001t0006g0200others(14): Show | 17 | HG02165.hp1 HG04115.hp2 NA18747.hp1 others(14): Show |
intron_variant | MODIFIER | c.1289-397C>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719011 | ||||||
chr15:51719021 | G | A | 1 | a0001c0002t0002g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1289-387G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719021 | ||||||
chr15:51719158 | A | C | 165 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1289-250A>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719158 | ||||||
chr15:51719215 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1289-193G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719215 | ||||||
chr15:51719229 | A | T | 7 | a0001c0001t0007g0063a0001c0001t0007g0064a0001c0001t0007g0065others(4): Show | 7 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-179A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719229 | ||||||
chr15:51719293 | G | A | 17 | a0001c0001t0005g0070a0001c0001t0005g0072a0001c0001t0005g0073others(14): Show | 17 | HG00140.hp1 HG02145.hp1 HG02922.hp1 others(14): Show |
intron_variant | MODIFIER | c.1289-115G>A | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719293 | ||||||
chr15:51719321 | T | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1289-87T>C | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719321 | ||||||
chr15:51719397 | A | T | 1 | a0002c0003t0003g0371 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1289-11A>T | SCG3 | ENSG00000104112.9 | transcript | ENST00000220478.8 | protein_coding | 11/11 | chr15 | 51719397 |