geneid | 22908 |
---|---|
ensemblid | ENSG00000211456.14 |
hgncid | 17059 |
symbol | SACM1L |
name | SAC1 like phosphatidylinositide phosphatase |
refseq_nuc | NM_014016.5 |
refseq_prot | NP_054735.3 |
ensembl_nuc | ENST00000389061.10 |
ensembl_prot | ENSP00000373713.4 |
mane_status | MANE Select |
chr | chr3 |
start | 45689396 |
end | 45745409 |
strand | + |
ver | v1.2 |
region | chr3:45689396-45745409 |
region5000 | chr3:45684396-45750409 |
regionname0 | SACM1L_chr3_45689396_45745409 |
regionname5000 | SACM1L_chr3_45684396_45750409 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 587 | 198 | 54 | 46 | 72 | 10 | 15 | 54 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0002 | 1/0 | 587 | 155 | 28 | 23 | 82 | 6 | 15 | 62 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0003 | 0/0 | 587 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1764 | 155 | 28 | 23 | 82 | 6 | 15 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
c0002 | 0/1 | 1764 | 141 | 35 | 31 | 53 | 10 | 11 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
c0003 | 0/0 | 1764 | 54 | 17 | 15 | 18 | 0 | 4 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
c0004 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
c0005 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
c0006 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1811 | 147 | 26 | 19 | 80 | 6 | 15 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0002 | 0/0 | 1812 | 127 | 35 | 42 | 32 | 6 | 12 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0003 | 0/0 | 1807 | 23 | 0 | 0 | 22 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0004 | 0/0 | 1812 | 19 | 16 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0005 | 0/0 | 1812 | 17 | 0 | 0 | 14 | 1 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0006 | 0/1 | 1812 | 4 | 0 | 1 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0007 | 0/0 | 1812 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0008 | 0/0 | 1811 | 3 | 0 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0009 | 0/0 | 1811 | 2 | 1 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0010 | 0/0 | 1811 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0011 | 0/0 | 1812 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0012 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0013 | 0/0 | 1812 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0014 | 0/0 | 1811 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
t0015 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 2 | 1 | 11 | 1 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0005 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0009 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0014 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/1 | 1764 | 141 | 35 | 31 | 53 | 10 | 11 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0003 | 0/0 | 1764 | 54 | 17 | 15 | 18 | 0 | 4 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0004 | 0/0 | 1764 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0006 | 0/0 | 1764 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0002c0001 | 1/0 | 1764 | 155 | 28 | 23 | 82 | 6 | 15 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0003c0005 | 0/0 | 1764 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 0/0 | 3575 | 70 | 17 | 26 | 13 | 6 | 8 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0003 | 0/0 | 3570 | 23 | 0 | 0 | 22 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0004 | 0/0 | 3575 | 19 | 16 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0005 | 0/0 | 3575 | 17 | 0 | 0 | 14 | 1 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0006 | 0/1 | 3575 | 4 | 0 | 1 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0007 | 0/0 | 3575 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0011 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0012 | 0/0 | 3575 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0002t0013 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0003t0002 | 0/0 | 3575 | 53 | 16 | 15 | 18 | 0 | 4 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0003t0015 | 0/0 | 3575 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0004t0002 | 0/0 | 3575 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0001c0006t0002 | 0/0 | 3575 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0002c0001t0001 | 1/0 | 3574 | 147 | 26 | 19 | 80 | 6 | 15 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0002c0001t0008 | 0/0 | 3574 | 3 | 0 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0002c0001t0009 | 0/0 | 3574 | 2 | 1 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0002c0001t0010 | 0/0 | 3574 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0002c0001t0014 | 0/0 | 3574 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
a0003c0005t0002 | 0/0 | 3575 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | copy fasta | chr3 | 45684396 | 45750409 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0009 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0014 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0006g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0006g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0011g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0012g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0002t0013g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0003 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0003t0015g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0004t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0004t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0001c0006t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0001 | 0/0 | 16 | 2 | 1 | 11 | 1 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0005 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0008g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0008g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0008g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0010g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0002c0001t0014g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
a0003c0005t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00099 | hp2 | a0002 | c0001 | t0001 | g0019 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0125 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00140 | hp2 | a0001 | c0002 | t0006 | g0016 | EUR | GBR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | FIN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00323 | hp2 | a0001 | c0002 | t0006 | g0016 | EUR | FIN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0226 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0166 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00558 | hp2 | a0002 | c0001 | t0001 | g0194 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00597 | hp1 | a0002 | c0001 | t0001 | g0193 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00597 | hp2 | a0001 | c0002 | t0007 | g0260 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00609 | hp2 | a0002 | c0001 | t0010 | g0023 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00621 | hp1 | a0001 | c0003 | t0002 | g0097 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00621 | hp2 | a0002 | c0001 | t0001 | g0222 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0186 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00733 | hp1 | a0002 | c0001 | t0001 | g0185 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00735 | hp1 | a0001 | c0002 | t0006 | g0150 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG00738 | hp2 | a0002 | c0001 | t0001 | g0067 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0146 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01069 | hp2 | a0002 | c0001 | t0001 | g0198 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01070 | hp2 | a0002 | c0001 | t0001 | g0189 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01074 | hp1 | a0002 | c0001 | t0001 | g0037 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0045 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0088 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01106 | hp2 | a0002 | c0001 | t0001 | g0215 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0106 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0025 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01167 | hp1 | a0001 | c0002 | t0004 | g0182 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01167 | hp2 | a0001 | c0003 | t0002 | g0084 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01168 | hp2 | a0001 | c0003 | t0002 | g0078 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0113 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01169 | hp2 | a0001 | c0002 | t0004 | g0183 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0208 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01243 | hp1 | a0002 | c0001 | t0009 | g0101 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0021 | AMR | PUR | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0063 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0131 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0098 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01257 | hp1 | a0001 | c0002 | t0013 | g0016 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01257 | hp2 | a0002 | c0001 | t0008 | g0190 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01258 | hp1 | a0002 | c0001 | t0008 | g0207 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01261 | hp2 | a0002 | c0001 | t0001 | g0249 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01346 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01358 | hp1 | a0002 | c0001 | t0008 | g0210 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01358 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01361 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01433 | hp1 | a0002 | c0001 | t0001 | g0074 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01433 | hp2 | a0001 | c0003 | t0002 | g0025 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01496 | hp1 | a0001 | c0003 | t0002 | g0091 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0040 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01515 | hp2 | a0001 | c0002 | t0012 | g0118 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0151 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0024 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01517 | hp2 | a0002 | c0001 | t0001 | g0024 | EUR | IBS | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01884 | hp1 | a0002 | c0001 | t0001 | g0052 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01891 | hp1 | a0001 | c0003 | t0002 | g0095 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01891 | hp2 | a0001 | c0003 | t0002 | g0107 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01928 | hp2 | a0002 | c0001 | t0001 | g0253 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01934 | hp2 | a0003 | c0005 | t0002 | g0013 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01943 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0122 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01975 | hp2 | a0002 | c0001 | t0001 | g0244 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01978 | hp2 | a0002 | c0001 | t0001 | g0038 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01993 | hp1 | a0002 | c0001 | t0001 | g0010 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02004 | hp1 | a0001 | c0003 | t0002 | g0087 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02004 | hp2 | a0002 | c0001 | t0001 | g0038 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0184 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02055 | hp1 | a0002 | c0001 | t0001 | g0056 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02055 | hp2 | a0001 | c0003 | t0002 | g0080 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02056 | hp1 | a0001 | c0002 | t0005 | g0174 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0246 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0228 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02080 | hp2 | a0001 | c0003 | t0002 | g0090 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02083 | hp1 | a0001 | c0003 | t0002 | g0026 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02129 | hp1 | a0002 | c0001 | t0010 | g0023 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02129 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02132 | hp1 | a0001 | c0002 | t0005 | g0149 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02135 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02145 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02148 | hp1 | a0002 | c0001 | t0001 | g0187 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02155 | hp1 | a0002 | c0001 | t0001 | g0199 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02155 | hp2 | a0001 | c0002 | t0005 | g0031 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0147 | EAS | CDX | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02257 | hp1 | a0001 | c0002 | t0004 | g0035 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02258 | hp1 | a0002 | c0001 | t0001 | g0211 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02280 | hp1 | a0001 | c0002 | t0004 | g0018 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02300 | hp2 | a0001 | c0002 | t0004 | g0180 | AMR | PEL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02451 | hp1 | a0001 | c0003 | t0002 | g0028 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02451 | hp2 | a0002 | c0001 | t0001 | g0104 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02523 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | KHV | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0079 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02622 | hp2 | a0002 | c0001 | t0001 | g0230 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0109 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02630 | hp2 | a0002 | c0001 | t0001 | g0027 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0142 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02647 | hp2 | a0002 | c0001 | t0001 | g0050 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02683 | hp2 | a0002 | c0001 | t0001 | g0039 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02735 | hp1 | a0002 | c0001 | t0001 | g0043 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02735 | hp2 | a0001 | c0002 | t0005 | g0148 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0116 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0218 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0047 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02886 | hp1 | a0001 | c0002 | t0011 | g0041 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02886 | hp2 | a0001 | c0003 | t0002 | g0094 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02895 | hp2 | a0002 | c0001 | t0001 | g0055 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0177 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02897 | hp2 | a0002 | c0001 | t0001 | g0054 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02965 | hp1 | a0001 | c0003 | t0002 | g0044 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02965 | hp2 | a0001 | c0003 | t0015 | g0046 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02970 | hp1 | a0001 | c0004 | t0002 | g0176 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02970 | hp2 | a0002 | c0001 | t0001 | g0005 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0022 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02976 | hp2 | a0001 | c0003 | t0002 | g0093 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03017 | hp1 | a0001 | c0003 | t0002 | g0076 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0141 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0178 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03098 | hp1 | a0001 | c0003 | t0002 | g0028 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03098 | hp2 | a0001 | c0002 | t0004 | g0100 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0110 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0144 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03139 | hp2 | a0001 | c0002 | t0011 | g0041 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03195 | hp1 | a0001 | c0003 | t0002 | g0096 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03195 | hp2 | a0001 | c0003 | t0002 | g0021 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03209 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03209 | hp2 | a0002 | c0001 | t0009 | g0102 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03225 | hp1 | a0002 | c0001 | t0001 | g0057 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03225 | hp2 | a0001 | c0002 | t0004 | g0033 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03453 | hp1 | a0002 | c0001 | t0001 | g0053 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03453 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03486 | hp1 | a0002 | c0001 | t0001 | g0058 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03486 | hp2 | a0002 | c0001 | t0001 | g0051 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03490 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03490 | hp2 | a0001 | c0003 | t0002 | g0083 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03491 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03516 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03516 | hp2 | a0002 | c0001 | t0001 | g0103 | AFR | ESN | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03540 | hp1 | a0001 | c0004 | t0002 | g0134 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0181 | AFR | GWD | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0145 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03579 | hp2 | a0002 | c0001 | t0001 | g0229 | AFR | MSL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03654 | hp1 | a0002 | c0001 | t0001 | g0232 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03669 | hp1 | a0002 | c0001 | t0001 | g0019 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03688 | hp1 | a0002 | c0001 | t0001 | g0019 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0120 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03704 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03704 | hp2 | a0002 | c0001 | t0001 | g0037 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0200 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03831 | hp1 | a0001 | c0002 | t0005 | g0161 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03831 | hp2 | a0002 | c0001 | t0001 | g0231 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0250 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0124 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG04184 | hp2 | a0002 | c0001 | t0001 | g0243 | SAS | BEB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0065 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0261 | SAS | STU | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18522 | hp1 | a0001 | c0003 | t0002 | g0105 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18522 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0263 | EAS | CHB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18747 | hp2 | a0002 | c0001 | t0001 | g0192 | EAS | CHB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18906 | hp1 | a0002 | c0001 | t0001 | g0022 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | YRI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0066 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18940 | hp1 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18940 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18941 | hp2 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18943 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18943 | hp2 | a0002 | c0001 | t0001 | g0069 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18944 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18944 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18946 | hp2 | a0002 | c0001 | t0001 | g0040 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18951 | hp1 | a0001 | c0003 | t0002 | g0086 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18951 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0039 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18952 | hp2 | a0001 | c0002 | t0005 | g0136 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0154 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18953 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18954 | hp1 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18954 | hp2 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18956 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18956 | hp2 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18957 | hp1 | a0001 | c0002 | t0005 | g0017 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18957 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18959 | hp1 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18959 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18960 | hp1 | a0001 | c0002 | t0005 | g0175 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18960 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18962 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18962 | hp2 | a0001 | c0002 | t0005 | g0031 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18963 | hp1 | a0002 | c0001 | t0001 | g0202 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18963 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18964 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18964 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18966 | hp1 | a0002 | c0001 | t0001 | g0060 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0073 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18967 | hp2 | a0002 | c0001 | t0001 | g0234 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18970 | hp1 | a0002 | c0001 | t0001 | g0225 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18970 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18974 | hp1 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18974 | hp2 | a0002 | c0001 | t0001 | g0209 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18977 | hp1 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18977 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18980 | hp1 | a0002 | c0001 | t0001 | g0247 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18980 | hp2 | a0002 | c0001 | t0001 | g0196 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18982 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18982 | hp2 | a0001 | c0003 | t0002 | g0077 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18983 | hp1 | a0002 | c0001 | t0001 | g0212 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18985 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18987 | hp1 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18987 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18988 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18989 | hp1 | a0001 | c0002 | t0005 | g0162 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18991 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18991 | hp2 | a0002 | c0001 | t0001 | g0061 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18992 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18992 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18993 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0026 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18994 | hp2 | a0001 | c0002 | t0005 | g0170 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18998 | hp1 | a0002 | c0001 | t0001 | g0204 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA18998 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0214 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19007 | hp2 | a0001 | c0002 | t0007 | g0258 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19009 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0219 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19010 | hp2 | a0001 | c0002 | t0007 | g0255 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19012 | hp2 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19030 | hp1 | a0002 | c0001 | t0014 | g0048 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19030 | hp2 | a0002 | c0001 | t0001 | g0111 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19054 | hp1 | a0002 | c0001 | t0001 | g0213 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19054 | hp2 | a0001 | c0002 | t0005 | g0158 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19055 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19055 | hp2 | a0001 | c0002 | t0005 | g0159 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19057 | hp1 | a0002 | c0001 | t0001 | g0191 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19057 | hp2 | a0001 | c0002 | t0007 | g0257 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19060 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19060 | hp2 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19062 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19062 | hp2 | a0001 | c0003 | t0002 | g0081 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19063 | hp1 | a0002 | c0001 | t0001 | g0241 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19063 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19065 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19065 | hp2 | a0001 | c0003 | t0002 | g0082 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19068 | hp1 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19068 | hp2 | a0001 | c0003 | t0002 | g0092 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19070 | hp1 | a0001 | c0002 | t0005 | g0017 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19070 | hp2 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19077 | hp1 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19077 | hp2 | a0001 | c0003 | t0002 | g0089 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19078 | hp2 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19079 | hp1 | a0001 | c0002 | t0005 | g0017 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19084 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19084 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19085 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19087 | hp1 | a0001 | c0002 | t0005 | g0171 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19087 | hp2 | a0002 | c0001 | t0001 | g0195 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0064 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19088 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA19091 | hp2 | a0002 | c0001 | t0001 | g0216 | EAS | JPT | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA20129 | hp1 | a0001 | c0002 | t0004 | g0035 | AFR | ASW | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0049 | AFR | ASW | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0251 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA20805 | hp1 | a0001 | c0002 | t0005 | g0160 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0029 | EUR | TSI | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0117 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG01123 | hp2 | a0001 | c0003 | t0002 | g0099 | AMR | CLM | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02109 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02486 | hp1 | a0002 | c0001 | t0001 | g0059 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02559 | hp1 | a0002 | c0001 | t0001 | g0062 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG02559 | hp2 | a0001 | c0002 | t0004 | g0179 | AFR | ACB | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | USA | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
HG06807 | hp2 | a0002 | c0001 | t0001 | g0206 | AFR | USA | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | LWK | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0006 | g0135 | REF | REF | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0001 | g0075 | REF | REF | SACM1L_chr3_45684396_45750409 | SACM1L | chr3 | 45684396 | 45750409 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:45732099
|
G | A | 1 | a0003 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.1048G>A | p.Asp350Asn | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/20 | 1118/3574 | 1048/1764 | 350/587 | chr3 | 45732099 | ||
chr3:45737644
|
A | T | 2 | a0001a0003 | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
missense_variant | MODERATE | c.1301A>T | p.Tyr434Phe | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 15/20 | 1371/3574 | 1301/1764 | 434/587 | chr3 | 45737644 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:45713193
|
A | G | 2 | a0001c0003a0001c0006 | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
synonymous_variant | LOW | c.540A>G | p.Pro180Pro | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/20 | 610/3574 | 540/1764 | 180/587 | chr3 | 45713193 | ||
chr3:45731339
|
A | G | 1 | a0001c0004 | 2 | HG02970.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.960A>G | p.Thr320Thr | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/20 | 1030/3574 | 960/1764 | 320/587 | chr3 | 45731339 | ||
chr3:45732074
|
T | C | 1 | a0001c0006 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.1023T>C | p.His341His | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/20 | 1093/3574 | 1023/1764 | 341/587 | chr3 | 45732074 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:45689427
|
G | A | 1 | a0002c0001t0008 | 3 | HG01257.hp2 HG01258.hp1 HG01358.hp1 |
5_prime_UTR_variant | MODIFIER | c.-39G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/20 | 39 | chr3 | 45689427 | |||||
chr3:45689445
|
G | A | 1 | a0001c0002t0012 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/20 | 21 | chr3 | 45689445 | |||||
chr3:45743965
|
A | G | 1 | a0001c0002t0011 | 2 | HG02886.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 296 | chr3 | 45743965 | |||||
chr3:45744274
|
G | A | 1 | a0001c0002t0013 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 605 | chr3 | 45744274 | |||||
chr3:45744423
|
T | G | 2 | a0001c0002t0006a0001c0002t0013 | 5 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*754T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 754 | chr3 | 45744423 | |||||
chr3:45744474
|
C | G | 2 | a0001c0002t0003a0001c0002t0005 | 40 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*805C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 805 | chr3 | 45744474 | |||||
chr3:45744556
|
C | G | 1 | a0001c0002t0007 | 4 | HG00597.hp2 NA19007.hp2 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*887C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 887 | chr3 | 45744556 | |||||
chr3:45744615
|
A | G | 1 | a0001c0003t0015 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*946A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 946 | chr3 | 45744615 | |||||
chr3:45744828
|
A | T | 1 | a0002c0001t0010 | 2 | HG00609.hp2 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1159A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1159 | chr3 | 45744828 | |||||
chr3:45744847
|
T | TA | 14 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(11): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1181dupA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1182 | INFO_REALIGN_3_PRIME | chr3 | 45744847 | ||||
chr3:45744851
|
T | C | 14 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(11): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1182T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1182 | chr3 | 45744851 | |||||
chr3:45744856
|
C | T | 1 | a0002c0001t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1187C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1187 | chr3 | 45744856 | |||||
chr3:45744913
|
T | C | 1 | a0002c0001t0009 | 2 | HG01243.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1244 | chr3 | 45744913 | |||||
chr3:45745006
|
TTAATA | T | 1 | a0001c0002t0003 | 23 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1341_*1345delTATA others(1): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1341 | INFO_REALIGN_3_PRIME | chr3 | 45745006 | ||||
chr3:45745012
|
T | G | 1 | a0002c0001t0010 | 2 | HG00609.hp2 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1343T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1343 | chr3 | 45745012 | |||||
chr3:45745108
|
A | T | 1 | a0001c0002t0004 | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1439A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1439 | chr3 | 45745108 | |||||
chr3:45745389
|
A | G | 1 | a0001c0002t0004 | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1720A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 20/20 | 1720 | chr3 | 45745389 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:45689584
|
G | C | 1 | a0002c0001t0001g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.32+87G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689584 | ||||||
chr3:45689771
|
G | T | 11 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(8): Show | 12 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.32+274G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689771 | ||||||
chr3:45689783
|
A | G | 80 | a0001c0002t0011g0041a0002c0001t0001g0001a0002c0001t0001g0005others(77): Show | 111 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.32+286A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689783 | ||||||
chr3:45689862
|
A | G | 23 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(20): Show | 30 | HG00438.hp1 HG00597.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.32+365A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689862 | ||||||
chr3:45689912
|
A | G | 1 | a0002c0001t0001g0253 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.32+415A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689912 | ||||||
chr3:45689959
|
C | T | 104 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(101): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.32+462C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689959 | ||||||
chr3:45689972
|
G | GC | 5 | a0001c0003t0002g0021a0001c0003t0002g0044a0001c0003t0002g0045others(2): Show | 6 | HG01074.hp2 HG01243.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.32+480dupC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45689972 | |||||
chr3:45689976
|
C | G | 1 | a0002c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.32+479C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45689976 | ||||||
chr3:45690089
|
A | G | 1 | a0001c0004t0002g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.32+592A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690089 | ||||||
chr3:45690152
|
C | G | 1 | a0002c0001t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.32+655C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690152 | ||||||
chr3:45690240
|
A | C | 48 | a0001c0002t0002g0004a0001c0002t0002g0137a0001c0002t0002g0138others(45): Show | 64 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.32+743A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690240 | ||||||
chr3:45690292
|
T | C | 103 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(100): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.32+795T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690292 | ||||||
chr3:45690297
|
T | C | 1 | a0002c0001t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.32+800T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690297 | ||||||
chr3:45690428
|
C | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+931C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690428 | ||||||
chr3:45690437
|
G | A | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+940G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690437 | ||||||
chr3:45690551
|
T | G | 1 | a0001c0002t0006g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.32+1054T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690551 | ||||||
chr3:45690552
|
T | C | 35 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0013others(32): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.32+1055T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690552 | ||||||
chr3:45690571
|
A | G | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+1074A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690571 | ||||||
chr3:45690710
|
C | T | 9 | a0001c0003t0002g0021a0001c0003t0002g0028a0001c0003t0002g0044others(6): Show | 11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.32+1213C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690710 | ||||||
chr3:45690716
|
CCTCCACA others(7): Show |
C | 125 | a0001c0002t0004g0100a0001c0003t0002g0003a0001c0003t0002g0006others(122): Show | 171 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.32+1226_32+1239del others(14): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45690716 | |||||
chr3:45690745
|
A | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+1248A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690745 | ||||||
chr3:45690917
|
G | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+1420G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690917 | ||||||
chr3:45690926
|
G | GT | 23 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0014others(20): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.32+1430dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45690926 | |||||
chr3:45690941
|
G | A | 1 | a0002c0001t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.32+1444G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690941 | ||||||
chr3:45690974
|
A | C | 1 | a0001c0003t0002g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.32+1477A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45690974 | ||||||
chr3:45691023
|
T | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+1526T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691023 | ||||||
chr3:45691074
|
T | C | 1 | a0001c0002t0002g0254 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.32+1577T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691074 | ||||||
chr3:45691105
|
C | G | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+1608C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691105 | ||||||
chr3:45691256
|
A | T | 1 | a0001c0002t0005g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.32+1759A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691256 | ||||||
chr3:45691328
|
G | A | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+1831G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691328 | ||||||
chr3:45691598
|
G | GT | 14 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(11): Show | 16 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.32+2111dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45691598 | |||||
chr3:45691598
|
G | GTT | 95 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(92): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.32+2110_32+2111dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45691598 | |||||
chr3:45691599
|
T | C | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+2102T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691599 | ||||||
chr3:45691759
|
T | A | 1 | a0002c0001t0001g0186 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.32+2262T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691759 | ||||||
chr3:45691938
|
A | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+2441A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691938 | ||||||
chr3:45691963
|
A | G | 1 | a0002c0001t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.32+2466A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45691963 | ||||||
chr3:45692026
|
C | T | 2 | a0001c0003t0002g0098a0001c0003t0002g0099 | 2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.32+2529C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692026 | ||||||
chr3:45692114
|
G | A | 1 | a0002c0001t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.32+2617G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692114 | ||||||
chr3:45692149
|
C | G | 3 | a0002c0001t0001g0249a0002c0001t0001g0250a0002c0001t0001g0251 | 3 | HG01261.hp2 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.32+2652C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692149 | ||||||
chr3:45692219
|
G | A | 95 | a0001c0002t0004g0100a0001c0003t0002g0021a0001c0003t0002g0028others(92): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.32+2722G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692219 | ||||||
chr3:45692316
|
GT | G | 32 | a0002c0001t0001g0011a0002c0001t0001g0022a0002c0001t0001g0024others(29): Show | 37 | HG00609.hp2 HG00738.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.32+2834delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45692316 | |||||
chr3:45692316
|
GTT | G | 233 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(230): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.32+2833_32+2834del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45692316 | |||||
chr3:45692335
|
A | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+2838A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692335 | ||||||
chr3:45692766
|
A | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+3269A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692766 | ||||||
chr3:45692912
|
G | A | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+3415G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692912 | ||||||
chr3:45692992
|
A | C | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.32+3495A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45692992 | ||||||
chr3:45693266
|
G | A | 7 | a0001c0002t0004g0033a0001c0002t0004g0034a0001c0002t0004g0035others(4): Show | 11 | HG02257.hp1 HG02559.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+3769G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693266 | ||||||
chr3:45693326
|
T | C | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+3829T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693326 | ||||||
chr3:45693416
|
G | T | 1 | a0001c0002t0004g0036 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.32+3919G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693416 | ||||||
chr3:45693483
|
A | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+3986A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693483 | ||||||
chr3:45693650
|
T | C | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+4153T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693650 | ||||||
chr3:45693660
|
A | G | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.32+4163A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693660 | ||||||
chr3:45693664
|
A | G | 1 | a0001c0002t0004g0179 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.32+4167A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693664 | ||||||
chr3:45693700
|
A | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+4203A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693700 | ||||||
chr3:45693726
|
G | A | 35 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0013others(32): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.32+4229G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693726 | ||||||
chr3:45693793
|
A | G | 1 | a0001c0003t0002g0097 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.32+4296A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45693793 | ||||||
chr3:45694025
|
G | A | 1 | a0002c0001t0001g0187 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.32+4528G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694025 | ||||||
chr3:45694087
|
G | A | 26 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(23): Show | 37 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.32+4590G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694087 | ||||||
chr3:45694118
|
T | C | 4 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0002t0002g0139others(1): Show | 4 | NA18939.hp2 NA18985.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+4621T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694118 | ||||||
chr3:45694126
|
A | C | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+4629A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694126 | ||||||
chr3:45694238
|
T | A | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+4741T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694238 | ||||||
chr3:45694409
|
A | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+4912A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694409 | ||||||
chr3:45694652
|
T | A | 1 | a0001c0003t0002g0076 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.32+5155T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694652 | ||||||
chr3:45694686
|
G | A | 3 | a0001c0002t0004g0100a0002c0001t0009g0101a0002c0001t0009g0102 | 3 | HG01243.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.32+5189G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694686 | ||||||
chr3:45694768
|
A | G | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.32+5271A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694768 | ||||||
chr3:45694931
|
A | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+5434A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694931 | ||||||
chr3:45694971
|
A | C | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+5474A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45694971 | ||||||
chr3:45695026
|
G | C | 1 | a0001c0003t0002g0077 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.32+5529G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695026 | ||||||
chr3:45695130
|
A | G | 1 | a0002c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.32+5633A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695130 | ||||||
chr3:45695266
|
CT | C | 81 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0010others(78): Show | 111 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.32+5781delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45695266 | |||||
chr3:45695330
|
G | A | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.32+5833G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695330 | ||||||
chr3:45695421
|
C | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+5924C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695421 | ||||||
chr3:45695469
|
C | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+5972C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695469 | ||||||
chr3:45695484
|
C | T | 12 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(9): Show | 18 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+5987C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695484 | ||||||
chr3:45695615
|
A | C | 1 | a0002c0001t0001g0246 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.32+6118A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695615 | ||||||
chr3:45695629
|
C | G | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+6132C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695629 | ||||||
chr3:45695768
|
C | T | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.32+6271C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695768 | ||||||
chr3:45695803
|
T | A | 3 | a0002c0001t0001g0050a0002c0001t0001g0051a0002c0001t0001g0052 | 3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.32+6306T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695803 | ||||||
chr3:45695858
|
G | A | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.32+6361G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695858 | ||||||
chr3:45695950
|
A | G | 2 | a0001c0004t0002g0134a0001c0004t0002g0176 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.32+6453A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695950 | ||||||
chr3:45695975
|
G | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+6478G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45695975 | ||||||
chr3:45695997
|
CTT | C | 46 | a0001c0002t0002g0004a0001c0002t0002g0137a0001c0002t0002g0138others(43): Show | 62 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.32+6517_32+6518del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45695997 | |||||
chr3:45695997
|
CTTTT | C | 7 | a0001c0002t0004g0100a0002c0001t0001g0027a0002c0001t0001g0103others(4): Show | 8 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.32+6515_32+6518del others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45695997 | |||||
chr3:45696137
|
T | G | 1 | a0001c0002t0003g0141 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.32+6640T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696137 | ||||||
chr3:45696221
|
T | C | 3 | a0001c0003t0002g0025a0001c0003t0002g0078a0001c0003t0002g0079 | 4 | HG01109.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+6724T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696221 | ||||||
chr3:45696233
|
G | A | 1 | a0001c0002t0012g0118 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.32+6736G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696233 | ||||||
chr3:45696310
|
C | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.32+6813C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696310 | ||||||
chr3:45696326
|
T | A | 1 | a0001c0002t0004g0018 | 3 | HG02109.hp2 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.32+6829T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696326 | ||||||
chr3:45696352
|
C | T | 48 | a0001c0002t0002g0004a0001c0002t0002g0137a0001c0002t0002g0138others(45): Show | 64 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.32+6855C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696352 | ||||||
chr3:45696399
|
G | A | 2 | a0002c0001t0001g0103a0002c0001t0001g0104 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.32+6902G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696399 | ||||||
chr3:45696522
|
A | G | 1 | a0001c0003t0015g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.33-6916A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696522 | ||||||
chr3:45696615
|
C | T | 35 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0013others(32): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-6823C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696615 | ||||||
chr3:45696741
|
A | G | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-6697A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696741 | ||||||
chr3:45696764
|
C | T | 12 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(9): Show | 18 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-6674C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45696764 | ||||||
chr3:45697141
|
T | G | 8 | a0002c0001t0001g0022a0002c0001t0001g0053a0002c0001t0001g0054others(5): Show | 9 | HG02055.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-6297T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697141 | ||||||
chr3:45697199
|
G | A | 4 | a0001c0002t0002g0142a0001c0002t0002g0143a0001c0002t0002g0144others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-6239G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697199 | ||||||
chr3:45697267
|
TC | T | 4 | a0001c0002t0002g0146a0001c0002t0003g0147a0001c0002t0003g0173others(1): Show | 4 | HG01069.hp1 HG02165.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-6169delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697267 | |||||
chr3:45697268
|
C | CT | 11 | a0001c0002t0002g0139a0001c0002t0002g0140a0001c0002t0002g0165others(8): Show | 12 | HG00558.hp1 HG01361.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.33-6170_33-6169ins others(1): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697268 | ||||||
chr3:45697269
|
C | CT | 15 | a0001c0002t0002g0117a0001c0002t0002g0131a0001c0002t0002g0132others(12): Show | 17 | HG01123.hp1 HG01255.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-6144dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
C | CTT | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.33-6145_33-6144dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
C | CTTTT | 14 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(11): Show | 15 | HG00438.hp1 HG00597.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.33-6147_33-6144dup others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
C | CTTTTT | 26 | a0001c0002t0002g0261a0001c0002t0002g0262a0001c0003t0002g0003others(23): Show | 38 | HG00438.hp2 HG00621.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.33-6148_33-6144dup others(5): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
C | CTTTTTTT others(4): Show |
1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-6154_33-6144dup others(11): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
C | CTTTTTTT others(5): Show |
1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33-6155_33-6144dup others(12): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
C | T | 44 | a0001c0002t0002g0004a0001c0002t0002g0137a0001c0002t0002g0138others(41): Show | 60 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.33-6169C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697269 | ||||||
chr3:45697269
|
CT | C | 7 | a0001c0002t0002g0119a0002c0001t0001g0037a0002c0001t0001g0188others(4): Show | 8 | HG00738.hp1 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-6144delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
CTTTTTTT others(2): Show |
C | 12 | a0001c0002t0004g0100a0001c0003t0002g0021a0001c0003t0002g0028others(9): Show | 14 | HG01074.hp2 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-6152_33-6144del others(9): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697269
|
CTTTTTTT others(3): Show |
C | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-6153_33-6144del others(10): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45697269 | |||||
chr3:45697655
|
G | T | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-5783G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45697655 | ||||||
chr3:45698119
|
A | G | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-5319A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698119 | ||||||
chr3:45698272
|
C | G | 3 | a0002c0001t0001g0241a0002c0001t0001g0242a0002c0001t0001g0248 | 3 | NA18977.hp1 NA19012.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.33-5166C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698272 | ||||||
chr3:45698315
|
G | T | 90 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(87): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.33-5123G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698315 | ||||||
chr3:45698355
|
C | G | 3 | a0002c0001t0001g0050a0002c0001t0001g0051a0002c0001t0001g0052 | 3 | HG01884.hp1 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.33-5083C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698355 | ||||||
chr3:45698623
|
T | TCACTGCA others(9): Show |
1 | a0002c0001t0001g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.33-4814_33-4799dup others(16): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45698623 | |||||
chr3:45698707
|
T | C | 81 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0013others(78): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.33-4731T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698707 | ||||||
chr3:45698786
|
T | C | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-4652T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698786 | ||||||
chr3:45698807
|
A | G | 91 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0013others(88): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.33-4631A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698807 | ||||||
chr3:45698896
|
G | A | 3 | a0001c0002t0002g0014a0001c0002t0002g0120a0001c0002t0002g0121 | 5 | HG00639.hp2 HG01192.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-4542G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698896 | ||||||
chr3:45698918
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-4520G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45698918 | ||||||
chr3:45699009
|
G | A | 1 | a0002c0001t0001g0193 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.33-4429G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699009 | ||||||
chr3:45699066
|
T | C | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-4372T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699066 | ||||||
chr3:45699257
|
A | G | 2 | a0001c0003t0002g0007a0001c0003t0002g0077 | 5 | NA18954.hp1 NA18964.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-4181A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699257 | ||||||
chr3:45699284
|
A | T | 26 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(23): Show | 37 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-4154A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699284 | ||||||
chr3:45699288
|
T | A | 153 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(150): Show | 206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.33-4150T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699288 | ||||||
chr3:45699304
|
A | T | 1 | a0001c0002t0003g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.33-4134A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699304 | ||||||
chr3:45699341
|
A | T | 1 | a0002c0001t0001g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.33-4097A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699341 | ||||||
chr3:45699371
|
G | A | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.33-4067G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699371 | ||||||
chr3:45699468
|
A | AAAATTAT | 246 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(243): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.33-3963_33-3957dup others(7): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45699468 | |||||
chr3:45699490
|
T | C | 1 | a0001c0002t0005g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.33-3948T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699490 | ||||||
chr3:45699551
|
T | G | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-3887T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699551 | ||||||
chr3:45699608
|
A | G | 154 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(151): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.33-3830A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699608 | ||||||
chr3:45699695
|
T | G | 3 | a0002c0001t0001g0249a0002c0001t0001g0250a0002c0001t0001g0251 | 3 | HG01261.hp2 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.33-3743T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699695 | ||||||
chr3:45699727
|
G | A | 2 | a0002c0001t0001g0060a0002c0001t0001g0247 | 2 | NA18966.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.33-3711G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699727 | ||||||
chr3:45699727
|
G | T | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.33-3711G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699727 | ||||||
chr3:45699765
|
G | T | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.33-3673G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699765 | ||||||
chr3:45699768
|
C | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-3670C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699768 | ||||||
chr3:45699905
|
T | C | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.33-3533T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45699905 | ||||||
chr3:45700150
|
C | T | 1 | a0002c0001t0009g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.33-3288C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700150 | ||||||
chr3:45700241
|
A | G | 1 | a0002c0001t0001g0235 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.33-3197A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700241 | ||||||
chr3:45700529
|
G | A | 1 | a0001c0002t0002g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.33-2909G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700529 | ||||||
chr3:45700753
|
A | G | 1 | a0002c0001t0001g0234 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.33-2685A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700753 | ||||||
chr3:45700826
|
C | T | 1 | a0001c0002t0002g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.33-2612C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700826 | ||||||
chr3:45700869
|
A | G | 1 | a0001c0003t0002g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.33-2569A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700869 | ||||||
chr3:45700932
|
A | C | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-2506A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45700932 | ||||||
chr3:45701312
|
C | G | 29 | a0001c0002t0003g0002a0001c0002t0003g0032a0001c0002t0003g0141others(26): Show | 40 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.33-2126C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701312 | ||||||
chr3:45701361
|
T | C | 3 | a0001c0002t0002g0112a0001c0002t0002g0113a0001c0002t0002g0116 | 3 | HG01168.hp1 HG01169.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.33-2077T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701361 | ||||||
chr3:45701502
|
G | A | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33-1936G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701502 | ||||||
chr3:45701559
|
T | C | 1 | a0002c0001t0001g0194 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.33-1879T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701559 | ||||||
chr3:45701621
|
A | G | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-1817A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701621 | ||||||
chr3:45701785
|
G | A | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.33-1653G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701785 | ||||||
chr3:45701857
|
C | T | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-1581C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701857 | ||||||
chr3:45701898
|
G | T | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-1540G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45701898 | ||||||
chr3:45702052
|
A | G | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.33-1386A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702052 | ||||||
chr3:45702146
|
A | C | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-1292A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702146 | ||||||
chr3:45702163
|
G | C | 1 | a0001c0002t0002g0122 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.33-1275G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702163 | ||||||
chr3:45702182
|
GT | G | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-1255delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702182 | ||||||
chr3:45702215
|
G | A | 246 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(243): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.33-1223G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702215 | ||||||
chr3:45702421
|
A | G | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-1017A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702421 | ||||||
chr3:45702424
|
C | A | 2 | a0001c0004t0002g0134a0001c0004t0002g0176 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.33-1014C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702424 | ||||||
chr3:45702596
|
A | G | 1 | a0002c0001t0001g0233 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.33-842A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702596 | ||||||
chr3:45702698
|
C | G | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.33-740C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702698 | ||||||
chr3:45702727
|
T | C | 4 | a0001c0002t0002g0142a0001c0002t0002g0143a0001c0002t0002g0144others(1): Show | 4 | HG02615.hp2 HG02647.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-711T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702727 | ||||||
chr3:45702756
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-682G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702756 | ||||||
chr3:45702785
|
A | G | 2 | a0001c0004t0002g0134a0001c0004t0002g0176 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.33-653A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702785 | ||||||
chr3:45702800
|
C | T | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.33-638C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45702800 | ||||||
chr3:45703014
|
C | T | 2 | a0001c0002t0002g0030a0001c0002t0002g0119 | 3 | HG00738.hp1 HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.33-424C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703014 | ||||||
chr3:45703019
|
G | A | 1 | a0002c0001t0001g0194 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.33-419G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703019 | ||||||
chr3:45703047
|
G | T | 1 | a0001c0003t0002g0099 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.33-391G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703047 | ||||||
chr3:45703106
|
C | T | 1 | a0001c0002t0003g0172 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.33-332C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703106 | ||||||
chr3:45703154
|
T | G | 1 | a0001c0002t0002g0008 | 4 | HG01106.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-284T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | chr3 | 45703154 | ||||||
chr3:45703201
|
AT | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.33-230delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr3 | 45703201 | |||||
chr3:45703582
|
A | C | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+47A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45703582 | ||||||
chr3:45703590
|
C | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+55C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45703590 | ||||||
chr3:45704227
|
C | T | 1 | a0002c0001t0001g0232 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130+692C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704227 | ||||||
chr3:45704281
|
G | A | 2 | a0002c0001t0001g0188a0002c0001t0001g0195 | 2 | NA18941.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.130+746G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704281 | ||||||
chr3:45704281
|
G | C | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.130+746G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704281 | ||||||
chr3:45704352
|
G | A | 1 | a0002c0001t0001g0196 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.131-783G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704352 | ||||||
chr3:45704353
|
G | A | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.131-782G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704353 | ||||||
chr3:45704368
|
G | A | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.131-767G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704368 | ||||||
chr3:45704400
|
G | A | 1 | a0002c0001t0001g0197 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.131-735G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704400 | ||||||
chr3:45704412
|
G | A | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.131-723G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704412 | ||||||
chr3:45704518
|
A | G | 9 | a0001c0003t0002g0021a0001c0003t0002g0028a0001c0003t0002g0044others(6): Show | 11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.131-617A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704518 | ||||||
chr3:45704872
|
T | G | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.131-263T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704872 | ||||||
chr3:45704873
|
T | C | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.131-262T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45704873 | ||||||
chr3:45705108
|
T | C | 1 | a0001c0003t0015g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.131-27T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 2/19 | chr3 | 45705108 | ||||||
chr3:45705344
|
A | G | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.205+135A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705344 | ||||||
chr3:45705496
|
A | AT | 48 | a0001c0002t0002g0116a0001c0002t0002g0117a0001c0002t0005g0162others(45): Show | 67 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.205+310dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 45705496 | |||||
chr3:45705496
|
AT | A | 33 | a0001c0002t0002g0123a0001c0002t0002g0137a0001c0002t0002g0139others(30): Show | 44 | HG00099.hp2 HG00558.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.205+310delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr3 | 45705496 | |||||
chr3:45705588
|
C | T | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.205+379C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705588 | ||||||
chr3:45705645
|
G | A | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.205+436G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705645 | ||||||
chr3:45705860
|
G | A | 2 | a0002c0001t0001g0103a0002c0001t0001g0104 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.205+651G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705860 | ||||||
chr3:45705933
|
G | A | 1 | a0002c0001t0001g0061 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.205+724G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45705933 | ||||||
chr3:45706005
|
C | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.206-775C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706005 | ||||||
chr3:45706172
|
G | T | 1 | a0001c0003t0002g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.206-608G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706172 | ||||||
chr3:45706408
|
G | T | 1 | a0002c0001t0001g0038 | 2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.206-372G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706408 | ||||||
chr3:45706460
|
C | T | 1 | a0002c0001t0001g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.206-320C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706460 | ||||||
chr3:45706517
|
C | G | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.206-263C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 3/19 | chr3 | 45706517 | ||||||
chr3:45706937
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.333+30G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45706937 | ||||||
chr3:45706943
|
A | G | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.333+36A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45706943 | ||||||
chr3:45707107
|
T | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.333+200T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707107 | ||||||
chr3:45707140
|
A | G | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.333+233A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707140 | ||||||
chr3:45707488
|
T | C | 1 | a0001c0002t0002g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.333+581T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707488 | ||||||
chr3:45707602
|
A | T | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.333+695A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707602 | ||||||
chr3:45707691
|
G | A | 13 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0002t0002g0139others(10): Show | 14 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.333+784G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707691 | ||||||
chr3:45707810
|
A | G | 1 | a0001c0002t0002g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.333+903A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707810 | ||||||
chr3:45707973
|
A | G | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.333+1066A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45707973 | ||||||
chr3:45708055
|
AC | A | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.333+1149delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708055 | ||||||
chr3:45708185
|
G | C | 1 | a0001c0003t0002g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.333+1278G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708185 | ||||||
chr3:45708230
|
T | C | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.334-1268T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708230 | ||||||
chr3:45708344
|
T | G | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.334-1154T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708344 | ||||||
chr3:45708406
|
A | G | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1092A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708406 | ||||||
chr3:45708488
|
G | T | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-1010G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708488 | ||||||
chr3:45708523
|
C | T | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.334-975C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708523 | ||||||
chr3:45708708
|
C | T | 13 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0002t0002g0139others(10): Show | 14 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.334-790C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708708 | ||||||
chr3:45708767
|
T | C | 19 | a0001c0002t0003g0002a0001c0002t0003g0032a0001c0002t0003g0141others(16): Show | 28 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.334-731T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708767 | ||||||
chr3:45708791
|
T | G | 1 | a0002c0001t0001g0237 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.334-707T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45708791 | ||||||
chr3:45709382
|
C | T | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.334-116C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45709382 | ||||||
chr3:45709494
|
A | G | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
splice_region_variant&intron_variant | LOW | c.334-4A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 4/19 | chr3 | 45709494 | ||||||
chr3:45709737
|
C | T | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.483+90C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45709737 | ||||||
chr3:45709944
|
A | G | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.483+297A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45709944 | ||||||
chr3:45710224
|
A | G | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.483+577A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710224 | ||||||
chr3:45710271
|
G | A | 2 | a0001c0002t0002g0125a0001c0002t0002g0131 | 2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.483+624G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710271 | ||||||
chr3:45710498
|
G | A | 3 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0110 | 3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483+851G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710498 | ||||||
chr3:45710500
|
C | CT | 91 | a0001c0003t0002g0021a0001c0003t0002g0028a0001c0003t0002g0044others(88): Show | 124 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.483+871dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | |||||
chr3:45710500
|
C | CTT | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 42 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.483+870_483+871dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | |||||
chr3:45710500
|
C | CTTT | 5 | a0001c0003t0002g0012a0001c0003t0002g0093a0001c0003t0002g0094others(2): Show | 7 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.483+869_483+871dup others(3): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | |||||
chr3:45710500
|
CT | C | 95 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(92): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.483+871delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45710500 | |||||
chr3:45710535
|
A | G | 1 | a0002c0001t0001g0186 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.483+888A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710535 | ||||||
chr3:45710597
|
G | A | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.483+950G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710597 | ||||||
chr3:45710737
|
G | T | 106 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(103): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.483+1090G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710737 | ||||||
chr3:45710801
|
C | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.483+1154C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710801 | ||||||
chr3:45710848
|
G | T | 1 | a0002c0001t0001g0027 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.483+1201G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710848 | ||||||
chr3:45710951
|
G | A | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.483+1304G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710951 | ||||||
chr3:45710979
|
C | T | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.483+1332C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45710979 | ||||||
chr3:45711119
|
T | C | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.483+1472T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711119 | ||||||
chr3:45711158
|
T | C | 1 | a0002c0001t0001g0202 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.483+1511T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711158 | ||||||
chr3:45711392
|
C | T | 2 | a0001c0002t0003g0168a0001c0002t0003g0169 | 2 | NA18944.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.483+1745C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711392 | ||||||
chr3:45711421
|
G | A | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-1716G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711421 | ||||||
chr3:45711542
|
C | T | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.484-1595C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711542 | ||||||
chr3:45711694
|
A | G | 3 | a0001c0002t0005g0148a0001c0002t0005g0160a0001c0002t0005g0161 | 3 | HG02735.hp2 HG03831.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.484-1443A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711694 | ||||||
chr3:45711719
|
A | G | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.484-1418A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711719 | ||||||
chr3:45711803
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.484-1334G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711803 | ||||||
chr3:45711995
|
C | T | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.484-1142C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45711995 | ||||||
chr3:45712047
|
A | G | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.484-1090A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712047 | ||||||
chr3:45712087
|
A | G | 246 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(243): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.484-1050A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712087 | ||||||
chr3:45712172
|
GC | G | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.484-964delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712172 | ||||||
chr3:45712173
|
C | G | 94 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(91): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.484-964C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712173 | ||||||
chr3:45712501
|
G | A | 1 | a0001c0002t0005g0160 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.484-636G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712501 | ||||||
chr3:45712528
|
G | A | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.484-609G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712528 | ||||||
chr3:45712715
|
A | G | 3 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0110 | 3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.484-422A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712715 | ||||||
chr3:45712740
|
C | T | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.484-397C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712740 | ||||||
chr3:45712810
|
T | TTAG | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.484-325_484-323dup others(3): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr3 | 45712810 | |||||
chr3:45712995
|
C | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.484-142C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45712995 | ||||||
chr3:45713067
|
G | A | 1 | a0002c0001t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.484-70G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 5/19 | chr3 | 45713067 | ||||||
chr3:45713257
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.543+61G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713257 | ||||||
chr3:45713267
|
G | A | 1 | a0002c0001t0001g0203 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.543+71G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713267 | ||||||
chr3:45713511
|
G | A | 3 | a0002c0001t0001g0204a0002c0001t0001g0205a0002c0001t0001g0252 | 3 | NA18991.hp1 NA18998.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.543+315G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713511 | ||||||
chr3:45713646
|
A | G | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.544-400A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 6/19 | chr3 | 45713646 | ||||||
chr3:45714144
|
G | C | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.577+65G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714144 | ||||||
chr3:45714238
|
T | G | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.577+159T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714238 | ||||||
chr3:45714239
|
TTG | T | 109 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(106): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.577+162_577+163del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45714239 | |||||
chr3:45714240
|
TG | T | 127 | a0001c0002t0007g0260a0001c0003t0002g0003a0001c0003t0002g0006others(124): Show | 174 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.577+162delG | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714240 | ||||||
chr3:45714241
|
G | T | 9 | a0002c0001t0001g0027a0002c0001t0001g0059a0002c0001t0001g0103others(6): Show | 10 | HG01243.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.577+162G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714241 | ||||||
chr3:45714246
|
T | G | 1 | a0001c0003t0002g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.577+167T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714246 | ||||||
chr3:45714436
|
A | C | 1 | a0002c0001t0001g0228 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.577+357A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714436 | ||||||
chr3:45714482
|
G | A | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.577+403G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714482 | ||||||
chr3:45714778
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.577+699G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714778 | ||||||
chr3:45714804
|
A | C | 1 | a0002c0001t0001g0236 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.577+725A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714804 | ||||||
chr3:45714818
|
A | C | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.577+739A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714818 | ||||||
chr3:45714858
|
C | G | 112 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(109): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.577+779C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714858 | ||||||
chr3:45714902
|
C | T | 1 | a0002c0001t0001g0234 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.577+823C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714902 | ||||||
chr3:45714903
|
G | A | 1 | a0001c0002t0002g0261 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.577+824G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714903 | ||||||
chr3:45714997
|
A | G | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577+918A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45714997 | ||||||
chr3:45715059
|
G | A | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.577+980G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715059 | ||||||
chr3:45715071
|
T | C | 1 | a0002c0001t0001g0206 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.577+992T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715071 | ||||||
chr3:45715081
|
C | T | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577+1002C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715081 | ||||||
chr3:45715088
|
C | T | 1 | a0001c0003t0002g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.577+1009C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715088 | ||||||
chr3:45715097
|
G | A | 1 | a0001c0002t0002g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.577+1018G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715097 | ||||||
chr3:45715158
|
C | T | 6 | a0002c0001t0001g0010a0002c0001t0001g0187a0002c0001t0001g0203others(3): Show | 9 | HG00423.hp2 HG01975.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.577+1079C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715158 | ||||||
chr3:45715191
|
G | C | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.577+1112G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715191 | ||||||
chr3:45715230
|
G | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.577+1151G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715230 | ||||||
chr3:45715233
|
G | C | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.577+1154G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715233 | ||||||
chr3:45715314
|
C | A | 1 | a0002c0001t0001g0204 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.577+1235C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715314 | ||||||
chr3:45715364
|
A | G | 2 | a0002c0001t0001g0192a0002c0001t0001g0225 | 2 | NA18747.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.577+1285A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715364 | ||||||
chr3:45715435
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.577+1356C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715435 | ||||||
chr3:45715494
|
A | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.577+1415A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715494 | ||||||
chr3:45715497
|
C | T | 1 | a0001c0002t0002g0164 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.577+1418C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715497 | ||||||
chr3:45715500
|
G | T | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.577+1421G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715500 | ||||||
chr3:45715547
|
C | T | 1 | a0002c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.577+1468C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715547 | ||||||
chr3:45715613
|
A | G | 1 | a0001c0002t0002g0153 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.577+1534A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715613 | ||||||
chr3:45715635
|
G | A | 1 | a0002c0001t0001g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.577+1556G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715635 | ||||||
chr3:45715706
|
G | A | 5 | a0001c0002t0002g0013a0001c0002t0002g0114a0001c0002t0002g0115others(2): Show | 6 | HG00735.hp2 HG01123.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.577+1627G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715706 | ||||||
chr3:45715773
|
CA | C | 137 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(134): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.577+1709delA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45715773 | |||||
chr3:45715790
|
T | C | 82 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0013others(79): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.577+1711T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715790 | ||||||
chr3:45715925
|
T | A | 107 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(104): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.577+1846T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45715925 | ||||||
chr3:45716099
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.577+2020C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716099 | ||||||
chr3:45716408
|
T | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.577+2329T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716408 | ||||||
chr3:45716504
|
G | T | 1 | a0002c0001t0001g0232 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.577+2425G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716504 | ||||||
chr3:45716528
|
T | G | 3 | a0001c0002t0002g0014a0001c0002t0002g0120a0001c0002t0002g0121 | 5 | HG00639.hp2 HG01192.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.577+2449T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716528 | ||||||
chr3:45716584
|
C | T | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.577+2505C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716584 | ||||||
chr3:45716889
|
C | A | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.578-2611C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45716889 | ||||||
chr3:45717029
|
G | A | 3 | a0002c0001t0001g0024a0002c0001t0001g0049a0002c0001t0001g0074 | 4 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-2471G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717029 | ||||||
chr3:45717037
|
T | C | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.578-2463T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717037 | ||||||
chr3:45717103
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.578-2397T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717103 | ||||||
chr3:45717359
|
G | A | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-2141G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717359 | ||||||
chr3:45717375
|
A | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.578-2125A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717375 | ||||||
chr3:45717454
|
G | C | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.578-2046G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717454 | ||||||
chr3:45717461
|
G | T | 1 | a0001c0002t0002g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.578-2039G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717461 | ||||||
chr3:45717519
|
C | T | 1 | a0001c0002t0002g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.578-1981C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717519 | ||||||
chr3:45717544
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.578-1956T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717544 | ||||||
chr3:45717615
|
A | G | 6 | a0002c0001t0001g0050a0002c0001t0001g0051a0002c0001t0001g0052others(3): Show | 6 | HG01884.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.578-1885A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717615 | ||||||
chr3:45717724
|
T | C | 1 | a0002c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.578-1776T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717724 | ||||||
chr3:45717791
|
C | T | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.578-1709C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717791 | ||||||
chr3:45717871
|
G | T | 1 | a0001c0003t0002g0045 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.578-1629G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717871 | ||||||
chr3:45717944
|
A | T | 1 | a0002c0001t0001g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.578-1556A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45717944 | ||||||
chr3:45718006
|
A | G | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.578-1494A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718006 | ||||||
chr3:45718046
|
T | C | 1 | a0002c0001t0001g0201 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.578-1454T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718046 | ||||||
chr3:45718084
|
A | G | 1 | a0001c0002t0002g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.578-1416A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718084 | ||||||
chr3:45718162
|
A | G | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.578-1338A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718162 | ||||||
chr3:45718294
|
TA | T | 56 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(53): Show | 72 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.578-1192delA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45718294 | |||||
chr3:45718294
|
TAA | T | 99 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(96): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.578-1193_578-1192d others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr3 | 45718294 | |||||
chr3:45718330
|
A | G | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.578-1170A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718330 | ||||||
chr3:45718383
|
T | C | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.578-1117T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718383 | ||||||
chr3:45718432
|
T | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.578-1068T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718432 | ||||||
chr3:45718495
|
A | C | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.578-1005A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718495 | ||||||
chr3:45718503
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.578-997C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718503 | ||||||
chr3:45718805
|
A | G | 1 | a0001c0002t0003g0172 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.578-695A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718805 | ||||||
chr3:45718991
|
A | G | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.578-509A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45718991 | ||||||
chr3:45719108
|
C | T | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.578-392C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719108 | ||||||
chr3:45719237
|
A | G | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.578-263A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719237 | ||||||
chr3:45719314
|
G | A | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.578-186G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719314 | ||||||
chr3:45719492
|
T | C | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.578-8T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 7/19 | chr3 | 45719492 | ||||||
chr3:45719623
|
G | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.679+22G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45719623 | ||||||
chr3:45719919
|
G | C | 9 | a0001c0003t0002g0021a0001c0003t0002g0028a0001c0003t0002g0044others(6): Show | 11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.679+318G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45719919 | ||||||
chr3:45719950
|
G | A | 5 | a0001c0003t0002g0012a0001c0003t0002g0093a0001c0003t0002g0094others(2): Show | 7 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+349G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45719950 | ||||||
chr3:45720019
|
T | C | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.679+418T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45720019 | ||||||
chr3:45720439
|
AC | A | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.679+843delC | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr3 | 45720439 | |||||
chr3:45720517
|
C | G | 1 | a0001c0002t0002g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.679+916C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45720517 | ||||||
chr3:45720596
|
T | C | 1 | a0002c0001t0001g0024 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.679+995T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45720596 | ||||||
chr3:45721229
|
T | C | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.680-771T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721229 | ||||||
chr3:45721233
|
C | T | 42 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0002t0002g0139others(39): Show | 54 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.680-767C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721233 | ||||||
chr3:45721271
|
C | G | 1 | a0001c0002t0003g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.680-729C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721271 | ||||||
chr3:45721383
|
G | A | 1 | a0001c0004t0002g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.680-617G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721383 | ||||||
chr3:45721391
|
G | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.680-609G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721391 | ||||||
chr3:45721553
|
T | C | 4 | a0002c0001t0001g0022a0002c0001t0001g0056a0002c0001t0001g0057others(1): Show | 5 | HG02055.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-447T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721553 | ||||||
chr3:45721554
|
A | G | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.680-446A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721554 | ||||||
chr3:45721577
|
G | A | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.680-423G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721577 | ||||||
chr3:45721643
|
C | T | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.680-357C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 8/19 | chr3 | 45721643 | ||||||
chr3:45722143
|
A | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.765+58A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722143 | ||||||
chr3:45722230
|
A | G | 1 | a0002c0001t0001g0231 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.765+145A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722230 | ||||||
chr3:45722407
|
A | G | 1 | a0002c0001t0009g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.765+322A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722407 | ||||||
chr3:45722443
|
C | T | 1 | a0002c0001t0001g0223 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.765+358C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722443 | ||||||
chr3:45722485
|
G | A | 81 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0013others(78): Show | 106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.766-384G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722485 | ||||||
chr3:45722672
|
A | G | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.766-197A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722672 | ||||||
chr3:45722754
|
A | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.766-115A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 9/19 | chr3 | 45722754 | ||||||
chr3:45723005
|
G | A | 1 | a0001c0002t0005g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.852+50G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723005 | ||||||
chr3:45723041
|
G | A | 2 | a0002c0001t0008g0190a0002c0001t0008g0207 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.852+86G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723041 | ||||||
chr3:45723052
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.852+97T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723052 | ||||||
chr3:45723078
|
C | T | 1 | a0001c0002t0004g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.852+123C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723078 | ||||||
chr3:45723187
|
A | C | 1 | a0001c0002t0002g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.852+232A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723187 | ||||||
chr3:45723200
|
A | G | 1 | a0001c0002t0002g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.852+245A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723200 | ||||||
chr3:45723233
|
A | G | 1 | a0001c0002t0002g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.853-242A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723233 | ||||||
chr3:45723437
|
A | G | 4 | a0002c0001t0001g0061a0002c0001t0001g0071a0002c0001t0001g0073others(1): Show | 4 | NA18747.hp1 NA18956.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.853-38A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 10/19 | chr3 | 45723437 | ||||||
chr3:45723640
|
T | G | 4 | a0001c0002t0006g0016a0001c0002t0006g0135a0001c0002t0006g0150others(1): Show | 5 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+97T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723640 | ||||||
chr3:45723696
|
T | A | 4 | a0001c0003t0002g0021a0001c0003t0002g0044a0001c0003t0002g0045others(1): Show | 5 | HG01074.hp2 HG01243.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+153T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723696 | ||||||
chr3:45723729
|
C | T | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.921+186C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723729 | ||||||
chr3:45723780
|
A | G | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.921+237A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723780 | ||||||
chr3:45723904
|
T | A | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.921+361T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723904 | ||||||
chr3:45723948
|
A | G | 1 | a0002c0001t0001g0243 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.921+405A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723948 | ||||||
chr3:45723959
|
C | G | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.921+416C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45723959 | ||||||
chr3:45723965
|
G | GAC | 95 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(92): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.921+440_921+441dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45723965 | |||||
chr3:45723965
|
G | GACAC | 51 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(48): Show | 67 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.921+438_921+441dup others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45723965 | |||||
chr3:45724216
|
C | T | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.921+673C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724216 | ||||||
chr3:45724243
|
A | G | 1 | a0001c0002t0005g0174 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.921+700A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724243 | ||||||
chr3:45724255
|
A | G | 2 | a0002c0001t0001g0103a0002c0001t0001g0104 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.921+712A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724255 | ||||||
chr3:45724256
|
G | A | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.921+713G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724256 | ||||||
chr3:45724298
|
G | GGT | 37 | a0001c0002t0002g0004a0001c0002t0002g0110a0001c0002t0002g0127others(34): Show | 50 | HG00621.hp2 HG01074.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.921+790_921+791dup others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGT | 55 | a0001c0002t0002g0008a0001c0002t0002g0013a0001c0002t0002g0029others(52): Show | 75 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.921+788_921+791dup others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGT | 91 | a0001c0002t0002g0138a0001c0002t0002g0140a0001c0002t0002g0153others(88): Show | 131 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.921+786_921+791dup others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGTG others(1): Show |
25 | a0001c0002t0002g0146a0001c0002t0002g0152a0001c0002t0002g0261others(22): Show | 30 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.921+784_921+791dup others(8): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGTG others(3): Show |
19 | a0001c0002t0002g0137a0001c0002t0002g0139a0001c0002t0002g0254others(16): Show | 19 | HG00609.hp1 HG00735.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.921+782_921+791dup others(10): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGTG others(5): Show |
4 | a0001c0002t0002g0151a0001c0002t0002g0165a0001c0002t0002g0259others(1): Show | 4 | HG01361.hp2 HG01516.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+780_921+791dup others(12): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGTG others(7): Show |
5 | a0001c0002t0002g0042a0001c0002t0002g0143a0001c0002t0002g0144others(2): Show | 6 | HG00438.hp1 HG00597.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.921+778_921+791dup others(14): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGTG others(9): Show |
4 | a0001c0002t0002g0262a0001c0002t0007g0255a0001c0002t0007g0257others(1): Show | 4 | NA18989.hp2 NA19007.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+776_921+791dup others(16): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGTG others(13): Show |
1 | a0001c0002t0002g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.921+772_921+791dup others(20): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
G | GGTGTGTG others(15): Show |
1 | a0001c0002t0002g0256 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.921+770_921+791dup others(22): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724298
|
GGT | G | 3 | a0001c0002t0011g0041a0001c0003t0002g0096a0002c0001t0001g0246 | 4 | HG02056.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+790_921+791del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45724298 | |||||
chr3:45724334
|
T | TGTGTG | 3 | a0001c0002t0012g0118a0002c0001t0001g0196a0002c0001t0001g0247 | 3 | HG01515.hp2 NA18980.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.921+791_921+792ins others(5): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724334 | ||||||
chr3:45724366
|
G | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.921+823G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724366 | ||||||
chr3:45724479
|
C | T | 2 | a0001c0002t0004g0035a0001c0002t0004g0177 | 3 | HG02257.hp1 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.921+936C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724479 | ||||||
chr3:45724563
|
C | T | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.921+1020C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724563 | ||||||
chr3:45724730
|
T | A | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.921+1187T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45724730 | ||||||
chr3:45725306
|
T | TTGTC | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.921+1763_921+1764i others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725306 | ||||||
chr3:45725328
|
TTTTA | T | 10 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0120others(7): Show | 14 | HG00140.hp1 HG00639.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.921+1795_921+1798d others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45725328 | |||||
chr3:45725526
|
T | C | 1 | a0001c0003t0002g0081 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.921+1983T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725526 | ||||||
chr3:45725581
|
A | T | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.921+2038A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725581 | ||||||
chr3:45725624
|
A | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.921+2081A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725624 | ||||||
chr3:45725684
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.921+2141C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725684 | ||||||
chr3:45725685
|
T | C | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.921+2142T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725685 | ||||||
chr3:45725696
|
CT | C | 3 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0110 | 3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.921+2155delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45725696 | |||||
chr3:45725995
|
G | A | 154 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(151): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.921+2452G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45725995 | ||||||
chr3:45726110
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.921+2567C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726110 | ||||||
chr3:45726640
|
T | C | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.921+3097T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726640 | ||||||
chr3:45726791
|
T | C | 1 | a0002c0001t0001g0064 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.921+3248T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726791 | ||||||
chr3:45726859
|
TGCTTTAT others(318): Show |
T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.921+3327_921+3651d others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45726859 | |||||
chr3:45726869
|
C | CT | 21 | a0002c0001t0001g0049a0002c0001t0001g0053a0002c0001t0001g0067others(18): Show | 21 | HG00423.hp2 HG00738.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.921+3353dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45726869 | |||||
chr3:45726869
|
CT | C | 6 | a0002c0001t0001g0027a0002c0001t0001g0040a0002c0001t0001g0103others(3): Show | 8 | HG01515.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+3353delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45726869 | |||||
chr3:45726873
|
T | C | 1 | a0002c0001t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.921+3330T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726873 | ||||||
chr3:45726902
|
G | A | 1 | a0002c0001t0001g0043 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.921+3359G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726902 | ||||||
chr3:45726909
|
C | T | 1 | a0002c0001t0001g0066 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.921+3366C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726909 | ||||||
chr3:45726918
|
A | G | 7 | a0002c0001t0001g0027a0002c0001t0001g0049a0002c0001t0001g0103others(4): Show | 8 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+3375A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726918 | ||||||
chr3:45726933
|
C | T | 1 | a0002c0001t0001g0027 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.921+3390C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45726933 | ||||||
chr3:45727047
|
G | A | 1 | a0002c0001t0001g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.921+3504G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727047 | ||||||
chr3:45727165
|
G | C | 1 | a0002c0001t0001g0027 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.921+3622G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727165 | ||||||
chr3:45727245
|
A | G | 1 | a0001c0002t0003g0147 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.921+3702A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727245 | ||||||
chr3:45727341
|
G | C | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.921+3798G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727341 | ||||||
chr3:45727489
|
G | A | 138 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(135): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.922-3812G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727489 | ||||||
chr3:45727497
|
C | T | 1 | a0002c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.922-3804C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727497 | ||||||
chr3:45727643
|
G | A | 5 | a0001c0003t0002g0012a0001c0003t0002g0093a0001c0003t0002g0094others(2): Show | 7 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.922-3658G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727643 | ||||||
chr3:45727675
|
G | A | 1 | a0002c0001t0001g0027 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.922-3626G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727675 | ||||||
chr3:45727740
|
C | T | 2 | a0001c0003t0002g0006a0001c0003t0002g0089 | 5 | HG01358.hp2 HG01943.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-3561C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727740 | ||||||
chr3:45727797
|
G | A | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.922-3504G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727797 | ||||||
chr3:45727847
|
G | A | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.922-3454G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45727847 | ||||||
chr3:45728171
|
T | C | 1 | a0002c0001t0001g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.922-3130T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728171 | ||||||
chr3:45728353
|
G | T | 1 | a0002c0001t0001g0211 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.922-2948G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728353 | ||||||
chr3:45728563
|
G | A | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.922-2738G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728563 | ||||||
chr3:45728595
|
A | C | 69 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0014others(66): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.922-2706A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728595 | ||||||
chr3:45728812
|
A | G | 1 | a0002c0001t0014g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.922-2489A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45728812 | ||||||
chr3:45729038
|
T | C | 1 | a0001c0002t0004g0177 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.922-2263T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729038 | ||||||
chr3:45729073
|
G | GATTT | 26 | a0001c0002t0002g0004a0001c0003t0002g0003a0001c0003t0002g0006others(23): Show | 41 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.922-2203_922-2200d others(6): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45729073 | |||||
chr3:45729098
|
A | T | 1 | a0002c0001t0001g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.922-2203A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729098 | ||||||
chr3:45729280
|
T | A | 1 | a0001c0003t0002g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.922-2021T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729280 | ||||||
chr3:45729283
|
T | TGC | 246 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(243): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.922-2018_922-2017i others(4): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729283 | ||||||
chr3:45729355
|
G | T | 2 | a0001c0002t0002g0112a0001c0002t0002g0113 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.922-1946G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729355 | ||||||
chr3:45729708
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.922-1593C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729708 | ||||||
chr3:45729730
|
C | T | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.922-1571C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729730 | ||||||
chr3:45729745
|
G | A | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.922-1556G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729745 | ||||||
chr3:45729904
|
A | G | 1 | a0002c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.922-1397A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729904 | ||||||
chr3:45729981
|
A | C | 1 | a0002c0001t0001g0235 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.922-1320A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45729981 | ||||||
chr3:45730109
|
C | G | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.922-1192C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730109 | ||||||
chr3:45730193
|
C | T | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.922-1108C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730193 | ||||||
chr3:45730296
|
G | A | 8 | a0002c0001t0001g0022a0002c0001t0001g0051a0002c0001t0001g0053others(5): Show | 9 | HG02055.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.922-1005G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730296 | ||||||
chr3:45730307
|
G | GT | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.922-986dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45730307 | |||||
chr3:45730307
|
G | T | 1 | a0001c0004t0002g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.922-994G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730307 | ||||||
chr3:45730349
|
AT | A | 9 | a0001c0002t0005g0148a0002c0001t0001g0027a0002c0001t0001g0049others(6): Show | 10 | HG01243.hp1 HG02630.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.922-938delT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45730349 | |||||
chr3:45730349
|
ATT | A | 145 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(142): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.922-939_922-938del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr3 | 45730349 | |||||
chr3:45730736
|
A | G | 21 | a0001c0002t0002g0008a0001c0002t0002g0009a0001c0002t0002g0014others(18): Show | 32 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.922-565A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730736 | ||||||
chr3:45730868
|
G | A | 3 | a0001c0002t0002g0108a0001c0002t0002g0109a0001c0002t0002g0110 | 3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.922-433G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45730868 | ||||||
chr3:45731250
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.922-51T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731250 | ||||||
chr3:45731252
|
C | T | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.922-49C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731252 | ||||||
chr3:45731280
|
G | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.922-21G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731280 | ||||||
chr3:45731295
|
T | C | 1 | a0001c0003t0002g0087 | 1 | HG02004.hp1 | splice_region_variant&intron_variant | LOW | c.922-6T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 11/19 | chr3 | 45731295 | ||||||
chr3:45731496
|
A | AGATCAAA others(12): Show |
1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1001+118_1001+136d others(21): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr3 | 45731496 | |||||
chr3:45731547
|
G | A | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1001+167G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731547 | ||||||
chr3:45731555
|
A | G | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1001+175A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731555 | ||||||
chr3:45731796
|
A | C | 31 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(28): Show | 44 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1002-257A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731796 | ||||||
chr3:45731828
|
A | C | 1 | a0002c0001t0001g0249 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1002-225A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731828 | ||||||
chr3:45731828
|
A | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1002-225A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731828 | ||||||
chr3:45731906
|
G | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002-147G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45731906 | ||||||
chr3:45732047
|
T | C | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | splice_region_variant&intron_variant | LOW | c.1002-6T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45732047 | ||||||
chr3:45732049
|
G | A | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | splice_region_variant&intron_variant | LOW | c.1002-4G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 12/19 | chr3 | 45732049 | ||||||
chr3:45732158
|
TATATTAT others(4): Show |
T | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | splice_region_variant&intron_variant | LOW | c.1100+8_1100+18delA others(10): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732158 | ||||||
chr3:45732171
|
T | A | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+20T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732171 | ||||||
chr3:45732172
|
A | G | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+21A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732172 | ||||||
chr3:45732177
|
G | T | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+26G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732177 | ||||||
chr3:45732178
|
G | A | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+27G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732178 | ||||||
chr3:45732185
|
G | C | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+34G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732185 | ||||||
chr3:45732205
|
C | A | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+54C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732205 | ||||||
chr3:45732211
|
T | A | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+60T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732211 | ||||||
chr3:45732213
|
A | C | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+62A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732213 | ||||||
chr3:45732215
|
T | A | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+64T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732215 | ||||||
chr3:45732216
|
A | T | 1 | a0002c0001t0001g0198 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1100+65A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732216 | ||||||
chr3:45732240
|
G | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1100+89G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732240 | ||||||
chr3:45732257
|
G | C | 1 | a0001c0002t0002g0256 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1100+106G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732257 | ||||||
chr3:45732295
|
C | A | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1100+144C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732295 | ||||||
chr3:45732395
|
T | A | 1 | a0002c0001t0001g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1100+244T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732395 | ||||||
chr3:45732471
|
A | G | 13 | a0002c0001t0001g0011a0002c0001t0001g0043a0002c0001t0001g0061others(10): Show | 16 | HG00609.hp2 HG01255.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100+320A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732471 | ||||||
chr3:45732499
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1100+348C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732499 | ||||||
chr3:45732616
|
A | G | 1 | a0001c0002t0003g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1100+465A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732616 | ||||||
chr3:45732686
|
T | A | 1 | a0002c0001t0001g0027 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100+535T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45732686 | ||||||
chr3:45733009
|
C | G | 246 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(243): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1100+858C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733009 | ||||||
chr3:45733204
|
G | A | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1100+1053G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733204 | ||||||
chr3:45733269
|
G | T | 1 | a0002c0001t0001g0232 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1100+1118G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733269 | ||||||
chr3:45733508
|
T | C | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1100+1357T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733508 | ||||||
chr3:45733526
|
G | A | 78 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0010others(75): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1100+1375G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733526 | ||||||
chr3:45733699
|
G | A | 1 | a0001c0002t0002g0256 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1101-1536G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733699 | ||||||
chr3:45733747
|
T | C | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1101-1488T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733747 | ||||||
chr3:45733854
|
C | T | 2 | a0002c0001t0001g0204a0002c0001t0001g0252 | 2 | NA18991.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1101-1381C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45733854 | ||||||
chr3:45734014
|
T | A | 5 | a0001c0002t0002g0030a0001c0002t0002g0119a0001c0002t0002g0123others(2): Show | 6 | HG00738.hp1 HG01070.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1101-1221T>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734014 | ||||||
chr3:45734037
|
G | A | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1101-1198G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734037 | ||||||
chr3:45734113
|
A | AT | 9 | a0002c0001t0001g0051a0002c0001t0001g0192a0002c0001t0001g0220others(6): Show | 9 | HG01243.hp1 HG01261.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1101-1105dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | |||||
chr3:45734113
|
A | ATTC | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1101-1120_1101-111 others(7): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | |||||
chr3:45734113
|
A | ATTT | 41 | a0001c0002t0002g0013a0001c0002t0002g0029a0001c0002t0002g0108others(38): Show | 56 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.1101-1107_1101-110 others(7): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | |||||
chr3:45734113
|
A | ATTTT | 92 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(89): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1101-1108_1101-110 others(8): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734113 | |||||
chr3:45734136
|
G | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1101-1099G>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734136 | ||||||
chr3:45734150
|
C | T | 3 | a0001c0003t0002g0093a0001c0003t0002g0094a0001c0003t0002g0096 | 3 | HG02886.hp2 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1101-1085C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734150 | ||||||
chr3:45734187
|
C | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1101-1048C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734187 | ||||||
chr3:45734386
|
C | G | 1 | a0001c0002t0002g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1101-849C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734386 | ||||||
chr3:45734412
|
C | CA | 11 | a0001c0002t0006g0016a0001c0002t0006g0135a0001c0002t0006g0150others(8): Show | 16 | HG00140.hp2 HG00323.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.1101-813dupA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr3 | 45734412 | |||||
chr3:45734439
|
A | T | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1101-796A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734439 | ||||||
chr3:45734460
|
A | T | 1 | a0001c0002t0002g0004 | 5 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1101-775A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734460 | ||||||
chr3:45734620
|
G | A | 1 | a0001c0002t0003g0168 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1101-615G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734620 | ||||||
chr3:45734772
|
A | G | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1101-463A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 13/19 | chr3 | 45734772 | ||||||
chr3:45735383
|
C | CT | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1239+23dupT | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr3 | 45735383 | |||||
chr3:45735408
|
A | G | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1239+35A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735408 | ||||||
chr3:45735567
|
A | G | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1239+194A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735567 | ||||||
chr3:45735621
|
G | A | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1239+248G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735621 | ||||||
chr3:45735949
|
C | G | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1239+576C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45735949 | ||||||
chr3:45736077
|
C | T | 1 | a0002c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1239+704C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736077 | ||||||
chr3:45736277
|
A | G | 4 | a0001c0002t0005g0017a0001c0002t0005g0159a0001c0002t0005g0170others(1): Show | 6 | NA18957.hp1 NA18994.hp2 NA19055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+904A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736277 | ||||||
chr3:45736369
|
A | G | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1239+996A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736369 | ||||||
chr3:45736796
|
C | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1240-787C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736796 | ||||||
chr3:45736837
|
C | G | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1240-746C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736837 | ||||||
chr3:45736856
|
A | G | 1 | a0002c0001t0001g0196 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1240-727A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736856 | ||||||
chr3:45736988
|
G | A | 2 | a0002c0001t0001g0213a0002c0001t0001g0217 | 2 | NA18992.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1240-595G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45736988 | ||||||
chr3:45737057
|
G | A | 1 | a0001c0002t0005g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1240-526G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737057 | ||||||
chr3:45737131
|
G | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1240-452G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737131 | ||||||
chr3:45737169
|
G | C | 3 | a0001c0002t0003g0032a0001c0002t0003g0167a0001c0002t0003g0172 | 4 | NA18946.hp1 NA18963.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-414G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737169 | ||||||
chr3:45737176
|
T | C | 1 | a0002c0001t0001g0221 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1240-407T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737176 | ||||||
chr3:45737280
|
G | A | 1 | a0002c0001t0001g0186 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1240-303G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737280 | ||||||
chr3:45737524
|
C | G | 1 | a0002c0001t0001g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1240-59C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 14/19 | chr3 | 45737524 | ||||||
chr3:45737953
|
C | A | 1 | a0001c0002t0007g0257 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1382+109C>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45737953 | ||||||
chr3:45738101
|
C | T | 1 | a0002c0001t0001g0185 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1382+257C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738101 | ||||||
chr3:45738220
|
A | G | 11 | a0002c0001t0001g0022a0002c0001t0001g0050a0002c0001t0001g0051others(8): Show | 12 | HG01884.hp1 HG02055.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383-358A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738220 | ||||||
chr3:45738451
|
G | A | 154 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(151): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1383-127G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738451 | ||||||
chr3:45738560
|
T | C | 2 | a0002c0001t0001g0199a0002c0001t0001g0235 | 2 | HG02155.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1383-18T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738560 | ||||||
chr3:45738565
|
C | T | 3 | a0002c0001t0001g0209a0002c0001t0001g0216a0002c0001t0001g0219 | 3 | NA18974.hp2 NA19010.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1383-13C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 16/19 | chr3 | 45738565 | ||||||
chr3:45738700
|
A | C | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1476+29A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 17/19 | chr3 | 45738700 | ||||||
chr3:45738899
|
A | G | 1 | a0002c0001t0001g0186 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1569+26A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45738899 | ||||||
chr3:45738954
|
C | T | 1 | a0001c0003t0002g0098 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1569+81C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45738954 | ||||||
chr3:45739049
|
G | C | 1 | a0002c0001t0001g0214 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1569+176G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739049 | ||||||
chr3:45739174
|
A | G | 1 | a0002c0001t0001g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1569+301A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739174 | ||||||
chr3:45739288
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1570-299T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739288 | ||||||
chr3:45739333
|
A | T | 1 | a0001c0002t0002g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1570-254A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739333 | ||||||
chr3:45739414
|
A | G | 78 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0010others(75): Show | 108 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1570-173A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739414 | ||||||
chr3:45739488
|
A | G | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1570-99A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739488 | ||||||
chr3:45739580
|
T | C | 3 | a0002c0001t0001g0027a0002c0001t0001g0103a0002c0001t0001g0104 | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1570-7T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 18/19 | chr3 | 45739580 | ||||||
chr3:45739656
|
C | T | 17 | a0001c0002t0002g0008a0001c0002t0002g0013a0001c0002t0002g0029others(14): Show | 23 | HG00735.hp2 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1627+12C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739656 | ||||||
chr3:45739696
|
T | G | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1627+52T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739696 | ||||||
chr3:45739724
|
G | A | 1 | a0001c0002t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1627+80G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739724 | ||||||
chr3:45739878
|
C | T | 1 | a0002c0001t0001g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1627+234C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739878 | ||||||
chr3:45739888
|
A | G | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1627+244A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739888 | ||||||
chr3:45739981
|
A | G | 4 | a0002c0001t0001g0204a0002c0001t0001g0205a0002c0001t0001g0224others(1): Show | 4 | NA18991.hp1 NA18998.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+337A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45739981 | ||||||
chr3:45740003
|
A | C | 1 | a0001c0002t0011g0041 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1627+359A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740003 | ||||||
chr3:45740023
|
C | T | 40 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(37): Show | 55 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1627+379C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740023 | ||||||
chr3:45740091
|
G | C | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1627+447G>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740091 | ||||||
chr3:45740094
|
A | C | 6 | a0001c0002t0003g0141a0001c0002t0003g0154a0001c0002t0003g0155others(3): Show | 6 | HG00609.hp1 HG03017.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+450A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740094 | ||||||
chr3:45740123
|
T | C | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627+479T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740123 | ||||||
chr3:45740163
|
G | A | 2 | a0001c0002t0002g0151a0001c0002t0002g0165 | 2 | HG01361.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1627+519G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740163 | ||||||
chr3:45740606
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1627+962T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740606 | ||||||
chr3:45740633
|
A | C | 1 | a0002c0001t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627+989A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45740633 | ||||||
chr3:45741025
|
A | G | 1 | a0001c0002t0005g0175 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1627+1381A>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741025 | ||||||
chr3:45741094
|
G | A | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1627+1450G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741094 | ||||||
chr3:45741174
|
C | T | 3 | a0002c0001t0001g0185a0002c0001t0001g0215a0002c0001t0001g0251 | 3 | HG00733.hp1 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1627+1530C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741174 | ||||||
chr3:45741262
|
T | G | 1 | a0001c0003t0002g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1627+1618T>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741262 | ||||||
chr3:45741271
|
G | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1627+1627G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741271 | ||||||
chr3:45741323
|
A | T | 2 | a0002c0001t0001g0024a0002c0001t0001g0074 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1627+1679A>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741323 | ||||||
chr3:45741652
|
G | A | 10 | a0001c0002t0002g0042a0001c0002t0002g0254a0001c0002t0002g0256others(7): Show | 11 | HG00438.hp1 HG00597.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1628-1881G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741652 | ||||||
chr3:45741980
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1628-1553T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45741980 | ||||||
chr3:45742132
|
C | T | 2 | a0002c0001t0009g0101a0002c0001t0009g0102 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1628-1401C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742132 | ||||||
chr3:45742316
|
T | C | 13 | a0001c0002t0004g0018a0001c0002t0004g0033a0001c0002t0004g0034others(10): Show | 19 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1628-1217T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742316 | ||||||
chr3:45742554
|
C | G | 97 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(94): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1628-979C>G | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742554 | ||||||
chr3:45742590
|
T | C | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1628-943T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742590 | ||||||
chr3:45742787
|
G | A | 1 | a0002c0001t0001g0193 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1628-746G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742787 | ||||||
chr3:45742792
|
A | C | 1 | a0002c0001t0001g0064 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1628-741A>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742792 | ||||||
chr3:45742925
|
T | C | 26 | a0001c0003t0002g0003a0001c0003t0002g0006a0001c0003t0002g0007others(23): Show | 37 | HG00621.hp1 HG01081.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1628-608T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45742925 | ||||||
chr3:45743093
|
T | TA | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1628-438dupA | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr3 | 45743093 | |||||
chr3:45743110
|
G | A | 147 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(144): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1628-423G>A | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743110 | ||||||
chr3:45743262
|
C | T | 9 | a0001c0003t0002g0021a0001c0003t0002g0028a0001c0003t0002g0044others(6): Show | 11 | HG01074.hp2 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1628-271C>T | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743262 | ||||||
chr3:45743471
|
T | C | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1628-62T>C | SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743471 | ||||||
chr3:45743480
|
GGT | G | 83 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0009others(80): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1628-52_1628-51del others(2): Show |
SACM1L | ENSG00000211456.14 | transcript | ENST00000389061.10 | protein_coding | 19/19 | chr3 | 45743480 |