geneid | 389432 |
---|---|
ensemblid | ENSG00000203727.4 |
hgncid | 21180 |
symbol | SAMD5 |
name | sterile alpha motif domain containing 5 |
refseq_nuc | NM_001030060.3 |
refseq_prot | NP_001025231.1 |
ensembl_nuc | ENST00000367474.2 |
ensembl_prot | ENSP00000356444.1 |
mane_status | MANE Select |
chr | chr6 |
start | 147508690 |
end | 147570021 |
strand | + |
ver | v1.2 |
region | chr6:147508690-147570021 |
region5000 | chr6:147503690-147575021 |
regionname0 | SAMD5_chr6_147508690_147570021 |
regionname5000 | SAMD5_chr6_147503690_147575021 |
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 | 173 | 331 | 73 | 71 | 129 | 15 | 41 | 92 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002 | 0/0 | 173 | 20 | 0 | 3 | 15 | 1 | 1 | 12 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003 | 0/0 | 173 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0004 | 0/0 | 173 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0005 | 0/0 | 173 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
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 | 522 | 215 | 39 | 46 | 98 | 9 | 21 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
c0002 | 0/0 | 522 | 113 | 33 | 23 | 31 | 6 | 20 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
c0003 | 0/0 | 522 | 20 | 0 | 3 | 15 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
c0004 | 0/0 | 522 | 8 | 8 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
c0005 | 0/0 | 522 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
c0006 | 0/0 | 522 | 3 | 1 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
c0007 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
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 | 0/0 | 5806 | 44 | 6 | 9 | 21 | 4 | 4 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0002 | 0/0 | 5807 | 30 | 0 | 5 | 24 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0003 | 0/1 | 5806 | 29 | 1 | 3 | 22 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0004 | 0/0 | 5806 | 25 | 5 | 7 | 8 | 2 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0005 | 0/0 | 5805 | 24 | 2 | 14 | 3 | 0 | 5 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0006 | 0/0 | 5807 | 16 | 0 | 10 | 1 | 1 | 4 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0007 | 0/0 | 5807 | 13 | 1 | 2 | 9 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0008 | 0/0 | 5806 | 12 | 8 | 2 | 0 | 2 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0009 | 0/0 | 5806 | 11 | 0 | 0 | 11 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0010 | 0/0 | 5806 | 9 | 0 | 2 | 5 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0011 | 0/0 | 5806 | 8 | 8 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0012 | 0/0 | 5806 | 7 | 7 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0013 | 0/0 | 5805 | 4 | 0 | 1 | 2 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0014 | 0/0 | 5805 | 4 | 1 | 1 | 1 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0015 | 0/0 | 5806 | 4 | 2 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0016 | 0/0 | 5804 | 4 | 3 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0017 | 0/0 | 5807 | 3 | 0 | 0 | 0 | 0 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0018 | 0/0 | 5806 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0019 | 0/0 | 5806 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0020 | 0/0 | 5804 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0021 | 0/0 | 5807 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0022 | 0/0 | 5804 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0023 | 0/0 | 5805 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0024 | 0/0 | 5805 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0025 | 0/0 | 5806 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0026 | 0/0 | 5804 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0027 | 0/0 | 5804 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0028 | 0/0 | 5804 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0029 | 0/0 | 5804 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0030 | 0/0 | 5806 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0031 | 0/0 | 5806 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0032 | 0/0 | 5806 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0033 | 0/0 | 5807 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0034 | 0/0 | 5804 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0035 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0036 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0037 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0038 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0039 | 0/0 | 5807 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0040 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0041 | 0/0 | 5807 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0042 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0043 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0044 | 0/0 | 5807 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0045 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0046 | 0/0 | 5807 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0047 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0048 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0049 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0050 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0051 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0052 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0053 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0054 | 0/0 | 5805 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0055 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0056 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0057 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0058 | 0/0 | 5807 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0059 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0060 | 0/0 | 5805 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0061 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0062 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0063 | 0/0 | 5805 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0064 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0065 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0066 | 0/0 | 5808 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0067 | 0/0 | 5804 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0068 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0069 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0070 | 0/0 | 5807 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0071 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0072 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0073 | 0/0 | 5805 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0074 | 0/0 | 5804 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0075 | 1/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0076 | 0/0 | 5807 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0077 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0078 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0079 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0080 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0081 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0082 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0083 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0084 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0085 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0086 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0087 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0088 | 0/0 | 5806 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0089 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0090 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0091 | 0/0 | 5807 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0092 | 0/0 | 5806 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0093 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0094 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0095 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0096 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0097 | 0/0 | 5805 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0098 | 0/0 | 5805 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0099 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0100 | 0/0 | 5804 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0101 | 0/0 | 5807 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0102 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0103 | 0/0 | 5807 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0104 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0105 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0106 | 0/0 | 5959 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0107 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0108 | 0/0 | 5805 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0109 | 0/0 | 5805 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0110 | 0/0 | 5806 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0111 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0112 | 0/0 | 5805 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
t0113 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
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 | 4 | 0 | 2 | 1 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0325 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
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 | 522 | 215 | 39 | 46 | 98 | 9 | 21 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002 | 0/0 | 522 | 113 | 33 | 23 | 31 | 6 | 20 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0006 | 0/0 | 522 | 3 | 1 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003 | 0/0 | 522 | 20 | 0 | 3 | 15 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004 | 0/0 | 522 | 8 | 8 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0004c0005 | 0/0 | 522 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0005c0007 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6327 | 38 | 5 | 8 | 19 | 3 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0002 | 0/0 | 6328 | 26 | 0 | 4 | 21 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0003 | 0/1 | 6327 | 27 | 1 | 3 | 20 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0005 | 0/0 | 6326 | 24 | 2 | 14 | 3 | 0 | 5 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0006 | 0/0 | 6328 | 16 | 0 | 10 | 1 | 1 | 4 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0009 | 0/0 | 6327 | 11 | 0 | 0 | 11 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0011 | 0/0 | 6327 | 7 | 7 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0012 | 0/0 | 6327 | 6 | 6 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0016 | 0/0 | 6325 | 2 | 1 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0017 | 0/0 | 6328 | 3 | 0 | 0 | 0 | 0 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0019 | 0/0 | 6327 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0020 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0021 | 0/0 | 6328 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0027 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0028 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0029 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0030 | 0/0 | 6327 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0033 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0035 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0071 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0072 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0074 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0075 | 1/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0076 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0077 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0079 | 0/0 | 6329 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0080 | 0/0 | 6329 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0081 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0082 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0083 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0084 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0085 | 0/0 | 6317 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0086 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0087 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0088 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0089 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0090 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0091 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0092 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0094 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0095 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0096 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0097 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0098 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0099 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0100 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0101 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0102 | 0/0 | 6329 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0103 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0104 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0105 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0106 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0108 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0109 | 0/0 | 6326 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0111 | 0/0 | 6329 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0112 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0001t0113 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0004 | 0/0 | 6327 | 25 | 5 | 7 | 8 | 2 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0007 | 0/0 | 6328 | 13 | 1 | 2 | 9 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0008 | 0/0 | 6327 | 12 | 8 | 2 | 0 | 2 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0010 | 0/0 | 6327 | 9 | 0 | 2 | 5 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0013 | 0/0 | 6326 | 4 | 0 | 1 | 2 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0014 | 0/0 | 6326 | 4 | 1 | 1 | 1 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0015 | 0/0 | 6327 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0022 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0023 | 0/0 | 6326 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0024 | 0/0 | 6326 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0025 | 0/0 | 6327 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0026 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0036 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0037 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0038 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0039 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0040 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0041 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0042 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0043 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0044 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0045 | 0/0 | 6329 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0046 | 0/0 | 6328 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0047 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0048 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0049 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0050 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0051 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0052 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0054 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0055 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0056 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0057 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0058 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0059 | 0/0 | 6465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0060 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0061 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0062 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0063 | 0/0 | 6326 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0064 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0065 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0066 | 0/0 | 6329 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0067 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0068 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0069 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0002t0070 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0006t0015 | 0/0 | 6327 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0001c0006t0053 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0001 | 0/0 | 6327 | 5 | 0 | 1 | 2 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0002 | 0/0 | 6328 | 4 | 0 | 1 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0003 | 0/0 | 6327 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0018 | 0/0 | 6327 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0031 | 0/0 | 6327 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0032 | 0/0 | 6327 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0033 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0002c0003t0073 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004t0001 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004t0016 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004t0020 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004t0078 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004t0093 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004t0107 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0003c0004t0110 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0004c0005t0012 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0004c0005t0029 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0004c0005t0034 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
a0005c0007t0011 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | copy fasta | chr6 | 147503690 | 147575021 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0325 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0016g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0017g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0017g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0019g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0019g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0020g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0020g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0021g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0021g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0021g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0027g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0027g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0028g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0028g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0029g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0030g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0030g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0033g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0035g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0071g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0072g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0074g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0075g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0076g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0077g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0079g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0080g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0081g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0082g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0083g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0084g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0085g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0086g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0087g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0088g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0089g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0090g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0091g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0092g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0094g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0095g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0096g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0097g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0098g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0099g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0100g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0101g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0102g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0103g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0104g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0105g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0106g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0108g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0109g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0111g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0112g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0113g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0022g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0023g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0023g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0024g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0024g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0025g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0025g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0026g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0026g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0036g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0037g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0038g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0039g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0040g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0041g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0042g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0043g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0044g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0045g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0046g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0047g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0048g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0049g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0050g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0051g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0052g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0054g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0055g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0056g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0057g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0058g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0059g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0060g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0061g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0062g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0063g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0064g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0065g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0066g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0067g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0068g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0069g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0070g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0006t0015g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0006t0015g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0006t0053g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0018g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0018g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0031g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0031g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0032g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0032g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0033g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0073g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0020g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0078g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0093g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0107g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0110g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0029g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0034g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0034g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0005c0007t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0057 | g0169 | EUR | GBR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00140 | hp2 | a0001 | c0001 | t0016 | g0246 | EUR | GBR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00280 | hp2 | a0001 | c0002 | t0004 | g0176 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0326 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00323 | hp2 | a0002 | c0003 | t0001 | g0021 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00408 | hp2 | a0001 | c0001 | t0009 | g0053 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00423 | hp1 | a0001 | c0001 | t0009 | g0331 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00544 | hp1 | a0001 | c0002 | t0007 | g0116 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00609 | hp1 | a0002 | c0003 | t0002 | g0022 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00609 | hp2 | a0001 | c0001 | t0009 | g0039 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00621 | hp2 | a0001 | c0001 | t0019 | g0263 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0313 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00639 | hp2 | a0001 | c0002 | t0014 | g0164 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00733 | hp1 | a0001 | c0001 | t0112 | g0254 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00733 | hp2 | a0001 | c0002 | t0054 | g0154 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0323 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0252 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00738 | hp1 | a0001 | c0006 | t0015 | g0141 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0207 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0267 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0161 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0307 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0023 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0295 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01081 | hp1 | a0001 | c0002 | t0046 | g0178 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01081 | hp2 | a0001 | c0006 | t0015 | g0140 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01106 | hp2 | a0001 | c0002 | t0004 | g0148 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0270 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0083 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01169 | hp1 | a0001 | c0002 | t0004 | g0168 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0235 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01192 | hp1 | a0001 | c0002 | t0004 | g0119 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01192 | hp2 | a0001 | c0001 | t0090 | g0199 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01243 | hp1 | a0002 | c0003 | t0073 | g0020 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01255 | hp1 | a0001 | c0002 | t0007 | g0105 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0345 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01256 | hp2 | a0001 | c0001 | t0030 | g0188 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01257 | hp1 | a0001 | c0002 | t0008 | g0110 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01258 | hp1 | a0001 | c0002 | t0008 | g0111 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01258 | hp2 | a0001 | c0001 | t0030 | g0189 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01261 | hp1 | a0001 | c0002 | t0051 | g0104 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01346 | hp2 | a0001 | c0002 | t0024 | g0162 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0276 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0329 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0330 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0260 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01433 | hp2 | a0001 | c0002 | t0013 | g0106 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0064 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01516 | hp1 | a0001 | c0001 | t0071 | g0211 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01516 | hp2 | a0001 | c0002 | t0008 | g0138 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01517 | hp2 | a0001 | c0002 | t0008 | g0139 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01884 | hp1 | a0001 | c0001 | t0086 | g0061 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0213 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01891 | hp1 | a0001 | c0002 | t0068 | g0067 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01928 | hp1 | a0002 | c0003 | t0002 | g0026 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01934 | hp1 | a0001 | c0001 | t0111 | g0013 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01934 | hp2 | a0001 | c0002 | t0049 | g0117 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01943 | hp1 | a0001 | c0001 | t0092 | g0217 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01975 | hp1 | a0001 | c0002 | t0048 | g0001 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01975 | hp2 | a0001 | c0001 | t0097 | g0065 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01978 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01981 | hp2 | a0001 | c0002 | t0010 | g0163 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02004 | hp2 | a0001 | c0002 | t0060 | g0124 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02027 | hp2 | a0001 | c0002 | t0007 | g0147 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02040 | hp1 | a0001 | c0001 | t0109 | g0037 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02040 | hp2 | a0001 | c0001 | t0009 | g0066 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0221 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02055 | hp2 | a0001 | c0001 | t0020 | g0152 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02056 | hp1 | a0002 | c0003 | t0033 | g0025 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02071 | hp2 | a0001 | c0002 | t0043 | g0158 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02074 | hp2 | a0001 | c0001 | t0009 | g0272 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02129 | hp1 | a0001 | c0001 | t0084 | g0318 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02129 | hp2 | a0001 | c0002 | t0041 | g0128 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02132 | hp1 | a0001 | c0001 | t0033 | g0013 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02132 | hp2 | a0001 | c0001 | t0100 | g0227 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02135 | hp1 | a0001 | c0002 | t0013 | g0137 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02145 | hp1 | a0005 | c0007 | t0011 | g0090 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02145 | hp2 | a0001 | c0006 | t0053 | g0142 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02148 | hp2 | a0001 | c0001 | t0006 | g0328 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02155 | hp2 | a0001 | c0002 | t0010 | g0145 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02165 | hp1 | a0001 | c0001 | t0091 | g0034 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02165 | hp2 | a0001 | c0001 | t0035 | g0300 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0282 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02273 | hp1 | a0001 | c0002 | t0024 | g0112 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0311 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02293 | hp1 | a0001 | c0002 | t0007 | g0114 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02451 | hp1 | a0001 | c0002 | t0004 | g0171 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02451 | hp2 | a0001 | c0002 | t0008 | g0174 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02523 | hp2 | a0001 | c0001 | t0089 | g0044 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0279 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02572 | hp2 | a0001 | c0001 | t0028 | g0253 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02615 | hp1 | a0003 | c0004 | t0016 | g0072 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02615 | hp2 | a0001 | c0001 | t0099 | g0062 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02622 | hp1 | a0001 | c0001 | t0020 | g0192 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02622 | hp2 | a0001 | c0002 | t0052 | g0095 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0264 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02630 | hp2 | a0001 | c0002 | t0026 | g0343 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0249 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02683 | hp2 | a0001 | c0001 | t0098 | g0187 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02698 | hp1 | a0001 | c0001 | t0017 | g0196 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02698 | hp2 | a0001 | c0002 | t0070 | g0143 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0197 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02723 | hp2 | a0001 | c0001 | t0027 | g0036 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02809 | hp1 | a0001 | c0001 | t0108 | g0059 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02809 | hp2 | a0001 | c0002 | t0015 | g0166 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02818 | hp1 | a0001 | c0002 | t0008 | g0340 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02886 | hp1 | a0001 | c0002 | t0026 | g0087 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02886 | hp2 | a0001 | c0002 | t0015 | g0172 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02895 | hp2 | a0001 | c0002 | t0004 | g0129 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02896 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02896 | hp2 | a0004 | c0005 | t0034 | g0047 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0130 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02897 | hp2 | a0004 | c0005 | t0034 | g0046 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02922 | hp1 | a0001 | c0001 | t0095 | g0074 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02922 | hp2 | a0004 | c0005 | t0029 | g0043 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0344 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02965 | hp2 | a0003 | c0004 | t0020 | g0077 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02970 | hp1 | a0001 | c0002 | t0069 | g0107 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0209 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02976 | hp1 | a0001 | c0002 | t0008 | g0181 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0089 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03017 | hp1 | a0001 | c0002 | t0064 | g0103 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0084 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03041 | hp2 | a0001 | c0002 | t0008 | g0342 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03098 | hp1 | a0001 | c0001 | t0105 | g0194 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03098 | hp2 | a0001 | c0002 | t0025 | g0341 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03130 | hp1 | a0001 | c0002 | t0014 | g0080 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03130 | hp2 | a0001 | c0002 | t0008 | g0180 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03139 | hp1 | a0001 | c0001 | t0029 | g0144 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03139 | hp2 | a0001 | c0002 | t0022 | g0167 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03195 | hp1 | a0001 | c0002 | t0023 | g0088 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03195 | hp2 | a0003 | c0004 | t0110 | g0070 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03209 | hp1 | a0001 | c0001 | t0104 | g0244 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03209 | hp2 | a0001 | c0002 | t0037 | g0081 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03225 | hp1 | a0003 | c0004 | t0001 | g0068 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0338 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03239 | hp1 | a0001 | c0002 | t0039 | g0133 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03239 | hp2 | a0001 | c0002 | t0062 | g0121 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0033 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03453 | hp2 | a0001 | c0001 | t0028 | g0297 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0226 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03486 | hp2 | a0001 | c0001 | t0096 | g0054 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03490 | hp1 | a0001 | c0001 | t0017 | g0007 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0238 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03491 | hp1 | a0001 | c0001 | t0103 | g0241 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03492 | hp1 | a0001 | c0001 | t0017 | g0007 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03516 | hp1 | a0001 | c0001 | t0027 | g0245 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03579 | hp1 | a0001 | c0002 | t0022 | g0086 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03579 | hp2 | a0001 | c0002 | t0042 | g0131 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03654 | hp1 | a0001 | c0002 | t0065 | g0135 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03654 | hp2 | a0001 | c0002 | t0014 | g0102 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0206 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03669 | hp2 | a0001 | c0002 | t0010 | g0170 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0239 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0078 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03710 | hp2 | a0001 | c0002 | t0058 | g0126 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03831 | hp1 | a0001 | c0002 | t0066 | g0094 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0336 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03834 | hp1 | a0001 | c0002 | t0013 | g0120 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03927 | hp1 | a0001 | c0002 | t0056 | g0092 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03927 | hp2 | a0001 | c0001 | t0081 | g0201 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03942 | hp2 | a0001 | c0002 | t0004 | g0127 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04115 | hp1 | a0001 | c0002 | t0040 | g0136 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04115 | hp2 | a0001 | c0002 | t0061 | g0125 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0298 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04184 | hp2 | a0001 | c0002 | t0038 | g0149 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0215 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04204 | hp1 | a0001 | c0002 | t0045 | g0091 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04204 | hp2 | a0002 | c0003 | t0001 | g0032 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0093 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04228 | hp2 | a0001 | c0002 | t0010 | g0165 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18522 | hp1 | a0001 | c0002 | t0059 | g0079 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18522 | hp2 | a0001 | c0002 | t0008 | g0179 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18612 | hp1 | a0001 | c0001 | t0072 | g0222 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18612 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18747 | hp1 | a0001 | c0001 | t0085 | g0288 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0281 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18943 | hp1 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18946 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18948 | hp1 | a0001 | c0002 | t0044 | g0098 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18957 | hp1 | a0001 | c0002 | t0063 | g0159 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18957 | hp2 | a0001 | c0001 | t0076 | g0233 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18960 | hp1 | a0001 | c0001 | t0074 | g0327 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18961 | hp2 | a0001 | c0001 | t0009 | g0200 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18963 | hp1 | a0001 | c0002 | t0007 | g0099 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18964 | hp1 | a0001 | c0002 | t0010 | g0097 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18964 | hp2 | a0001 | c0001 | t0083 | g0234 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18965 | hp1 | a0002 | c0003 | t0018 | g0004 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18966 | hp1 | a0001 | c0001 | t0019 | g0040 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18966 | hp2 | a0001 | c0001 | t0087 | g0275 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18968 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18970 | hp1 | a0001 | c0002 | t0013 | g0123 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18970 | hp2 | a0002 | c0003 | t0031 | g0018 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18974 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18974 | hp2 | a0001 | c0001 | t0009 | g0259 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18977 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18980 | hp1 | a0001 | c0002 | t0047 | g0118 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18980 | hp2 | a0001 | c0002 | t0007 | g0156 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18981 | hp2 | a0001 | c0002 | t0004 | g0100 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18984 | hp1 | a0001 | c0002 | t0014 | g0003 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18987 | hp1 | a0002 | c0003 | t0002 | g0017 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18987 | hp2 | a0001 | c0002 | t0004 | g0115 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18988 | hp1 | a0001 | c0001 | t0079 | g0321 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18988 | hp2 | a0001 | c0001 | t0019 | g0055 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18990 | hp2 | a0001 | c0001 | t0009 | g0273 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0109 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18997 | hp1 | a0001 | c0002 | t0010 | g0160 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18997 | hp2 | a0001 | c0001 | t0101 | g0277 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0292 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18998 | hp2 | a0001 | c0002 | t0004 | g0108 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19000 | hp1 | a0001 | c0001 | t0021 | g0049 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19001 | hp2 | a0002 | c0003 | t0018 | g0015 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19002 | hp1 | a0001 | c0002 | t0007 | g0157 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19004 | hp1 | a0002 | c0003 | t0032 | g0030 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19010 | hp1 | a0002 | c0003 | t0031 | g0019 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19012 | hp1 | a0002 | c0003 | t0018 | g0004 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19030 | hp1 | a0001 | c0001 | t0082 | g0243 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19030 | hp2 | a0001 | c0001 | t0106 | g0058 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0208 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19054 | hp2 | a0001 | c0001 | t0102 | g0333 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19057 | hp2 | a0001 | c0002 | t0050 | g0146 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19064 | hp1 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19070 | hp1 | a0001 | c0002 | t0010 | g0113 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19070 | hp2 | a0001 | c0001 | t0009 | g0271 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19078 | hp2 | a0001 | c0001 | t0080 | g0268 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19079 | hp1 | a0001 | c0002 | t0007 | g0122 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19080 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19083 | hp1 | a0001 | c0001 | t0021 | g0220 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19088 | hp1 | a0001 | c0001 | t0021 | g0262 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19088 | hp2 | a0002 | c0003 | t0002 | g0028 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19090 | hp2 | a0001 | c0002 | t0010 | g0101 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19091 | hp1 | a0001 | c0002 | t0007 | g0096 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19091 | hp2 | a0002 | c0003 | t0032 | g0027 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19240 | hp1 | a0001 | c0002 | t0008 | g0173 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19240 | hp2 | a0001 | c0001 | t0113 | g0151 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | ASW | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20129 | hp2 | a0003 | c0004 | t0016 | g0071 | AFR | ASW | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20752 | hp1 | a0001 | c0001 | t0088 | g0314 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20752 | hp2 | a0001 | c0002 | t0067 | g0175 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20805 | hp1 | a0001 | c0002 | t0004 | g0001 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20805 | hp2 | a0001 | c0001 | t0094 | g0210 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20905 | hp1 | a0001 | c0002 | t0007 | g0134 | SAS | GIH | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20905 | hp2 | a0001 | c0001 | t0077 | g0193 | SAS | GIH | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01123 | hp1 | a0001 | c0002 | t0010 | g0177 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0073 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02109 | hp1 | a0001 | c0002 | t0055 | g0182 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02109 | hp2 | a0003 | c0004 | t0107 | g0069 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02486 | hp1 | a0003 | c0004 | t0093 | g0075 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0153 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02559 | hp1 | a0001 | c0002 | t0023 | g0082 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02559 | hp2 | a0001 | c0002 | t0036 | g0132 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG06807 | hp1 | a0004 | c0005 | t0012 | g0048 | AFR | USA | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG06807 | hp2 | a0003 | c0004 | t0078 | g0076 | AFR | USA | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA21309 | hp1 | a0001 | c0002 | t0008 | g0150 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA21309 | hp2 | a0001 | c0002 | t0025 | g0085 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0325 | REF | REF | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0075 | g0212 | REF | REF | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147509076
|
G | C | 1 | a0002 | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
missense_variant | MODERATE | c.148G>C | p.Ala50Pro | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 387/6326 | 148/522 | 50/173 | chr6 | 147509076 | ||
chr6:147509088
|
C | G | 1 | a0005 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.160C>G | p.Arg54Gly | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 399/6326 | 160/522 | 54/173 | chr6 | 147509088 | ||
chr6:147509167
|
C | T | 1 | a0004 | 4 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.239C>T | p.Pro80Leu | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 478/6326 | 239/522 | 80/173 | chr6 | 147509167 | ||
chr6:147509172
|
C | T | 1 | a0003 | 8 | HG02109.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
missense_variant | MODERATE | c.244C>T | p.Pro82Ser | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 483/6326 | 244/522 | 82/173 | chr6 | 147509172 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147508937
|
C | T | 2 | a0001c0002a0001c0006 | 116 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
synonymous_variant | LOW | c.9C>T | p.Thr3Thr | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 248/6326 | 9/522 | 3/173 | chr6 | 147508937 | ||
chr6:147509144
|
C | G | 1 | a0001c0006 | 3 | HG00738.hp1 HG01081.hp2 HG02145.hp2 |
synonymous_variant | LOW | c.216C>G | p.Leu72Leu | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 455/6326 | 216/522 | 72/173 | chr6 | 147509144 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147508692
|
T | A | 1 | a0001c0001t0035 | 1 | HG02165.hp2 | 5_prime_UTR_variant | MODIFIER | c.-237T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 237 | chr6 | 147508692 | |||||
chr6:147508708
|
T | G | 48 | a0001c0002t0004a0001c0002t0007a0001c0002t0008others(45): Show | 116 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-221T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 221 | chr6 | 147508708 | |||||
chr6:147508759
|
C | T | 1 | a0001c0001t0113 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-170C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 170 | chr6 | 147508759 | |||||
chr6:147508783
|
C | T | 1 | a0001c0002t0070 | 1 | HG02698.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-146C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | chr6 | 147508783 | ||||||
chr6:147508887
|
G | A | 1 | a0001c0001t0071 | 1 | HG01516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 42 | chr6 | 147508887 | |||||
chr6:147508890
|
G | T | 1 | a0001c0002t0069 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 39 | chr6 | 147508890 | |||||
chr6:147564658
|
G | A | 1 | a0001c0001t0072 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*202G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 202 | chr6 | 147564658 | |||||
chr6:147564667
|
C | T | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0016others(31): Show | 96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*211C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 211 | chr6 | 147564667 | |||||
chr6:147564822
|
A | T | 5 | a0001c0001t0100a0001c0001t0101a0001c0001t0102others(2): Show | 5 | HG02132.hp2 HG03491.hp1 HG03710.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*366A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 366 | chr6 | 147564822 | |||||
chr6:147564856
|
A | G | 22 | a0001c0001t0011a0001c0001t0016a0001c0001t0097others(19): Show | 43 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*400A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 400 | chr6 | 147564856 | |||||
chr6:147564971
|
C | G | 33 | a0001c0001t0002a0001c0001t0006a0001c0001t0020others(30): Show | 92 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*515C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 515 | chr6 | 147564971 | |||||
chr6:147565195
|
T | C | 1 | a0001c0002t0036 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 739 | chr6 | 147565195 | |||||
chr6:147565381
|
T | A | 1 | a0001c0001t0105 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*925T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 925 | chr6 | 147565381 | |||||
chr6:147565456
|
T | C | 18 | a0001c0001t0016a0001c0001t0020a0001c0001t0027others(15): Show | 26 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1000T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1000 | chr6 | 147565456 | |||||
chr6:147565464
|
G | GT | 57 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(54): Show | 202 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*1021dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1022 | INFO_REALIGN_3_PRIME | chr6 | 147565464 | ||||
chr6:147565500
|
C | A | 1 | a0003c0004t0107 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1044C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1044 | chr6 | 147565500 | |||||
chr6:147565545
|
G | A | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1089 | chr6 | 147565545 | |||||
chr6:147565582
|
T | C | 58 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(55): Show | 169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1126T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1126 | chr6 | 147565582 | |||||
chr6:147565591
|
G | A | 5 | a0001c0001t0009a0001c0001t0035a0001c0001t0079others(2): Show | 15 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1135G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1135 | chr6 | 147565591 | |||||
chr6:147565684
|
T | C | 1 | a0001c0002t0038 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1228T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1228 | chr6 | 147565684 | |||||
chr6:147565715
|
C | T | 2 | a0001c0002t0052a0003c0004t0093 | 2 | HG02486.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1259C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1259 | chr6 | 147565715 | |||||
chr6:147565744
|
G | A | 1 | a0001c0001t0087 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1288G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1288 | chr6 | 147565744 | |||||
chr6:147565794
|
C | T | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1338C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1338 | chr6 | 147565794 | |||||
chr6:147565862
|
T | A | 4 | a0001c0001t0100a0001c0001t0108a0001c0002t0061others(1): Show | 4 | HG02132.hp2 HG02809.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1406T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1406 | chr6 | 147565862 | |||||
chr6:147565905
|
T | C | 7 | a0001c0001t0016a0001c0001t0088a0001c0001t0112others(4): Show | 10 | HG00140.hp2 HG00733.hp1 HG01891.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1449T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1449 | chr6 | 147565905 | |||||
chr6:147565956
|
C | A | 2 | a0001c0001t0097a0001c0002t0054 | 2 | HG00733.hp2 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1500 | chr6 | 147565956 | |||||
chr6:147565991
|
A | G | 1 | a0001c0002t0025 | 2 | HG03098.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1535A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1535 | chr6 | 147565991 | |||||
chr6:147566082
|
A | G | 113 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(110): Show | 326 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*1626A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1626 | chr6 | 147566082 | |||||
chr6:147566213
|
G | A | 5 | a0001c0001t0021a0001c0001t0071a0001c0001t0079others(2): Show | 8 | HG01243.hp1 HG01346.hp2 HG01516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1757G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1757 | chr6 | 147566213 | |||||
chr6:147566214
|
C | A | 3 | a0001c0001t0017a0001c0002t0039a0001c0002t0040 | 5 | HG02698.hp1 HG03239.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1758C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1758 | chr6 | 147566214 | |||||
chr6:147566393
|
A | C | 1 | a0003c0004t0110 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1937A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1937 | chr6 | 147566393 | |||||
chr6:147566433
|
C | T | 51 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(48): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1977C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1977 | chr6 | 147566433 | |||||
chr6:147566594
|
A | G | 1 | a0002c0003t0031 | 2 | NA18970.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2138A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2138 | chr6 | 147566594 | |||||
chr6:147566628
|
G | A | 123 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(120): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*2172G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2172 | chr6 | 147566628 | |||||
chr6:147566754
|
G | A | 19 | a0001c0001t0016a0001c0001t0020a0001c0001t0027others(16): Show | 27 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2298G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2298 | chr6 | 147566754 | |||||
chr6:147566886
|
G | A | 113 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(110): Show | 326 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*2430G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2430 | chr6 | 147566886 | |||||
chr6:147567095
|
G | A | 2 | a0001c0001t0089a0002c0003t0032 | 3 | HG02523.hp2 NA19004.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2639G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2639 | chr6 | 147567095 | |||||
chr6:147567187
|
G | A | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2731G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2731 | chr6 | 147567187 | |||||
chr6:147567191
|
T | G | 1 | a0001c0001t0090 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2735 | chr6 | 147567191 | |||||
chr6:147567232
|
T | C | 31 | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(28): Show | 90 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2776T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2776 | chr6 | 147567232 | |||||
chr6:147567358
|
A | C | 20 | a0001c0001t0016a0001c0001t0020a0001c0001t0027others(17): Show | 28 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2902A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2902 | chr6 | 147567358 | |||||
chr6:147567586
|
TTACACCC others(3): Show |
T | 1 | a0001c0001t0085 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3135_*3144delCCCA others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3135 | INFO_REALIGN_3_PRIME | chr6 | 147567586 | ||||
chr6:147567646
|
C | T | 1 | a0001c0001t0084 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3190C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3190 | chr6 | 147567646 | |||||
chr6:147567660
|
T | C | 2 | a0001c0001t0098a0001c0002t0056 | 2 | HG02683.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3204T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3204 | chr6 | 147567660 | |||||
chr6:147567791
|
C | T | 51 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(48): Show | 160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*3335C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3335 | chr6 | 147567791 | |||||
chr6:147567801
|
A | G | 40 | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(37): Show | 99 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*3345A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3345 | chr6 | 147567801 | |||||
chr6:147567808
|
G | A | 1 | a0001c0002t0043 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3352G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3352 | chr6 | 147567808 | |||||
chr6:147567825
|
T | C | 1 | a0001c0001t0082 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3369T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3369 | chr6 | 147567825 | |||||
chr6:147567907
|
C | A | 1 | a0004c0005t0034 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3451C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3451 | chr6 | 147567907 | |||||
chr6:147567934
|
A | G | 4 | a0001c0001t0029a0001c0002t0042a0001c0002t0069others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3478A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3478 | chr6 | 147567934 | |||||
chr6:147567980
|
G | T | 7 | a0001c0001t0012a0001c0001t0090a0001c0002t0015others(4): Show | 14 | HG00738.hp1 HG01081.hp2 HG01192.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3524G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3524 | chr6 | 147567980 | |||||
chr6:147568139
|
G | T | 3 | a0001c0001t0077a0001c0001t0092a0001c0002t0051 | 3 | HG01261.hp1 HG01943.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3683G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3683 | chr6 | 147568139 | |||||
chr6:147568172
|
T | C | 6 | a0001c0001t0006a0001c0001t0033a0001c0002t0062others(3): Show | 21 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3716T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3716 | chr6 | 147568172 | |||||
chr6:147568194
|
T | A | 1 | a0001c0002t0047 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3738T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3738 | chr6 | 147568194 | |||||
chr6:147568195
|
G | T | 1 | a0001c0002t0025 | 2 | HG03098.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3739G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3739 | chr6 | 147568195 | |||||
chr6:147568314
|
G | A | 1 | a0001c0001t0077 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3858G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3858 | chr6 | 147568314 | |||||
chr6:147568580
|
G | A | 1 | a0001c0002t0048 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4124G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4124 | chr6 | 147568580 | |||||
chr6:147568628
|
A | G | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4172A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4172 | chr6 | 147568628 | |||||
chr6:147568676
|
G | T | 1 | a0001c0001t0089 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4220G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4220 | chr6 | 147568676 | |||||
chr6:147568791
|
T | G | 1 | a0001c0001t0083 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4335T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4335 | chr6 | 147568791 | |||||
chr6:147569032
|
G | A | 2 | a0001c0001t0033a0002c0003t0033 | 2 | HG02056.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4576G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4576 | chr6 | 147569032 | |||||
chr6:147569072
|
C | CA | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(20): Show | 82 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*4624dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4625 | INFO_REALIGN_3_PRIME | chr6 | 147569072 | ||||
chr6:147569159
|
C | T | 17 | a0001c0001t0016a0001c0001t0020a0001c0001t0028others(14): Show | 23 | HG00140.hp2 HG00733.hp2 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4703C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4703 | chr6 | 147569159 | |||||
chr6:147569206
|
G | T | 4 | a0001c0001t0096a0001c0002t0036a0001c0002t0046others(1): Show | 4 | HG01081.hp1 HG02145.hp2 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4750G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4750 | chr6 | 147569206 | |||||
chr6:147569219
|
T | TA | 26 | a0001c0001t0002a0001c0001t0006a0001c0001t0017others(23): Show | 85 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*4779dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4780 | INFO_REALIGN_3_PRIME | chr6 | 147569219 | ||||
chr6:147569219
|
TA | T | 8 | a0001c0001t0029a0001c0001t0074a0001c0002t0014others(5): Show | 11 | HG00639.hp2 HG02922.hp2 HG02970.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4779delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4779 | INFO_REALIGN_3_PRIME | chr6 | 147569219 | ||||
chr6:147569233
|
A | G | 2 | a0001c0001t0097a0001c0002t0054 | 2 | HG00733.hp2 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4777A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4777 | chr6 | 147569233 | |||||
chr6:147569234
|
A | G | 18 | a0001c0001t0016a0001c0001t0020a0001c0001t0027others(15): Show | 26 | HG00140.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4778A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4778 | chr6 | 147569234 | |||||
chr6:147569235
|
AG | A | 18 | a0001c0001t0016a0001c0001t0020a0001c0001t0027others(15): Show | 26 | HG00140.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4780delG | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4780 | chr6 | 147569235 | |||||
chr6:147569285
|
A | AGATAATT others(133): Show |
1 | a0001c0002t0059 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4840_*4841insTTTT others(136): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4841 | INFO_REALIGN_3_PRIME | chr6 | 147569285 | ||||
chr6:147569285
|
A | AGATAATT others(148): Show |
1 | a0001c0001t0106 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4840_*4841insTTTT others(151): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4841 | INFO_REALIGN_3_PRIME | chr6 | 147569285 | ||||
chr6:147569471
|
A | G | 1 | a0001c0001t0030 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5015A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5015 | chr6 | 147569471 | |||||
chr6:147569479
|
T | A | 1 | a0001c0002t0049 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5023T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5023 | chr6 | 147569479 | |||||
chr6:147569686
|
T | C | 1 | a0001c0001t0094 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5230T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5230 | chr6 | 147569686 | |||||
chr6:147569696
|
A | G | 1 | a0001c0001t0081 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5240A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5240 | chr6 | 147569696 | |||||
chr6:147569844
|
A | G | 1 | a0001c0001t0085 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5388A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5388 | chr6 | 147569844 | |||||
chr6:147569889
|
A | T | 2 | a0001c0001t0019a0001c0002t0050 | 4 | HG00621.hp2 NA18966.hp1 NA18988.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5433A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5433 | chr6 | 147569889 | |||||
chr6:147569933
|
G | A | 1 | a0001c0002t0045 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5477G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5477 | chr6 | 147569933 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147509565
|
G | C | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+178G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509565 | ||||||
chr6:147509614
|
T | C | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+227T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509614 | ||||||
chr6:147509694
|
A | G | 1 | a0001c0002t0007g0014 | 2 | NA18974.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.459+307A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509694 | ||||||
chr6:147509856
|
A | G | 1 | a0001c0001t0005g0345 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.459+469A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509856 | ||||||
chr6:147509873
|
T | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(27): Show | 33 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.459+486T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509873 | ||||||
chr6:147509925
|
A | G | 29 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(26): Show | 31 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+538A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509925 | ||||||
chr6:147510146
|
G | A | 32 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(29): Show | 34 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.459+759G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510146 | ||||||
chr6:147510230
|
T | A | 1 | a0001c0001t0005g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.459+843T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510230 | ||||||
chr6:147510332
|
T | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(25): Show | 30 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+945T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510332 | ||||||
chr6:147510341
|
C | A | 2 | a0001c0001t0003g0064a0001c0001t0097g0065 | 2 | HG01515.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.459+954C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510341 | ||||||
chr6:147510508
|
A | C | 4 | a0001c0002t0008g0340a0001c0002t0008g0342a0001c0002t0025g0341others(1): Show | 4 | HG02630.hp2 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+1121A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510508 | ||||||
chr6:147510710
|
G | A | 1 | a0001c0001t0009g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.459+1323G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510710 | ||||||
chr6:147510856
|
G | A | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+1469G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510856 | ||||||
chr6:147510933
|
G | A | 1 | a0001c0002t0068g0067 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.459+1546G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510933 | ||||||
chr6:147511020
|
G | A | 178 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(175): Show | 186 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.459+1633G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511020 | ||||||
chr6:147511030
|
G | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459+1643G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511030 | ||||||
chr6:147511226
|
A | G | 124 | a0001c0001t0001g0005a0001c0001t0002g0337a0001c0001t0012g0033others(121): Show | 129 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.459+1839A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511226 | ||||||
chr6:147511308
|
C | T | 55 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294others(52): Show | 60 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.459+1921C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511308 | ||||||
chr6:147511365
|
G | T | 2 | a0001c0001t0106g0058a0001c0001t0108g0059 | 2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.459+1978G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511365 | ||||||
chr6:147511390
|
A | G | 21 | a0001c0002t0004g0168a0001c0002t0004g0171a0001c0002t0004g0176others(18): Show | 21 | HG00140.hp1 HG00280.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.459+2003A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511390 | ||||||
chr6:147511452
|
T | C | 1 | a0001c0001t0091g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.459+2065T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511452 | ||||||
chr6:147511502
|
T | G | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.459+2115T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511502 | ||||||
chr6:147511612
|
C | T | 1 | a0001c0001t0012g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459+2225C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511612 | ||||||
chr6:147511627
|
CA | C | 171 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(168): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+2254delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147511627 | |||||
chr6:147511840
|
T | A | 1 | a0001c0002t0004g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.459+2453T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511840 | ||||||
chr6:147512102
|
C | T | 8 | a0003c0004t0001g0068a0003c0004t0016g0071a0003c0004t0016g0072others(5): Show | 8 | HG02109.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+2715C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512102 | ||||||
chr6:147512146
|
C | T | 1 | a0001c0002t0010g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459+2759C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512146 | ||||||
chr6:147512173
|
A | G | 180 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(177): Show | 188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.459+2786A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512173 | ||||||
chr6:147512245
|
C | T | 108 | a0001c0001t0003g0336a0001c0001t0012g0338a0001c0001t0020g0152others(105): Show | 112 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.459+2858C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512245 | ||||||
chr6:147512277
|
G | A | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+2890G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512277 | ||||||
chr6:147512713
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.459+3326A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512713 | ||||||
chr6:147512756
|
T | C | 2 | a0001c0001t0001g0291a0001c0001t0002g0290 | 2 | HG00423.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.459+3369T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512756 | ||||||
chr6:147512888
|
A | G | 1 | a0001c0001t0002g0337 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.459+3501A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512888 | ||||||
chr6:147513194
|
T | C | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+3807T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513194 | ||||||
chr6:147513269
|
T | C | 2 | a0002c0003t0018g0004a0002c0003t0018g0015 | 3 | NA18965.hp1 NA19001.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.459+3882T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513269 | ||||||
chr6:147513301
|
C | T | 28 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(25): Show | 30 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+3914C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513301 | ||||||
chr6:147513513
|
G | C | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+4126G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513513 | ||||||
chr6:147513604
|
C | G | 1 | a0002c0003t0001g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.459+4217C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513604 | ||||||
chr6:147513691
|
A | G | 128 | a0001c0001t0001g0005a0001c0001t0012g0033a0001c0001t0012g0338others(125): Show | 133 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.459+4304A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513691 | ||||||
chr6:147513733
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.459+4346G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513733 | ||||||
chr6:147513981
|
T | C | 1 | a0001c0002t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459+4594T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513981 | ||||||
chr6:147514002
|
C | T | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+4615C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514002 | ||||||
chr6:147514204
|
C | T | 7 | a0001c0001t0001g0283a0001c0001t0002g0286a0001c0001t0002g0289others(4): Show | 7 | HG00558.hp1 NA18747.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+4817C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514204 | ||||||
chr6:147514211
|
G | T | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4824G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514211 | ||||||
chr6:147514216
|
T | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4829T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514216 | ||||||
chr6:147514219
|
C | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4832C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514219 | ||||||
chr6:147514223
|
T | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4836T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514223 | ||||||
chr6:147514227
|
T | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4840T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514227 | ||||||
chr6:147514228
|
A | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4841A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514228 | ||||||
chr6:147514229
|
G | GGCGGGGG others(22): Show |
1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4842_459+4843i others(31): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514229 | ||||||
chr6:147514415
|
GTGGGATC others(50): Show |
G | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5032_459+5088d others(59): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147514415 | |||||
chr6:147514419
|
G | A | 178 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(175): Show | 186 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.459+5032G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514419 | ||||||
chr6:147514513
|
C | T | 3 | a0001c0002t0004g0161a0001c0002t0010g0163a0001c0002t0024g0162 | 3 | HG01069.hp2 HG01346.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.459+5126C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514513 | ||||||
chr6:147514532
|
C | T | 5 | a0002c0003t0001g0031a0002c0003t0002g0028a0002c0003t0003g0029others(2): Show | 5 | NA18961.hp1 NA18968.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+5145C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514532 | ||||||
chr6:147514788
|
C | G | 2 | a0001c0001t0011g0281a0001c0001t0011g0282 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.459+5401C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514788 | ||||||
chr6:147514789
|
G | A | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+5402G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514789 | ||||||
chr6:147514799
|
T | C | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+5412T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514799 | ||||||
chr6:147514852
|
G | A | 153 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(150): Show | 159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+5465G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514852 | ||||||
chr6:147514862
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5475C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514862 | ||||||
chr6:147515061
|
C | A | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5674C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515061 | ||||||
chr6:147515081
|
C | T | 1 | a0001c0001t0002g0280 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.459+5694C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515081 | ||||||
chr6:147515082
|
G | A | 153 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(150): Show | 159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+5695G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515082 | ||||||
chr6:147515146
|
C | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(150): Show | 159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+5759C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515146 | ||||||
chr6:147515176
|
G | GT | 51 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0251others(48): Show | 56 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.459+5820dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515176
|
G | GTT | 17 | a0001c0001t0001g0274a0001c0001t0002g0269a0001c0001t0002g0335others(14): Show | 17 | HG00609.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+5819_459+5820d others(4): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515176
|
G | GTTTT | 6 | a0001c0001t0003g0278a0001c0001t0011g0279a0001c0001t0101g0277others(3): Show | 6 | HG01106.hp1 HG01928.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+5817_459+5820d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515176
|
GTTTTTTT others(1): Show |
G | 31 | a0001c0001t0001g0005a0001c0001t0002g0056a0001c0001t0009g0057others(28): Show | 33 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.459+5813_459+5820d others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515176
|
GTTTTTTT others(2): Show |
G | 117 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(114): Show | 122 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.459+5812_459+5820d others(11): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515176
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0002t0004g0161a0001c0002t0045g0091 | 2 | HG01069.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.459+5811_459+5820d others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515176
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5810_459+5820d others(13): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515176
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0012g0338 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.459+5804_459+5820d others(19): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | |||||
chr6:147515188
|
T | C | 1 | a0005c0007t0011g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+5801T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515188 | ||||||
chr6:147515275
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.459+5888G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515275 | ||||||
chr6:147515362
|
C | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+5975C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515362 | ||||||
chr6:147515410
|
TATCC | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6028_459+6031d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515410 | |||||
chr6:147515431
|
A | ACCAT | 25 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0247others(22): Show | 26 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.459+6085_459+6088d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | |||||
chr6:147515431
|
ACCAT | A | 108 | a0001c0001t0009g0053a0001c0001t0011g0281a0001c0001t0011g0282others(105): Show | 112 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.459+6085_459+6088d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | |||||
chr6:147515431
|
ACCATCCA others(1): Show |
A | 11 | a0001c0001t0001g0005a0001c0002t0004g0083a0001c0002t0004g0084others(8): Show | 12 | HG01109.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+6081_459+6088d others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | |||||
chr6:147515431
|
ACCATCCA others(5): Show |
A | 1 | a0001c0001t0012g0344 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.459+6077_459+6088d others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | |||||
chr6:147515431
|
ACCATCCA others(9): Show |
A | 4 | a0001c0002t0068g0067a0003c0004t0016g0071a0003c0004t0016g0072others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+6073_459+6088d others(18): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | |||||
chr6:147515576
|
C | G | 2 | a0001c0001t0001g0242a0001c0001t0080g0268 | 2 | NA19010.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.459+6189C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515576 | ||||||
chr6:147515656
|
GC | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6272delC | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515656 | |||||
chr6:147515703
|
C | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6316C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515703 | ||||||
chr6:147515727
|
G | A | 153 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(150): Show | 159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+6340G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515727 | ||||||
chr6:147515921
|
T | A | 1 | a0001c0002t0004g0073 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.459+6534T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515921 | ||||||
chr6:147515989
|
A | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6602A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515989 | ||||||
chr6:147516062
|
C | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(150): Show | 159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+6675C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516062 | ||||||
chr6:147516079
|
T | C | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6692T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516079 | ||||||
chr6:147516202
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+6815C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516202 | ||||||
chr6:147516279
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+6892T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516279 | ||||||
chr6:147516366
|
C | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6979C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516366 | ||||||
chr6:147516383
|
C | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0248a0001c0001t0005g0008 | 4 | HG00642.hp2 HG00741.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+6996C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516383 | ||||||
chr6:147516397
|
C | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0003c0004t0020g0077others(2): Show | 5 | HG02486.hp1 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+7010C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516397 | ||||||
chr6:147516425
|
C | G | 4 | a0001c0001t0002g0334a0001c0001t0003g0320a0001c0001t0003g0332others(1): Show | 4 | NA18946.hp2 NA19054.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+7038C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516425 | ||||||
chr6:147516457
|
A | C | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+7070A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516457 | ||||||
chr6:147516467
|
A | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7080A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516467 | ||||||
chr6:147516470
|
A | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7083A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516470 | ||||||
chr6:147516475
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7088G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516475 | ||||||
chr6:147516517
|
T | C | 115 | a0001c0001t0001g0005a0001c0001t0012g0033a0001c0001t0012g0338others(112): Show | 119 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.459+7130T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516517 | ||||||
chr6:147516532
|
T | A | 4 | a0001c0001t0002g0334a0001c0001t0003g0320a0001c0001t0003g0332others(1): Show | 4 | NA18946.hp2 NA19054.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+7145T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516532 | ||||||
chr6:147516555
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459+7168A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516555 | ||||||
chr6:147516594
|
A | G | 1 | a0001c0002t0010g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459+7207A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516594 | ||||||
chr6:147516644
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7257G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516644 | ||||||
chr6:147516756
|
C | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7369C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516756 | ||||||
chr6:147516762
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.459+7375A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516762 | ||||||
chr6:147516791
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+7404C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516791 | ||||||
chr6:147516861
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+7474C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516861 | ||||||
chr6:147516888
|
C | T | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+7501C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516888 | ||||||
chr6:147517046
|
G | A | 36 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(33): Show | 38 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.459+7659G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517046 | ||||||
chr6:147517057
|
T | G | 1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.459+7670T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517057 | ||||||
chr6:147517133
|
C | T | 1 | a0001c0001t0009g0057 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.459+7746C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517133 | ||||||
chr6:147517236
|
T | C | 1 | a0001c0001t0006g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.459+7849T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517236 | ||||||
chr6:147517279
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7892G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517279 | ||||||
chr6:147517345
|
G | A | 1 | a0001c0001t0005g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.459+7958G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517345 | ||||||
chr6:147517370
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7983G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517370 | ||||||
chr6:147517409
|
G | C | 2 | a0001c0001t0006g0295a0001c0001t0006g0323 | 2 | HG00735.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.459+8022G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517409 | ||||||
chr6:147517426
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.459+8039C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517426 | ||||||
chr6:147517492
|
G | C | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8105G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517492 | ||||||
chr6:147517502
|
T | TGATAAAT others(8): Show |
172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8118_459+8119i others(17): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147517502 | |||||
chr6:147517542
|
C | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8155C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517542 | ||||||
chr6:147517562
|
C | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8175C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517562 | ||||||
chr6:147517598
|
A | C | 28 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(25): Show | 30 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+8211A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517598 | ||||||
chr6:147517600
|
T | C | 1 | a0001c0002t0057g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.459+8213T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517600 | ||||||
chr6:147517728
|
G | A | 2 | a0001c0001t0011g0281a0001c0001t0011g0282 | 2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.459+8341G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517728 | ||||||
chr6:147517742
|
A | G | 1 | a0001c0002t0023g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.459+8355A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517742 | ||||||
chr6:147517742
|
A | T | 1 | a0001c0002t0070g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.459+8355A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517742 | ||||||
chr6:147517780
|
A | C | 1 | a0001c0001t0002g0319 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.459+8393A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517780 | ||||||
chr6:147517873
|
G | GT | 9 | a0001c0001t0002g0056a0001c0001t0080g0268a0001c0002t0007g0153others(6): Show | 9 | HG00738.hp1 HG01081.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+8498dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147517873 | |||||
chr6:147517897
|
T | C | 1 | a0001c0001t0012g0344 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.459+8510T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517897 | ||||||
chr6:147517991
|
A | G | 11 | a0001c0002t0004g0083a0001c0002t0004g0084a0001c0002t0014g0080others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.459+8604A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517991 | ||||||
chr6:147518039
|
A | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8652A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518039 | ||||||
chr6:147518168
|
C | T | 2 | a0001c0001t0005g0267a0001c0001t0103g0241 | 2 | HG00741.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.459+8781C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518168 | ||||||
chr6:147518199
|
C | T | 1 | a0001c0001t0002g0337 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.459+8812C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518199 | ||||||
chr6:147518244
|
A | C | 1 | a0001c0001t0003g0287 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.459+8857A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518244 | ||||||
chr6:147518369
|
C | A | 1 | a0001c0001t0001g0291 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.459+8982C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518369 | ||||||
chr6:147518543
|
G | A | 1 | a0003c0004t0001g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.459+9156G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518543 | ||||||
chr6:147518555
|
G | A | 171 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(168): Show | 178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.459+9168G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518555 | ||||||
chr6:147518572
|
T | G | 1 | a0001c0001t0003g0186 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.459+9185T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518572 | ||||||
chr6:147518613
|
C | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(169): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+9226C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518613 | ||||||
chr6:147518638
|
G | A | 171 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0051others(168): Show | 178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.459+9251G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518638 | ||||||
chr6:147518966
|
A | C | 3 | a0003c0004t0020g0077a0003c0004t0078g0076a0003c0004t0093g0075 | 3 | HG02486.hp1 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.459+9579A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518966 | ||||||
chr6:147519443
|
A | C | 1 | a0001c0001t0084g0318 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.459+10056A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519443 | ||||||
chr6:147519459
|
T | G | 108 | a0001c0001t0001g0038a0001c0001t0012g0338a0001c0001t0020g0192others(105): Show | 111 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.459+10072T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519459 | ||||||
chr6:147519480
|
C | G | 1 | a0001c0001t0012g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459+10093C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519480 | ||||||
chr6:147519609
|
T | C | 1 | a0001c0002t0010g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.459+10222T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519609 | ||||||
chr6:147519660
|
A | G | 31 | a0001c0001t0003g0060a0001c0001t0012g0344a0001c0002t0023g0088others(28): Show | 32 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.459+10273A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519660 | ||||||
chr6:147519717
|
G | T | 1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.459+10330G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519717 | ||||||
chr6:147519800
|
A | T | 1 | a0001c0001t0011g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.459+10413A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519800 | ||||||
chr6:147519897
|
C | T | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+10510C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519897 | ||||||
chr6:147519949
|
C | T | 28 | a0001c0001t0003g0060a0001c0001t0012g0344a0002c0003t0001g0016others(25): Show | 29 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+10562C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519949 | ||||||
chr6:147520117
|
G | GT | 31 | a0001c0001t0001g0248a0001c0001t0002g0334a0001c0001t0003g0285others(28): Show | 32 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.459+10747dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | |||||
chr6:147520117
|
G | GTT | 124 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(121): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+10746_459+1074 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | |||||
chr6:147520117
|
G | GTTT | 10 | a0001c0001t0009g0057a0001c0001t0012g0338a0001c0001t0020g0192others(7): Show | 10 | HG00738.hp1 HG01081.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+10745_459+1074 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | |||||
chr6:147520117
|
GT | G | 10 | a0001c0001t0003g0060a0001c0001t0009g0292a0001c0001t0012g0344others(7): Show | 10 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+10747delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | |||||
chr6:147520139
|
A | G | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+10752A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520139 | ||||||
chr6:147520196
|
C | A | 1 | a0001c0001t0096g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+10809C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520196 | ||||||
chr6:147520220
|
C | T | 7 | a0001c0002t0004g0083a0001c0002t0004g0084a0001c0002t0014g0080others(4): Show | 7 | HG01109.hp2 HG02559.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+10833C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520220 | ||||||
chr6:147520377
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.459+10990C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520377 | ||||||
chr6:147520517
|
G | C | 4 | a0001c0001t0001g0324a0001c0001t0002g0335a0001c0001t0003g0296others(1): Show | 4 | NA18963.hp2 NA18988.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+11130G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520517 | ||||||
chr6:147520625
|
A | C | 158 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(155): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.459+11238A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520625 | ||||||
chr6:147520625
|
A | G | 2 | a0001c0001t0005g0238a0001c0001t0005g0239 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.459+11238A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520625 | ||||||
chr6:147520747
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.459+11360A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520747 | ||||||
chr6:147520788
|
T | A | 1 | a0001c0002t0050g0146 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.459+11401T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520788 | ||||||
chr6:147520915
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+11528G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520915 | ||||||
chr6:147521049
|
T | C | 27 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0002g0006others(24): Show | 29 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+11662T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521049 | ||||||
chr6:147521123
|
A | G | 1 | a0005c0007t0011g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+11736A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521123 | ||||||
chr6:147521135
|
TA | T | 27 | a0001c0001t0012g0344a0002c0003t0001g0016a0002c0003t0001g0021others(24): Show | 28 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.459+11749delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521135 | ||||||
chr6:147521136
|
A | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+11749A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521136 | ||||||
chr6:147521151
|
G | T | 1 | a0001c0002t0040g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+11764G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521151 | ||||||
chr6:147521161
|
C | T | 2 | a0001c0001t0020g0152a0001c0001t0113g0151 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+11774C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521161 | ||||||
chr6:147521163
|
T | C | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+11776T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521163 | ||||||
chr6:147521469
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+12082A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521469 | ||||||
chr6:147521775
|
T | A | 1 | a0001c0001t0005g0317 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.459+12388T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521775 | ||||||
chr6:147521868
|
C | CT | 107 | a0001c0001t0005g0063a0001c0001t0012g0338a0001c0001t0020g0192others(104): Show | 110 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.459+12488dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147521868 | |||||
chr6:147521882
|
A | G | 8 | a0001c0001t0012g0344a0003c0004t0001g0068a0003c0004t0016g0071others(5): Show | 8 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+12495A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521882 | ||||||
chr6:147521889
|
T | G | 27 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0002g0006others(24): Show | 29 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+12502T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521889 | ||||||
chr6:147521983
|
C | A | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+12596C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521983 | ||||||
chr6:147522029
|
C | T | 111 | a0001c0001t0005g0063a0001c0001t0012g0338a0001c0001t0020g0192others(108): Show | 114 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.459+12642C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522029 | ||||||
chr6:147522326
|
C | T | 2 | a0001c0001t0020g0152a0001c0001t0113g0151 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+12939C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522326 | ||||||
chr6:147522422
|
C | A | 1 | a0001c0001t0077g0193 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.459+13035C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522422 | ||||||
chr6:147522537
|
G | A | 3 | a0003c0004t0016g0071a0003c0004t0016g0072a0003c0004t0110g0070 | 3 | HG02615.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.459+13150G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522537 | ||||||
chr6:147522614
|
C | G | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+13227C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522614 | ||||||
chr6:147522621
|
C | T | 5 | a0001c0002t0008g0179a0001c0002t0008g0180a0001c0002t0008g0181others(2): Show | 5 | HG01081.hp1 HG02109.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+13234C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522621 | ||||||
chr6:147522720
|
A | G | 113 | a0001c0001t0001g0185a0001c0001t0001g0247a0001c0001t0003g0284others(110): Show | 116 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.459+13333A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522720 | ||||||
chr6:147522799
|
A | G | 163 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(160): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.459+13412A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522799 | ||||||
chr6:147522870
|
G | C | 2 | a0001c0001t0011g0279a0001c0001t0105g0194 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.459+13483G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522870 | ||||||
chr6:147522920
|
G | A | 2 | a0001c0002t0052g0095a0003c0004t0093g0075 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.459+13533G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522920 | ||||||
chr6:147523013
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG01074.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.459+13626A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523013 | ||||||
chr6:147523058
|
C | G | 3 | a0001c0001t0003g0060a0001c0001t0086g0061a0001c0001t0099g0062 | 3 | HG01884.hp1 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.459+13671C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523058 | ||||||
chr6:147523091
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0240 | 2 | NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.459+13704C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523091 | ||||||
chr6:147523091
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459+13704C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523091 | ||||||
chr6:147523117
|
C | T | 1 | a0001c0002t0065g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.459+13730C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523117 | ||||||
chr6:147523123
|
C | A | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+13736C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523123 | ||||||
chr6:147523142
|
C | G | 2 | a0001c0001t0002g0315a0001c0001t0003g0316 | 2 | NA18965.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.459+13755C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523142 | ||||||
chr6:147523155
|
T | C | 2 | a0001c0001t0005g0267a0001c0001t0103g0241 | 2 | HG00741.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.459+13768T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523155 | ||||||
chr6:147523295
|
A | G | 1 | a0001c0001t0005g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.459+13908A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523295 | ||||||
chr6:147523538
|
A | G | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+14151A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523538 | ||||||
chr6:147523747
|
C | T | 122 | a0001c0001t0005g0063a0001c0001t0020g0192a0001c0001t0027g0036others(119): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.459+14360C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523747 | ||||||
chr6:147523778
|
G | T | 1 | a0001c0001t0083g0234 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.459+14391G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523778 | ||||||
chr6:147523863
|
C | T | 18 | a0001c0001t0003g0060a0001c0001t0011g0279a0001c0001t0011g0281others(15): Show | 18 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.459+14476C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523863 | ||||||
chr6:147523864
|
G | A | 1 | a0005c0007t0011g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+14477G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523864 | ||||||
chr6:147524170
|
C | T | 155 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0002g0006others(152): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.459+14783C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524170 | ||||||
chr6:147524242
|
C | A | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+14855C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524242 | ||||||
chr6:147524252
|
G | C | 153 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0002g0006others(150): Show | 158 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.459+14865G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524252 | ||||||
chr6:147524419
|
G | GT | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+15034dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147524419 | |||||
chr6:147524422
|
G | GT | 26 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0002g0006others(23): Show | 28 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.459+15047dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147524422 | |||||
chr6:147524422
|
G | T | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+15035G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524422 | ||||||
chr6:147524480
|
C | T | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+15093C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524480 | ||||||
chr6:147524540
|
ACTT | A | 4 | a0001c0001t0011g0279a0001c0001t0020g0152a0001c0001t0105g0194others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+15161_459+1516 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147524540 | |||||
chr6:147524563
|
G | A | 2 | a0001c0002t0008g0138a0001c0002t0008g0139 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.459+15176G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524563 | ||||||
chr6:147524637
|
A | C | 153 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0002g0006others(150): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+15250A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524637 | ||||||
chr6:147524690
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+15303C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524690 | ||||||
chr6:147525025
|
G | A | 24 | a0001c0001t0012g0344a0002c0003t0001g0016a0002c0003t0001g0021others(21): Show | 25 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.459+15638G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525025 | ||||||
chr6:147525111
|
A | G | 162 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0185others(159): Show | 168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.459+15724A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525111 | ||||||
chr6:147525439
|
A | G | 182 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(179): Show | 189 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.459+16052A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525439 | ||||||
chr6:147525513
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+16126C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525513 | ||||||
chr6:147525624
|
G | A | 6 | a0001c0002t0007g0096a0001c0002t0007g0099a0001c0002t0007g0147others(3): Show | 6 | HG02027.hp2 HG02135.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+16237G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525624 | ||||||
chr6:147525933
|
A | G | 3 | a0003c0004t0020g0077a0003c0004t0078g0076a0003c0004t0107g0069 | 3 | HG02109.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.459+16546A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525933 | ||||||
chr6:147525965
|
G | T | 19 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0023others(16): Show | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+16578G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525965 | ||||||
chr6:147526024
|
A | C | 2 | a0002c0003t0001g0023a0002c0003t0073g0020 | 2 | HG01071.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.459+16637A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526024 | ||||||
chr6:147526099
|
G | A | 1 | a0001c0001t0098g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.459+16712G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526099 | ||||||
chr6:147526240
|
A | G | 8 | a0001c0001t0002g0230a0001c0001t0002g0232a0001c0001t0002g0265others(5): Show | 8 | HG00558.hp2 HG00597.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+16853A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526240 | ||||||
chr6:147526254
|
C | T | 1 | a0001c0002t0025g0341 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459+16867C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526254 | ||||||
chr6:147526279
|
T | C | 1 | a0001c0001t0017g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.459+16892T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526279 | ||||||
chr6:147526387
|
C | T | 148 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(145): Show | 154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.459+17000C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526387 | ||||||
chr6:147526416
|
T | C | 19 | a0001c0001t0027g0036a0001c0001t0086g0061a0001c0001t0099g0062others(16): Show | 19 | HG01081.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.459+17029T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526416 | ||||||
chr6:147526453
|
A | G | 16 | a0002c0003t0001g0016a0002c0003t0001g0021a0002c0003t0001g0031others(13): Show | 17 | HG00323.hp2 HG00609.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+17066A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526453 | ||||||
chr6:147526466
|
C | T | 1 | a0001c0001t0099g0062 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.459+17079C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526466 | ||||||
chr6:147526533
|
T | C | 7 | a0001c0002t0004g0161a0001c0002t0007g0105a0001c0002t0007g0153others(4): Show | 7 | HG01069.hp2 HG01243.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+17146T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526533 | ||||||
chr6:147526562
|
G | A | 17 | a0001c0001t0002g0337a0002c0003t0001g0016a0002c0003t0001g0021others(14): Show | 18 | HG00323.hp2 HG00609.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.459+17175G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526562 | ||||||
chr6:147526582
|
G | A | 77 | a0001c0001t0001g0038a0001c0001t0001g0251a0001c0001t0002g0250others(74): Show | 80 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.459+17195G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526582 | ||||||
chr6:147526610
|
T | C | 1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.459+17223T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526610 | ||||||
chr6:147526752
|
C | A | 6 | a0001c0001t0002g0337a0002c0003t0001g0016a0002c0003t0002g0017others(3): Show | 7 | HG02155.hp1 NA18612.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+17365C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526752 | ||||||
chr6:147526770
|
C | T | 1 | a0001c0002t0041g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.459+17383C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526770 | ||||||
chr6:147526803
|
C | T | 1 | a0002c0003t0001g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.459+17416C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526803 | ||||||
chr6:147526819
|
G | GACAGTAG others(11): Show |
18 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0190others(15): Show | 20 | HG00323.hp2 HG01074.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+17433_459+1743 others(22): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147526819 | |||||
chr6:147526855
|
A | C | 10 | a0001c0001t0002g0337a0001c0001t0100g0227a0002c0003t0001g0016others(7): Show | 11 | HG00323.hp2 HG02056.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.459+17468A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526855 | ||||||
chr6:147527082
|
T | C | 38 | a0001c0001t0001g0038a0001c0001t0003g0255a0001c0001t0003g0336others(35): Show | 38 | HG00733.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.459+17695T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527082 | ||||||
chr6:147527136
|
A | G | 3 | a0001c0002t0004g0129a0001c0002t0004g0130a0003c0004t0016g0071 | 3 | HG02895.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+17749A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527136 | ||||||
chr6:147527148
|
C | T | 1 | a0001c0001t0017g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.459+17761C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527148 | ||||||
chr6:147527225
|
A | G | 37 | a0001c0001t0001g0184a0001c0001t0001g0225a0001c0001t0003g0060others(34): Show | 37 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.459+17838A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527225 | ||||||
chr6:147527548
|
G | A | 1 | a0001c0002t0008g0340 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.459+18161G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527548 | ||||||
chr6:147527575
|
G | C | 19 | a0001c0001t0001g0005a0001c0001t0027g0036a0001c0001t0028g0253others(16): Show | 20 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+18188G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527575 | ||||||
chr6:147527624
|
A | G | 106 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0183others(103): Show | 110 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.459+18237A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527624 | ||||||
chr6:147527631
|
T | C | 296 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(293): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.459+18244T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527631 | ||||||
chr6:147527675
|
C | A | 1 | a0001c0002t0004g0155 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.459+18288C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527675 | ||||||
chr6:147527804
|
G | GT | 17 | a0001c0001t0011g0208a0001c0001t0011g0209a0001c0001t0011g0281others(14): Show | 17 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+18425dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147527804 | |||||
chr6:147527847
|
T | C | 1 | a0001c0001t0094g0210 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.459+18460T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527847 | ||||||
chr6:147527949
|
G | C | 6 | a0001c0001t0027g0036a0001c0001t0028g0297a0001c0001t0082g0243others(3): Show | 6 | HG02723.hp2 HG02818.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+18562G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527949 | ||||||
chr6:147527958
|
A | G | 1 | a0001c0002t0004g0093 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.459+18571A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527958 | ||||||
chr6:147527985
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0191a0001c0001t0001g0198others(9): Show | 13 | HG00280.hp1 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+18598G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527985 | ||||||
chr6:147528145
|
A | G | 176 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0052others(173): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.459+18758A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528145 | ||||||
chr6:147528227
|
C | G | 107 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0256others(104): Show | 110 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.459+18840C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528227 | ||||||
chr6:147528274
|
C | T | 105 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0256others(102): Show | 108 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.459+18887C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528274 | ||||||
chr6:147528357
|
C | T | 1 | a0001c0002t0060g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.459+18970C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528357 | ||||||
chr6:147528373
|
C | T | 30 | a0001c0001t0001g0256a0001c0001t0003g0060a0001c0001t0003g0299others(27): Show | 30 | HG00609.hp2 HG02040.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+18986C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528373 | ||||||
chr6:147528479
|
G | T | 2 | a0001c0002t0008g0342a0005c0007t0011g0090 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459+19092G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528479 | ||||||
chr6:147528573
|
T | C | 1 | a0001c0001t0017g0007 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.459+19186T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528573 | ||||||
chr6:147528905
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0027g0036a0001c0001t0028g0253others(16): Show | 20 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+19518T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528905 | ||||||
chr6:147528937
|
A | G | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+19550A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528937 | ||||||
chr6:147529014
|
T | C | 21 | a0001c0001t0001g0005a0001c0001t0027g0036a0001c0001t0028g0253others(18): Show | 22 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+19627T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529014 | ||||||
chr6:147529112
|
A | G | 3 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0100g0227 | 3 | HG02132.hp2 NA18984.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.459+19725A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529112 | ||||||
chr6:147529145
|
G | A | 1 | a0001c0002t0004g0100 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.459+19758G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529145 | ||||||
chr6:147529232
|
T | G | 315 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(312): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.459+19845T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529232 | ||||||
chr6:147529293
|
T | C | 1 | a0002c0003t0001g0021 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.459+19906T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529293 | ||||||
chr6:147529397
|
C | T | 6 | a0001c0001t0003g0060a0001c0001t0029g0144a0001c0001t0086g0061others(3): Show | 6 | HG01884.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+20010C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529397 | ||||||
chr6:147529416
|
T | G | 2 | a0001c0001t0086g0061a0001c0002t0022g0167 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.459+20029T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529416 | ||||||
chr6:147529461
|
G | A | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+20074G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529461 | ||||||
chr6:147529500
|
C | T | 1 | a0002c0003t0001g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.459+20113C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529500 | ||||||
chr6:147529598
|
G | T | 2 | a0001c0001t0001g0224a0001c0002t0041g0128 | 2 | HG02129.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.459+20211G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529598 | ||||||
chr6:147529628
|
A | C | 4 | a0001c0001t0027g0036a0001c0001t0028g0297a0001c0002t0008g0340others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+20241A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529628 | ||||||
chr6:147529650
|
T | C | 1 | a0001c0002t0010g0177 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.459+20263T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529650 | ||||||
chr6:147529846
|
G | A | 8 | a0001c0001t0003g0186a0001c0001t0003g0228a0001c0001t0003g0229others(5): Show | 9 | NA18612.hp2 NA18939.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+20459G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529846 | ||||||
chr6:147529855
|
A | G | 246 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0051others(243): Show | 258 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.459+20468A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529855 | ||||||
chr6:147529949
|
A | C | 2 | a0001c0002t0008g0342a0005c0007t0011g0090 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459+20562A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529949 | ||||||
chr6:147530010
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.459+20623T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530010 | ||||||
chr6:147530085
|
T | A | 1 | a0001c0001t0081g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.459+20698T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530085 | ||||||
chr6:147530087
|
T | C | 14 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0002g0337others(11): Show | 15 | HG02132.hp2 HG02155.hp1 HG04204.hp2 others(12): Show |
intron_variant | MODIFIER | c.459+20700T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530087 | ||||||
chr6:147530155
|
G | A | 267 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0051others(264): Show | 279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.459+20768G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530155 | ||||||
chr6:147530314
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0028g0253a0001c0001t0106g0058others(9): Show | 13 | HG01891.hp2 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+20927C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530314 | ||||||
chr6:147530363
|
C | T | 7 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0011g0197others(4): Show | 7 | HG01891.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+20976C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530363 | ||||||
chr6:147530399
|
G | A | 2 | a0001c0001t0003g0011a0001c0002t0010g0097 | 3 | NA18943.hp2 NA18964.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.459+21012G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530399 | ||||||
chr6:147530406
|
C | G | 1 | a0001c0001t0003g0287 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.459+21019C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530406 | ||||||
chr6:147530442
|
T | C | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.459+21055T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530442 | ||||||
chr6:147530494
|
C | G | 3 | a0001c0001t0092g0217a0001c0002t0004g0176a0002c0003t0001g0021 | 3 | HG00280.hp2 HG00323.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.459+21107C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530494 | ||||||
chr6:147530599
|
C | T | 2 | a0001c0002t0008g0342a0005c0007t0011g0090 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459+21212C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530599 | ||||||
chr6:147530679
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0106g0058a0001c0002t0004g0129others(8): Show | 12 | HG01891.hp2 HG02451.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+21292C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530679 | ||||||
chr6:147530838
|
T | G | 75 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0266others(72): Show | 78 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.459+21451T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530838 | ||||||
chr6:147531032
|
C | A | 13 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0003g0186others(10): Show | 14 | HG02132.hp2 HG04204.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.459+21645C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531032 | ||||||
chr6:147531155
|
GT | G | 7 | a0001c0001t0020g0192a0001c0001t0102g0333a0001c0001t0105g0194others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+21784delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147531155 | |||||
chr6:147531155
|
GTT | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0256a0001c0001t0001g0291others(59): Show | 64 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.459+21783_459+2178 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147531155 | |||||
chr6:147531155
|
GTTT | G | 222 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0051others(219): Show | 234 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.459+21782_459+2178 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147531155 | |||||
chr6:147531162
|
T | G | 2 | a0001c0001t0002g0269a0001c0002t0007g0105 | 2 | HG01255.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.459+21775T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531162 | ||||||
chr6:147531561
|
G | A | 129 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0183others(126): Show | 135 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.459+22174G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531561 | ||||||
chr6:147531841
|
C | T | 2 | a0001c0001t0029g0144a0003c0004t0020g0077 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459+22454C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531841 | ||||||
chr6:147531913
|
A | G | 2 | a0001c0002t0004g0127a0002c0003t0001g0032 | 2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.459+22526A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531913 | ||||||
chr6:147532014
|
T | A | 2 | a0001c0001t0005g0307a0001c0001t0005g0308 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.459+22627T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532014 | ||||||
chr6:147532279
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.459+22892C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532279 | ||||||
chr6:147532281
|
C | T | 6 | a0001c0001t0106g0058a0001c0002t0042g0131a0001c0002t0069g0107others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+22894C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532281 | ||||||
chr6:147532303
|
C | G | 5 | a0001c0001t0003g0060a0001c0001t0029g0144a0001c0002t0059g0079others(2): Show | 5 | HG02965.hp2 HG03139.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+22916C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532303 | ||||||
chr6:147532329
|
T | G | 3 | a0001c0001t0001g0005a0001c0002t0004g0129a0001c0002t0004g0130 | 4 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+22942T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532329 | ||||||
chr6:147532856
|
G | A | 1 | a0001c0002t0010g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459+23469G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532856 | ||||||
chr6:147532951
|
T | A | 1 | a0001c0001t0017g0007 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.459+23564T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532951 | ||||||
chr6:147532995
|
A | G | 18 | a0001c0001t0001g0256a0001c0001t0009g0039a0001c0001t0009g0066others(15): Show | 18 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.459+23608A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532995 | ||||||
chr6:147533136
|
A | G | 16 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(13): Show | 16 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.459+23749A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533136 | ||||||
chr6:147533165
|
C | T | 1 | a0001c0001t0076g0233 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.459+23778C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533165 | ||||||
chr6:147533330
|
C | T | 18 | a0001c0001t0001g0256a0001c0001t0009g0039a0001c0001t0009g0066others(15): Show | 18 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.459+23943C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533330 | ||||||
chr6:147533447
|
A | C | 1 | a0001c0002t0045g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.459+24060A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533447 | ||||||
chr6:147533462
|
C | CA | 90 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0266others(87): Show | 94 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.459+24093dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147533462 | |||||
chr6:147533462
|
CA | C | 73 | a0001c0001t0001g0256a0001c0001t0003g0060a0001c0001t0003g0064others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.459+24093delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147533462 | |||||
chr6:147533477
|
A | G | 9 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+24090A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533477 | ||||||
chr6:147533553
|
T | C | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.459+24166T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533553 | ||||||
chr6:147533587
|
C | T | 3 | a0001c0001t0086g0061a0001c0002t0022g0167a0001c0002t0025g0341 | 3 | HG01884.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.459+24200C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533587 | ||||||
chr6:147533991
|
C | G | 1 | a0001c0001t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.459+24604C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533991 | ||||||
chr6:147534300
|
C | T | 1 | a0001c0001t0006g0207 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.459+24913C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534300 | ||||||
chr6:147534350
|
A | T | 192 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(189): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.459+24963A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534350 | ||||||
chr6:147534406
|
C | G | 6 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0001t0102g0333others(3): Show | 6 | HG02132.hp2 HG03209.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+25019C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534406 | ||||||
chr6:147534443
|
G | A | 7 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+25056G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534443 | ||||||
chr6:147534487
|
C | T | 5 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0001t0102g0333others(2): Show | 5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25100C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534487 | ||||||
chr6:147534488
|
A | G | 5 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0001t0102g0333others(2): Show | 5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25101A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534488 | ||||||
chr6:147534512
|
A | G | 5 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0001t0102g0333others(2): Show | 5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25125A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534512 | ||||||
chr6:147534617
|
T | C | 1 | a0001c0001t0017g0007 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.459+25230T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534617 | ||||||
chr6:147534712
|
T | G | 5 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0001t0102g0333others(2): Show | 5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25325T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534712 | ||||||
chr6:147534790
|
G | C | 5 | a0001c0001t0002g0258a0001c0001t0009g0053a0001c0001t0009g0057others(2): Show | 5 | HG00408.hp2 HG00423.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+25403G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534790 | ||||||
chr6:147535235
|
G | C | 314 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(311): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.459+25848G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535235 | ||||||
chr6:147535241
|
G | A | 2 | a0001c0001t0011g0279a0001c0001t0012g0033 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.459+25854G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535241 | ||||||
chr6:147535375
|
A | G | 17 | a0001c0001t0001g0256a0001c0001t0009g0039a0001c0001t0009g0066others(14): Show | 17 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+25988A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535375 | ||||||
chr6:147535376
|
A | T | 192 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(189): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.459+25989A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535376 | ||||||
chr6:147535409
|
T | C | 13 | a0001c0001t0011g0197a0001c0001t0011g0208a0001c0001t0011g0209others(10): Show | 13 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+26022T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535409 | ||||||
chr6:147535721
|
C | T | 8 | a0001c0001t0095g0074a0001c0001t0106g0058a0001c0002t0008g0174others(5): Show | 8 | HG02451.hp2 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+26334C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535721 | ||||||
chr6:147535898
|
C | T | 1 | a0001c0001t0005g0216 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.459+26511C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535898 | ||||||
chr6:147536205
|
A | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(218): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.459+26818A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536205 | ||||||
chr6:147536263
|
G | A | 2 | a0001c0002t0008g0150a0001c0002t0008g0340 | 2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.459+26876G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536263 | ||||||
chr6:147536383
|
G | A | 185 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(182): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.459+26996G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536383 | ||||||
chr6:147536474
|
A | T | 223 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(220): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.459+27087A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536474 | ||||||
chr6:147536531
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.459+27144G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536531 | ||||||
chr6:147536560
|
T | G | 1 | a0001c0002t0010g0177 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.459+27173T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536560 | ||||||
chr6:147536627
|
C | G | 1 | a0001c0001t0102g0333 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.459+27240C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536627 | ||||||
chr6:147536826
|
C | T | 21 | a0001c0001t0011g0197a0001c0001t0011g0208a0001c0001t0011g0209others(18): Show | 21 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.459+27439C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536826 | ||||||
chr6:147536866
|
A | G | 1 | a0004c0005t0029g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.459+27479A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536866 | ||||||
chr6:147537039
|
A | C | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-27355A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537039 | ||||||
chr6:147537103
|
A | T | 1 | a0001c0001t0001g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.460-27291A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537103 | ||||||
chr6:147537107
|
C | A | 5 | a0001c0001t0027g0036a0001c0001t0086g0061a0001c0002t0022g0086others(2): Show | 5 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-27287C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537107 | ||||||
chr6:147537168
|
A | T | 2 | a0001c0002t0004g0108a0001c0002t0004g0109 | 2 | NA18995.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.460-27226A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537168 | ||||||
chr6:147537430
|
C | A | 1 | a0001c0001t0009g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.460-26964C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537430 | ||||||
chr6:147537567
|
C | A | 8 | a0001c0001t0011g0279a0001c0001t0012g0033a0001c0001t0106g0058others(5): Show | 8 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.460-26827C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537567 | ||||||
chr6:147537567
|
C | T | 12 | a0001c0001t0009g0039a0001c0001t0009g0066a0001c0001t0009g0200others(9): Show | 12 | HG00609.hp2 HG02040.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-26827C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537567 | ||||||
chr6:147537584
|
C | T | 186 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(183): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.460-26810C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537584 | ||||||
chr6:147537596
|
C | CA | 184 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(181): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.460-26789dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147537596 | |||||
chr6:147537630
|
T | C | 1 | a0001c0002t0008g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-26764T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537630 | ||||||
chr6:147537636
|
C | T | 13 | a0001c0001t0001g0266a0001c0001t0011g0279a0001c0001t0012g0033others(10): Show | 13 | HG02132.hp2 HG02572.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.460-26758C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537636 | ||||||
chr6:147537645
|
T | G | 1 | a0001c0002t0010g0163 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.460-26749T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537645 | ||||||
chr6:147537721
|
C | A | 174 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(171): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.460-26673C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537721 | ||||||
chr6:147537755
|
CA | C | 287 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(284): Show | 302 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.460-26625delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147537755 | |||||
chr6:147537755
|
CAA | C | 24 | a0001c0001t0001g0306a0001c0001t0009g0039a0001c0001t0009g0066others(21): Show | 24 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-26626_460-2662 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147537755 | |||||
chr6:147537821
|
A | G | 22 | a0001c0001t0011g0197a0001c0001t0011g0208a0001c0001t0011g0209others(19): Show | 22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-26573A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537821 | ||||||
chr6:147537872
|
T | C | 6 | a0001c0001t0106g0058a0001c0002t0042g0131a0001c0002t0069g0107others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-26522T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537872 | ||||||
chr6:147537962
|
T | C | 2 | a0001c0001t0098g0187a0001c0002t0056g0092 | 2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.460-26432T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537962 | ||||||
chr6:147538073
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.460-26321T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538073 | ||||||
chr6:147538192
|
T | C | 1 | a0001c0002t0023g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.460-26202T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538192 | ||||||
chr6:147538257
|
T | A | 2 | a0001c0001t0009g0066a0001c0001t0009g0200 | 2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.460-26137T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538257 | ||||||
chr6:147538270
|
G | T | 209 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(206): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.460-26124G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538270 | ||||||
chr6:147538349
|
C | G | 22 | a0001c0001t0011g0197a0001c0001t0011g0208a0001c0001t0011g0209others(19): Show | 22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-26045C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538349 | ||||||
chr6:147538377
|
C | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(188): Show | 202 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.460-26017C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538377 | ||||||
chr6:147538462
|
A | G | 22 | a0001c0001t0011g0197a0001c0001t0011g0208a0001c0001t0011g0209others(19): Show | 22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-25932A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538462 | ||||||
chr6:147538512
|
T | G | 164 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(161): Show | 175 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.460-25882T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538512 | ||||||
chr6:147538988
|
G | A | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-25406G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538988 | ||||||
chr6:147539049
|
G | A | 11 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-25345G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539049 | ||||||
chr6:147539057
|
C | A | 8 | a0001c0001t0016g0226a0001c0001t0028g0297a0001c0001t0096g0054others(5): Show | 8 | HG02145.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-25337C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539057 | ||||||
chr6:147539077
|
G | A | 11 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-25317G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539077 | ||||||
chr6:147539274
|
C | CTAT | 200 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(197): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.460-25120_460-2511 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539274 | ||||||
chr6:147539329
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.460-25065A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539329 | ||||||
chr6:147539549
|
C | A | 10 | a0001c0001t0012g0010a0001c0001t0012g0338a0001c0001t0027g0245others(7): Show | 11 | HG00738.hp1 HG01081.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-24845C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539549 | ||||||
chr6:147539658
|
A | C | 7 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0223others(4): Show | 7 | HG00597.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-24736A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539658 | ||||||
chr6:147539702
|
G | GA | 24 | a0001c0001t0009g0039a0001c0001t0009g0066a0001c0001t0009g0200others(21): Show | 24 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-24679dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147539702 | |||||
chr6:147539821
|
T | C | 1 | a0001c0002t0007g0096 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.460-24573T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539821 | ||||||
chr6:147539907
|
C | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(156): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.460-24487C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539907 | ||||||
chr6:147540027
|
A | G | 26 | a0001c0001t0001g0266a0001c0001t0011g0197a0001c0001t0011g0208others(23): Show | 26 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-24367A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540027 | ||||||
chr6:147540077
|
C | CT | 22 | a0001c0001t0011g0197a0001c0001t0011g0208a0001c0001t0011g0209others(19): Show | 22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-24309dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540077 | |||||
chr6:147540161
|
G | A | 10 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-24233G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540161 | ||||||
chr6:147540175
|
TA | T | 8 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-24218delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540175 | ||||||
chr6:147540183
|
A | T | 4 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0002t0004g0127others(1): Show | 4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-24211A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540183 | ||||||
chr6:147540223
|
G | A | 10 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-24171G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540223 | ||||||
chr6:147540767
|
C | CAG | 5 | a0001c0001t0001g0306a0001c0001t0003g0202a0001c0001t0087g0275others(2): Show | 5 | HG02132.hp2 NA18966.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-23618_460-2361 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540767 | |||||
chr6:147540777
|
G | GA | 309 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(306): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.460-23617_460-2361 others(5): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540777 | ||||||
chr6:147540784
|
G | T | 2 | a0001c0006t0015g0140a0001c0006t0015g0141 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.460-23610G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540784 | ||||||
chr6:147540843
|
C | T | 1 | a0001c0002t0008g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-23551C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540843 | ||||||
chr6:147540903
|
C | T | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-23491C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540903 | ||||||
chr6:147540931
|
G | A | 7 | a0001c0001t0029g0144a0001c0001t0106g0058a0001c0002t0042g0131others(4): Show | 7 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-23463G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540931 | ||||||
chr6:147540933
|
G | GT | 66 | a0001c0001t0001g0183a0001c0001t0001g0283a0001c0001t0002g0006others(63): Show | 70 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.460-23434dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | |||||
chr6:147540933
|
G | GTT | 67 | a0001c0001t0001g0038a0001c0001t0001g0293a0001c0001t0001g0312others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.460-23435_460-2343 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | |||||
chr6:147540933
|
GT | G | 86 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0184others(83): Show | 89 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.460-23434delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | |||||
chr6:147540933
|
GTT | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0190others(67): Show | 78 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.460-23435_460-2343 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | |||||
chr6:147540933
|
GTTT | G | 9 | a0001c0001t0001g0256a0001c0001t0020g0152a0001c0001t0029g0144others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-23436_460-2343 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | |||||
chr6:147540933
|
GTTTT | G | 12 | a0001c0001t0012g0344a0001c0001t0020g0192a0001c0001t0096g0054others(9): Show | 12 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-23437_460-2343 others(8): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | |||||
chr6:147540941
|
T | A | 4 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0002t0004g0127others(1): Show | 4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-23453T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540941 | ||||||
chr6:147540941
|
T | G | 3 | a0001c0001t0020g0152a0001c0002t0036g0132a0003c0004t0107g0069 | 3 | HG02055.hp2 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.460-23453T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540941 | ||||||
chr6:147540942
|
T | G | 15 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(12): Show | 15 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-23452T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540942 | ||||||
chr6:147540943
|
T | G | 12 | a0001c0001t0012g0344a0001c0001t0020g0192a0001c0001t0096g0054others(9): Show | 12 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-23451T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540943 | ||||||
chr6:147540944
|
T | A | 4 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0002t0004g0127others(1): Show | 4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-23450T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540944 | ||||||
chr6:147540944
|
T | TG | 2 | a0001c0001t0003g0011a0001c0002t0010g0097 | 3 | NA18943.hp2 NA18964.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.460-23450_460-2344 others(5): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540944 | ||||||
chr6:147540945
|
T | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-23449T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540945 | ||||||
chr6:147541021
|
C | T | 1 | a0001c0002t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.460-23373C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541021 | ||||||
chr6:147541230
|
G | A | 15 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(12): Show | 15 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-23164G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541230 | ||||||
chr6:147541232
|
A | G | 15 | a0001c0001t0012g0344a0001c0001t0020g0152a0001c0001t0020g0192others(12): Show | 15 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-23162A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541232 | ||||||
chr6:147541338
|
G | T | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-23056G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541338 | ||||||
chr6:147541390
|
C | T | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-23004C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541390 | ||||||
chr6:147541498
|
C | T | 2 | a0001c0001t0005g0235a0001c0002t0023g0088 | 2 | HG01169.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.460-22896C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541498 | ||||||
chr6:147541499
|
G | A | 1 | a0001c0001t0005g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.460-22895G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541499 | ||||||
chr6:147541577
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0002g0304a0001c0001t0002g0305 | 3 | HG00621.hp1 NA19007.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.460-22817G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541577 | ||||||
chr6:147541685
|
T | C | 1 | a0001c0002t0008g0342 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.460-22709T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541685 | ||||||
chr6:147541687
|
C | T | 1 | a0001c0002t0024g0162 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.460-22707C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541687 | ||||||
chr6:147541704
|
G | A | 5 | a0001c0001t0002g0335a0001c0001t0003g0231a0001c0001t0003g0296others(2): Show | 5 | NA18939.hp1 NA18963.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-22690G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541704 | ||||||
chr6:147541810
|
T | C | 1 | a0001c0001t0002g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.460-22584T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541810 | ||||||
chr6:147541852
|
T | A | 4 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0002t0004g0127others(1): Show | 4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-22542T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541852 | ||||||
chr6:147541968
|
C | A | 2 | a0001c0001t0096g0054a0001c0006t0053g0142 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.460-22426C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541968 | ||||||
chr6:147541997
|
G | A | 27 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0009g0039others(24): Show | 27 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-22397G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541997 | ||||||
chr6:147542079
|
A | G | 1 | a0001c0001t0098g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.460-22315A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542079 | ||||||
chr6:147542109
|
G | A | 3 | a0001c0001t0097g0065a0001c0002t0010g0163a0001c0002t0057g0169 | 3 | HG00140.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.460-22285G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542109 | ||||||
chr6:147542232
|
A | C | 1 | a0001c0001t0006g0326 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.460-22162A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542232 | ||||||
chr6:147542257
|
C | G | 1 | a0001c0001t0098g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.460-22137C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542257 | ||||||
chr6:147542315
|
C | T | 2 | a0001c0001t0002g0319a0001c0002t0007g0116 | 2 | HG00408.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.460-22079C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542315 | ||||||
chr6:147542317
|
C | T | 2 | a0001c0001t0005g0322a0001c0002t0013g0123 | 2 | NA18944.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.460-22077C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542317 | ||||||
chr6:147542362
|
G | A | 128 | a0001c0001t0001g0225a0001c0001t0001g0283a0001c0001t0001g0293others(125): Show | 133 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.460-22032G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542362 | ||||||
chr6:147542524
|
G | A | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-21870G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542524 | ||||||
chr6:147542567
|
A | T | 4 | a0001c0001t0011g0279a0001c0001t0012g0033a0001c0001t0095g0074others(1): Show | 4 | HG02572.hp1 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-21827A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542567 | ||||||
chr6:147542599
|
C | T | 35 | a0001c0001t0001g0225a0001c0001t0002g0286a0001c0001t0003g0064others(32): Show | 35 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.460-21795C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542599 | ||||||
chr6:147542620
|
G | A | 27 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0009g0039others(24): Show | 27 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-21774G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542620 | ||||||
chr6:147542789
|
C | T | 3 | a0001c0001t0011g0279a0001c0001t0012g0033a0001c0001t0113g0151 | 3 | HG02572.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.460-21605C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542789 | ||||||
chr6:147543040
|
TC | T | 6 | a0001c0001t0029g0144a0001c0001t0106g0058a0001c0002t0042g0131others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-21350delC | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147543040 | |||||
chr6:147543071
|
T | C | 1 | a0001c0001t0005g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.460-21323T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543071 | ||||||
chr6:147543164
|
A | C | 238 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(235): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.460-21230A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543164 | ||||||
chr6:147543271
|
C | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-21123C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543271 | ||||||
chr6:147543283
|
G | A | 235 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(232): Show | 250 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.460-21111G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543283 | ||||||
chr6:147543358
|
A | C | 2 | a0001c0001t0095g0074a0001c0001t0103g0241 | 2 | HG02922.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.460-21036A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543358 | ||||||
chr6:147543526
|
A | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(236): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.460-20868A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543526 | ||||||
chr6:147543864
|
T | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(291): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.460-20530T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543864 | ||||||
chr6:147543911
|
G | A | 6 | a0001c0001t0029g0144a0001c0001t0106g0058a0001c0002t0042g0131others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-20483G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543911 | ||||||
chr6:147544061
|
C | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-20333C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544061 | ||||||
chr6:147544063
|
T | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-20331T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544063 | ||||||
chr6:147544106
|
T | A | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-20288T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544106 | ||||||
chr6:147544387
|
A | C | 3 | a0001c0001t0097g0065a0001c0002t0010g0163a0001c0002t0057g0169 | 3 | HG00140.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.460-20007A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544387 | ||||||
chr6:147544685
|
G | A | 303 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(300): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.460-19709G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544685 | ||||||
chr6:147544694
|
C | T | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-19700C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544694 | ||||||
chr6:147544778
|
G | A | 2 | a0001c0002t0008g0110a0001c0002t0008g0111 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.460-19616G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544778 | ||||||
chr6:147544807
|
T | C | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-19587T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544807 | ||||||
chr6:147544840
|
T | C | 1 | a0001c0002t0014g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.460-19554T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544840 | ||||||
chr6:147545076
|
G | C | 9 | a0001c0001t0011g0279a0001c0001t0012g0033a0001c0001t0029g0144others(6): Show | 9 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-19318G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545076 | ||||||
chr6:147545088
|
C | T | 34 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0009g0039others(31): Show | 34 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.460-19306C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545088 | ||||||
chr6:147545299
|
C | T | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-19095C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545299 | ||||||
chr6:147545480
|
T | C | 307 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(304): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.460-18914T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545480 | ||||||
chr6:147545562
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.460-18832G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545562 | ||||||
chr6:147545566
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.460-18828C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545566 | ||||||
chr6:147545690
|
A | T | 3 | a0001c0002t0008g0150a0001c0002t0008g0181a0001c0002t0008g0340 | 3 | HG02818.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.460-18704A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545690 | ||||||
chr6:147546017
|
T | C | 2 | a0001c0001t0001g0242a0001c0001t0080g0268 | 2 | NA19010.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.460-18377T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546017 | ||||||
chr6:147546259
|
G | T | 2 | a0001c0001t0003g0060a0001c0001t0028g0253 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.460-18135G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546259 | ||||||
chr6:147546306
|
G | T | 1 | a0001c0001t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.460-18088G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546306 | ||||||
chr6:147546356
|
C | T | 3 | a0001c0002t0004g0089a0001c0002t0068g0067a0003c0004t0016g0072 | 3 | HG01891.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.460-18038C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546356 | ||||||
chr6:147546393
|
G | C | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-18001G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546393 | ||||||
chr6:147546399
|
G | A | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-17995G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546399 | ||||||
chr6:147546406
|
T | G | 1 | a0001c0001t0087g0275 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.460-17988T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546406 | ||||||
chr6:147546466
|
T | G | 308 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(305): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.460-17928T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546466 | ||||||
chr6:147546471
|
G | A | 2 | a0001c0001t0020g0192a0001c0002t0026g0087 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.460-17923G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546471 | ||||||
chr6:147546530
|
C | CAAAAAAA | 22 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0012g0264others(19): Show | 22 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-17857_460-1785 others(11): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | |||||
chr6:147546530
|
C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0185a0001c0001t0009g0057a0001c0001t0009g0066others(12): Show | 15 | HG01081.hp1 HG02040.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-17858_460-1785 others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | |||||
chr6:147546530
|
C | CAAAAAAA others(2): Show |
24 | a0001c0001t0001g0266a0001c0001t0003g0284a0001c0001t0005g0313others(21): Show | 24 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-17859_460-1785 others(13): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | |||||
chr6:147546530
|
C | CAAAAAAA others(3): Show |
231 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(228): Show | 245 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.460-17860_460-1785 others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | |||||
chr6:147546530
|
C | CAAAAAAA others(4): Show |
12 | a0001c0001t0001g0302a0001c0001t0002g0290a0001c0001t0005g0317others(9): Show | 13 | HG00140.hp1 HG01975.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.460-17861_460-1785 others(15): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | |||||
chr6:147546541
|
A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0312a0001c0002t0007g0122 | 2 | HG02027.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.460-17851_460-1785 others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546541 | |||||
chr6:147546574
|
T | C | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-17820T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546574 | ||||||
chr6:147546635
|
C | G | 303 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(300): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.460-17759C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546635 | ||||||
chr6:147546684
|
C | A | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-17710C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546684 | ||||||
chr6:147546698
|
T | C | 1 | a0001c0001t0091g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.460-17696T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546698 | ||||||
chr6:147547478
|
A | G | 6 | a0001c0001t0029g0144a0001c0001t0106g0058a0001c0002t0042g0131others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-16916A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547478 | ||||||
chr6:147547483
|
CT | C | 347 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(344): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.460-16909delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147547483 | |||||
chr6:147547520
|
C | T | 245 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(242): Show | 260 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.460-16874C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547520 | ||||||
chr6:147547553
|
G | C | 6 | a0001c0001t0029g0144a0001c0001t0106g0058a0001c0002t0042g0131others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-16841G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547553 | ||||||
chr6:147547586
|
T | C | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-16808T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547586 | ||||||
chr6:147547649
|
C | T | 8 | a0001c0001t0002g0035a0001c0001t0002g0230a0001c0001t0002g0289others(5): Show | 8 | HG01255.hp2 HG02155.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-16745C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547649 | ||||||
chr6:147547674
|
T | C | 5 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0001t0102g0333others(2): Show | 5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-16720T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547674 | ||||||
chr6:147547698
|
C | A | 3 | a0001c0001t0005g0218a0001c0001t0005g0276a0001c0002t0054g0154 | 3 | HG00733.hp2 HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.460-16696C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547698 | ||||||
chr6:147547998
|
A | G | 1 | a0003c0004t0110g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.460-16396A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547998 | ||||||
chr6:147548043
|
T | G | 249 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(246): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.460-16351T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548043 | ||||||
chr6:147548101
|
A | G | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-16293A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548101 | ||||||
chr6:147548112
|
TATA | T | 38 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0185others(35): Show | 38 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.460-16275_460-1627 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147548112 | |||||
chr6:147548147
|
G | A | 264 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(261): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.460-16247G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548147 | ||||||
chr6:147548655
|
T | C | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-15739T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548655 | ||||||
chr6:147548922
|
A | G | 3 | a0001c0001t0011g0279a0001c0001t0012g0033a0001c0001t0113g0151 | 3 | HG02572.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.460-15472A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548922 | ||||||
chr6:147549095
|
T | C | 1 | a0001c0002t0065g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.460-15299T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549095 | ||||||
chr6:147549115
|
A | C | 252 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(249): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.460-15279A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549115 | ||||||
chr6:147549264
|
G | C | 1 | a0001c0001t0089g0044 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.460-15130G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549264 | ||||||
chr6:147549370
|
G | A | 38 | a0001c0001t0001g0038a0001c0001t0001g0183a0001c0001t0001g0185others(35): Show | 38 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.460-15024G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549370 | ||||||
chr6:147549558
|
T | C | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-14836T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549558 | ||||||
chr6:147549859
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.460-14535C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549859 | ||||||
chr6:147549889
|
G | C | 237 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(234): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.460-14505G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549889 | ||||||
chr6:147549937
|
C | T | 2 | a0001c0001t0096g0054a0001c0006t0053g0142 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.460-14457C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549937 | ||||||
chr6:147550101
|
T | C | 252 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(249): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.460-14293T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550101 | ||||||
chr6:147550234
|
G | A | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-14160G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550234 | ||||||
chr6:147550398
|
A | G | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13996A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550398 | ||||||
chr6:147550528
|
T | C | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13866T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550528 | ||||||
chr6:147550548
|
T | C | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-13846T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550548 | ||||||
chr6:147550709
|
C | CA | 307 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(304): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.460-13683dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147550709 | |||||
chr6:147550768
|
A | T | 252 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(249): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.460-13626A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550768 | ||||||
chr6:147550868
|
G | A | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13526G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550868 | ||||||
chr6:147550900
|
T | TTA | 251 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(248): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.460-13481_460-1348 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147550900 | |||||
chr6:147550991
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0100g0227a0001c0002t0004g0127others(1): Show | 4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-13403T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550991 | ||||||
chr6:147551012
|
G | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(242): Show | 260 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.460-13382G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551012 | ||||||
chr6:147551045
|
G | A | 247 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0051others(244): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.460-13349G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551045 | ||||||
chr6:147551080
|
A | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0225a0001c0001t0001g0283others(173): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.460-13314A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551080 | ||||||
chr6:147551138
|
A | G | 3 | a0001c0001t0097g0065a0001c0002t0010g0163a0001c0002t0057g0169 | 3 | HG00140.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.460-13256A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551138 | ||||||
chr6:147551151
|
G | C | 7 | a0001c0001t0029g0144a0001c0001t0104g0244a0001c0001t0106g0058others(4): Show | 7 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-13243G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551151 | ||||||
chr6:147551158
|
G | A | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13236G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551158 | ||||||
chr6:147551174
|
A | G | 328 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(325): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.460-13220A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551174 | ||||||
chr6:147551176
|
T | G | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13218T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551176 | ||||||
chr6:147551350
|
C | A | 188 | a0001c0001t0001g0225a0001c0001t0001g0266a0001c0001t0001g0293others(185): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.460-13044C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551350 | ||||||
chr6:147551485
|
AC | A | 3 | a0001c0001t0106g0058a0001c0002t0023g0082a0003c0004t0110g0070 | 3 | HG02559.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.460-12907delC | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551485 | |||||
chr6:147551643
|
G | A | 306 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(303): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.460-12751G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551643 | ||||||
chr6:147551734
|
T | A | 2 | a0001c0001t0005g0322a0001c0002t0013g0123 | 2 | NA18944.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.460-12660T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551734 | ||||||
chr6:147551747
|
G | A | 6 | a0001c0001t0029g0144a0001c0001t0106g0058a0001c0002t0042g0131others(3): Show | 6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-12647G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551747 | ||||||
chr6:147551812
|
T | TTATA | 10 | a0001c0001t0001g0038a0001c0001t0001g0185a0001c0001t0001g0283others(7): Show | 11 | HG00558.hp1 HG02683.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-12560_460-1255 others(8): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATA | 16 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0302others(13): Show | 17 | HG01192.hp1 HG01261.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.460-12562_460-1255 others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(1): Show |
47 | a0001c0001t0001g0009a0001c0001t0001g0184a0001c0001t0001g0190others(44): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.460-12564_460-1255 others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(3): Show |
22 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(19): Show | 23 | HG01891.hp2 HG02040.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.460-12566_460-1255 others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(5): Show |
10 | a0001c0001t0001g0266a0001c0001t0002g0056a0001c0001t0002g0265others(7): Show | 10 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-12568_460-1255 others(16): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(7): Show |
5 | a0001c0001t0001g0291a0001c0002t0004g0084a0001c0002t0004g0171others(2): Show | 5 | HG00423.hp2 HG01071.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-12570_460-1255 others(18): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(9): Show |
4 | a0001c0001t0009g0273a0001c0002t0023g0082a0003c0004t0110g0070others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-12572_460-1255 others(20): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(11): Show |
4 | a0001c0001t0106g0058a0001c0002t0004g0083a0001c0002t0042g0131others(1): Show | 4 | HG01081.hp1 HG01109.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-12574_460-1255 others(22): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.460-12576_460-1255 others(24): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(15): Show |
1 | a0001c0002t0069g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.460-12578_460-1255 others(26): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
T | TTATATAT others(19): Show |
1 | a0001c0002t0004g0073 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.460-12557_460-1255 others(30): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
TTA | T | 6 | a0001c0001t0005g0214a0001c0001t0016g0226a0001c0002t0061g0125others(3): Show | 6 | HG01243.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-12558_460-1255 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
TTATA | T | 10 | a0001c0001t0020g0152a0001c0001t0020g0192a0001c0001t0104g0244others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-12560_460-1255 others(8): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
TTATATA | T | 11 | a0001c0001t0002g0223a0001c0001t0027g0036a0001c0001t0086g0061others(8): Show | 11 | HG01884.hp1 HG02056.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-12562_460-1255 others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551812
|
TTATATAT others(1): Show |
T | 168 | a0001c0001t0001g0225a0001c0001t0001g0293a0001c0001t0001g0312others(165): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.460-12564_460-1255 others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | |||||
chr6:147551816
|
A | T | 4 | a0001c0001t0016g0226a0003c0004t0016g0071a0004c0005t0034g0046others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-12578A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551816 | ||||||
chr6:147551820
|
A | ATATATAT others(65): Show |
1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-12561_460-1256 others(76): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551820 | |||||
chr6:147551820
|
A | T | 7 | a0001c0001t0002g0223a0001c0001t0027g0036a0001c0001t0086g0061others(4): Show | 7 | HG01884.hp1 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-12574A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551820 | ||||||
chr6:147551822
|
A | T | 168 | a0001c0001t0001g0225a0001c0001t0001g0293a0001c0001t0001g0312others(165): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.460-12572A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551822 | ||||||
chr6:147551897
|
C | CCAAATT | 174 | a0001c0001t0001g0225a0001c0001t0001g0293a0001c0001t0001g0312others(171): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.460-12495_460-1249 others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551897 | |||||
chr6:147551901
|
T | C | 1 | a0001c0002t0066g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.460-12493T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551901 | ||||||
chr6:147551955
|
G | A | 177 | a0001c0001t0001g0225a0001c0001t0001g0293a0001c0001t0001g0312others(174): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.460-12439G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551955 | ||||||
chr6:147551976
|
G | C | 182 | a0001c0001t0001g0225a0001c0001t0001g0293a0001c0001t0001g0312others(179): Show | 191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.460-12418G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551976 | ||||||
chr6:147552042
|
C | T | 1 | a0001c0001t0011g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.460-12352C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552042 | ||||||
chr6:147552144
|
T | C | 1 | a0001c0002t0022g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.460-12250T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552144 | ||||||
chr6:147552803
|
T | C | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.460-11591T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552803 | ||||||
chr6:147552976
|
T | A | 5 | a0001c0001t0029g0144a0001c0001t0106g0058a0001c0002t0042g0131others(2): Show | 5 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-11418T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552976 | ||||||
chr6:147553000
|
G | A | 2 | a0001c0001t0100g0227a0001c0001t0103g0241 | 2 | HG02132.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.460-11394G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553000 | ||||||
chr6:147553245
|
C | G | 167 | a0001c0001t0001g0225a0001c0001t0001g0312a0001c0001t0001g0339others(164): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.460-11149C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553245 | ||||||
chr6:147553251
|
C | G | 21 | a0001c0001t0016g0226a0001c0001t0020g0152a0001c0001t0020g0192others(18): Show | 21 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.460-11143C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553251 | ||||||
chr6:147553743
|
C | T | 7 | a0001c0001t0001g0224a0001c0001t0001g0242a0001c0001t0001g0247others(4): Show | 7 | HG00597.hp2 HG02129.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-10651C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553743 | ||||||
chr6:147553803
|
A | G | 102 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0052others(99): Show | 107 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.460-10591A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553803 | ||||||
chr6:147553986
|
T | C | 1 | a0001c0002t0069g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.460-10408T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553986 | ||||||
chr6:147553987
|
A | G | 2 | a0001c0001t0027g0036a0001c0002t0022g0086 | 2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.460-10407A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553987 | ||||||
chr6:147554001
|
G | A | 8 | a0001c0001t0002g0050a0001c0001t0002g0056a0001c0001t0002g0203others(5): Show | 8 | HG00597.hp1 HG02040.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.460-10393G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554001 | ||||||
chr6:147554162
|
C | T | 1 | a0001c0002t0004g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.460-10232C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554162 | ||||||
chr6:147554214
|
C | T | 2 | a0001c0001t0082g0243a0003c0004t0110g0070 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.460-10180C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554214 | ||||||
chr6:147554329
|
A | G | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-10065A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554329 | ||||||
chr6:147554361
|
C | T | 2 | a0001c0001t0082g0243a0003c0004t0110g0070 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.460-10033C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554361 | ||||||
chr6:147554377
|
G | A | 14 | a0001c0001t0001g0185a0001c0001t0001g0283a0001c0001t0009g0039others(11): Show | 14 | HG00558.hp1 HG00609.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-10017G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554377 | ||||||
chr6:147554477
|
A | G | 1 | a0001c0001t0087g0275 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.460-9917A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554477 | ||||||
chr6:147554483
|
C | G | 2 | a0001c0001t0082g0243a0003c0004t0110g0070 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.460-9911C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554483 | ||||||
chr6:147554588
|
GT | G | 10 | a0001c0001t0020g0152a0001c0001t0020g0192a0001c0001t0105g0194others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-9800delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147554588 | |||||
chr6:147554595
|
C | G | 10 | a0001c0001t0020g0152a0001c0001t0020g0192a0001c0001t0105g0194others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-9799C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554595 | ||||||
chr6:147554621
|
C | T | 1 | a0001c0002t0060g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.460-9773C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554621 | ||||||
chr6:147554662
|
G | T | 10 | a0001c0001t0002g0258a0001c0001t0002g0304a0001c0001t0002g0305others(7): Show | 11 | HG00621.hp1 HG01928.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-9732G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554662 | ||||||
chr6:147554731
|
C | T | 6 | a0001c0001t0002g0232a0001c0001t0002g0334a0001c0002t0008g0179others(3): Show | 6 | HG00558.hp2 HG00609.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-9663C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554731 | ||||||
chr6:147554798
|
C | T | 1 | a0001c0002t0007g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.460-9596C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554798 | ||||||
chr6:147554875
|
C | T | 203 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0183others(200): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.460-9519C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554875 | ||||||
chr6:147554887
|
C | T | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-9507C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554887 | ||||||
chr6:147554902
|
T | C | 171 | a0001c0001t0001g0225a0001c0001t0001g0312a0001c0001t0001g0339others(168): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.460-9492T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554902 | ||||||
chr6:147555028
|
A | G | 2 | a0001c0001t0100g0227a0001c0001t0103g0241 | 2 | HG02132.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.460-9366A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555028 | ||||||
chr6:147555124
|
T | G | 7 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0082g0243others(4): Show | 7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-9270T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555124 | ||||||
chr6:147555245
|
C | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0183others(28): Show | 32 | HG00558.hp1 HG00609.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.460-9149C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555245 | ||||||
chr6:147555333
|
A | G | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-9061A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555333 | ||||||
chr6:147555334
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.460-9060C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555334 | ||||||
chr6:147555500
|
T | C | 1 | a0001c0001t0080g0268 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.460-8894T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555500 | ||||||
chr6:147555511
|
C | T | 1 | a0001c0002t0056g0092 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.460-8883C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555511 | ||||||
chr6:147555552
|
G | A | 4 | a0001c0001t0009g0039a0001c0001t0009g0271a0001c0001t0009g0272others(1): Show | 4 | HG00609.hp2 HG02074.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-8842G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555552 | ||||||
chr6:147555705
|
T | C | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-8689T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555705 | ||||||
chr6:147555850
|
A | G | 3 | a0001c0001t0003g0011a0001c0001t0003g0285a0001c0002t0010g0097 | 4 | NA18943.hp2 NA18964.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-8544A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555850 | ||||||
chr6:147555891
|
T | C | 7 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0082g0243others(4): Show | 7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-8503T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555891 | ||||||
chr6:147556097
|
A | AT | 6 | a0001c0001t0016g0226a0001c0002t0068g0067a0003c0004t0016g0071others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-8284dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147556097 | |||||
chr6:147556100
|
T | A | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-8294T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556100 | ||||||
chr6:147556121
|
C | T | 1 | a0001c0002t0007g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.460-8273C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556121 | ||||||
chr6:147556131
|
C | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0183others(29): Show | 33 | HG00558.hp1 HG00609.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.460-8263C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556131 | ||||||
chr6:147556132
|
G | A | 1 | a0001c0002t0024g0112 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.460-8262G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556132 | ||||||
chr6:147556218
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.460-8176G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556218 | ||||||
chr6:147556237
|
C | T | 3 | a0001c0002t0008g0150a0001c0002t0008g0181a0001c0002t0008g0340 | 3 | HG02818.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.460-8157C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556237 | ||||||
chr6:147556313
|
C | T | 6 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0086g0061others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-8081C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556313 | ||||||
chr6:147556401
|
A | C | 6 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0086g0061others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-7993A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556401 | ||||||
chr6:147556559
|
C | T | 2 | a0001c0001t0005g0214a0001c0002t0038g0149 | 2 | HG01243.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.460-7835C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556559 | ||||||
chr6:147556778
|
A | G | 2 | a0001c0001t0113g0151a0003c0004t0107g0069 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.460-7616A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556778 | ||||||
chr6:147556837
|
C | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0183others(27): Show | 31 | HG00558.hp1 HG00609.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.460-7557C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556837 | ||||||
chr6:147556861
|
A | G | 1 | a0002c0003t0001g0031 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.460-7533A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556861 | ||||||
chr6:147556908
|
A | G | 7 | a0001c0001t0020g0152a0001c0001t0020g0192a0001c0001t0105g0194others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-7486A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556908 | ||||||
chr6:147556950
|
G | A | 1 | a0001c0001t0005g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.460-7444G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556950 | ||||||
chr6:147557080
|
T | A | 12 | a0001c0001t0001g0339a0001c0001t0011g0279a0001c0001t0028g0297others(9): Show | 12 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.460-7314T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557080 | ||||||
chr6:147557277
|
C | T | 27 | a0001c0001t0001g0339a0001c0001t0011g0208a0001c0001t0011g0209others(24): Show | 27 | HG00140.hp1 HG00733.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-7117C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557277 | ||||||
chr6:147557280
|
T | C | 74 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0052others(71): Show | 79 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.460-7114T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557280 | ||||||
chr6:147557362
|
T | C | 1 | a0001c0002t0036g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.460-7032T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557362 | ||||||
chr6:147557515
|
G | A | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-6879G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557515 | ||||||
chr6:147557654
|
T | C | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-6740T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557654 | ||||||
chr6:147557826
|
G | A | 2 | a0001c0001t0009g0066a0001c0001t0009g0200 | 2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.460-6568G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557826 | ||||||
chr6:147557952
|
C | A | 7 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0082g0243others(4): Show | 7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-6442C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557952 | ||||||
chr6:147558043
|
G | A | 1 | a0001c0001t0003g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.460-6351G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558043 | ||||||
chr6:147558134
|
A | C | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-6260A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558134 | ||||||
chr6:147558302
|
G | A | 6 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0086g0061others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-6092G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558302 | ||||||
chr6:147558334
|
G | A | 1 | a0001c0001t0006g0328 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.460-6060G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558334 | ||||||
chr6:147558573
|
C | T | 76 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0052others(73): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.460-5821C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558573 | ||||||
chr6:147558704
|
C | T | 1 | a0001c0001t0027g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460-5690C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558704 | ||||||
chr6:147558899
|
C | T | 8 | a0001c0001t0082g0243a0001c0001t0095g0074a0001c0001t0096g0054others(5): Show | 8 | HG02132.hp2 HG02145.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.460-5495C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558899 | ||||||
chr6:147558903
|
A | T | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-5491A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558903 | ||||||
chr6:147558939
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0248 | 2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.460-5455G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558939 | ||||||
chr6:147559084
|
A | G | 14 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0082g0243others(11): Show | 14 | HG01884.hp1 HG02132.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-5310A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559084 | ||||||
chr6:147559528
|
G | A | 2 | a0001c0001t0001g0225a0001c0002t0004g0161 | 2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.460-4866G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559528 | ||||||
chr6:147559627
|
C | A | 2 | a0001c0001t0082g0243a0001c0002t0023g0088 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.460-4767C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559627 | ||||||
chr6:147559690
|
C | G | 29 | a0001c0001t0001g0339a0001c0001t0011g0197a0001c0001t0011g0208others(26): Show | 29 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-4704C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559690 | ||||||
chr6:147559716
|
T | C | 12 | a0001c0001t0011g0208a0001c0001t0011g0209a0001c0001t0011g0221others(9): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.460-4678T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559716 | ||||||
chr6:147559865
|
A | C | 213 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(210): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.460-4529A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559865 | ||||||
chr6:147560035
|
A | G | 181 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(178): Show | 189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.460-4359A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560035 | ||||||
chr6:147560181
|
T | G | 1 | a0001c0001t0103g0241 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.460-4213T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560181 | ||||||
chr6:147560223
|
T | C | 1 | a0001c0001t0082g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-4171T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560223 | ||||||
chr6:147560227
|
A | G | 1 | a0001c0001t0079g0321 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.460-4167A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560227 | ||||||
chr6:147560239
|
T | C | 2 | a0001c0001t0003g0060a0001c0001t0028g0253 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.460-4155T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560239 | ||||||
chr6:147560380
|
G | T | 2 | a0001c0001t0001g0324a0001c0002t0047g0118 | 2 | NA18980.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.460-4014G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560380 | ||||||
chr6:147560456
|
A | G | 7 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0028g0297others(4): Show | 7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-3938A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560456 | ||||||
chr6:147560586
|
A | T | 3 | a0001c0001t0003g0042a0001c0001t0003g0284a0001c0001t0003g0287 | 3 | NA18944.hp2 NA18975.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.460-3808A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560586 | ||||||
chr6:147560618
|
C | A | 1 | a0001c0002t0004g0161 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.460-3776C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560618 | ||||||
chr6:147560702
|
A | T | 1 | a0003c0004t0110g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.460-3692A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560702 | ||||||
chr6:147560743
|
G | A | 1 | a0002c0003t0002g0017 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.460-3651G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560743 | ||||||
chr6:147560825
|
A | G | 1 | a0001c0002t0036g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.460-3569A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560825 | ||||||
chr6:147560885
|
A | G | 2 | a0001c0001t0003g0186a0001c0001t0003g0229 | 2 | NA18939.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.460-3509A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560885 | ||||||
chr6:147560947
|
C | T | 9 | a0001c0001t0016g0226a0001c0001t0016g0246a0001c0001t0112g0254others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-3447C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560947 | ||||||
chr6:147561046
|
G | T | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.460-3348G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561046 | ||||||
chr6:147561186
|
A | AATTT | 4 | a0001c0001t0100g0227a0001c0001t0101g0277a0001c0001t0102g0333others(1): Show | 4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3187_460-3184d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147561186 | |||||
chr6:147561216
|
C | T | 4 | a0001c0001t0100g0227a0001c0001t0101g0277a0001c0001t0102g0333others(1): Show | 4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3178C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561216 | ||||||
chr6:147561256
|
C | T | 4 | a0001c0001t0100g0227a0001c0001t0101g0277a0001c0001t0102g0333others(1): Show | 4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3138C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561256 | ||||||
chr6:147561273
|
C | T | 4 | a0001c0001t0100g0227a0001c0001t0101g0277a0001c0001t0102g0333others(1): Show | 4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3121C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561273 | ||||||
chr6:147561362
|
A | G | 3 | a0001c0001t0108g0059a0001c0002t0061g0125a0003c0004t0110g0070 | 3 | HG02809.hp1 HG03195.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.460-3032A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561362 | ||||||
chr6:147561507
|
A | C | 30 | a0001c0001t0001g0339a0001c0001t0011g0197a0001c0001t0011g0208others(27): Show | 30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-2887A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561507 | ||||||
chr6:147561709
|
T | G | 304 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(301): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.460-2685T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561709 | ||||||
chr6:147561747
|
A | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.460-2647A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561747 | ||||||
chr6:147561872
|
C | T | 1 | a0001c0002t0051g0104 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.460-2522C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561872 | ||||||
chr6:147562000
|
G | A | 29 | a0001c0001t0001g0339a0001c0001t0011g0208a0001c0001t0011g0209others(26): Show | 29 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2394G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562000 | ||||||
chr6:147562160
|
T | G | 1 | a0001c0001t0003g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.460-2234T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562160 | ||||||
chr6:147562273
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.460-2121G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562273 | ||||||
chr6:147562298
|
A | G | 3 | a0001c0001t0002g0258a0001c0002t0007g0099a0001c0002t0007g0147 | 3 | HG02027.hp2 NA18948.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.460-2096A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562298 | ||||||
chr6:147562323
|
T | C | 2 | a0001c0001t0005g0307a0001c0001t0005g0308 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.460-2071T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562323 | ||||||
chr6:147562324
|
G | C | 1 | a0001c0001t0003g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.460-2070G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562324 | ||||||
chr6:147562652
|
C | T | 1 | a0003c0004t0110g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.460-1742C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562652 | ||||||
chr6:147562694
|
C | A | 30 | a0001c0001t0001g0339a0001c0001t0011g0197a0001c0001t0011g0208others(27): Show | 30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-1700C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562694 | ||||||
chr6:147562777
|
G | A | 1 | a0001c0001t0009g0271 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.460-1617G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562777 | ||||||
chr6:147562809
|
G | A | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.460-1585G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562809 | ||||||
chr6:147562821
|
C | CA | 6 | a0001c0001t0003g0231a0001c0001t0003g0296a0001c0001t0009g0057others(3): Show | 6 | HG01261.hp1 HG02451.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-1564dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147562821 | |||||
chr6:147562821
|
C | CAA | 30 | a0001c0001t0001g0339a0001c0001t0011g0197a0001c0001t0011g0208others(27): Show | 30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-1565_460-1564d others(4): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147562821 | |||||
chr6:147562827
|
A | T | 85 | a0001c0001t0002g0006a0001c0001t0002g0035a0001c0001t0002g0050others(82): Show | 91 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.460-1567A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562827 | ||||||
chr6:147562831
|
T | A | 206 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(203): Show | 214 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.460-1563T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562831 | ||||||
chr6:147563073
|
G | A | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-1321G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563073 | ||||||
chr6:147563090
|
C | A | 5 | a0001c0001t0003g0255a0001c0001t0003g0278a0001c0001t0003g0330others(2): Show | 5 | HG01106.hp1 HG01361.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-1304C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563090 | ||||||
chr6:147563099
|
A | T | 211 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(208): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.460-1295A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563099 | ||||||
chr6:147563161
|
GT | G | 30 | a0001c0001t0001g0339a0001c0001t0011g0197a0001c0001t0011g0208others(27): Show | 30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-1232delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563161 | ||||||
chr6:147563347
|
T | G | 1 | a0001c0002t0036g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.460-1047T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563347 | ||||||
chr6:147563356
|
A | C | 10 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0028g0297others(7): Show | 10 | HG01884.hp1 HG02132.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-1038A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563356 | ||||||
chr6:147563366
|
G | T | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-1028G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563366 | ||||||
chr6:147563469
|
C | A | 3 | a0001c0001t0021g0049a0001c0001t0021g0220a0001c0001t0021g0262 | 3 | NA19000.hp1 NA19083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.460-925C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563469 | ||||||
chr6:147563703
|
A | G | 1 | a0001c0002t0014g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.460-691A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563703 | ||||||
chr6:147563788
|
ATACT | A | 3 | a0001c0001t0097g0065a0001c0002t0054g0154a0001c0002t0057g0169 | 3 | HG00140.hp1 HG00733.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.460-603_460-600del others(4): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147563788 | |||||
chr6:147563815
|
C | A | 1 | a0001c0002t0008g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-579C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563815 | ||||||
chr6:147563971
|
G | A | 1 | a0001c0001t0005g0218 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.460-423G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563971 | ||||||
chr6:147564104
|
A | AT | 6 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0028g0297others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-281dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147564104 | |||||
chr6:147564104
|
AT | A | 95 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0038others(92): Show | 99 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.460-281delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147564104 | |||||
chr6:147564175
|
A | G | 6 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0028g0297others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-219A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147564175 | ||||||
chr6:147564197
|
G | A | 6 | a0001c0001t0027g0036a0001c0001t0027g0245a0001c0001t0028g0297others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-197G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147564197 | ||||||
chr6:147564288
|
G | A | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-106G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147564288 |