geneid | 130013 |
---|---|
ensemblid | ENSG00000153086.14 |
hgncid | 19288 |
symbol | ACMSD |
name | aminocarboxymuconate semialdehyde decarboxylase |
refseq_nuc | NM_138326.3 |
refseq_prot | NP_612199.2 |
ensembl_nuc | ENST00000356140.10 |
ensembl_prot | ENSP00000348459.5 |
mane_status | MANE Select |
chr | chr2 |
start | 134838616 |
end | 134902034 |
strand | + |
ver | v1.2 |
region | chr2:134838616-134902034 |
region5000 | chr2:134833616-134907034 |
regionname0 | ACMSD_chr2_134838616_134902034 |
regionname5000 | ACMSD_chr2_134833616_134907034 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 336 | 369 | 75 | 66 | 178 | 10 | 38 | 145 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0002 | 0/0 | 336 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0003 | 0/0 | 49 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0004 | 0/0 | 336 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0005 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0006 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0007 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0008 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1011 | 365 | 72 | 66 | 178 | 10 | 37 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0002 | 0/0 | 1011 | 4 | 4 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0003 | 0/0 | 1011 | 3 | 0 | 0 | 3 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0004 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0005 | 0/0 | 1011 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0007 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0008 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0009 | 0/0 | 1011 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
c0010 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 242 | 382 | 80 | 66 | 186 | 10 | 38 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 6 | 0 | 4 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
g0370 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1011 | 365 | 72 | 66 | 178 | 10 | 37 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0001c0004 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0001c0009 | 0/0 | 1011 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0002c0002 | 0/0 | 1011 | 4 | 4 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0003c0003 | 0/0 | 1011 | 3 | 0 | 0 | 3 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0004c0005 | 0/0 | 1011 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0005c0007 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0006c0008 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0007c0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0008c0010 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1252 | 365 | 72 | 66 | 178 | 10 | 37 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0001c0004t0001 | 0/0 | 1252 | 3 | 3 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0001c0009t0001 | 0/0 | 1252 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0002c0002t0001 | 0/0 | 1252 | 4 | 4 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0003c0003t0001 | 0/0 | 1252 | 3 | 0 | 0 | 3 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0004c0005t0001 | 0/0 | 1252 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0005c0007t0001 | 0/0 | 1252 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0006c0008t0001 | 0/0 | 1252 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0007c0006t0001 | 0/0 | 1252 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
a0008c0010t0001 | 0/0 | 1252 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | copy fasta | chr2 | 134833616 | 134907034 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 6 | 0 | 4 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0001t0001g0370 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0001c0009t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0003c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0003c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0004c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0004c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0005c0007t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0006c0008t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0007c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
a0008c0010t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | GBR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0369 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0334 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0333 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02027 | hp2 | a0008 | c0010 | t0001 | g0107 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02040 | hp2 | a0007 | c0006 | t0001 | g0244 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02155 | hp2 | a0005 | c0007 | t0001 | g0157 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0191 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0147 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02735 | hp2 | a0001 | c0009 | t0001 | g0169 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02809 | hp2 | a0006 | c0008 | t0001 | g0348 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0345 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18952 | hp2 | a0004 | c0005 | t0001 | g0173 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18962 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18988 | hp2 | a0004 | c0005 | t0001 | g0143 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0274 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ASW | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | GIH | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0370 | REF | REF | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | ACMSD_chr2_134833616_134907034 | ACMSD | chr2 | 134833616 | 134907034 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134845277
|
G | T | 1 | a0008 | 1 | HG02027.hp2 | missense_variant&splice_region_variant | MODERATE | c.102G>T | p.Lys34Asn | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/10 | 169/1252 | 102/1011 | 34/336 | chr2 | 134845277 | ||
chr2:134859306
|
C | T | 1 | a0003 | 3 | NA18962.hp2 NA19070.hp1 NA19084.hp2 |
stop_gained | HIGH | c.148C>T | p.Arg50* | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/10 | 215/1252 | 148/1011 | 50/336 | chr2 | 134859306 | ||
chr2:134859307
|
G | A | 1 | a0002 | 4 | HG02145.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.149G>A | p.Arg50Gln | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/10 | 216/1252 | 149/1011 | 50/336 | chr2 | 134859307 | ||
chr2:134859321
|
G | C | 1 | a0004 | 2 | NA18952.hp2 NA18988.hp2 |
missense_variant | MODERATE | c.163G>C | p.Asp55His | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/10 | 230/1252 | 163/1011 | 55/336 | chr2 | 134859321 | ||
chr2:134870986
|
T | C | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.602T>C | p.Ile201Thr | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/10 | 669/1252 | 602/1011 | 201/336 | chr2 | 134870986 | ||
chr2:134871015
|
G | A | 1 | a0005 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.631G>A | p.Val211Ile | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/10 | 698/1252 | 631/1011 | 211/336 | chr2 | 134871015 | ||
chr2:134901813
|
G | A | 1 | a0006 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.964G>A | p.Gly322Ser | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 10/10 | 1031/1252 | 964/1011 | 322/336 | chr2 | 134901813 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134838715
|
A | T | 1 | a0001c0004 | 3 | HG02257.hp2 HG02572.hp1 HG02647.hp2 |
synonymous_variant | LOW | c.33A>T | p.Pro11Pro | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/10 | 100/1252 | 33/1011 | 11/336 | chr2 | 134838715 | ||
chr2:134871050
|
C | T | 1 | a0001c0009 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.666C>T | p.Phe222Phe | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/10 | 733/1252 | 666/1011 | 222/336 | chr2 | 134871050 |
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 |
---|
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:134838838
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.57+99T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134838838 | ||||||
chr2:134839032
|
A | C | 4 | a0001c0001t0001g0367a0001c0001t0001g0368a0001c0001t0001g0369others(1): Show | 4 | HG01255.hp1 HG01361.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+293A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839032 | ||||||
chr2:134839120
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.57+381G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839120 | ||||||
chr2:134839170
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02896.hp1 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.57+431A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839170 | ||||||
chr2:134839206
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.57+467T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839206 | ||||||
chr2:134839396
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+657T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839396 | ||||||
chr2:134839407
|
A | T | 3 | a0001c0001t0001g0362a0001c0001t0001g0363a0001c0001t0001g0364 | 3 | HG02630.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.57+668A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839407 | ||||||
chr2:134839693
|
G | A | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+954G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839693 | ||||||
chr2:134839694
|
T | C | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+955T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839694 | ||||||
chr2:134839695
|
A | C | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+956A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839695 | ||||||
chr2:134839696
|
T | C | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57+957T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839696 | ||||||
chr2:134839756
|
C | G | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.57+1017C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839756 | ||||||
chr2:134839863
|
A | G | 1 | a0001c0001t0001g0361 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.57+1124A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839863 | ||||||
chr2:134839918
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.57+1179G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134839918 | ||||||
chr2:134840058
|
T | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.57+1319T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840058 | ||||||
chr2:134840087
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.57+1348T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840087 | ||||||
chr2:134840166
|
G | GAAAAAAA others(3): Show |
1 | a0001c0001t0001g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.57+1427_57+1428ins others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840166 | ||||||
chr2:134840167
|
C | A | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02486.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.57+1428C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840167 | ||||||
chr2:134840167
|
C | CA | 25 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0137others(22): Show | 27 | HG00558.hp2 HG01123.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.57+1454dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAA | 6 | a0001c0001t0001g0136a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 6 | HG00438.hp1 HG02040.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+1453_57+1454dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA | 12 | a0001c0001t0001g0134a0001c0001t0001g0268a0001c0001t0001g0269others(9): Show | 12 | HG01346.hp1 NA18951.hp1 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+1448_57+1454dup others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(1): Show |
18 | a0001c0001t0001g0014a0001c0001t0001g0133a0001c0001t0001g0252others(15): Show | 18 | HG00741.hp1 HG01168.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.57+1447_57+1454dup others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0011a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG00438.hp2 HG00597.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1446_57+1454dup others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(3): Show |
11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(8): Show | 13 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1445_57+1454dup others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(4): Show |
21 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(18): Show | 21 | HG01361.hp1 HG01361.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+1444_57+1454dup others(11): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(5): Show |
16 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(13): Show | 16 | HG01255.hp1 HG02015.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.57+1443_57+1454dup others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(6): Show |
15 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(12): Show | 15 | HG00140.hp2 HG01070.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.57+1442_57+1454dup others(13): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(7): Show |
11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG01192.hp2 HG01243.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.57+1441_57+1454dup others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(8): Show |
13 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1440_57+1454dup others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(9): Show |
14 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.57+1439_57+1454dup others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(10): Show |
7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG03041.hp2 HG03471.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1438_57+1454dup others(17): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG01081.hp2 NA19079.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.57+1437_57+1454dup others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG01257.hp2 NA18612.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.57+1436_57+1454dup others(19): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0023 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+1435_57+1454dup others(20): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022 | 3 | HG01261.hp2 HG01993.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.57+1434_57+1454dup others(21): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.57+1430_57+1454dup others(25): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0001g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.57+1429_57+1454dup others(26): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
CA | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0236a0001c0001t0001g0343others(9): Show | 12 | HG00639.hp2 HG01070.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+1454delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840167
|
CAA | C | 8 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355others(5): Show | 8 | HG00735.hp2 HG01243.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1453_57+1454del others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840167 | |||||
chr2:134840180
|
A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG03654.hp1 NA18943.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+1454_57+1455ins others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840180 | |||||
chr2:134840180
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18970.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.57+1449_57+1450ins others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840180 | |||||
chr2:134840180
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0203 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.57+1448_57+1449ins others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840180 | |||||
chr2:134840181
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG00558.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.57+1451_57+1452ins others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840181 | |||||
chr2:134840183
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840183 | |||||
chr2:134840183
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0235 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.57+1445_57+1455del others(11): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840183 | ||||||
chr2:134840184
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840184 | |||||
chr2:134840184
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.57+1446_57+1455del others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840184 | ||||||
chr2:134840185
|
AAAAAAAA others(2): Show |
A | 23 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(20): Show | 23 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+1447_57+1455del others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840185 | ||||||
chr2:134840186
|
AAAAAAAA others(1): Show |
A | 8 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 8 | HG02165.hp2 HG02293.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1448_57+1455del others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840186 | ||||||
chr2:134840187
|
A | C | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.57+1448A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840187 | ||||||
chr2:134840189
|
AAAAAC | A | 7 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(4): Show | 7 | HG01168.hp1 HG02698.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+1451_57+1455del others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840189 | ||||||
chr2:134840192
|
A | C | 2 | a0001c0004t0001g0190a0001c0004t0001g0191 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.57+1453A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840192 | ||||||
chr2:134840193
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(38): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840193 | ||||||
chr2:134840193
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(37): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840193 | ||||||
chr2:134840193
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.57+1454_57+1455ins others(35): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840193 | ||||||
chr2:134840193
|
AC | A | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0307others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+1456delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840193 | |||||
chr2:134840194
|
C | A | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 206 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.57+1455C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840194 | ||||||
chr2:134840194
|
C | CAAAAAAA others(7): Show |
22 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(19): Show | 22 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.57+1455_57+1456ins others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840194 | ||||||
chr2:134840194
|
C | CAAAACAA others(8): Show |
1 | a0001c0001t0001g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+1455_57+1456ins others(15): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840194 | ||||||
chr2:134840242
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.57+1503A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840242 | ||||||
chr2:134840267
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.57+1528C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840267 | ||||||
chr2:134840336
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18939.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.57+1597C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840336 | ||||||
chr2:134840497
|
G | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0236others(18): Show | 21 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.57+1758G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840497 | ||||||
chr2:134840559
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.57+1820G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840559 | ||||||
chr2:134840597
|
G | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0251 | 2 | HG00597.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.57+1858G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840597 | ||||||
chr2:134840738
|
TTTC | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 234 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.57+2008_57+2010del others(3): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 134840738 | |||||
chr2:134840815
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+2076A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840815 | ||||||
chr2:134840888
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+2149A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840888 | ||||||
chr2:134840929
|
C | T | 54 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0237others(51): Show | 55 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.57+2190C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134840929 | ||||||
chr2:134841001
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.57+2262G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841001 | ||||||
chr2:134841343
|
G | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 79 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+2604G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841343 | ||||||
chr2:134841439
|
G | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.57+2700G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841439 | ||||||
chr2:134841537
|
G | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+2798G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841537 | ||||||
chr2:134841694
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0236 | 3 | HG00741.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.57+2955C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841694 | ||||||
chr2:134841743
|
G | A | 52 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0237others(49): Show | 53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.57+3004G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841743 | ||||||
chr2:134841794
|
A | T | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.57+3055A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841794 | ||||||
chr2:134841811
|
G | A | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.57+3072G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841811 | ||||||
chr2:134841837
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 287 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.57+3098T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841837 | ||||||
chr2:134841947
|
G | C | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.57+3208G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841947 | ||||||
chr2:134841956
|
T | C | 1 | a0001c0001t0001g0353 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.57+3217T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841956 | ||||||
chr2:134841980
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.57+3241G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134841980 | ||||||
chr2:134842068
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.58-3165G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842068 | ||||||
chr2:134842158
|
T | C | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-3075T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842158 | ||||||
chr2:134842164
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 234 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.58-3069C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842164 | ||||||
chr2:134842169
|
C | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 289 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.58-3064C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842169 | ||||||
chr2:134842172
|
C | G | 5 | a0001c0001t0001g0308a0001c0001t0001g0349a0001c0001t0001g0350others(2): Show | 5 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-3061C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842172 | ||||||
chr2:134842289
|
G | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.58-2944G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842289 | ||||||
chr2:134842306
|
T | C | 18 | a0001c0001t0001g0012a0001c0001t0001g0308a0001c0001t0001g0343others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.58-2927T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842306 | ||||||
chr2:134842371
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58-2862C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842371 | ||||||
chr2:134842423
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.58-2810G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842423 | ||||||
chr2:134842455
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0009 | 3 | HG02559.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.58-2778G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842455 | ||||||
chr2:134842466
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(39): Show | 43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.58-2767C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842466 | ||||||
chr2:134842538
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0093a0001c0001t0001g0103others(1): Show | 4 | HG02717.hp1 HG03453.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-2695C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842538 | ||||||
chr2:134842843
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-2390C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842843 | ||||||
chr2:134842847
|
T | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0001g0182 | 3 | HG02258.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.58-2386T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842847 | ||||||
chr2:134842848
|
C | T | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(303): Show | 311 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(308): Show |
intron_variant | MODIFIER | c.58-2385C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842848 | ||||||
chr2:134842855
|
G | A | 1 | a0008c0010t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.58-2378G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134842855 | ||||||
chr2:134843031
|
T | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0253 | 2 | NA18940.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.58-2202T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843031 | ||||||
chr2:134843058
|
C | A | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.58-2175C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843058 | ||||||
chr2:134843109
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.58-2124T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843109 | ||||||
chr2:134843127
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.58-2106T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843127 | ||||||
chr2:134843179
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.58-2054A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843179 | ||||||
chr2:134843355
|
T | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 79 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.58-1878T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843355 | ||||||
chr2:134843735
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-1498T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843735 | ||||||
chr2:134843793
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.58-1440G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843793 | ||||||
chr2:134843937
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58-1296C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843937 | ||||||
chr2:134843954
|
T | A | 78 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 79 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.58-1279T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843954 | ||||||
chr2:134843979
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(39): Show | 43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.58-1254C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134843979 | ||||||
chr2:134844187
|
A | G | 17 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.58-1046A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844187 | ||||||
chr2:134844211
|
G | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0192others(1): Show | 4 | HG00558.hp1 NA18989.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1022G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844211 | ||||||
chr2:134844222
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0177 | 2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.58-1011T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844222 | ||||||
chr2:134844586
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.58-647G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844586 | ||||||
chr2:134844624
|
C | T | 49 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(46): Show | 50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-609C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844624 | ||||||
chr2:134844839
|
T | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.58-394T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844839 | ||||||
chr2:134844881
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58-352A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844881 | ||||||
chr2:134844941
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-292C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844941 | ||||||
chr2:134844974
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-259T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844974 | ||||||
chr2:134844998
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.58-235G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134844998 | ||||||
chr2:134845031
|
T | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.58-202T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 1/9 | chr2 | 134845031 | ||||||
chr2:134845361
|
G | A | 17 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.102+84G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845361 | ||||||
chr2:134845509
|
G | GTC | 42 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0051others(39): Show | 43 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.102+277_102+278dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTC | 22 | a0001c0001t0001g0031a0001c0001t0001g0064a0001c0001t0001g0076others(19): Show | 22 | HG00609.hp2 HG01361.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.102+275_102+278dup others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTCTC | 21 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0065others(18): Show | 21 | HG01070.hp1 HG01257.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.102+273_102+278dup others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTCTCT others(1): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0025others(13): Show | 16 | HG00140.hp2 HG01192.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.102+271_102+278dup others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTCTCT others(3): Show |
14 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0027others(11): Show | 15 | HG01081.hp2 HG01192.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.102+269_102+278dup others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTCTCT others(5): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG00639.hp1 HG01243.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+267_102+278dup others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTCTCT others(7): Show |
8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+265_102+278dup others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTCTCT others(9): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0061 | 2 | HG00738.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.102+263_102+278dup others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
G | GTCTCTCT others(11): Show |
1 | a0001c0001t0001g0081 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.102+261_102+278dup others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
GTC | G | 51 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0018others(48): Show | 51 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.102+277_102+278del others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
GTCTC | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0028others(64): Show | 68 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.102+275_102+278del others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
GTCTCTC | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0015others(47): Show | 52 | HG00408.hp2 HG00741.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.102+273_102+278del others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
GTCTCTCT others(1): Show |
G | 10 | a0001c0001t0001g0017a0001c0001t0001g0074a0001c0001t0001g0089others(7): Show | 10 | HG02559.hp2 HG02717.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+271_102+278del others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
GTCTCTCT others(3): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102+269_102+278del others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
GTCTCTCT others(5): Show |
G | 3 | a0001c0001t0001g0030a0001c0001t0001g0137a0001c0001t0001g0194 | 3 | HG03041.hp2 HG03831.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.102+267_102+278del others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845509
|
GTCTCTCT others(7): Show |
G | 1 | a0001c0001t0001g0005 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.102+265_102+278del others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134845509 | |||||
chr2:134845554
|
T | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(1): Show | 4 | HG01978.hp2 NA18961.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+277T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845554 | ||||||
chr2:134845555
|
C | CTCTCTCT others(2): Show |
3 | a0001c0001t0001g0054a0001c0001t0001g0180a0001c0001t0001g0339 | 3 | HG01123.hp2 HG01175.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.102+278_102+279ins others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845555 | ||||||
chr2:134845555
|
C | CTCTCTCT others(10): Show |
1 | a0001c0001t0001g0181 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.102+278_102+279ins others(17): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845555 | ||||||
chr2:134845640
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.102+363A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845640 | ||||||
chr2:134845728
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+451A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845728 | ||||||
chr2:134845854
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.102+577T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134845854 | ||||||
chr2:134846120
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.102+843A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846120 | ||||||
chr2:134846227
|
T | C | 78 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 79 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.102+950T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846227 | ||||||
chr2:134846389
|
C | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.102+1112C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846389 | ||||||
chr2:134846613
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.102+1336T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846613 | ||||||
chr2:134846820
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.102+1543G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846820 | ||||||
chr2:134846847
|
A | C | 1 | a0001c0001t0001g0275 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.102+1570A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846847 | ||||||
chr2:134846911
|
G | C | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+1634G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846911 | ||||||
chr2:134846919
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+1642C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846919 | ||||||
chr2:134846922
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0200a0001c0001t0001g0205others(17): Show | 20 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.102+1645G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134846922 | ||||||
chr2:134847169
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(39): Show | 43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.102+1892G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847169 | ||||||
chr2:134847264
|
G | C | 1 | a0001c0001t0001g0205 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.102+1987G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847264 | ||||||
chr2:134847290
|
C | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2013C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847290 | ||||||
chr2:134847331
|
T | C | 3 | a0001c0001t0001g0087a0001c0001t0001g0101a0001c0001t0001g0128 | 3 | HG02015.hp1 HG02074.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.102+2054T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847331 | ||||||
chr2:134847393
|
GATACAGA others(9): Show |
G | 1 | a0001c0001t0001g0254 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.102+2118_102+2133d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847393 | |||||
chr2:134847395
|
T | TATAG | 14 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0072others(11): Show | 14 | HG00735.hp2 HG01256.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+2119_102+2120i others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | |||||
chr2:134847395
|
TACAG | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(60): Show | 65 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.102+2120_102+2123d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | |||||
chr2:134847395
|
TACAGATA others(1): Show |
T | 92 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(89): Show | 93 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.102+2120_102+2127d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | |||||
chr2:134847395
|
TACAGATA others(5): Show |
T | 79 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0017others(76): Show | 81 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.102+2120_102+2131d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | |||||
chr2:134847395
|
TACAGATA others(9): Show |
T | 15 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0029others(12): Show | 15 | HG00741.hp1 HG01175.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.102+2120_102+2135d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847395 | |||||
chr2:134847397
|
C | CAGAT | 18 | a0001c0001t0001g0008a0001c0001t0001g0153a0001c0001t0001g0296others(15): Show | 19 | HG01099.hp1 HG01169.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.102+2170_102+2173d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | |||||
chr2:134847397
|
C | CAGATAGA others(1): Show |
20 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0280others(17): Show | 21 | HG01123.hp1 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.102+2166_102+2173d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | |||||
chr2:134847397
|
C | CAGATAGA others(5): Show |
4 | a0001c0001t0001g0279a0001c0001t0001g0306a0001c0001t0001g0329others(1): Show | 4 | HG00438.hp1 HG02922.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+2162_102+2173d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | |||||
chr2:134847397
|
C | CAGATAGA others(9): Show |
6 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(3): Show | 6 | HG03098.hp2 HG03453.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2158_102+2173d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | |||||
chr2:134847397
|
C | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0033others(48): Show | 51 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.102+2120C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847397 | ||||||
chr2:134847397
|
CAGAT | C | 4 | a0001c0001t0001g0298a0001c0001t0001g0303a0001c0001t0001g0328others(1): Show | 4 | HG00140.hp1 HG02155.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+2170_102+2173d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847397 | |||||
chr2:134847443
|
G | GATAGATA others(11): Show |
1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.102+2173_102+2174i others(20): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847443 | |||||
chr2:134847444
|
A | G | 78 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(75): Show | 79 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.102+2167A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847444 | ||||||
chr2:134847449
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0030 | 2 | HG01261.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.102+2172T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847449 | ||||||
chr2:134847451
|
T | G | 52 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0031others(49): Show | 53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.102+2174T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847451 | ||||||
chr2:134847558
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0099 | 2 | HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.102+2281C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847558 | ||||||
chr2:134847601
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0130 | 3 | HG02109.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.102+2324C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847601 | ||||||
chr2:134847646
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+2369T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847646 | ||||||
chr2:134847707
|
G | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+2430G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847707 | ||||||
chr2:134847850
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+2573T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847850 | ||||||
chr2:134847855
|
C | CT | 48 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(45): Show | 49 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.102+2591dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847855 | |||||
chr2:134847855
|
CT | C | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 254 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(251): Show |
intron_variant | MODIFIER | c.102+2591delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134847855 | |||||
chr2:134847856
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+2579T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847856 | ||||||
chr2:134847914
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102+2637C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134847914 | ||||||
chr2:134848130
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102+2853C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848130 | ||||||
chr2:134848249
|
T | C | 12 | a0001c0001t0001g0308a0001c0001t0001g0349a0001c0001t0001g0350others(9): Show | 12 | HG00735.hp2 HG01358.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.102+2972T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848249 | ||||||
chr2:134848418
|
T | C | 7 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG02145.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+3141T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848418 | ||||||
chr2:134848604
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.102+3327C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848604 | ||||||
chr2:134848635
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.102+3358T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134848635 | ||||||
chr2:134849027
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.102+3750G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849027 | ||||||
chr2:134849056
|
C | T | 10 | a0001c0001t0001g0141a0001c0001t0001g0154a0001c0001t0001g0156others(7): Show | 10 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+3779C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849056 | ||||||
chr2:134849228
|
C | T | 14 | a0001c0001t0001g0254a0001c0001t0001g0258a0001c0001t0001g0263others(11): Show | 15 | NA18951.hp1 NA18952.hp1 NA18962.hp2 others(12): Show |
intron_variant | MODIFIER | c.102+3951C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849228 | ||||||
chr2:134849272
|
C | CTTAT | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.102+3998_102+4001d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849272 | |||||
chr2:134849309
|
T | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.102+4032T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849309 | ||||||
chr2:134849330
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.102+4053T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849330 | ||||||
chr2:134849525
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.102+4248C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849525 | ||||||
chr2:134849689
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+4412G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849689 | ||||||
chr2:134849703
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0177 | 2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.102+4426C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849703 | ||||||
chr2:134849763
|
G | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.102+4486G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849763 | ||||||
chr2:134849773
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.102+4496G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849773 | ||||||
chr2:134849882
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.102+4605G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849882 | ||||||
chr2:134849902
|
T | C | 1 | a0001c0001t0001g0321 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.102+4625T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134849902 | ||||||
chr2:134849963
|
A | AAC | 40 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0035others(37): Show | 40 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.102+4721_102+4722d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | |||||
chr2:134849963
|
A | AACAC | 4 | a0001c0001t0001g0063a0001c0001t0001g0170a0001c0001t0001g0188others(1): Show | 4 | HG02602.hp2 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+4719_102+4722d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | |||||
chr2:134849963
|
AAC | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 139 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.102+4721_102+4722d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | |||||
chr2:134849963
|
AACAC | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0020others(84): Show | 89 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.102+4719_102+4722d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | |||||
chr2:134849963
|
AACACAC | A | 46 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(43): Show | 47 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.102+4717_102+4722d others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | |||||
chr2:134849963
|
AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0012a0001c0001t0001g0265a0001c0001t0001g0286 | 3 | HG02027.hp1 NA18962.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.102+4715_102+4722d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | |||||
chr2:134849963
|
AACACACA others(3): Show |
A | 18 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.102+4713_102+4722d others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134849963 | |||||
chr2:134850102
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.102+4825T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850102 | ||||||
chr2:134850205
|
C | G | 31 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0027others(28): Show | 31 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.102+4928C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850205 | ||||||
chr2:134850206
|
T | A | 1 | a0001c0001t0001g0034 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+4929T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850206 | ||||||
chr2:134850269
|
C | CT | 9 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(6): Show | 9 | HG02145.hp2 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+5006dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134850269 | |||||
chr2:134850282
|
TTC | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0131a0001c0001t0001g0133others(5): Show | 9 | HG01168.hp2 HG01169.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+5007_102+5008d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134850282 | |||||
chr2:134850283
|
TC | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 215 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.102+5007delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850283 | ||||||
chr2:134850284
|
C | T | 83 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(80): Show | 84 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.102+5007C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850284 | ||||||
chr2:134850287
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.102+5010A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850287 | ||||||
chr2:134850299
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0126 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.102+5022G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850299 | ||||||
chr2:134850371
|
C | T | 1 | a0001c0001t0001g0369 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.102+5094C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850371 | ||||||
chr2:134850618
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.102+5341A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850618 | ||||||
chr2:134850631
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.102+5354A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850631 | ||||||
chr2:134850641
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.102+5364A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850641 | ||||||
chr2:134850658
|
T | TTTA | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.102+5395_102+5397d others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134850658 | |||||
chr2:134850807
|
A | G | 68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(65): Show | 69 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.102+5530A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850807 | ||||||
chr2:134850916
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+5639A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850916 | ||||||
chr2:134850965
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | NA18985.hp1 NA18991.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.102+5688T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850965 | ||||||
chr2:134850973
|
A | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0130 | 3 | HG02109.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.102+5696A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134850973 | ||||||
chr2:134851209
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0056 | 2 | HG00639.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.102+5932C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851209 | ||||||
chr2:134851231
|
A | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.102+5954A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851231 | ||||||
chr2:134851283
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.102+6006G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851283 | ||||||
chr2:134851325
|
C | G | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.102+6048C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851325 | ||||||
chr2:134851346
|
G | T | 4 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346others(1): Show | 4 | HG00639.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6069G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851346 | ||||||
chr2:134851434
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.102+6157G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851434 | ||||||
chr2:134851459
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.102+6182T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851459 | ||||||
chr2:134851460
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.102+6183T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851460 | ||||||
chr2:134851539
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.102+6262T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851539 | ||||||
chr2:134851597
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.102+6320C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851597 | ||||||
chr2:134851633
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+6356G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851633 | ||||||
chr2:134851677
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 185 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.102+6400G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851677 | ||||||
chr2:134851688
|
C | A | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.102+6411C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134851688 | ||||||
chr2:134852084
|
G | T | 3 | a0002c0002t0001g0179a0002c0002t0001g0183a0002c0002t0001g0185 | 3 | HG02145.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.102+6807G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852084 | ||||||
chr2:134852125
|
G | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.102+6848G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852125 | ||||||
chr2:134852176
|
G | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.102+6899G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852176 | ||||||
chr2:134852208
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.102+6931T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852208 | ||||||
chr2:134852226
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.102+6949G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852226 | ||||||
chr2:134852342
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-6919G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852342 | ||||||
chr2:134852436
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-6825C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852436 | ||||||
chr2:134852437
|
G | A | 56 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0046others(53): Show | 56 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.103-6824G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852437 | ||||||
chr2:134852458
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.103-6803G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852458 | ||||||
chr2:134852536
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.103-6725C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852536 | ||||||
chr2:134852584
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.103-6677A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852584 | ||||||
chr2:134852632
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.103-6629G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852632 | ||||||
chr2:134852662
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.103-6599G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852662 | ||||||
chr2:134852793
|
G | A | 2 | a0004c0005t0001g0143a0004c0005t0001g0173 | 2 | NA18952.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.103-6468G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852793 | ||||||
chr2:134852868
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-6393T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852868 | ||||||
chr2:134852874
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0136 | 3 | NA18957.hp2 NA19062.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.103-6387T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852874 | ||||||
chr2:134852992
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-6269G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852992 | ||||||
chr2:134852995
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.103-6266T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134852995 | ||||||
chr2:134853047
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0126 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.103-6214C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853047 | ||||||
chr2:134853112
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.103-6149G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853112 | ||||||
chr2:134853167
|
T | TA | 181 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 184 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(181): Show |
intron_variant | MODIFIER | c.103-6075dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | |||||
chr2:134853167
|
T | TAA | 11 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0001g0079others(8): Show | 11 | HG02145.hp2 HG02572.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-6076_103-6075d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | |||||
chr2:134853167
|
TA | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0254a0001c0001t0001g0258others(7): Show | 11 | HG01515.hp2 HG02647.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-6075delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | |||||
chr2:134853167
|
TAAAAAAA others(1): Show |
T | 42 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(39): Show | 43 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.103-6082_103-6075d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134853167 | |||||
chr2:134853169
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.103-6092A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853169 | ||||||
chr2:134853311
|
T | C | 49 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(46): Show | 50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.103-5950T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853311 | ||||||
chr2:134853428
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.103-5833A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853428 | ||||||
chr2:134853478
|
G | A | 4 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346others(1): Show | 4 | HG00639.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5783G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853478 | ||||||
chr2:134853550
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-5711G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853550 | ||||||
chr2:134853559
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.103-5702T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853559 | ||||||
chr2:134853701
|
T | C | 1 | a0001c0001t0001g0344 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.103-5560T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853701 | ||||||
chr2:134853736
|
T | G | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.103-5525T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853736 | ||||||
chr2:134853740
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-5521C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853740 | ||||||
chr2:134853751
|
G | T | 1 | a0001c0009t0001g0169 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.103-5510G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853751 | ||||||
chr2:134853927
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-5334G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134853927 | ||||||
chr2:134854387
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-4874T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854387 | ||||||
chr2:134854740
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.103-4521C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854740 | ||||||
chr2:134854811
|
AT | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 95 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.103-4446delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134854811 | |||||
chr2:134854819
|
G | GCCTC | 94 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(91): Show | 95 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.103-4442_103-4441i others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854819 | ||||||
chr2:134854852
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(171): Show | 176 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.103-4409C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854852 | ||||||
chr2:134854869
|
G | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.103-4392G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854869 | ||||||
chr2:134854878
|
C | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.103-4383C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134854878 | ||||||
chr2:134855014
|
T | G | 1 | a0001c0001t0001g0034 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.103-4247T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855014 | ||||||
chr2:134855039
|
C | CT | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 232 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(229): Show |
intron_variant | MODIFIER | c.103-4212dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134855039 | |||||
chr2:134855149
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.103-4112G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855149 | ||||||
chr2:134855187
|
G | A | 49 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(46): Show | 50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.103-4074G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855187 | ||||||
chr2:134855347
|
T | C | 56 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(53): Show | 57 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.103-3914T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855347 | ||||||
chr2:134855812
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.103-3449T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855812 | ||||||
chr2:134855982
|
G | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | HG00741.hp2 HG01256.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-3279G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134855982 | ||||||
chr2:134856005
|
C | T | 6 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-3256C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856005 | ||||||
chr2:134856113
|
A | T | 5 | a0001c0001t0001g0189a0002c0002t0001g0013a0002c0002t0001g0179others(2): Show | 5 | HG02145.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-3148A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856113 | ||||||
chr2:134856364
|
C | T | 1 | a0001c0001t0001g0337 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-2897C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856364 | ||||||
chr2:134856432
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-2829G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856432 | ||||||
chr2:134856659
|
CCT | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG02698.hp2 HG03490.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-2601_103-2600d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134856659 | ||||||
chr2:134856905
|
G | GT | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 236 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(233): Show |
intron_variant | MODIFIER | c.103-2347dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 134856905 | |||||
chr2:134857097
|
C | G | 1 | a0001c0001t0001g0368 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.103-2164C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857097 | ||||||
chr2:134857269
|
C | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.103-1992C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857269 | ||||||
chr2:134857295
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-1966G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857295 | ||||||
chr2:134857306
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 237 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(234): Show |
intron_variant | MODIFIER | c.103-1955C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857306 | ||||||
chr2:134857387
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG02965.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-1874G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857387 | ||||||
chr2:134857864
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.103-1397T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857864 | ||||||
chr2:134857941
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.103-1320A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134857941 | ||||||
chr2:134858072
|
T | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0301a0001c0001t0001g0302others(5): Show | 9 | HG02257.hp1 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.103-1189T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858072 | ||||||
chr2:134858085
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0126 | 2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.103-1176G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858085 | ||||||
chr2:134858126
|
A | T | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.103-1135A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858126 | ||||||
chr2:134858322
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.103-939T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858322 | ||||||
chr2:134858363
|
G | A | 7 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0123others(4): Show | 7 | HG00558.hp1 HG00609.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-898G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858363 | ||||||
chr2:134858474
|
T | C | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103-787T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858474 | ||||||
chr2:134858614
|
T | C | 1 | a0001c0001t0001g0368 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.103-647T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858614 | ||||||
chr2:134858630
|
T | C | 77 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(74): Show | 78 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.103-631T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858630 | ||||||
chr2:134858643
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.103-618T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858643 | ||||||
chr2:134858776
|
A | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.103-485A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858776 | ||||||
chr2:134858815
|
C | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.103-446C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134858815 | ||||||
chr2:134859046
|
T | C | 2 | a0001c0001t0001g0166a0001c0009t0001g0169 | 2 | HG02735.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.103-215T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134859046 | ||||||
chr2:134859051
|
G | A | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.103-210G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134859051 | ||||||
chr2:134859065
|
C | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(94): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.103-196C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 2/9 | chr2 | 134859065 | ||||||
chr2:134859443
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.199+86T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134859443 | ||||||
chr2:134859563
|
C | T | 19 | a0001c0001t0001g0012a0001c0001t0001g0308a0001c0001t0001g0343others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.199+206C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134859563 | ||||||
chr2:134859586
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0001g0127others(1): Show | 4 | HG01175.hp2 HG02258.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+229T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134859586 | ||||||
chr2:134859623
|
T | TAAAAATT others(317): Show |
1 | a0001c0001t0001g0366 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.199+279_199+280ins others(324): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134859623 | |||||
chr2:134859623
|
T | TAAAAATT others(318): Show |
1 | a0001c0001t0001g0365 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.199+279_199+280ins others(325): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134859623 | |||||
chr2:134860194
|
C | T | 3 | a0001c0001t0001g0263a0003c0003t0001g0006a0003c0003t0001g0274 | 4 | NA18952.hp1 NA18962.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+837C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860194 | ||||||
chr2:134860212
|
G | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG01099.hp2 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+855G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860212 | ||||||
chr2:134860234
|
G | C | 49 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(46): Show | 50 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.199+877G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860234 | ||||||
chr2:134860265
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.199+908A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860265 | ||||||
chr2:134860368
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.199+1011A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860368 | ||||||
chr2:134860450
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0260a0001c0001t0001g0273 | 3 | HG01255.hp2 HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.199+1093A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860450 | ||||||
chr2:134860637
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.199+1280G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860637 | ||||||
chr2:134860671
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.200-1298G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860671 | ||||||
chr2:134860749
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.200-1220G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860749 | ||||||
chr2:134860856
|
C | CA | 17 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(14): Show | 17 | HG01169.hp1 HG01261.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.200-1089dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
C | CAAA | 36 | a0001c0001t0001g0010a0001c0001t0001g0035a0001c0001t0001g0048others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.200-1091_200-1089d others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
C | CAAAA | 19 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0036others(16): Show | 20 | HG00609.hp2 HG01175.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.200-1092_200-1089d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
C | CAAAAA | 48 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0022others(45): Show | 49 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.200-1093_200-1089d others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
C | CAAAAAA | 35 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0096others(32): Show | 36 | HG01243.hp1 HG01255.hp2 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.200-1094_200-1089d others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
C | CAAAAAAA | 37 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(34): Show | 38 | HG00597.hp2 HG00642.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.200-1095_200-1089d others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0011a0001c0001t0001g0083a0001c0001t0001g0086others(12): Show | 15 | HG00408.hp2 HG00438.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.200-1096_200-1089d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
CA | C | 9 | a0001c0001t0001g0327a0001c0001t0001g0329a0001c0001t0001g0340others(6): Show | 9 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.200-1089delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860856
|
CAAAAAA | C | 79 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(76): Show | 80 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.200-1094_200-1089d others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134860856 | |||||
chr2:134860965
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.200-1004G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134860965 | ||||||
chr2:134861412
|
T | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.200-557T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861412 | ||||||
chr2:134861445
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.200-524A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861445 | ||||||
chr2:134861446
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.200-523G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861446 | ||||||
chr2:134861787
|
T | TA | 77 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(74): Show | 78 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.200-181dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134861787 | |||||
chr2:134861817
|
A | AG | 17 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(14): Show | 17 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.200-146dupG | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 134861817 | |||||
chr2:134861829
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.200-140G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861829 | ||||||
chr2:134861915
|
A | C | 3 | a0002c0002t0001g0179a0002c0002t0001g0183a0002c0002t0001g0185 | 3 | HG02145.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.200-54A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861915 | ||||||
chr2:134861930
|
C | A | 7 | a0001c0001t0001g0062a0001c0001t0001g0217a0001c0001t0001g0227others(4): Show | 7 | HG00741.hp2 HG01256.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-39C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 3/9 | chr2 | 134861930 | ||||||
chr2:134862075
|
A | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.249+57A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862075 | ||||||
chr2:134862247
|
T | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0308a0001c0001t0001g0343others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+229T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862247 | ||||||
chr2:134862311
|
A | T | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.249+293A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862311 | ||||||
chr2:134862541
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.249+523G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862541 | ||||||
chr2:134862585
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.249+567G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862585 | ||||||
chr2:134862615
|
G | C | 150 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(147): Show | 152 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.249+597G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862615 | ||||||
chr2:134862731
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.250-664C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862731 | ||||||
chr2:134862995
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250-400T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134862995 | ||||||
chr2:134863017
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.250-378T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134863017 | ||||||
chr2:134863057
|
A | AG | 96 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(93): Show | 97 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.250-332dupG | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 134863057 | |||||
chr2:134863064
|
C | A | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.250-331C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 4/9 | chr2 | 134863064 | ||||||
chr2:134863809
|
TC | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+180delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 134863809 | |||||
chr2:134863953
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+322G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134863953 | ||||||
chr2:134863986
|
T | C | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 309 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.486+355T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134863986 | ||||||
chr2:134864044
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.486+413G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864044 | ||||||
chr2:134864132
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.486+501G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864132 | ||||||
chr2:134864265
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.486+634T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864265 | ||||||
chr2:134864268
|
C | CA | 76 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0014others(73): Show | 77 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.486+652dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 134864268 | |||||
chr2:134864333
|
T | A | 1 | a0001c0001t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.486+702T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864333 | ||||||
chr2:134864348
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.486+717G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864348 | ||||||
chr2:134864372
|
G | T | 3 | a0001c0001t0001g0077a0001c0001t0001g0146a0001c0001t0001g0178 | 3 | HG02572.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.486+741G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864372 | ||||||
chr2:134864475
|
T | G | 2 | a0001c0001t0001g0302a0001c0001t0001g0330 | 2 | HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.486+844T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864475 | ||||||
chr2:134864586
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.486+955C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864586 | ||||||
chr2:134864624
|
A | AT | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 307 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.486+998dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 134864624 | |||||
chr2:134864953
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.486+1322T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134864953 | ||||||
chr2:134865032
|
C | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.486+1401C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865032 | ||||||
chr2:134865158
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.486+1527G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865158 | ||||||
chr2:134865238
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 234 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.486+1607C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865238 | ||||||
chr2:134865290
|
T | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(171): Show | 176 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.486+1659T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865290 | ||||||
chr2:134865330
|
A | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0306a0001c0001t0001g0321others(1): Show | 5 | NA18966.hp1 NA18967.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1699A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865330 | ||||||
chr2:134865354
|
G | A | 2 | a0001c0001t0001g0189a0002c0002t0001g0013 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.486+1723G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865354 | ||||||
chr2:134865541
|
T | C | 1 | a0001c0001t0001g0369 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.486+1910T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865541 | ||||||
chr2:134865550
|
A | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(49): Show | 53 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.486+1919A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865550 | ||||||
chr2:134865814
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.487-1765C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865814 | ||||||
chr2:134865947
|
C | T | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.487-1632C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134865947 | ||||||
chr2:134866039
|
T | C | 16 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.487-1540T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866039 | ||||||
chr2:134866259
|
C | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.487-1320C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866259 | ||||||
chr2:134866438
|
A | C | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(300): Show | 308 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.487-1141A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866438 | ||||||
chr2:134866507
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487-1072G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866507 | ||||||
chr2:134866596
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.487-983T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866596 | ||||||
chr2:134866797
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.487-782A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866797 | ||||||
chr2:134866991
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0078 | 2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.487-588C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134866991 | ||||||
chr2:134867251
|
G | C | 1 | a0002c0002t0001g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.487-328G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867251 | ||||||
chr2:134867312
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.487-267T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867312 | ||||||
chr2:134867479
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.487-100C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867479 | ||||||
chr2:134867552
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487-27T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 5/9 | chr2 | 134867552 | ||||||
chr2:134867709
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.580+37C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867709 | ||||||
chr2:134867803
|
T | G | 1 | a0001c0001t0001g0353 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.580+131T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867803 | ||||||
chr2:134867821
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.580+149G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867821 | ||||||
chr2:134867829
|
C | CTA | 4 | a0001c0001t0001g0036a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG02071.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+172_580+173dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134867829 | |||||
chr2:134867838
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+166T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867838 | ||||||
chr2:134867848
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+176C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134867848 | ||||||
chr2:134868102
|
A | G | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.580+430A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868102 | ||||||
chr2:134868257
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0056 | 2 | HG00639.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.580+585C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868257 | ||||||
chr2:134868279
|
G | A | 1 | a0008c0010t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.580+607G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868279 | ||||||
chr2:134868331
|
T | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.580+659T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868331 | ||||||
chr2:134868347
|
T | TA | 6 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 6 | NA18959.hp1 NA18983.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.580+676dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134868347 | |||||
chr2:134868386
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.580+714A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868386 | ||||||
chr2:134868451
|
C | CT | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 231 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(228): Show |
intron_variant | MODIFIER | c.580+798dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134868451 | |||||
chr2:134868451
|
C | CTT | 11 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0142others(8): Show | 11 | HG01243.hp1 HG01978.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.580+797_580+798dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134868451 | |||||
chr2:134868456
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.580+784T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868456 | ||||||
chr2:134868805
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.580+1133C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868805 | ||||||
chr2:134868969
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.580+1297G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134868969 | ||||||
chr2:134869019
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.580+1347T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869019 | ||||||
chr2:134869041
|
GC | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.580+1370delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869041 | ||||||
chr2:134869205
|
C | CATTT | 166 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(163): Show | 168 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.580+1555_580+1558d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869205 | |||||
chr2:134869205
|
C | CATTTATT others(1): Show |
8 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0065others(5): Show | 8 | HG03831.hp1 NA18959.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.580+1551_580+1558d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869205 | |||||
chr2:134869340
|
G | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.581-1625G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869340 | ||||||
chr2:134869358
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.581-1607G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869358 | ||||||
chr2:134869369
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.581-1596C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869369 | ||||||
chr2:134869443
|
CCTCAAGT others(15): Show |
C | 1 | a0001c0001t0001g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.581-1521_581-1500d others(24): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869443 | ||||||
chr2:134869548
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.581-1417G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869548 | ||||||
chr2:134869605
|
G | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 234 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.581-1360G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869605 | ||||||
chr2:134869706
|
G | GTA | 83 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0012others(80): Show | 85 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.581-1239_581-1238d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869706 | |||||
chr2:134869706
|
G | GTATA | 6 | a0001c0001t0001g0035a0001c0001t0001g0140a0001c0001t0001g0186others(3): Show | 6 | HG02155.hp2 HG03195.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.581-1241_581-1238d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869706 | |||||
chr2:134869706
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.581-1247_581-1238d others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 134869706 | |||||
chr2:134869826
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.581-1139C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869826 | ||||||
chr2:134869880
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.581-1085G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134869880 | ||||||
chr2:134870179
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.581-786C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870179 | ||||||
chr2:134870253
|
G | A | 4 | a0001c0001t0001g0344a0001c0001t0001g0345a0001c0001t0001g0346others(1): Show | 4 | HG00639.hp2 HG03710.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.581-712G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870253 | ||||||
chr2:134870351
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.581-614G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870351 | ||||||
chr2:134870393
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.581-572G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870393 | ||||||
chr2:134870460
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.581-505C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870460 | ||||||
chr2:134870504
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.581-461G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870504 | ||||||
chr2:134870570
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.581-395G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870570 | ||||||
chr2:134870601
|
C | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.581-364C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870601 | ||||||
chr2:134870643
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.581-322G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870643 | ||||||
chr2:134870800
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-165G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870800 | ||||||
chr2:134870836
|
C | T | 30 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(27): Show | 30 | HG00558.hp1 HG00609.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.581-129C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870836 | ||||||
chr2:134870903
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0079 | 2 | HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.581-62A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 6/9 | chr2 | 134870903 | ||||||
chr2:134871124
|
T | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.676+64T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871124 | ||||||
chr2:134871263
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.676+203T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871263 | ||||||
chr2:134871511
|
G | GT | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(239): Show | 245 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.676+463dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871511 | |||||
chr2:134871511
|
G | GTT | 6 | a0001c0001t0001g0075a0001c0001t0001g0095a0001c0001t0001g0099others(3): Show | 6 | HG02602.hp1 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+462_676+463dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871511 | |||||
chr2:134871582
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.676+522C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871582 | ||||||
chr2:134871678
|
G | GAC | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(101): Show | 106 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.676+620_676+621dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | |||||
chr2:134871678
|
G | GACAC | 19 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0063others(16): Show | 20 | HG00642.hp1 HG00735.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | |||||
chr2:134871678
|
G | GACACAC | 13 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0084others(10): Show | 13 | HG01978.hp2 HG02717.hp2 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | |||||
chr2:134871678
|
G | GACACACA others(1): Show |
49 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0029others(46): Show | 50 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | |||||
chr2:134871678
|
G | GACACACA others(3): Show |
30 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0081others(27): Show | 30 | HG00544.hp2 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.676+621_676+622ins others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | |||||
chr2:134871678
|
G | GACACACA others(5): Show |
3 | a0001c0001t0001g0151a0001c0001t0001g0220a0001c0001t0001g0225 | 3 | HG00597.hp1 NA18949.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.676+621_676+622ins others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871678 | |||||
chr2:134871680
|
CAG | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(7): Show | 10 | HG02109.hp1 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+622_676+623del others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871680 | |||||
chr2:134871682
|
G | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 228 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.676+622G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871682 | ||||||
chr2:134871682
|
G | GAC | 8 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0236others(5): Show | 9 | HG02647.hp1 HG02922.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+652_676+653dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871682
|
G | GACAC | 9 | a0001c0001t0001g0189a0001c0001t0001g0302a0001c0001t0001g0303others(6): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.676+650_676+653dup others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871682
|
G | GACACAC | 3 | a0001c0001t0001g0009a0001c0001t0001g0014a0006c0008t0001g0348 | 3 | HG00741.hp1 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.676+648_676+653dup others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871682
|
G | GACACACA others(1): Show |
43 | a0001c0001t0001g0011a0001c0001t0001g0240a0001c0001t0001g0241others(40): Show | 44 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.676+646_676+653dup others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871682
|
G | GACACACA others(3): Show |
12 | a0001c0001t0001g0278a0001c0001t0001g0287a0001c0001t0001g0308others(9): Show | 12 | HG01243.hp1 HG01358.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.676+644_676+653dup others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871682
|
G | GACACACA others(5): Show |
6 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG00639.hp2 HG03710.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.676+642_676+653dup others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871682
|
G | GACACACA others(9): Show |
1 | a0001c0001t0001g0277 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.676+638_676+653dup others(16): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871682
|
G | GACAGACA others(11): Show |
1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.676+625_676+626ins others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871682 | |||||
chr2:134871735
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.676+675G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871735 | ||||||
chr2:134871736
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(100): Show | 104 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.676+676C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871736 | ||||||
chr2:134871760
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG02559.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.676+700G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871760 | ||||||
chr2:134871763
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.676+703T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871763 | ||||||
chr2:134871865
|
A | G | 7 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0123others(4): Show | 7 | HG00558.hp1 HG00609.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.677-604A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871865 | ||||||
chr2:134871869
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 234 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.677-600C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871869 | ||||||
chr2:134871890
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.677-579A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134871890 | ||||||
chr2:134871960
|
C | CT | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 270 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(267): Show |
intron_variant | MODIFIER | c.677-495dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871960 | |||||
chr2:134871960
|
C | CTT | 28 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0085others(25): Show | 29 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.677-496_677-495dup others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 134871960 | |||||
chr2:134872025
|
C | T | 2 | a0001c0001t0001g0012a0002c0002t0001g0183 | 2 | HG02027.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.677-444C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872025 | ||||||
chr2:134872069
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.677-400G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872069 | ||||||
chr2:134872104
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.677-365G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872104 | ||||||
chr2:134872337
|
T | C | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.677-132T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872337 | ||||||
chr2:134872357
|
C | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.677-112C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 7/9 | chr2 | 134872357 | ||||||
chr2:134872928
|
A | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(66): Show | 70 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.849+287A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134872928 | ||||||
chr2:134873078
|
A | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0129 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.849+437A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873078 | ||||||
chr2:134873130
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.849+489C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873130 | ||||||
chr2:134873295
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+654C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873295 | ||||||
chr2:134873356
|
GC | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+716delC | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873356 | ||||||
chr2:134873400
|
A | T | 1 | a0001c0001t0001g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.849+759A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873400 | ||||||
chr2:134873483
|
G | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0308a0001c0001t0001g0343others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.849+842G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873483 | ||||||
chr2:134873512
|
T | C | 1 | a0001c0001t0001g0003 | 2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.849+871T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873512 | ||||||
chr2:134873761
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 314 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(311): Show |
intron_variant | MODIFIER | c.849+1120A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873761 | ||||||
chr2:134873830
|
C | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 234 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.849+1189C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873830 | ||||||
chr2:134873863
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+1222G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873863 | ||||||
chr2:134873989
|
T | C | 3 | a0001c0001t0001g0263a0003c0003t0001g0006a0003c0003t0001g0274 | 4 | NA18952.hp1 NA18962.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1348T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134873989 | ||||||
chr2:134874149
|
G | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.849+1508G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874149 | ||||||
chr2:134874237
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0078a0001c0001t0001g0180 | 3 | HG01070.hp1 HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.849+1596T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874237 | ||||||
chr2:134874301
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.849+1660T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874301 | ||||||
chr2:134874447
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+1806C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874447 | ||||||
chr2:134874495
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.849+1854G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874495 | ||||||
chr2:134874570
|
C | T | 2 | a0001c0004t0001g0190a0001c0004t0001g0191 | 2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.849+1929C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874570 | ||||||
chr2:134874588
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+1947T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874588 | ||||||
chr2:134874621
|
T | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.849+1980T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874621 | ||||||
chr2:134874666
|
T | C | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+2025T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874666 | ||||||
chr2:134874864
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.849+2223A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874864 | ||||||
chr2:134874983
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.849+2342A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134874983 | ||||||
chr2:134875008
|
G | C | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.849+2367G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875008 | ||||||
chr2:134875053
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+2412C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875053 | ||||||
chr2:134875169
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.849+2528T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875169 | ||||||
chr2:134875184
|
A | G | 16 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.849+2543A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875184 | ||||||
chr2:134875292
|
C | A | 308 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(305): Show | 313 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(310): Show |
intron_variant | MODIFIER | c.849+2651C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875292 | ||||||
chr2:134875411
|
C | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(283): Show | 291 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(288): Show |
intron_variant | MODIFIER | c.849+2770C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875411 | ||||||
chr2:134875581
|
G | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0089a0001c0001t0001g0090others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+2940G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875581 | ||||||
chr2:134875744
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.849+3103G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875744 | ||||||
chr2:134875899
|
A | C | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.849+3258A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134875899 | ||||||
chr2:134876025
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+3384T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876025 | ||||||
chr2:134876115
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.849+3474G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876115 | ||||||
chr2:134876252
|
A | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.849+3611A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876252 | ||||||
chr2:134876424
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+3783G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876424 | ||||||
chr2:134876558
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+3917G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876558 | ||||||
chr2:134876574
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.849+3933C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876574 | ||||||
chr2:134876578
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+3937A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876578 | ||||||
chr2:134876684
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.849+4043C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876684 | ||||||
chr2:134876707
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.849+4066C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876707 | ||||||
chr2:134876767
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+4126G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876767 | ||||||
chr2:134876821
|
A | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0306a0001c0001t0001g0321others(1): Show | 5 | NA18966.hp1 NA18967.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+4180A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134876821 | ||||||
chr2:134877011
|
G | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 233 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.849+4370G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877011 | ||||||
chr2:134877150
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+4509G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877150 | ||||||
chr2:134877157
|
A | C | 1 | a0006c0008t0001g0348 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.849+4516A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877157 | ||||||
chr2:134877208
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.849+4567T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877208 | ||||||
chr2:134877523
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+4882T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877523 | ||||||
chr2:134877577
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+4936G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877577 | ||||||
chr2:134877697
|
AAG | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+5059_849+5060d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134877697 | |||||
chr2:134877700
|
A | AG | 52 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0123others(49): Show | 53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+5067dupG | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134877700 | |||||
chr2:134877700
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.849+5059A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877700 | ||||||
chr2:134877709
|
A | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0014others(52): Show | 57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.849+5068A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877709 | ||||||
chr2:134877712
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0091a0001c0001t0001g0093others(2): Show | 5 | HG02717.hp1 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+5071A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877712 | ||||||
chr2:134877908
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.849+5267C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134877908 | ||||||
chr2:134878384
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.849+5743C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134878384 | ||||||
chr2:134879556
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+6915A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879556 | ||||||
chr2:134879622
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.849+6981T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879622 | ||||||
chr2:134879768
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.849+7127G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879768 | ||||||
chr2:134879779
|
C | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.849+7138C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879779 | ||||||
chr2:134879800
|
T | A | 4 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0294others(1): Show | 4 | NA18970.hp2 NA18978.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+7159T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879800 | ||||||
chr2:134879813
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+7172A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134879813 | ||||||
chr2:134880277
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.849+7636G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880277 | ||||||
chr2:134880322
|
G | C | 1 | a0001c0001t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.849+7681G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880322 | ||||||
chr2:134880474
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 227 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(224): Show |
intron_variant | MODIFIER | c.849+7833C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880474 | ||||||
chr2:134880478
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+7837C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880478 | ||||||
chr2:134880532
|
A | G | 1 | a0001c0001t0001g0353 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.849+7891A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880532 | ||||||
chr2:134880790
|
A | G | 11 | a0001c0001t0001g0308a0001c0001t0001g0349a0001c0001t0001g0350others(8): Show | 11 | HG00735.hp2 HG01358.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.849+8149A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880790 | ||||||
chr2:134880891
|
C | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.849+8250C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880891 | ||||||
chr2:134880904
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0001g0223 | 2 | HG01496.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.849+8263G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134880904 | ||||||
chr2:134881029
|
T | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.849+8388T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881029 | ||||||
chr2:134881260
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.849+8619C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881260 | ||||||
chr2:134881301
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+8660C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881301 | ||||||
chr2:134881440
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.849+8799T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881440 | ||||||
chr2:134881567
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+8926C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881567 | ||||||
chr2:134881807
|
G | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.849+9166G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881807 | ||||||
chr2:134881855
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0258 | 2 | NA19010.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.849+9214C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881855 | ||||||
chr2:134881860
|
G | C | 16 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.849+9219G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881860 | ||||||
chr2:134881948
|
T | A | 18 | a0001c0001t0001g0012a0001c0001t0001g0308a0001c0001t0001g0343others(15): Show | 18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.849+9307T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134881948 | ||||||
chr2:134882039
|
A | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+9398A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882039 | ||||||
chr2:134882324
|
T | C | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+9683T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882324 | ||||||
chr2:134882405
|
C | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.849+9764C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882405 | ||||||
chr2:134882588
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+9947A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882588 | ||||||
chr2:134882642
|
G | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.849+10001G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882642 | ||||||
chr2:134882652
|
A | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+10011A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134882652 | ||||||
chr2:134883065
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.849+10424T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883065 | ||||||
chr2:134883162
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0040 | 2 | NA18963.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.849+10521A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883162 | ||||||
chr2:134883243
|
G | T | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.849+10602G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883243 | ||||||
chr2:134883265
|
C | CA | 11 | a0001c0001t0001g0082a0001c0001t0001g0110a0001c0001t0001g0111others(8): Show | 11 | HG01099.hp2 HG01361.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+10634dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134883265 | |||||
chr2:134883332
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.849+10691A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883332 | ||||||
chr2:134883443
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.849+10802T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883443 | ||||||
chr2:134883564
|
C | G | 1 | a0001c0001t0001g0277 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.849+10923C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883564 | ||||||
chr2:134883699
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.849+11058C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883699 | ||||||
chr2:134883744
|
C | A | 1 | a0001c0001t0001g0145 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.849+11103C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883744 | ||||||
chr2:134883904
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+11263A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134883904 | ||||||
chr2:134884014
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.849+11373G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884014 | ||||||
chr2:134884238
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.849+11597T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884238 | ||||||
chr2:134884410
|
A | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+11769A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884410 | ||||||
chr2:134884589
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.849+11948C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884589 | ||||||
chr2:134884610
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(304): Show | 312 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.849+11969A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884610 | ||||||
chr2:134884833
|
G | T | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.849+12192G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884833 | ||||||
chr2:134884849
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.849+12208G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884849 | ||||||
chr2:134884952
|
T | TC | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+12311_849+1231 others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884952 | ||||||
chr2:134884965
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+12324G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134884965 | ||||||
chr2:134885012
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.849+12371A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885012 | ||||||
chr2:134885144
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(102): Show | 106 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.849+12503G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885144 | ||||||
chr2:134885149
|
T | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 228 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.849+12508T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885149 | ||||||
chr2:134885208
|
C | T | 3 | a0001c0001t0001g0340a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02896.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.849+12567C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885208 | ||||||
chr2:134885236
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+12595G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885236 | ||||||
chr2:134885244
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+12603A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885244 | ||||||
chr2:134885246
|
AT | A | 19 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0161others(16): Show | 19 | HG00735.hp2 HG01243.hp1 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.849+12608delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885246 | |||||
chr2:134885255
|
T | A | 1 | a0001c0001t0001g0344 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.849+12614T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885255 | ||||||
chr2:134885255
|
TA | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+12616delA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885255 | |||||
chr2:134885256
|
A | T | 1 | a0001c0001t0001g0344 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.849+12615A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885256 | ||||||
chr2:134885256
|
AAT | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01358.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+12625_849+1262 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885256 | |||||
chr2:134885277
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12636A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885277 | ||||||
chr2:134885278
|
T | A | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12637T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885278 | ||||||
chr2:134885284
|
A | ATAATATA others(3): Show |
1 | a0001c0001t0001g0145 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.849+12644_849+1264 others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885284 | |||||
chr2:134885285
|
T | A | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12644T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885285 | ||||||
chr2:134885285
|
T | TAATA | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(290): Show | 298 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(295): Show |
intron_variant | MODIFIER | c.849+12644_849+1264 others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885285 | ||||||
chr2:134885285
|
TTATATTT others(39): Show |
T | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.849+12645_849+1269 others(50): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885285 | ||||||
chr2:134885286
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+12645T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885286 | ||||||
chr2:134885290
|
T | TATATTTA others(51): Show |
1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+12649_849+1265 others(62): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885290 | ||||||
chr2:134885291
|
T | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0264 | 2 | HG02083.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.849+12650T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885291 | ||||||
chr2:134885292
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.849+12651T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885292 | ||||||
chr2:134885292
|
T | TATATATA | 167 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(164): Show | 169 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.849+12652_849+1265 others(11): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885292 | |||||
chr2:134885292
|
T | TATATATA others(1): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12658_849+1265 others(12): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885292 | |||||
chr2:134885293
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.849+12652A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885293 | ||||||
chr2:134885298
|
T | TA | 46 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(43): Show | 47 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.849+12658dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885298 | |||||
chr2:134885301
|
A | G | 52 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(49): Show | 53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+12660A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885301 | ||||||
chr2:134885303
|
T | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(45): Show | 49 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.849+12662T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885303 | ||||||
chr2:134885303
|
T | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 252 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.849+12662T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885303 | ||||||
chr2:134885305
|
A | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0264 | 3 | HG02083.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+12664A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885305 | ||||||
chr2:134885306
|
A | AAT | 33 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0044others(30): Show | 34 | HG00642.hp2 HG00673.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.849+12677_849+1267 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885306 | |||||
chr2:134885306
|
A | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(46): Show | 50 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.849+12665A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885306 | ||||||
chr2:134885306
|
AAT | A | 56 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0014others(53): Show | 57 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.849+12677_849+1267 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885306 | |||||
chr2:134885308
|
T | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0264 | 3 | HG02083.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.849+12667T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885308 | ||||||
chr2:134885308
|
T | TGTAA | 46 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(43): Show | 47 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.849+12667_849+1266 others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885308 | ||||||
chr2:134885309
|
A | ATATATAT others(42): Show |
3 | a0001c0001t0001g0362a0001c0001t0001g0363a0001c0001t0001g0364 | 3 | HG02630.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.849+12671_849+1271 others(53): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885309 | |||||
chr2:134885311
|
A | ATAT | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12671_849+1267 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885311 | |||||
chr2:134885316
|
TATA | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0340a0001c0001t0001g0365others(1): Show | 4 | HG02027.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+12677_849+1267 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885316 | |||||
chr2:134885317
|
ATAAATAT others(52): Show |
A | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.849+12677_849+1273 others(63): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885317 | ||||||
chr2:134885319
|
A | AT | 17 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0096others(14): Show | 17 | HG00544.hp2 HG00609.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.849+12678_849+1267 others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885319 | ||||||
chr2:134885319
|
A | ATAT | 39 | a0001c0001t0001g0028a0001c0001t0001g0046a0001c0001t0001g0047others(36): Show | 39 | HG00558.hp1 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.849+12678_849+1267 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885319 | ||||||
chr2:134885319
|
A | ATATAT | 5 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0106others(2): Show | 5 | HG02258.hp1 NA18906.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12678_849+1267 others(9): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885319 | ||||||
chr2:134885320
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.849+12679A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885320 | ||||||
chr2:134885329
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12688G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885329 | ||||||
chr2:134885332
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+12691A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885332 | ||||||
chr2:134885339
|
AT | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0361 | 3 | NA18949.hp2 NA18992.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.849+12701delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885339 | |||||
chr2:134885346
|
TATA | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0091others(6): Show | 10 | HG02486.hp1 HG02717.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.849+12709_849+1271 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885346 | |||||
chr2:134885349
|
A | AATATATA others(36): Show |
52 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(49): Show | 53 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.849+12719_849+1272 others(47): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885349 | |||||
chr2:134885359
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.849+12718T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885359 | ||||||
chr2:134885359
|
T | TAA | 50 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(47): Show | 51 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.849+12719_849+1272 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885359 | |||||
chr2:134885361
|
C | A | 65 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(62): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.849+12720C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885361 | ||||||
chr2:134885361
|
C | CAT | 4 | a0001c0001t0001g0091a0001c0001t0001g0136a0001c0001t0001g0168others(1): Show | 4 | HG03139.hp1 NA19005.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+12727_849+1272 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885361 | |||||
chr2:134885361
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.849+12720C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885361 | ||||||
chr2:134885368
|
A | AT | 3 | a0001c0001t0001g0010a0001c0001t0001g0236a0001c0001t0001g0360 | 3 | HG01243.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.849+12729dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885368 | |||||
chr2:134885368
|
A | ATTTATAT others(23): Show |
1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.849+12729_849+1273 others(34): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885368 | |||||
chr2:134885368
|
ATT | A | 13 | a0001c0001t0001g0204a0001c0001t0001g0212a0001c0001t0001g0213others(10): Show | 13 | HG02015.hp2 HG02451.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.849+12728_849+1272 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885368 | ||||||
chr2:134885369
|
T | TTATATAT others(25): Show |
2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.849+12737_849+1273 others(36): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885369 | |||||
chr2:134885377
|
A | T | 1 | a0001c0001t0001g0311 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.849+12736A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885377 | ||||||
chr2:134885389
|
A | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.849+12748A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885389 | ||||||
chr2:134885398
|
AT | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(101): Show | 105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.849+12760delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885398 | |||||
chr2:134885488
|
T | TAC | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 302 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.849+12848_849+1284 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134885488 | |||||
chr2:134885728
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 302 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.850-12613C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885728 | ||||||
chr2:134885745
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-12596C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885745 | ||||||
chr2:134885805
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | NA18939.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.850-12536G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885805 | ||||||
chr2:134885851
|
G | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-12490G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134885851 | ||||||
chr2:134886097
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.850-12244G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886097 | ||||||
chr2:134886233
|
C | CATT | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-12095_850-1209 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886233 | |||||
chr2:134886243
|
A | AT | 4 | a0001c0001t0001g0126a0001c0001t0001g0204a0001c0001t0001g0301others(1): Show | 4 | HG02895.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-12096dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | |||||
chr2:134886243
|
A | ATT | 3 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0253 | 3 | NA18985.hp2 NA18987.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.850-12097_850-1209 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | |||||
chr2:134886243
|
A | ATTT | 38 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(35): Show | 39 | HG00408.hp2 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.850-12096_850-1209 others(7): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | |||||
chr2:134886243
|
A | ATTTT | 13 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0246others(10): Show | 13 | HG00438.hp2 HG01346.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-12096_850-1209 others(8): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886243 | |||||
chr2:134886246
|
A | AT | 18 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0097others(15): Show | 18 | HG00544.hp2 HG01175.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.850-12073dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(20): Show |
1 | a0001c0001t0001g0351 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.850-12093_850-1209 others(31): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(21): Show |
2 | a0001c0001t0001g0350a0001c0001t0001g0358 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(15): Show |
1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(26): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(19): Show |
2 | a0001c0001t0001g0346a0001c0001t0001g0347 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(30): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(20): Show |
1 | a0001c0001t0001g0356 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(31): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(21): Show |
2 | a0001c0001t0001g0354a0001c0001t0001g0355 | 2 | HG00735.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(22): Show |
1 | a0001c0001t0001g0359 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.850-12093_850-1209 others(33): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(18): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0344 | 2 | HG00639.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(29): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(21): Show |
2 | a0001c0001t0001g0308a0001c0001t0001g0349 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(6): Show |
1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(17): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(17): Show |
1 | a0001c0001t0001g0345 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(28): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(20): Show |
1 | a0001c0001t0001g0353 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(31): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(21): Show |
1 | a0001c0001t0001g0357 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | ATTATTAT others(15): Show |
1 | a0001c0001t0001g0343 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.850-12093_850-1209 others(26): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886246 | |||||
chr2:134886246
|
A | T | 74 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014others(71): Show | 76 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.850-12095A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886246 | ||||||
chr2:134886248
|
T | TA | 11 | a0001c0001t0001g0041a0001c0001t0001g0062a0001c0001t0001g0064others(8): Show | 11 | HG01496.hp2 HG03579.hp1 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-12093_850-1209 others(5): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886248 | ||||||
chr2:134886249
|
T | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 158 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.850-12092T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886249 | ||||||
chr2:134886250
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0132 | 2 | HG01515.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.850-12091T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886250 | ||||||
chr2:134886251
|
T | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0064 | 2 | HG03927.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.850-12090T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886251 | ||||||
chr2:134886252
|
T | A | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(72): Show | 77 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.850-12089T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886252 | ||||||
chr2:134886255
|
T | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 20 | HG01257.hp2 HG01261.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.850-12086T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886255 | ||||||
chr2:134886258
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0137others(2): Show | 6 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-12083T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886258 | ||||||
chr2:134886275
|
GTC | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-12063_850-1206 others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134886275 | |||||
chr2:134886279
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-12062C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886279 | ||||||
chr2:134886287
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.850-12054C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886287 | ||||||
chr2:134886484
|
G | A | 16 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-11857G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886484 | ||||||
chr2:134886699
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.850-11642T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886699 | ||||||
chr2:134886751
|
C | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-11590C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886751 | ||||||
chr2:134886901
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-11440G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134886901 | ||||||
chr2:134887077
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-11264C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887077 | ||||||
chr2:134887194
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-11147C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887194 | ||||||
chr2:134887408
|
C | T | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 300 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(297): Show |
intron_variant | MODIFIER | c.850-10933C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887408 | ||||||
chr2:134887500
|
T | C | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-10841T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887500 | ||||||
chr2:134887737
|
C | A | 1 | a0001c0001t0001g0269 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.850-10604C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887737 | ||||||
chr2:134887749
|
A | C | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-10592A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134887749 | ||||||
chr2:134888213
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-10128G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134888213 | ||||||
chr2:134888343
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-9998T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134888343 | ||||||
chr2:134888665
|
G | GAAAAAAA others(310): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-9661_850-9660i others(319): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134888665 | |||||
chr2:134889162
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850-9179G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889162 | ||||||
chr2:134889184
|
G | A | 5 | a0001c0001t0001g0300a0001c0001t0001g0316a0001c0001t0001g0318others(2): Show | 5 | HG01123.hp1 HG01192.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-9157G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889184 | ||||||
chr2:134889209
|
G | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(222): Show | 229 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.850-9132G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889209 | ||||||
chr2:134889252
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.850-9089T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889252 | ||||||
chr2:134889428
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.850-8913A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889428 | ||||||
chr2:134889742
|
G | C | 1 | a0001c0001t0001g0353 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-8599G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889742 | ||||||
chr2:134889867
|
C | T | 15 | a0001c0001t0001g0308a0001c0001t0001g0344a0001c0001t0001g0345others(12): Show | 15 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.850-8474C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889867 | ||||||
chr2:134889959
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.850-8382C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134889959 | ||||||
chr2:134890043
|
A | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(42): Show | 46 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.850-8298A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890043 | ||||||
chr2:134890089
|
A | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 302 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.850-8252A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890089 | ||||||
chr2:134890428
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-7913G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890428 | ||||||
chr2:134890510
|
C | A | 1 | a0001c0001t0001g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.850-7831C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890510 | ||||||
chr2:134890738
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0023 | 2 | HG01358.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.850-7603A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890738 | ||||||
chr2:134890909
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-7432G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134890909 | ||||||
chr2:134891053
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.850-7288G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891053 | ||||||
chr2:134891300
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-7041T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891300 | ||||||
chr2:134891324
|
T | C | 1 | a0001c0001t0001g0353 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.850-7017T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891324 | ||||||
chr2:134891333
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-7008G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891333 | ||||||
chr2:134891362
|
A | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-6979A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891362 | ||||||
chr2:134891493
|
T | C | 64 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(61): Show | 65 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.850-6848T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891493 | ||||||
chr2:134891530
|
A | C | 1 | a0001c0001t0001g0340 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.850-6811A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891530 | ||||||
chr2:134891625
|
G | C | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.850-6716G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891625 | ||||||
chr2:134891689
|
A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0306others(2): Show | 6 | HG04204.hp2 NA18966.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-6652A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891689 | ||||||
chr2:134891769
|
T | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0083a0001c0001t0001g0084others(3): Show | 6 | HG01978.hp2 NA18940.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-6572T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891769 | ||||||
chr2:134891831
|
G | A | 1 | a0002c0002t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.850-6510G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891831 | ||||||
chr2:134891955
|
T | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-6386T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134891955 | ||||||
chr2:134892083
|
G | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(165): Show | 170 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.850-6258G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892083 | ||||||
chr2:134892143
|
G | T | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.850-6198G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892143 | ||||||
chr2:134892225
|
AT | A | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 299 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(296): Show |
intron_variant | MODIFIER | c.850-6106delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892225 | |||||
chr2:134892235
|
T | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(293): Show | 301 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.850-6106T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892235 | ||||||
chr2:134892401
|
A | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-5940A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892401 | ||||||
chr2:134892462
|
A | AAAAT | 40 | a0001c0001t0001g0014a0001c0001t0001g0189a0001c0001t0001g0240others(37): Show | 41 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.850-5842_850-5839d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | |||||
chr2:134892462
|
A | AAAATAAA others(1): Show |
21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0241others(18): Show | 21 | HG00597.hp2 HG01255.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.850-5846_850-5839d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | |||||
chr2:134892462
|
A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0256a0001c0001t0001g0284 | 2 | HG02148.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.850-5850_850-5839d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | |||||
chr2:134892462
|
AAAAT | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(19): Show | 22 | HG00639.hp2 HG01099.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.850-5842_850-5839d others(6): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | |||||
chr2:134892462
|
AAAATAAA others(1): Show |
A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 210 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.850-5846_850-5839d others(10): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | |||||
chr2:134892462
|
AAAATAAA others(5): Show |
A | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-5850_850-5839d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | |||||
chr2:134892462
|
AAAATAAA others(9): Show |
A | 1 | a0001c0001t0001g0364 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.850-5854_850-5839d others(18): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134892462 | |||||
chr2:134892655
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.850-5686T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892655 | ||||||
chr2:134892663
|
T | A | 16 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-5678T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892663 | ||||||
chr2:134892983
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.850-5358G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134892983 | ||||||
chr2:134893196
|
T | C | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 175 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.850-5145T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893196 | ||||||
chr2:134893198
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.850-5143T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893198 | ||||||
chr2:134893209
|
A | AT | 10 | a0001c0001t0001g0189a0001c0001t0001g0240a0001c0001t0001g0243others(7): Show | 11 | HG02809.hp2 HG03130.hp2 HG03471.hp1 others(8): Show |
intron_variant | MODIFIER | c.850-5114dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | |||||
chr2:134893209
|
A | ATT | 43 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0241others(40): Show | 43 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.850-5115_850-5114d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | |||||
chr2:134893209
|
AT | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(160): Show | 165 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.850-5114delT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | |||||
chr2:134893209
|
ATT | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0015others(67): Show | 72 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.850-5115_850-5114d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134893209 | |||||
chr2:134893299
|
T | G | 1 | a0001c0001t0001g0003 | 2 | NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.850-5042T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893299 | ||||||
chr2:134893339
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-5002C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893339 | ||||||
chr2:134893552
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-4789T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893552 | ||||||
chr2:134893602
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.850-4739C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893602 | ||||||
chr2:134893743
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-4598C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893743 | ||||||
chr2:134893986
|
A | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-4355A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134893986 | ||||||
chr2:134894142
|
T | A | 1 | a0001c0001t0001g0023 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.850-4199T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894142 | ||||||
chr2:134894144
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.850-4197T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894144 | ||||||
chr2:134894304
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0177 | 2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.850-4037G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894304 | ||||||
chr2:134894437
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-3904A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894437 | ||||||
chr2:134894782
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.850-3559G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894782 | ||||||
chr2:134894829
|
C | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 302 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.850-3512C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894829 | ||||||
chr2:134894985
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-3356C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134894985 | ||||||
chr2:134895088
|
A | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.850-3253A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895088 | ||||||
chr2:134895158
|
T | C | 1 | a0001c0004t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.850-3183T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895158 | ||||||
chr2:134895165
|
G | C | 16 | a0001c0001t0001g0308a0001c0001t0001g0343a0001c0001t0001g0344others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.850-3176G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895165 | ||||||
chr2:134895226
|
C | T | 1 | a0002c0002t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.850-3115C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895226 | ||||||
chr2:134895316
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0045 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.850-3025_850-3024i others(29): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895316 | ||||||
chr2:134895316
|
A | T | 57 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(54): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.850-3025A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895316 | ||||||
chr2:134895328
|
T | TTACATAT others(23): Show |
1 | a0001c0001t0001g0044 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.850-3011_850-3010i others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | |||||
chr2:134895328
|
T | TTACATAT others(25): Show |
12 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(9): Show | 12 | HG00673.hp2 HG01496.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-3011_850-3010i others(34): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | |||||
chr2:134895328
|
T | TTACATAT others(21): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.850-3011_850-3010i others(30): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | |||||
chr2:134895328
|
T | TTACATAT others(23): Show |
200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 203 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.850-3011_850-3010i others(32): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | |||||
chr2:134895328
|
T | TTACATAT others(25): Show |
1 | a0004c0005t0001g0173 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.850-3011_850-3010i others(34): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | |||||
chr2:134895328
|
T | TTACATAT others(24): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0101 | 2 | HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.850-3011_850-3010i others(33): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895328 | |||||
chr2:134895331
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-3010T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895331 | ||||||
chr2:134895335
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.850-3006T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895335 | ||||||
chr2:134895356
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-2985A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895356 | ||||||
chr2:134895358
|
A | AAT | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-2972_850-2971d others(4): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134895358 | |||||
chr2:134895358
|
A | T | 1 | a0001c0001t0001g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-2983A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895358 | ||||||
chr2:134895368
|
TATGTTAC others(183): Show |
T | 1 | a0001c0001t0001g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.850-2972_850-2783d others(2): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895368 | ||||||
chr2:134895375
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-2966C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895375 | ||||||
chr2:134895524
|
T | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(41): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.850-2817T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895524 | ||||||
chr2:134895638
|
A | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0075others(1): Show | 4 | NA18988.hp1 NA19058.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-2703A>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895638 | ||||||
chr2:134895785
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(165): Show | 170 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.850-2556C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134895785 | ||||||
chr2:134896013
|
A | T | 1 | a0001c0001t0001g0223 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.850-2328A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896013 | ||||||
chr2:134896278
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.850-2063C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896278 | ||||||
chr2:134896374
|
C | T | 2 | a0001c0001t0001g0189a0002c0002t0001g0013 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.850-1967C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896374 | ||||||
chr2:134896598
|
G | A | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(298): Show | 306 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(303): Show |
intron_variant | MODIFIER | c.850-1743G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896598 | ||||||
chr2:134896689
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0078 | 2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.850-1652T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896689 | ||||||
chr2:134896768
|
T | C | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 302 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.850-1573T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896768 | ||||||
chr2:134896924
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.850-1417C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896924 | ||||||
chr2:134896931
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.850-1410T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896931 | ||||||
chr2:134896962
|
G | T | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.850-1379G>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134896962 | ||||||
chr2:134897010
|
TGTGGTTA others(5): Show |
T | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-1329_850-1318d others(14): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897010 | |||||
chr2:134897065
|
G | GATTACAC others(29): Show |
1 | a0001c0001t0001g0226 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.850-1271_850-1236d others(38): Show |
ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897065 | |||||
chr2:134897119
|
G | C | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-1222G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897119 | ||||||
chr2:134897437
|
A | AT | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-901dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897437 | |||||
chr2:134897603
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.850-738C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897603 | ||||||
chr2:134897814
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0129 | 2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.850-527T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897814 | ||||||
chr2:134897885
|
G | GT | 97 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0014others(94): Show | 99 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.850-443dupT | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134897885 | |||||
chr2:134897891
|
T | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-450T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134897891 | ||||||
chr2:134898149
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.850-192G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134898149 | ||||||
chr2:134898149
|
G | GA | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0240others(50): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.850-183dupA | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 134898149 | |||||
chr2:134898189
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.850-152T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134898189 | ||||||
chr2:134898236
|
G | A | 1 | a0001c0001t0001g0311 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.850-105G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 8/9 | chr2 | 134898236 | ||||||
chr2:134898537
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 5 | HG02486.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+98G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898537 | ||||||
chr2:134898544
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.948+105T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898544 | ||||||
chr2:134898572
|
C | G | 1 | a0002c0002t0001g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.948+133C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898572 | ||||||
chr2:134898684
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.948+245T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898684 | ||||||
chr2:134898712
|
T | C | 4 | a0001c0001t0001g0354a0001c0001t0001g0355a0001c0001t0001g0356others(1): Show | 4 | HG00735.hp2 HG02145.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.948+273T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898712 | ||||||
chr2:134898779
|
G | C | 3 | a0001c0001t0001g0340a0001c0001t0001g0365a0001c0001t0001g0366 | 3 | HG02896.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.948+340G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898779 | ||||||
chr2:134898876
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.948+437T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898876 | ||||||
chr2:134898920
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0091a0001c0001t0001g0093others(2): Show | 5 | HG02717.hp1 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.948+481G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898920 | ||||||
chr2:134898933
|
C | G | 9 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0056others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.948+494C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898933 | ||||||
chr2:134898935
|
T | A | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.948+496T>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134898935 | ||||||
chr2:134899025
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.948+586C>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899025 | ||||||
chr2:134899053
|
T | G | 1 | a0001c0001t0001g0359 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.948+614T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899053 | ||||||
chr2:134899080
|
C | A | 3 | a0001c0001t0001g0256a0001c0001t0001g0260a0001c0001t0001g0273 | 3 | HG01255.hp2 HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.948+641C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899080 | ||||||
chr2:134899303
|
T | C | 5 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0255others(2): Show | 5 | NA18939.hp2 NA18941.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+864T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899303 | ||||||
chr2:134899874
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.948+1435G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899874 | ||||||
chr2:134899901
|
C | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(294): Show | 302 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(299): Show |
intron_variant | MODIFIER | c.948+1462C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899901 | ||||||
chr2:134899917
|
A | C | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.948+1478A>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134899917 | ||||||
chr2:134900378
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.949-1420T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900378 | ||||||
chr2:134900505
|
G | A | 1 | a0002c0002t0001g0013 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.949-1293G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900505 | ||||||
chr2:134900621
|
C | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0196a0001c0001t0001g0198 | 3 | HG02698.hp2 HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.949-1177C>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900621 | ||||||
chr2:134900677
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.949-1121T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900677 | ||||||
chr2:134900763
|
A | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0236 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.949-1035A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900763 | ||||||
chr2:134900926
|
G | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0319 | 2 | HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.949-872G>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134900926 | ||||||
chr2:134901281
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.949-517G>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901281 | ||||||
chr2:134901303
|
A | T | 1 | a0001c0001t0001g0343 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.949-495A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901303 | ||||||
chr2:134901491
|
T | G | 3 | a0001c0001t0001g0350a0001c0001t0001g0351a0001c0001t0001g0358 | 3 | HG02886.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.949-307T>G | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901491 | ||||||
chr2:134901610
|
A | T | 1 | a0001c0001t0001g0360 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.949-188A>T | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901610 | ||||||
chr2:134901692
|
T | C | 2 | a0002c0002t0001g0179a0002c0002t0001g0183 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.949-106T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901692 | ||||||
chr2:134901702
|
T | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0035others(7): Show | 11 | HG02080.hp1 HG03704.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.949-96T>C | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901702 | ||||||
chr2:134901740
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.949-58C>A | ACMSD | ENSG00000153086.14 | transcript | ENST00000356140.10 | protein_coding | 9/9 | chr2 | 134901740 |