geneid | 148418 |
---|---|
ensemblid | ENSG00000203943.9 |
hgncid | 24582 |
symbol | SAMD13 |
name | sterile alpha motif domain containing 13 |
refseq_nuc | NM_001134663.2 |
refseq_prot | NP_001128135.1 |
ensembl_nuc | ENST00000394834.8 |
ensembl_prot | ENSP00000378311.3 |
mane_status | MANE Select |
chr | chr1 |
start | 84301708 |
end | 84350798 |
strand | + |
ver | v1.2 |
region | chr1:84301708-84350798 |
region5000 | chr1:84296708-84355798 |
regionname0 | SAMD13_chr1_84301708_84350798 |
regionname5000 | SAMD13_chr1_84296708_84355798 |
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 | 102 | 316 | 82 | 64 | 122 | 14 | 32 | 98 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
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 | 309 | 297 | 73 | 64 | 122 | 11 | 25 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
c0002 | 0/0 | 309 | 18 | 8 | 0 | 0 | 3 | 7 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
c0003 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
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 | 0/1 | 1151 | 288 | 75 | 59 | 118 | 11 | 24 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
t0002 | 0/0 | 1153 | 12 | 0 | 1 | 0 | 3 | 8 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
t0003 | 0/0 | 1151 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
t0004 | 0/0 | 1151 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
t0005 | 1/0 | 1151 | 3 | 1 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
t0006 | 0/0 | 1153 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
t0007 | 0/0 | 1151 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
t0008 | 0/0 | 1151 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
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 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0002 | 0/0 | 6 | 0 | 0 | 0 | 1 | 5 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
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 | 309 | 297 | 73 | 64 | 122 | 11 | 25 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0002 | 0/0 | 309 | 18 | 8 | 0 | 0 | 3 | 7 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0003 | 0/0 | 309 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1459 | 281 | 68 | 59 | 118 | 11 | 24 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0001t0002 | 0/0 | 1461 | 2 | 0 | 1 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0001t0003 | 0/0 | 1459 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0001t0004 | 0/0 | 1459 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0001t0005 | 1/0 | 1459 | 3 | 1 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0001t0007 | 0/0 | 1459 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0001t0008 | 0/0 | 1459 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0002t0001 | 0/0 | 1459 | 6 | 6 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0002t0002 | 0/0 | 1461 | 10 | 0 | 0 | 0 | 3 | 7 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0002t0006 | 0/0 | 1461 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
a0001c0003t0001 | 0/0 | 1459 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | copy fasta | chr1 | 84296708 | 84355798 |
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 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0005g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0007g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0001t0008g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0002 | 0/0 | 6 | 0 | 0 | 0 | 1 | 5 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0002t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0181 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0051 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0237 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0086 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0087 | EUR | IBS | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0101 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03516 | hp1 | a0001 | c0002 | t0006 | g0252 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03540 | hp1 | a0001 | c0002 | t0006 | g0251 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0173 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | GIH | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | GIH | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0039 | AFR | MSL | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0215 | REF | REF | SAMD13_chr1_84296708_84355798 | SAMD13 | chr1 | 84296708 | 84355798 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84325691
|
C | T | 1 | a0001c0002 | 18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
synonymous_variant | LOW | c.108C>T | p.Val36Val | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/4 | 234/1459 | 108/309 | 36/102 | chr1 | 84325691 | ||
chr1:84325709
|
C | T | 1 | a0001c0003 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.126C>T | p.Thr42Thr | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/4 | 252/1459 | 126/309 | 42/102 | chr1 | 84325709 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84349785
|
T | C | 3 | a0001c0001t0002a0001c0002t0002a0001c0002t0006 | 14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*11T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 11 | chr1 | 84349785 | |||||
chr1:84349879
|
G | A | 1 | a0001c0001t0003 | 4 | NA18944.hp1 NA18957.hp1 NA18985.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*105G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 105 | chr1 | 84349879 | |||||
chr1:84349899
|
G | A | 1 | a0001c0001t0004 | 4 | HG02809.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*125G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 125 | chr1 | 84349899 | |||||
chr1:84350203
|
C | T | 1 | a0001c0001t0008 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*429C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 429 | chr1 | 84350203 | |||||
chr1:84350246
|
C | A | 1 | a0001c0002t0006 | 2 | HG03516.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 472 | chr1 | 84350246 | |||||
chr1:84350388
|
G | A | 3 | a0001c0001t0002a0001c0002t0002a0001c0002t0006 | 14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*614G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 614 | chr1 | 84350388 | |||||
chr1:84350440
|
C | T | 10 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | 313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*666C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 666 | chr1 | 84350440 | |||||
chr1:84350565
|
A | C | 4 | a0001c0001t0002a0001c0001t0007a0001c0002t0002others(1): Show | 16 | HG00639.hp1 HG01175.hp2 HG01516.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*791A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 791 | chr1 | 84350565 | |||||
chr1:84350643
|
C | CTT | 3 | a0001c0001t0002a0001c0002t0002a0001c0002t0006 | 14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*871_*872dupTT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 4/4 | 873 | INFO_REALIGN_3_PRIME | chr1 | 84350643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:84302308
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-33+507G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84302308 | ||||||
chr1:84302337
|
CT | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.-33+554delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302337 | |||||
chr1:84302337
|
CTT | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0048others(8): Show | 13 | HG00099.hp1 HG01099.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33+553_-33+554del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302337 | |||||
chr1:84302337
|
CTTT | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0038others(9): Show | 15 | HG01081.hp2 HG01169.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+552_-33+554del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302337 | |||||
chr1:84302541
|
T | TAC | 24 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0071others(21): Show | 25 | HG00323.hp1 HG00544.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-32-627_-32-626dup others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302541
|
T | TACAC | 14 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 15 | HG00741.hp2 HG01109.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32-629_-32-626dup others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302541
|
TAC | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(39): Show | 57 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.-32-627_-32-626del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302541
|
TACAC | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0049others(14): Show | 19 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-32-629_-32-626del others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302541
|
TACACAC | T | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(18): Show | 29 | HG00099.hp1 HG01081.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32-631_-32-626del others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302541
|
TACACACA others(1): Show |
T | 8 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0201others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32-633_-32-626del others(8): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302541
|
TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(2): Show | 5 | HG02559.hp1 HG02965.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-635_-32-626del others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302541
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-32-639_-32-626del others(14): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 84302541 | |||||
chr1:84302782
|
C | A | 4 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0069others(1): Show | 4 | HG02809.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-421C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84302782 | ||||||
chr1:84303072
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-32-131T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84303072 | ||||||
chr1:84303178
|
C | T | 9 | a0001c0001t0001g0048a0001c0001t0001g0088a0001c0001t0001g0089others(6): Show | 9 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-25C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 1/3 | chr1 | 84303178 | ||||||
chr1:84303596
|
C | T | 1 | a0001c0001t0001g0029 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.53+309C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303596 | ||||||
chr1:84303644
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.53+357T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303644 | ||||||
chr1:84303650
|
G | T | 8 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG01109.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+363G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303650 | ||||||
chr1:84303739
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+452C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303739 | ||||||
chr1:84303847
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0093 | 3 | HG02257.hp2 HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.53+560G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84303847 | ||||||
chr1:84304219
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.53+932C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304219 | ||||||
chr1:84304284
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0175a0001c0001t0001g0176 | 4 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+997A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304284 | ||||||
chr1:84304362
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.53+1075A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304362 | ||||||
chr1:84304666
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.53+1379T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304666 | ||||||
chr1:84304672
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.53+1385G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304672 | ||||||
chr1:84304735
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(177): Show | 218 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.53+1448A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304735 | ||||||
chr1:84304785
|
A | G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.53+1498A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304785 | ||||||
chr1:84304926
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+1639T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84304926 | ||||||
chr1:84305315
|
A | T | 6 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210others(3): Show | 6 | HG01175.hp2 HG01981.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+2028A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84305315 | ||||||
chr1:84305553
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.53+2266T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84305553 | ||||||
chr1:84305816
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.53+2529T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84305816 | ||||||
chr1:84306072
|
T | A | 1 | a0001c0001t0002g0044 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.53+2785T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306072 | ||||||
chr1:84306312
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.53+3025T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306312 | ||||||
chr1:84306368
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+3081G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306368 | ||||||
chr1:84306381
|
C | A | 1 | a0001c0001t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53+3094C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306381 | ||||||
chr1:84306523
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.53+3236G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306523 | ||||||
chr1:84306634
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+3347C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306634 | ||||||
chr1:84306644
|
C | CA | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.53+3376dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306644 | |||||
chr1:84306661
|
AAAG | A | 14 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0199others(11): Show | 20 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.53+3376_53+3378del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306661 | |||||
chr1:84306662
|
AAG | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(54): Show | 76 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.53+3391_53+3392del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306662 | |||||
chr1:84306664
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.53+3377G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306664 | ||||||
chr1:84306685
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0245a0001c0001t0001g0246others(4): Show | 9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+3398G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306685 | ||||||
chr1:84306830
|
A | AAAT | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.53+3567_53+3569dup others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306830 | |||||
chr1:84306830
|
A | AAATAATA others(8): Show |
1 | a0001c0001t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+3555_53+3569dup others(15): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306830 | |||||
chr1:84306830
|
AAAT | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0058others(9): Show | 15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+3567_53+3569del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84306830 | |||||
chr1:84306831
|
A | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(37): Show | 55 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.53+3544A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306831 | ||||||
chr1:84306834
|
A | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0058others(9): Show | 15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+3547A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306834 | ||||||
chr1:84306856
|
A | ATAAT | 8 | a0001c0001t0001g0028a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 9 | HG01109.hp2 HG02559.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+3569_53+3570ins others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306856 | ||||||
chr1:84306856
|
A | ATAATAAT others(3): Show |
1 | a0001c0001t0001g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.53+3569_53+3570ins others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306856 | ||||||
chr1:84306859
|
T | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0029others(43): Show | 51 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.53+3572T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84306859 | ||||||
chr1:84307159
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02630.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.53+3872G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307159 | ||||||
chr1:84307208
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.53+3921T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307208 | ||||||
chr1:84307235
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.53+3948T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307235 | ||||||
chr1:84307414
|
A | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 8 | HG01099.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+4127A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307414 | ||||||
chr1:84307454
|
T | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210 | 3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.53+4167T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307454 | ||||||
chr1:84307624
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53+4337G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307624 | ||||||
chr1:84307788
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.53+4501A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84307788 | ||||||
chr1:84308130
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+4843G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308130 | ||||||
chr1:84308135
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0164 | 2 | NA18965.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.53+4848G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308135 | ||||||
chr1:84308202
|
T | G | 13 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0242others(10): Show | 19 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.53+4915T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308202 | ||||||
chr1:84308292
|
A | T | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.53+5005A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308292 | ||||||
chr1:84308366
|
T | C | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.53+5079T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308366 | ||||||
chr1:84308387
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+5100C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308387 | ||||||
chr1:84308650
|
GCTTT | G | 8 | a0001c0001t0001g0036a0001c0002t0002g0002a0001c0002t0002g0085others(5): Show | 14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+5372_53+5375del others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84308650 | |||||
chr1:84308790
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+5503T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84308790 | ||||||
chr1:84309017
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+5730A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309017 | ||||||
chr1:84309068
|
A | G | 13 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0242others(10): Show | 19 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.53+5781A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309068 | ||||||
chr1:84309121
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.53+5834A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309121 | ||||||
chr1:84309216
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+5929C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309216 | ||||||
chr1:84309274
|
G | A | 8 | a0001c0001t0001g0036a0001c0002t0002g0002a0001c0002t0002g0085others(5): Show | 14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+5987G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309274 | ||||||
chr1:84309378
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.53+6091A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309378 | ||||||
chr1:84309442
|
A | C | 11 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210others(8): Show | 12 | HG01175.hp2 HG01891.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+6155A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309442 | ||||||
chr1:84309444
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.53+6157T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309444 | ||||||
chr1:84309585
|
A | G | 8 | a0001c0001t0001g0036a0001c0002t0002g0002a0001c0002t0002g0085others(5): Show | 14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+6298A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309585 | ||||||
chr1:84309711
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.53+6424A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309711 | ||||||
chr1:84309713
|
A | G | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210 | 3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.53+6426A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309713 | ||||||
chr1:84309860
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.53+6573A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309860 | ||||||
chr1:84309862
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.53+6575G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309862 | ||||||
chr1:84309908
|
A | G | 8 | a0001c0001t0001g0036a0001c0002t0002g0002a0001c0002t0002g0085others(5): Show | 14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+6621A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84309908 | ||||||
chr1:84310241
|
T | C | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.53+6954T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310241 | ||||||
chr1:84310342
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.53+7055T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310342 | ||||||
chr1:84310361
|
G | GA | 7 | a0001c0001t0001g0031a0001c0001t0001g0169a0001c0001t0001g0170others(4): Show | 8 | HG01099.hp1 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+7085dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84310361 | |||||
chr1:84310428
|
TC | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0070a0001c0001t0001g0071 | 4 | HG01243.hp2 HG01952.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+7143delC | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84310428 | |||||
chr1:84310779
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53+7492G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310779 | ||||||
chr1:84310804
|
C | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0058others(9): Show | 15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+7517C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310804 | ||||||
chr1:84310858
|
T | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.53+7571T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310858 | ||||||
chr1:84310866
|
T | C | 3 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0001t0007g0101 | 3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.53+7579T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310866 | ||||||
chr1:84310932
|
T | C | 8 | a0001c0001t0001g0036a0001c0002t0002g0002a0001c0002t0002g0085others(5): Show | 14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+7645T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310932 | ||||||
chr1:84310998
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53+7711A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84310998 | ||||||
chr1:84311101
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.53+7814C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311101 | ||||||
chr1:84311133
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.53+7846C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311133 | ||||||
chr1:84311157
|
GAAATCCC others(10): Show |
G | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+7874_53+7890del others(17): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311157 | |||||
chr1:84311189
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53+7902A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311189 | ||||||
chr1:84311332
|
T | TA | 17 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 23 | HG01099.hp2 HG01516.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.53+8063dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311332 | |||||
chr1:84311332
|
TA | T | 5 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(2): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+8063delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311332 | |||||
chr1:84311341
|
AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+8059_53+8068del others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311341 | |||||
chr1:84311346
|
A | AG | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.53+8059_53+8060ins others(1): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311346 | ||||||
chr1:84311346
|
A | G | 64 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0021others(61): Show | 72 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+8059A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311346 | ||||||
chr1:84311346
|
AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.53+8074_53+8083del others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84311346 | |||||
chr1:84311357
|
A | G | 8 | a0001c0001t0001g0036a0001c0002t0002g0002a0001c0002t0002g0085others(5): Show | 14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+8070A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311357 | ||||||
chr1:84311393
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+8106C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311393 | ||||||
chr1:84311624
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53+8337C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311624 | ||||||
chr1:84311694
|
C | T | 10 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0001g0242others(7): Show | 16 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.53+8407C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311694 | ||||||
chr1:84311823
|
T | C | 5 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(2): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+8536T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311823 | ||||||
chr1:84311860
|
A | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA19082.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.53+8573A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311860 | ||||||
chr1:84311992
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.53+8705T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84311992 | ||||||
chr1:84312008
|
G | C | 2 | a0001c0002t0006g0251a0001c0002t0006g0252 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.53+8721G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312008 | ||||||
chr1:84312148
|
GT | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.53+8869delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84312148 | |||||
chr1:84312226
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0007g0181 | 2 | HG00639.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.53+8939T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312226 | ||||||
chr1:84312538
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.53+9251C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312538 | ||||||
chr1:84312548
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0201 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.53+9261A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312548 | ||||||
chr1:84312614
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0002t0002g0002others(6): Show | 15 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+9327C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312614 | ||||||
chr1:84312615
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0058others(9): Show | 15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+9328G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312615 | ||||||
chr1:84312690
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.53+9403G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312690 | ||||||
chr1:84312743
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.53+9456A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312743 | ||||||
chr1:84312950
|
G | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0059others(3): Show | 7 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.53+9663G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84312950 | ||||||
chr1:84313187
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.53+9900T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313187 | ||||||
chr1:84313216
|
A | T | 5 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(2): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+9929A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313216 | ||||||
chr1:84313339
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53+10052T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313339 | ||||||
chr1:84313345
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.53+10058C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313345 | ||||||
chr1:84313446
|
T | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 9 | HG01099.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+10159T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313446 | ||||||
chr1:84313816
|
G | A | 5 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(2): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+10529G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313816 | ||||||
chr1:84313924
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.53+10637A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313924 | ||||||
chr1:84313958
|
T | C | 8 | a0001c0001t0001g0036a0001c0002t0002g0002a0001c0002t0002g0085others(5): Show | 14 | HG01516.hp2 HG01517.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+10671T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84313958 | ||||||
chr1:84314311
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.53+11024A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314311 | ||||||
chr1:84314333
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 9 | HG01099.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+11046C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314333 | ||||||
chr1:84314335
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.53+11048G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314335 | ||||||
chr1:84314405
|
A | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0058others(9): Show | 15 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.53+11118A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314405 | ||||||
chr1:84314592
|
C | G | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210 | 3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54-11045C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314592 | ||||||
chr1:84314961
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210 | 3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54-10676C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84314961 | ||||||
chr1:84315009
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-10628T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315009 | ||||||
chr1:84315145
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.54-10492A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315145 | ||||||
chr1:84315160
|
G | T | 1 | a0001c0001t0003g0156 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.54-10477G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315160 | ||||||
chr1:84315169
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.54-10468A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315169 | ||||||
chr1:84315308
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.54-10329A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315308 | ||||||
chr1:84315332
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.54-10305T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315332 | ||||||
chr1:84315542
|
C | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0247 | 4 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-10095C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315542 | ||||||
chr1:84315700
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0201 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.54-9937G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315700 | ||||||
chr1:84315750
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.54-9887G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315750 | ||||||
chr1:84315875
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54-9762A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315875 | ||||||
chr1:84315909
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.54-9728A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84315909 | ||||||
chr1:84316039
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.54-9598T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316039 | ||||||
chr1:84316120
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0182others(1): Show | 4 | HG00639.hp1 HG01884.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-9517C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316120 | ||||||
chr1:84316134
|
T | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-9503T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316134 | ||||||
chr1:84316144
|
A | G | 23 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(20): Show | 27 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.54-9493A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316144 | ||||||
chr1:84316263
|
CT | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.54-9369delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84316263 | |||||
chr1:84316309
|
G | T | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.54-9328G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316309 | ||||||
chr1:84316359
|
A | T | 1 | a0001c0001t0004g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.54-9278A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316359 | ||||||
chr1:84316400
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.54-9237A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316400 | ||||||
chr1:84316410
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.54-9227A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316410 | ||||||
chr1:84316645
|
G | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0055others(11): Show | 17 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.54-8992G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316645 | ||||||
chr1:84316958
|
C | T | 3 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0001t0007g0101 | 3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.54-8679C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84316958 | ||||||
chr1:84317177
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0004g0056others(3): Show | 7 | HG01891.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-8460C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317177 | ||||||
chr1:84317232
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.54-8405C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317232 | ||||||
chr1:84317518
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.54-8119A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317518 | ||||||
chr1:84317563
|
A | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(11): Show | 16 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-8074A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317563 | ||||||
chr1:84317578
|
T | C | 3 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0001t0007g0101 | 3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.54-8059T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317578 | ||||||
chr1:84317687
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.54-7950T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317687 | ||||||
chr1:84317871
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.54-7766T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84317871 | ||||||
chr1:84318060
|
G | A | 3 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0001t0007g0101 | 3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.54-7577G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318060 | ||||||
chr1:84318079
|
T | G | 14 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(11): Show | 16 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-7558T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318079 | ||||||
chr1:84318287
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-7350A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318287 | ||||||
chr1:84318389
|
T | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-7248T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318389 | ||||||
chr1:84318430
|
C | G | 4 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0069others(1): Show | 4 | HG02809.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-7207C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318430 | ||||||
chr1:84318442
|
A | G | 7 | a0001c0002t0002g0002a0001c0002t0002g0085a0001c0002t0002g0086others(4): Show | 12 | HG01516.hp2 HG01517.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.54-7195A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318442 | ||||||
chr1:84318546
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.54-7091A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318546 | ||||||
chr1:84318971
|
G | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG00741.hp2 HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.54-6666G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84318971 | ||||||
chr1:84319111
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54-6526A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319111 | ||||||
chr1:84319157
|
T | C | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210 | 3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.54-6480T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319157 | ||||||
chr1:84319181
|
C | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-6456C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319181 | ||||||
chr1:84319549
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0196a0001c0001t0001g0198 | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-6088C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319549 | ||||||
chr1:84319624
|
GA | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(45): Show | 63 | HG00544.hp2 HG00673.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.54-5996delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84319624 | |||||
chr1:84319624
|
GAA | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(12): Show | 19 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.54-5997_54-5996del others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84319624 | |||||
chr1:84319624
|
GAAA | G | 10 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0066others(7): Show | 12 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-5998_54-5996del others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84319624 | |||||
chr1:84319645
|
G | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0053others(7): Show | 12 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.54-5992G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319645 | ||||||
chr1:84319723
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.54-5914G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319723 | ||||||
chr1:84319887
|
G | A | 3 | a0001c0002t0002g0085a0001c0002t0002g0086a0001c0002t0002g0087 | 3 | HG01516.hp2 HG01517.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.54-5750G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84319887 | ||||||
chr1:84320110
|
C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0004g0056others(3): Show | 7 | HG01891.hp2 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-5527C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320110 | ||||||
chr1:84320211
|
T | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0199others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.54-5426T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320211 | ||||||
chr1:84320243
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0071 | 3 | NA18949.hp2 NA18956.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.54-5394G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320243 | ||||||
chr1:84320273
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.54-5364C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320273 | ||||||
chr1:84320293
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.54-5344G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320293 | ||||||
chr1:84320314
|
G | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0044 | 2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.54-5323G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320314 | ||||||
chr1:84320407
|
T | G | 3 | a0001c0001t0003g0026a0001c0001t0003g0149a0001c0001t0003g0156 | 4 | NA18944.hp1 NA18957.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-5230T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320407 | ||||||
chr1:84320530
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.54-5107C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320530 | ||||||
chr1:84320540
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-5097G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320540 | ||||||
chr1:84320585
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-5052A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320585 | ||||||
chr1:84320742
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.54-4895A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320742 | ||||||
chr1:84320914
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.54-4723C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84320914 | ||||||
chr1:84321135
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-4502G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321135 | ||||||
chr1:84321345
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.54-4292T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321345 | ||||||
chr1:84321351
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.54-4286T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321351 | ||||||
chr1:84321365
|
A | AAT | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-4263_54-4262dup others(2): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr1 | 84321365 | |||||
chr1:84321518
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.54-4119A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321518 | ||||||
chr1:84321566
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.54-4071A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321566 | ||||||
chr1:84321628
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.54-4009G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321628 | ||||||
chr1:84321629
|
A | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.54-4008A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321629 | ||||||
chr1:84321657
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0183 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.54-3980A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321657 | ||||||
chr1:84321700
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0144a0001c0001t0001g0167 | 3 | NA18971.hp2 NA18988.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.54-3937A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321700 | ||||||
chr1:84321995
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02027.hp1 HG03704.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.54-3642C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84321995 | ||||||
chr1:84322069
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.54-3568G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322069 | ||||||
chr1:84322465
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.54-3172G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322465 | ||||||
chr1:84322475
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-3162C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322475 | ||||||
chr1:84322521
|
A | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-3116A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322521 | ||||||
chr1:84322525
|
T | A | 1 | a0001c0001t0001g0097 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.54-3112T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322525 | ||||||
chr1:84322762
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0236 | 5 | NA18954.hp1 NA18962.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-2875C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322762 | ||||||
chr1:84322773
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.54-2864G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322773 | ||||||
chr1:84322853
|
A | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-2784A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322853 | ||||||
chr1:84322853
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.54-2784A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84322853 | ||||||
chr1:84323031
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.54-2606G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323031 | ||||||
chr1:84323107
|
T | C | 12 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(9): Show | 18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-2530T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323107 | ||||||
chr1:84323189
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.54-2448A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323189 | ||||||
chr1:84323206
|
G | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0055others(10): Show | 16 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-2431G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323206 | ||||||
chr1:84323307
|
T | A | 1 | a0001c0001t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.54-2330T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323307 | ||||||
chr1:84323308
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.54-2329A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323308 | ||||||
chr1:84323309
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54-2328A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323309 | ||||||
chr1:84323536
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.54-2101G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323536 | ||||||
chr1:84323583
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.54-2054C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323583 | ||||||
chr1:84323733
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(33): Show | 42 | HG01109.hp2 HG01175.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.54-1904A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323733 | ||||||
chr1:84323772
|
T | G | 1 | a0001c0001t0001g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.54-1865T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84323772 | ||||||
chr1:84324122
|
C | G | 12 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(9): Show | 18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-1515C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324122 | ||||||
chr1:84324435
|
C | T | 1 | a0001c0001t0002g0037 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.54-1202C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324435 | ||||||
chr1:84324477
|
T | G | 1 | a0001c0001t0001g0022 | 2 | NA18978.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.54-1160T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324477 | ||||||
chr1:84324572
|
G | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.54-1065G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324572 | ||||||
chr1:84324672
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0201 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.54-965G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324672 | ||||||
chr1:84324742
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.54-895C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324742 | ||||||
chr1:84324743
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.54-894G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84324743 | ||||||
chr1:84325257
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0133others(1): Show | 5 | HG02071.hp1 NA18974.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.54-380G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84325257 | ||||||
chr1:84325556
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.54-81T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 2/3 | chr1 | 84325556 | ||||||
chr1:84325918
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+170T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84325918 | ||||||
chr1:84326032
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.165+284G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326032 | ||||||
chr1:84326374
|
G | A | 2 | a0001c0001t0001g0177a0001c0003t0001g0039 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.165+626G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326374 | ||||||
chr1:84326379
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+631T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326379 | ||||||
chr1:84326420
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+672T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326420 | ||||||
chr1:84326574
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+826G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326574 | ||||||
chr1:84326798
|
G | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0058others(8): Show | 14 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+1050G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326798 | ||||||
chr1:84326804
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+1056G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326804 | ||||||
chr1:84326923
|
G | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(33): Show | 42 | HG01109.hp2 HG01175.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.165+1175G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84326923 | ||||||
chr1:84327114
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+1366A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327114 | ||||||
chr1:84327290
|
G | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.165+1542G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327290 | ||||||
chr1:84327293
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+1545T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327293 | ||||||
chr1:84327313
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.165+1565C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327313 | ||||||
chr1:84327450
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.165+1702C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327450 | ||||||
chr1:84327506
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0044 | 2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.165+1758A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327506 | ||||||
chr1:84327579
|
TG | T | 12 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(9): Show | 18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+1832delG | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327579 | ||||||
chr1:84327645
|
GGTATAAA others(7): Show |
G | 1 | a0001c0001t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+1900_165+1913d others(16): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84327645 | |||||
chr1:84327739
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0178 | 3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+1991G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327739 | ||||||
chr1:84327911
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.165+2163C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84327911 | ||||||
chr1:84328012
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.165+2264A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328012 | ||||||
chr1:84328060
|
C | A | 34 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+2312C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328060 | ||||||
chr1:84328069
|
C | A | 34 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+2321C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328069 | ||||||
chr1:84328236
|
C | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0199others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2488C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328236 | ||||||
chr1:84328248
|
C | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+2500C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328248 | ||||||
chr1:84328274
|
C | G | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.165+2526C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328274 | ||||||
chr1:84328448
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.165+2700G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328448 | ||||||
chr1:84328587
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165+2839C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328587 | ||||||
chr1:84328616
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.165+2868A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328616 | ||||||
chr1:84328661
|
A | G | 1 | a0001c0002t0006g0252 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.165+2913A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328661 | ||||||
chr1:84328721
|
A | G | 1 | a0001c0001t0001g0036 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.165+2973A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84328721 | ||||||
chr1:84329026
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0044 | 2 | HG01175.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.165+3278C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329026 | ||||||
chr1:84329243
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.165+3495A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329243 | ||||||
chr1:84329326
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0178 | 3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+3578A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329326 | ||||||
chr1:84329503
|
C | A | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165+3755C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329503 | ||||||
chr1:84329541
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0133others(1): Show | 5 | HG02071.hp1 NA18974.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+3793A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329541 | ||||||
chr1:84329600
|
G | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.165+3852G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329600 | ||||||
chr1:84329823
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+4075G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329823 | ||||||
chr1:84329915
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.165+4167G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84329915 | ||||||
chr1:84330085
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.165+4337A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330085 | ||||||
chr1:84330103
|
G | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+4355G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330103 | ||||||
chr1:84330154
|
T | C | 2 | a0001c0002t0006g0251a0001c0002t0006g0252 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.165+4406T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330154 | ||||||
chr1:84330231
|
A | G | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+4483A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330231 | ||||||
chr1:84330362
|
A | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.165+4614A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330362 | ||||||
chr1:84330519
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA19007.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.165+4771A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330519 | ||||||
chr1:84330524
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165+4776G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330524 | ||||||
chr1:84330797
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.165+5049G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330797 | ||||||
chr1:84330819
|
G | A | 7 | a0001c0002t0002g0002a0001c0002t0002g0085a0001c0002t0002g0086others(4): Show | 12 | HG01516.hp2 HG01517.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+5071G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330819 | ||||||
chr1:84330965
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.165+5217T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84330965 | ||||||
chr1:84331045
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+5297A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331045 | ||||||
chr1:84331275
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0196a0001c0001t0001g0198 | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+5527A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331275 | ||||||
chr1:84331286
|
T | C | 12 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(9): Show | 18 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+5538T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331286 | ||||||
chr1:84331328
|
T | TA | 12 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0032others(9): Show | 16 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+5610dupA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331328 | |||||
chr1:84331328
|
TA | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0106others(12): Show | 20 | HG00544.hp2 HG00673.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.165+5610delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331328 | |||||
chr1:84331352
|
A | AT | 17 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0058others(14): Show | 20 | HG01261.hp2 HG01361.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+5604_165+5605i others(3): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331352 | ||||||
chr1:84331352
|
A | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0050others(3): Show | 8 | HG01106.hp2 HG01891.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+5604A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331352 | ||||||
chr1:84331354
|
A | AAAAAAAA others(3): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0145a0001c0001t0001g0191 | 3 | HG02738.hp2 NA18906.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.165+5610_165+5611i others(12): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | |||||
chr1:84331354
|
A | AAAAAAAT others(2): Show |
20 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0020others(17): Show | 27 | HG00099.hp1 HG01081.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.165+5610_165+5611i others(11): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | |||||
chr1:84331354
|
A | AAAAAATA others(1): Show |
98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(95): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.165+5610_165+5611i others(10): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | |||||
chr1:84331354
|
A | AAAAATAC | 51 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(48): Show | 58 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.165+5611_165+5612i others(9): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | |||||
chr1:84331354
|
A | AAAATAC | 2 | a0001c0002t0002g0002a0001c0002t0002g0087 | 7 | HG01517.hp2 HG02698.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+5609_165+5610i others(8): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84331354 | |||||
chr1:84331354
|
A | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(22): Show | 30 | HG01106.hp2 HG01261.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.165+5606A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331354 | ||||||
chr1:84331512
|
G | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+5764G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331512 | ||||||
chr1:84331548
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0221 | 3 | HG01255.hp1 HG01358.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.165+5800G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331548 | ||||||
chr1:84331633
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.165+5885T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84331633 | ||||||
chr1:84332354
|
C | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0245a0001c0001t0001g0246others(4): Show | 9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6606C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332354 | ||||||
chr1:84332371
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.165+6623C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332371 | ||||||
chr1:84332576
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.165+6828G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332576 | ||||||
chr1:84332780
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.165+7032G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332780 | ||||||
chr1:84332934
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 113 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.165+7186A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332934 | ||||||
chr1:84332959
|
C | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(33): Show | 42 | HG01109.hp2 HG01175.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.165+7211C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84332959 | ||||||
chr1:84333182
|
C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.165+7434C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333182 | ||||||
chr1:84333186
|
G | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0074 | 2 | NA18954.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.165+7438G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333186 | ||||||
chr1:84333203
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.165+7455G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333203 | ||||||
chr1:84333239
|
T | C | 1 | a0001c0001t0001g0223 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.165+7491T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333239 | ||||||
chr1:84333432
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+7684G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333432 | ||||||
chr1:84333471
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.165+7723A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333471 | ||||||
chr1:84333603
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.165+7855C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333603 | ||||||
chr1:84333734
|
C | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+7986C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333734 | ||||||
chr1:84333829
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+8081G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333829 | ||||||
chr1:84333859
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.165+8111T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333859 | ||||||
chr1:84333891
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.165+8143C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84333891 | ||||||
chr1:84334002
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+8254G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334002 | ||||||
chr1:84334056
|
T | C | 3 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0001t0007g0101 | 3 | HG01175.hp2 HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.165+8308T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334056 | ||||||
chr1:84334147
|
A | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.165+8399A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334147 | ||||||
chr1:84334158
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.165+8410A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334158 | ||||||
chr1:84334309
|
T | C | 13 | a0001c0001t0001g0048a0001c0002t0001g0014a0001c0002t0001g0202others(10): Show | 19 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.165+8561T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334309 | ||||||
chr1:84334539
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0178 | 3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+8791T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334539 | ||||||
chr1:84334565
|
G | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0245a0001c0001t0001g0246others(4): Show | 9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+8817G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334565 | ||||||
chr1:84334570
|
G | C | 2 | a0001c0001t0001g0177a0001c0003t0001g0039 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.165+8822G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334570 | ||||||
chr1:84334581
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.165+8833T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334581 | ||||||
chr1:84334775
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.165+9027T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334775 | ||||||
chr1:84334882
|
T | C | 14 | a0001c0001t0001g0048a0001c0001t0001g0182a0001c0002t0001g0014others(11): Show | 20 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.165+9134T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84334882 | ||||||
chr1:84335250
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.165+9502G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335250 | ||||||
chr1:84335314
|
T | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0245a0001c0001t0001g0246others(4): Show | 9 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+9566T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335314 | ||||||
chr1:84335321
|
G | A | 1 | a0001c0001t0001g0022 | 2 | NA18978.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.165+9573G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335321 | ||||||
chr1:84335339
|
G | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.165+9591G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335339 | ||||||
chr1:84335403
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.165+9655T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335403 | ||||||
chr1:84335411
|
T | A | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.165+9663T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335411 | ||||||
chr1:84335535
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.165+9787C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335535 | ||||||
chr1:84335595
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.165+9847G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335595 | ||||||
chr1:84335745
|
A | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0199others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+9997A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335745 | ||||||
chr1:84335879
|
A | G | 7 | a0001c0001t0001g0063a0001c0001t0001g0074a0001c0001t0001g0115others(4): Show | 7 | HG00438.hp1 HG00673.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+10131A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335879 | ||||||
chr1:84335987
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.165+10239T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84335987 | ||||||
chr1:84336118
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0231 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.165+10370C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336118 | ||||||
chr1:84336249
|
A | C | 1 | a0001c0001t0001g0219 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165+10501A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336249 | ||||||
chr1:84336502
|
CCT | C | 5 | a0001c0002t0002g0002a0001c0002t0002g0085a0001c0002t0002g0086others(2): Show | 10 | HG01516.hp2 HG01517.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+10757_165+1075 others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84336502 | |||||
chr1:84336561
|
T | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.165+10813T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336561 | ||||||
chr1:84336638
|
G | A | 1 | a0001c0002t0006g0251 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+10890G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336638 | ||||||
chr1:84336640
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.165+10892T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336640 | ||||||
chr1:84336747
|
C | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+10999C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336747 | ||||||
chr1:84336838
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0196a0001c0001t0001g0198 | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+11090G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84336838 | ||||||
chr1:84337069
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0201 | 2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.165+11321C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337069 | ||||||
chr1:84337193
|
A | G | 1 | a0001c0002t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.165+11445A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337193 | ||||||
chr1:84337428
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+11680C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337428 | ||||||
chr1:84337471
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.165+11723C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337471 | ||||||
chr1:84337489
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.165+11741G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337489 | ||||||
chr1:84337837
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.166-11794A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337837 | ||||||
chr1:84337859
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0070others(4): Show | 9 | HG01243.hp2 HG01952.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-11772A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337859 | ||||||
chr1:84337885
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.166-11746C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337885 | ||||||
chr1:84337930
|
C | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.166-11701C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337930 | ||||||
chr1:84337965
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0241 | 3 | HG01515.hp1 HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.166-11666A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337965 | ||||||
chr1:84337994
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-11637C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84337994 | ||||||
chr1:84338036
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-11595C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338036 | ||||||
chr1:84338216
|
G | T | 5 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(2): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-11415G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338216 | ||||||
chr1:84338432
|
C | CT | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 142 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.166-11176dupT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | |||||
chr1:84338432
|
C | CTT | 7 | a0001c0001t0001g0055a0001c0001t0001g0092a0001c0001t0001g0138others(4): Show | 7 | HG01099.hp2 HG02055.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-11177_166-1117 others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | |||||
chr1:84338432
|
CTT | C | 15 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0036others(12): Show | 18 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-11177_166-1117 others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | |||||
chr1:84338432
|
CTTTTTTT others(2): Show |
C | 19 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(16): Show | 29 | HG00733.hp2 HG01192.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.166-11184_166-1117 others(13): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338432 | |||||
chr1:84338452
|
T | TTTTC | 9 | a0001c0001t0001g0031a0001c0001t0001g0153a0001c0001t0001g0157others(6): Show | 10 | HG01099.hp1 HG02145.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-11176_166-1117 others(8): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84338452 | |||||
chr1:84338531
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.166-11100G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338531 | ||||||
chr1:84338693
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.166-10938C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338693 | ||||||
chr1:84338760
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.166-10871A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338760 | ||||||
chr1:84338795
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0178 | 3 | HG02922.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.166-10836A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338795 | ||||||
chr1:84338872
|
C | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0179 | 3 | HG01884.hp2 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.166-10759C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338872 | ||||||
chr1:84338901
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.166-10730A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84338901 | ||||||
chr1:84339249
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.166-10382G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339249 | ||||||
chr1:84339560
|
G | A | 2 | a0001c0001t0001g0177a0001c0003t0001g0039 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.166-10071G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339560 | ||||||
chr1:84339626
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.166-10005C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339626 | ||||||
chr1:84339829
|
TACTC | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0050 | 3 | HG01891.hp2 HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.166-9799_166-9796d others(6): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84339829 | |||||
chr1:84339893
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0196a0001c0001t0001g0198 | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-9738G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339893 | ||||||
chr1:84339932
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0196a0001c0001t0001g0198 | 5 | HG02451.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-9699G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84339932 | ||||||
chr1:84340175
|
T | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 6 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-9456T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340175 | ||||||
chr1:84340200
|
T | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0036others(15): Show | 21 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-9431T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340200 | ||||||
chr1:84340279
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.166-9352C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340279 | ||||||
chr1:84340374
|
A | T | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-9257A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340374 | ||||||
chr1:84340545
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0195a0001c0003t0001g0039 | 3 | HG03195.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.166-9086G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340545 | ||||||
chr1:84340549
|
A | G | 34 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.166-9082A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340549 | ||||||
chr1:84340632
|
A | G | 5 | a0001c0002t0001g0014a0001c0002t0001g0202a0001c0002t0001g0203others(2): Show | 6 | HG01891.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-8999A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340632 | ||||||
chr1:84340837
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0189 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-8794G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84340837 | ||||||
chr1:84341017
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.166-8614C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341017 | ||||||
chr1:84341129
|
C | T | 34 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 40 | HG01109.hp2 HG01261.hp2 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.166-8502C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341129 | ||||||
chr1:84341209
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.166-8422C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341209 | ||||||
chr1:84341451
|
C | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.166-8180C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341451 | ||||||
chr1:84341532
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.166-8099G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341532 | ||||||
chr1:84341563
|
G | T | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-8068G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341563 | ||||||
chr1:84341740
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.166-7891A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341740 | ||||||
chr1:84341950
|
A | G | 1 | a0001c0002t0001g0202 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.166-7681A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84341950 | ||||||
chr1:84342094
|
A | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0141 | 2 | NA18950.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.166-7537A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342094 | ||||||
chr1:84342315
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.166-7316A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342315 | ||||||
chr1:84342476
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-7155C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342476 | ||||||
chr1:84342495
|
G | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0189 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7136G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342495 | ||||||
chr1:84342500
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.166-7131A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342500 | ||||||
chr1:84342500
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-7131A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342500 | ||||||
chr1:84342501
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0189 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7130A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342501 | ||||||
chr1:84342502
|
A | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0189 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7129A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342502 | ||||||
chr1:84342503
|
A | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0189 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7128A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342503 | ||||||
chr1:84342504
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0189 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.166-7127C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342504 | ||||||
chr1:84342742
|
C | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.166-6889C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342742 | ||||||
chr1:84342888
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210 | 3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-6743G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342888 | ||||||
chr1:84342891
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0060 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.166-6740A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342891 | ||||||
chr1:84342916
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.166-6715G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342916 | ||||||
chr1:84342924
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0024others(6): Show | 13 | HG00099.hp1 HG01081.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-6707A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342924 | ||||||
chr1:84342990
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.166-6641G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84342990 | ||||||
chr1:84343086
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.166-6545G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343086 | ||||||
chr1:84343144
|
C | G | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-6487C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343144 | ||||||
chr1:84343174
|
G | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0021others(65): Show | 76 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.166-6457G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343174 | ||||||
chr1:84343302
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166-6329C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343302 | ||||||
chr1:84343384
|
A | G | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-6247A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343384 | ||||||
chr1:84343524
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(12): Show | 24 | HG00733.hp2 HG01192.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-6107C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343524 | ||||||
chr1:84343873
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.166-5758A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343873 | ||||||
chr1:84343879
|
A | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0199others(6): Show | 10 | HG01891.hp2 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-5752A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343879 | ||||||
chr1:84343897
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0177a0001c0001t0001g0195others(1): Show | 4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-5734G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343897 | ||||||
chr1:84343945
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.166-5686T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84343945 | ||||||
chr1:84344015
|
TG | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0186others(9): Show | 17 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-5613delG | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84344015 | |||||
chr1:84344067
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0201 | 3 | HG02257.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.166-5564T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344067 | ||||||
chr1:84344078
|
CT | C | 44 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 56 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.166-5541delT | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84344078 | |||||
chr1:84344084
|
T | C | 10 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0001g0072others(7): Show | 11 | HG00621.hp2 NA18612.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-5547T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344084 | ||||||
chr1:84344213
|
G | A | 4 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG03688.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-5418G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344213 | ||||||
chr1:84344466
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.166-5165A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344466 | ||||||
chr1:84344479
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.166-5152G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344479 | ||||||
chr1:84344615
|
C | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-5016C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344615 | ||||||
chr1:84344653
|
G | C | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-4978G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344653 | ||||||
chr1:84344662
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.166-4969G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344662 | ||||||
chr1:84344713
|
A | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.166-4918A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344713 | ||||||
chr1:84344911
|
A | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0075 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.166-4720A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84344911 | ||||||
chr1:84345088
|
C | A | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.166-4543C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345088 | ||||||
chr1:84345132
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.166-4499A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345132 | ||||||
chr1:84345534
|
G | A | 9 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0002t0002g0002others(6): Show | 14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-4097G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345534 | ||||||
chr1:84345577
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166-4054C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345577 | ||||||
chr1:84345586
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.166-4045C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345586 | ||||||
chr1:84345617
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0243 | 2 | NA18945.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.166-4014A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345617 | ||||||
chr1:84345919
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.166-3712G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345919 | ||||||
chr1:84345979
|
C | G | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3652C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84345979 | ||||||
chr1:84346219
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.166-3412A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346219 | ||||||
chr1:84346257
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.166-3374T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346257 | ||||||
chr1:84346304
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.166-3327C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346304 | ||||||
chr1:84346379
|
C | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0065others(8): Show | 13 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-3252C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346379 | ||||||
chr1:84346419
|
T | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.166-3212T>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346419 | ||||||
chr1:84346543
|
G | A | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-3088G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346543 | ||||||
chr1:84346558
|
G | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0058a0001c0001t0001g0059others(4): Show | 8 | HG01261.hp2 HG01361.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-3073G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346558 | ||||||
chr1:84346638
|
G | C | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-2993G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346638 | ||||||
chr1:84346724
|
A | G | 1 | a0001c0002t0001g0204 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.166-2907A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346724 | ||||||
chr1:84346751
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.166-2880T>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346751 | ||||||
chr1:84346913
|
GA | G | 9 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0002t0002g0002others(6): Show | 14 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-2716delA | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84346913 | |||||
chr1:84346955
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0148a0001c0001t0001g0160 | 3 | HG02523.hp1 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.166-2676G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346955 | ||||||
chr1:84346981
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0028others(30): Show | 43 | HG01099.hp2 HG01109.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.166-2650T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346981 | ||||||
chr1:84346989
|
C | A | 2 | a0001c0001t0005g0051a0001c0001t0005g0052 | 2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-2642C>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84346989 | ||||||
chr1:84347018
|
C | G | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.166-2613C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347018 | ||||||
chr1:84347070
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.166-2561C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347070 | ||||||
chr1:84347135
|
G | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.166-2496G>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347135 | ||||||
chr1:84347402
|
A | C | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.166-2229A>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347402 | ||||||
chr1:84347676
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.166-1955G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347676 | ||||||
chr1:84347744
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.166-1887C>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347744 | ||||||
chr1:84347747
|
C | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0110a0001c0001t0001g0148others(1): Show | 4 | HG02080.hp1 HG02523.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1884C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347747 | ||||||
chr1:84347754
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.166-1877G>A | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347754 | ||||||
chr1:84347788
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-1843C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347788 | ||||||
chr1:84347852
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.166-1779A>G | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347852 | ||||||
chr1:84347979
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.166-1652G>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84347979 | ||||||
chr1:84348181
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0210 | 3 | HG02109.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-1450C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348181 | ||||||
chr1:84348283
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.166-1348A>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348283 | ||||||
chr1:84348396
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.166-1235C>T | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348396 | ||||||
chr1:84348506
|
G | GCA | 10 | a0001c0001t0002g0037a0001c0001t0002g0044a0001c0001t0007g0101others(7): Show | 15 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-1122_166-1121d others(4): Show |
SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr1 | 84348506 | |||||
chr1:84348747
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.166-884T>C | SAMD13 | ENSG00000203943.9 | transcript | ENST00000394834.8 | protein_coding | 3/3 | chr1 | 84348747 |