geneid | 148398 |
---|---|
ensemblid | ENSG00000187634.13 |
hgncid | 28706 |
symbol | SAMD11 |
name | sterile alpha motif domain containing 11 |
refseq_nuc | NM_001385641.1 |
refseq_prot | NP_001372570.1 |
ensembl_nuc | ENST00000616016.5 |
ensembl_prot | ENSP00000478421.2 |
mane_status | MANE Select |
chr | chr1 |
start | 923923 |
end | 944574 |
strand | + |
ver | v1.2 |
region | chr1:923923-944574 |
region5000 | chr1:918923-949574 |
regionname0 | SAMD11_chr1_923923_944574 |
regionname5000 | SAMD11_chr1_918923_949574 |
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 | 0/1 | 844 | 321 | 54 | 57 | 146 | 17 | 46 | 111 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002 | 0/0 | 844 | 40 | 3 | 8 | 29 | 0 | 0 | 24 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0003 | 0/0 | 611 | 10 | 2 | 6 | 0 | 1 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0004 | 0/0 | 876 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0005 | 0/0 | 876 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0006 | 0/0 | 844 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0007 | 0/0 | 860 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0008 | 0/0 | 844 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0009 | 0/0 | 892 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0010 | 0/0 | 844 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0011 | 0/0 | 860 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0012 | 0/0 | 844 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0013 | 0/0 | 892 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0014 | 0/0 | 844 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0015 | 0/0 | 844 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0016 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0017 | 0/0 | 844 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0018 | 0/0 | 892 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0019 | 0/0 | 844 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0020 | 0/0 | 844 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0021 | 0/0 | 844 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0022 | 1/0 | 844 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0023 | 0/0 | 844 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0024 | 0/0 | 431 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0025 | 0/0 | 611 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0026 | 0/0 | 844 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0027 | 0/0 | 844 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0028 | 0/0 | 844 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0029 | 0/0 | 844 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
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 | 0/1 | 2535 | 183 | 10 | 39 | 82 | 14 | 37 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0002 | 0/0 | 2535 | 69 | 17 | 2 | 45 | 0 | 5 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0003 | 0/0 | 2535 | 34 | 2 | 8 | 24 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0004 | 0/0 | 2535 | 23 | 9 | 5 | 9 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0005 | 0/0 | 2535 | 14 | 3 | 5 | 0 | 3 | 3 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0006 | 0/0 | 2521 | 9 | 1 | 6 | 0 | 1 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0007 | 0/0 | 2631 | 8 | 8 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0008 | 0/0 | 2631 | 8 | 7 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0009 | 0/0 | 2535 | 7 | 0 | 0 | 6 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0010 | 0/0 | 2535 | 6 | 3 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0011 | 0/0 | 2535 | 6 | 6 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0012 | 0/0 | 2583 | 5 | 5 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0013 | 0/0 | 2679 | 4 | 3 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0014 | 0/0 | 2535 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0015 | 0/0 | 2535 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0016 | 0/0 | 2535 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0017 | 0/0 | 2535 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0018 | 0/0 | 2535 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0019 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0020 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0021 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0022 | 0/0 | 2535 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0023 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0024 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0025 | 0/0 | 2535 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0026 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0027 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0028 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0029 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0030 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0031 | 0/0 | 2521 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0032 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0033 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0034 | 1/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0035 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0036 | 0/0 | 2631 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0037 | 0/0 | 2728 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0038 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0039 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0040 | 0/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0041 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0042 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0043 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0044 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0045 | 0/0 | 2521 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0046 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0047 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0048 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0049 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0050 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
c0051 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
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 | 931 | 155 | 21 | 34 | 61 | 14 | 25 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0002 | 0/0 | 931 | 77 | 20 | 2 | 50 | 0 | 5 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0003 | 0/1 | 931 | 66 | 3 | 26 | 19 | 4 | 13 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0004 | 0/0 | 925 | 46 | 3 | 8 | 35 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0005 | 0/0 | 931 | 15 | 0 | 5 | 9 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0006 | 0/0 | 931 | 9 | 9 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0007 | 0/0 | 931 | 9 | 6 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0008 | 0/0 | 931 | 8 | 8 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0009 | 1/0 | 931 | 6 | 3 | 0 | 1 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0010 | 0/0 | 931 | 6 | 0 | 0 | 6 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0011 | 0/0 | 931 | 4 | 3 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0012 | 0/0 | 931 | 4 | 3 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0013 | 0/0 | 931 | 3 | 2 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0014 | 0/0 | 925 | 3 | 1 | 0 | 1 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0015 | 0/0 | 931 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0016 | 0/0 | 931 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0017 | 0/0 | 931 | 2 | 1 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0018 | 0/0 | 931 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0019 | 0/0 | 931 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0020 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0021 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0022 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0023 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0024 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0025 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0026 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0027 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0028 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0029 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0030 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0031 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0032 | 0/0 | 931 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
t0033 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
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 | 16 | 0 | 0 | 15 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0002 | 0/0 | 8 | 0 | 6 | 0 | 0 | 2 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0005 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0006 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0326 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
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 | 0/1 | 2535 | 183 | 10 | 39 | 82 | 14 | 37 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002 | 0/0 | 2535 | 69 | 17 | 2 | 45 | 0 | 5 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0004 | 0/0 | 2535 | 23 | 9 | 5 | 9 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0005 | 0/0 | 2535 | 14 | 3 | 5 | 0 | 3 | 3 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0009 | 0/0 | 2535 | 7 | 0 | 0 | 6 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0010 | 0/0 | 2535 | 6 | 3 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0011 | 0/0 | 2535 | 6 | 6 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0017 | 0/0 | 2535 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0019 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0021 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0023 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0029 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0032 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0033 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0046 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0003 | 0/0 | 2535 | 34 | 2 | 8 | 24 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0018 | 0/0 | 2535 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0026 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0049 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0003c0006 | 0/0 | 2521 | 9 | 1 | 6 | 0 | 1 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0003c0031 | 0/0 | 2521 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0004c0008 | 0/0 | 2631 | 8 | 7 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0004c0036 | 0/0 | 2631 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0005c0007 | 0/0 | 2631 | 8 | 8 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0006c0016 | 0/0 | 2535 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0006c0024 | 0/0 | 2535 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0007c0012 | 0/0 | 2583 | 5 | 5 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0008c0014 | 0/0 | 2535 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0009c0013 | 0/0 | 2679 | 4 | 3 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0010c0015 | 0/0 | 2535 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0011c0035 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0011c0043 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0011c0044 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0012c0025 | 0/0 | 2535 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0013c0020 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0014c0027 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0015c0022 | 0/0 | 2535 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0016c0028 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0017c0051 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0018c0030 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0019c0041 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0020c0039 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0021c0040 | 0/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0022c0034 | 1/0 | 2535 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0023c0042 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0024c0037 | 0/0 | 2728 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0025c0045 | 0/0 | 2521 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0026c0038 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0027c0047 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0028c0048 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0029c0050 | 0/0 | 2535 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3465 | 103 | 2 | 17 | 52 | 10 | 22 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0003 | 0/1 | 3465 | 51 | 0 | 17 | 18 | 4 | 11 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0005 | 0/0 | 3465 | 14 | 0 | 4 | 9 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0012 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0013 | 0/0 | 3465 | 3 | 2 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0014 | 0/0 | 3459 | 2 | 0 | 0 | 1 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0018 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0019 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0029 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0030 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0032 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0001t0033 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0002 | 0/0 | 3465 | 51 | 5 | 1 | 41 | 0 | 4 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0004 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0007 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0009 | 0/0 | 3465 | 4 | 3 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0011 | 0/0 | 3465 | 4 | 3 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0016 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0020 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0023 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0025 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0002t0026 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0004t0001 | 0/0 | 3465 | 20 | 8 | 5 | 7 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0004t0003 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0004t0012 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0004t0027 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0005t0001 | 0/0 | 3465 | 14 | 3 | 5 | 0 | 3 | 3 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0009t0003 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0009t0010 | 0/0 | 3465 | 6 | 0 | 0 | 6 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0010t0007 | 0/0 | 3465 | 6 | 3 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0011t0002 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0011t0006 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0011t0028 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0017t0001 | 0/0 | 3465 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0019t0006 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0021t0002 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0021t0004 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0023t0001 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0029t0002 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0032t0002 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0033t0002 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0001c0046t0014 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0003t0004 | 0/0 | 3459 | 32 | 2 | 7 | 23 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0003t0009 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0003t0024 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0018t0004 | 0/0 | 3459 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0026t0002 | 0/0 | 3465 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0002c0049t0004 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0003c0006t0001 | 0/0 | 3451 | 2 | 0 | 1 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0003c0006t0002 | 0/0 | 3451 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0003c0006t0003 | 0/0 | 3451 | 6 | 1 | 5 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0003c0031t0002 | 0/0 | 3451 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0004c0008t0002 | 0/0 | 3561 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0004c0008t0006 | 0/0 | 3561 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0004c0008t0017 | 0/0 | 3561 | 2 | 1 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0004c0036t0002 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0005c0007t0008 | 0/0 | 3561 | 7 | 7 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0005c0007t0022 | 0/0 | 3561 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0006c0016t0002 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0006c0016t0015 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0006c0024t0003 | 0/0 | 3465 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0007c0012t0001 | 0/0 | 3513 | 5 | 5 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0008c0014t0004 | 0/0 | 3459 | 4 | 0 | 0 | 4 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0009c0013t0002 | 0/0 | 3609 | 4 | 3 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0010c0015t0002 | 0/0 | 3465 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0011c0035t0021 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0011c0043t0001 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0011c0044t0031 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0012c0025t0003 | 0/0 | 3465 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0013c0020t0002 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0013c0020t0006 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0014c0027t0004 | 0/0 | 3459 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0015c0022t0001 | 0/0 | 3465 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0016c0028t0008 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0017c0051t0001 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0018c0030t0006 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0019c0041t0003 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0020c0039t0005 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0021c0040t0003 | 0/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0022c0034t0009 | 1/0 | 3465 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0023c0042t0001 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0024c0037t0006 | 0/0 | 3658 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0025c0045t0003 | 0/0 | 3451 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0026c0038t0002 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0027c0047t0001 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0028c0048t0004 | 0/0 | 3459 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
a0029c0050t0004 | 0/0 | 3459 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | copy fasta | chr1 | 918923 | 949574 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0012g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0012g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0012g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0013g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0014g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0018g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0019g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0029g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0030g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0032g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0001t0033g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0001 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0009g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0009g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0011g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0011g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0011g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0011g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0016g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0016g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0020g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0023g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0025g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0002t0026g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0004t0027g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0009t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0009t0010g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0009t0010g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0009t0010g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0009t0010g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0009t0010g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0009t0010g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0010t0007g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0010t0007g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0010t0007g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0010t0007g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0010t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0011t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0011t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0011t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0011t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0011t0028g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0017t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0017t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0019t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0019t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0021t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0021t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0023t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0023t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0029t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0032t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0033t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0001c0046t0014g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0003t0024g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0018t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0018t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0018t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0026t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0002c0049t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0006t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0003c0031t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0017g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0008t0017g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0004c0036t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0005c0007t0022g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0006c0016t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0006c0016t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0006c0016t0015g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0006c0024t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0006c0024t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0007c0012t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0007c0012t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0007c0012t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0008c0014t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0008c0014t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0008c0014t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0008c0014t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0009c0013t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0009c0013t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0009c0013t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0009c0013t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0010c0015t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0010c0015t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0011c0035t0021g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0011c0043t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0011c0044t0031g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0012c0025t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0012c0025t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0013c0020t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0013c0020t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0014c0027t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0014c0027t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0015c0022t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0016c0028t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0017c0051t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0018c0030t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0019c0041t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0020c0039t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0021c0040t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0022c0034t0009g0326 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0023c0042t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0024c0037t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0025c0045t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0026c0038t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0027c0047t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0028c0048t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
a0029c0050t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0001 | g0066 | EUR | GBR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00099 | hp2 | a0001 | c0005 | t0001 | g0019 | EUR | GBR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0161 | EUR | GBR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00280 | hp2 | a0001 | c0005 | t0001 | g0017 | EUR | FIN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00423 | hp2 | a0001 | c0001 | t0014 | g0045 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00438 | hp1 | a0001 | c0001 | t0029 | g0170 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00558 | hp1 | a0001 | c0033 | t0002 | g0004 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0367 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00609 | hp1 | a0002 | c0003 | t0004 | g0255 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00621 | hp2 | a0001 | c0002 | t0026 | g0001 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00642 | hp2 | a0001 | c0002 | t0011 | g0274 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00673 | hp2 | a0001 | c0004 | t0001 | g0096 | EAS | CHS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00733 | hp2 | a0001 | c0005 | t0001 | g0054 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00735 | hp2 | a0003 | c0006 | t0003 | g0213 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG00741 | hp2 | a0001 | c0004 | t0001 | g0057 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01069 | hp2 | a0001 | c0010 | t0007 | g0294 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0125 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01081 | hp1 | a0003 | c0006 | t0003 | g0183 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0320 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01099 | hp2 | a0004 | c0008 | t0017 | g0361 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0069 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01106 | hp2 | a0019 | c0041 | t0003 | g0160 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0134 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01167 | hp1 | a0012 | c0025 | t0003 | g0195 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01169 | hp1 | a0001 | c0001 | t0032 | g0100 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01169 | hp2 | a0012 | c0025 | t0003 | g0196 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01175 | hp1 | a0015 | c0022 | t0001 | g0002 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01175 | hp2 | a0001 | c0005 | t0001 | g0019 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01192 | hp1 | a0011 | c0043 | t0001 | g0130 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01243 | hp1 | a0009 | c0013 | t0002 | g0287 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01243 | hp2 | a0001 | c0010 | t0007 | g0293 | AMR | PUR | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01255 | hp2 | a0002 | c0003 | t0004 | g0022 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01256 | hp1 | a0020 | c0039 | t0005 | g0111 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01257 | hp1 | a0001 | c0017 | t0001 | g0005 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01258 | hp1 | a0001 | c0017 | t0001 | g0005 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01261 | hp2 | a0001 | c0017 | t0001 | g0059 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01358 | hp1 | a0002 | c0003 | t0004 | g0022 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01358 | hp2 | a0001 | c0004 | t0001 | g0062 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01361 | hp2 | a0002 | c0003 | t0004 | g0229 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01433 | hp1 | a0001 | c0005 | t0001 | g0077 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01433 | hp2 | a0001 | c0004 | t0001 | g0056 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01496 | hp2 | a0002 | c0003 | t0024 | g0233 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01515 | hp2 | a0003 | c0006 | t0001 | g0089 | EUR | IBS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0166 | EUR | IBS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0165 | EUR | IBS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01884 | hp1 | a0005 | c0007 | t0008 | g0276 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01884 | hp2 | a0004 | c0036 | t0002 | g0346 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01891 | hp1 | a0007 | c0012 | t0001 | g0009 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01891 | hp2 | a0001 | c0002 | t0007 | g0297 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01934 | hp1 | a0001 | c0005 | t0001 | g0070 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01943 | hp1 | a0001 | c0004 | t0001 | g0061 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01978 | hp2 | a0003 | c0006 | t0003 | g0193 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01981 | hp2 | a0002 | c0003 | t0004 | g0011 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01993 | hp1 | a0003 | c0006 | t0001 | g0102 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01993 | hp2 | a0003 | c0006 | t0003 | g0181 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02004 | hp1 | a0002 | c0003 | t0004 | g0011 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02004 | hp2 | a0015 | c0022 | t0001 | g0002 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0330 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02055 | hp1 | a0003 | c0006 | t0003 | g0221 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02055 | hp2 | a0001 | c0004 | t0001 | g0133 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02071 | hp2 | a0002 | c0003 | t0004 | g0236 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02074 | hp2 | a0010 | c0015 | t0002 | g0001 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02080 | hp1 | a0001 | c0021 | t0004 | g0328 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0334 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02129 | hp1 | a0010 | c0015 | t0002 | g0001 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0356 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02132 | hp1 | a0010 | c0015 | t0002 | g0335 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02132 | hp2 | a0002 | c0003 | t0004 | g0243 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0364 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02145 | hp2 | a0004 | c0008 | t0002 | g0271 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02148 | hp1 | a0003 | c0006 | t0003 | g0194 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | CDX | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | CDX | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0331 | EAS | CDX | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02165 | hp2 | a0002 | c0003 | t0004 | g0235 | EAS | CDX | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02257 | hp1 | a0001 | c0011 | t0006 | g0025 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02257 | hp2 | a0001 | c0005 | t0001 | g0052 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02258 | hp1 | a0004 | c0008 | t0002 | g0317 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0363 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02273 | hp1 | a0002 | c0003 | t0004 | g0011 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02280 | hp1 | a0009 | c0013 | t0002 | g0285 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0315 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02293 | hp2 | a0025 | c0045 | t0003 | g0192 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02300 | hp1 | a0002 | c0003 | t0004 | g0230 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02451 | hp1 | a0001 | c0011 | t0006 | g0025 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0358 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02523 | hp2 | a0002 | c0003 | t0004 | g0254 | EAS | KHV | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02572 | hp1 | a0001 | c0002 | t0009 | g0323 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02572 | hp2 | a0004 | c0008 | t0017 | g0354 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02622 | hp1 | a0001 | c0004 | t0027 | g0362 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02622 | hp2 | a0001 | c0002 | t0011 | g0275 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02630 | hp1 | a0001 | c0002 | t0011 | g0272 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02630 | hp2 | a0001 | c0011 | t0002 | g0291 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02647 | hp1 | a0001 | c0002 | t0007 | g0296 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02647 | hp2 | a0007 | c0012 | t0001 | g0115 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0343 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02717 | hp2 | a0002 | c0049 | t0004 | g0223 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02723 | hp1 | a0001 | c0019 | t0006 | g0269 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02723 | hp2 | a0001 | c0011 | t0028 | g0316 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0345 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02738 | hp2 | a0003 | c0006 | t0002 | g0261 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02809 | hp1 | a0007 | c0012 | t0001 | g0009 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02809 | hp2 | a0001 | c0023 | t0001 | g0150 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0319 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02818 | hp2 | a0007 | c0012 | t0001 | g0131 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0064 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02886 | hp2 | a0016 | c0028 | t0008 | g0268 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02895 | hp1 | a0001 | c0010 | t0007 | g0295 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0365 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02896 | hp1 | a0009 | c0013 | t0002 | g0286 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02896 | hp2 | a0004 | c0008 | t0002 | g0270 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02922 | hp1 | a0001 | c0019 | t0006 | g0282 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02922 | hp2 | a0024 | c0037 | t0006 | g0307 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02965 | hp1 | a0001 | c0002 | t0011 | g0273 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02965 | hp2 | a0001 | c0002 | t0016 | g0265 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02970 | hp1 | a0013 | c0020 | t0006 | g0302 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02970 | hp2 | a0005 | c0007 | t0008 | g0277 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02976 | hp1 | a0002 | c0003 | t0004 | g0222 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02976 | hp2 | a0006 | c0016 | t0015 | g0263 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0333 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03041 | hp1 | a0004 | c0008 | t0006 | g0281 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0049 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03098 | hp1 | a0001 | c0002 | t0009 | g0321 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03098 | hp2 | a0006 | c0024 | t0003 | g0208 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03130 | hp1 | a0001 | c0002 | t0020 | g0304 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03130 | hp2 | a0003 | c0031 | t0002 | g0299 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03139 | hp1 | a0005 | c0007 | t0008 | g0279 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03139 | hp2 | a0006 | c0016 | t0015 | g0264 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03195 | hp1 | a0005 | c0007 | t0008 | g0300 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03195 | hp2 | a0001 | c0002 | t0016 | g0266 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03209 | hp1 | a0001 | c0001 | t0018 | g0151 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03209 | hp2 | a0001 | c0002 | t0009 | g0322 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0200 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03225 | hp2 | a0005 | c0007 | t0008 | g0280 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03453 | hp1 | a0004 | c0008 | t0006 | g0303 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03453 | hp2 | a0001 | c0010 | t0007 | g0024 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03486 | hp1 | a0011 | c0035 | t0021 | g0267 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03486 | hp2 | a0007 | c0012 | t0001 | g0009 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03490 | hp2 | a0001 | c0005 | t0001 | g0017 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0359 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03516 | hp2 | a0005 | c0007 | t0008 | g0284 | AFR | ESN | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03540 | hp1 | a0013 | c0020 | t0002 | g0318 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0132 | AFR | GWD | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03579 | hp1 | a0001 | c0011 | t0002 | g0314 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03579 | hp2 | a0001 | c0046 | t0014 | g0028 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03654 | hp1 | a0001 | c0009 | t0003 | g0180 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0126 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03669 | hp1 | a0021 | c0040 | t0003 | g0174 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03710 | hp1 | a0001 | c0001 | t0013 | g0175 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03831 | hp1 | a0001 | c0001 | t0019 | g0190 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0206 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03927 | hp1 | a0001 | c0001 | t0014 | g0080 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0191 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04184 | hp1 | a0001 | c0002 | t0009 | g0325 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04184 | hp2 | a0001 | c0005 | t0001 | g0076 | SAS | BEB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04199 | hp2 | a0001 | c0005 | t0001 | g0078 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | STU | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18522 | hp1 | a0004 | c0008 | t0002 | g0290 | AFR | YRI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18522 | hp2 | a0009 | c0013 | t0002 | g0288 | AFR | YRI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18612 | hp2 | a0001 | c0002 | t0004 | g0327 | EAS | CHB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18747 | hp1 | a0008 | c0014 | t0004 | g0257 | EAS | CHB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18906 | hp1 | a0006 | c0016 | t0002 | g0289 | AFR | YRI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18906 | hp2 | a0001 | c0004 | t0001 | g0135 | AFR | YRI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18940 | hp2 | a0002 | c0003 | t0004 | g0241 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18942 | hp1 | a0001 | c0009 | t0010 | g0308 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0366 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18948 | hp2 | a0001 | c0009 | t0010 | g0312 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18949 | hp1 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0347 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18952 | hp1 | a0002 | c0003 | t0004 | g0252 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18953 | hp1 | a0001 | c0009 | t0010 | g0309 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18956 | hp1 | a0001 | c0021 | t0002 | g0342 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18959 | hp1 | a0002 | c0003 | t0004 | g0250 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18960 | hp2 | a0002 | c0003 | t0004 | g0248 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18962 | hp2 | a0002 | c0003 | t0004 | g0242 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18964 | hp2 | a0002 | c0003 | t0004 | g0238 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18966 | hp2 | a0001 | c0002 | t0025 | g0344 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18967 | hp1 | a0001 | c0009 | t0010 | g0313 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18971 | hp1 | a0008 | c0014 | t0004 | g0259 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18971 | hp2 | a0001 | c0001 | t0033 | g0008 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18972 | hp1 | a0002 | c0003 | t0004 | g0239 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18974 | hp2 | a0026 | c0038 | t0002 | g0350 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18975 | hp1 | a0001 | c0004 | t0001 | g0145 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18975 | hp2 | a0008 | c0014 | t0004 | g0258 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18980 | hp1 | a0002 | c0026 | t0002 | g0023 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0351 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18981 | hp2 | a0002 | c0003 | t0004 | g0246 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18983 | hp1 | a0002 | c0003 | t0004 | g0306 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18984 | hp1 | a0001 | c0002 | t0023 | g0336 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18986 | hp1 | a0002 | c0003 | t0004 | g0245 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0360 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0357 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18992 | hp1 | a0002 | c0003 | t0004 | g0305 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18993 | hp1 | a0002 | c0003 | t0004 | g0256 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18995 | hp1 | a0002 | c0018 | t0004 | g0227 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18998 | hp1 | a0008 | c0014 | t0004 | g0260 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0338 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18999 | hp1 | a0002 | c0003 | t0004 | g0237 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA18999 | hp2 | a0002 | c0003 | t0004 | g0249 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19001 | hp1 | a0001 | c0004 | t0012 | g0055 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19002 | hp1 | a0001 | c0009 | t0010 | g0311 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0341 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19005 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0005 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19010 | hp2 | a0014 | c0027 | t0004 | g0232 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19011 | hp2 | a0002 | c0003 | t0004 | g0240 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19012 | hp1 | a0001 | c0029 | t0002 | g0349 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19030 | hp1 | a0001 | c0032 | t0002 | g0353 | AFR | LWK | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0063 | AFR | LWK | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19043 | hp1 | a0005 | c0007 | t0022 | g0283 | AFR | LWK | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0065 | AFR | LWK | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19054 | hp1 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19056 | hp1 | a0002 | c0018 | t0004 | g0225 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19056 | hp2 | a0027 | c0047 | t0001 | g0053 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19057 | hp2 | a0014 | c0027 | t0004 | g0231 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19063 | hp2 | a0002 | c0003 | t0009 | g0228 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19064 | hp2 | a0001 | c0009 | t0010 | g0310 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19065 | hp1 | a0002 | c0018 | t0004 | g0226 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19066 | hp1 | a0002 | c0003 | t0004 | g0251 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19067 | hp1 | a0002 | c0003 | t0004 | g0253 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19068 | hp1 | a0002 | c0003 | t0004 | g0247 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19068 | hp2 | a0002 | c0026 | t0002 | g0023 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0348 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19074 | hp2 | a0028 | c0048 | t0004 | g0244 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19079 | hp1 | a0001 | c0004 | t0003 | g0153 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19090 | hp1 | a0023 | c0042 | t0001 | g0046 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19240 | hp1 | a0011 | c0044 | t0031 | g0156 | AFR | YRI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA19240 | hp2 | a0001 | c0001 | t0018 | g0152 | AFR | YRI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20129 | hp1 | a0001 | c0005 | t0001 | g0109 | AFR | ASW | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20129 | hp2 | a0006 | c0024 | t0003 | g0207 | AFR | ASW | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0173 | EUR | TSI | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01123 | hp1 | a0001 | c0010 | t0007 | g0292 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG01123 | hp2 | a0029 | c0050 | t0004 | g0234 | AMR | CLM | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02109 | hp1 | a0005 | c0007 | t0008 | g0278 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02486 | hp1 | a0001 | c0005 | t0001 | g0067 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02559 | hp1 | a0001 | c0011 | t0002 | g0324 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG02559 | hp2 | a0018 | c0030 | t0006 | g0301 | AFR | ACB | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03471 | hp1 | a0001 | c0001 | t0013 | g0157 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG03471 | hp2 | a0001 | c0010 | t0007 | g0024 | AFR | MSL | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG06807 | hp1 | a0001 | c0002 | t0007 | g0298 | AFR | USA | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
HG06807 | hp2 | a0001 | c0001 | t0030 | g0205 | AFR | USA | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20300 | hp1 | a0001 | c0023 | t0001 | g0091 | AFR | USA | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | USA | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA21309 | hp1 | a0002 | c0003 | t0004 | g0224 | AFR | LWK | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
NA21309 | hp2 | a0017 | c0051 | t0001 | g0104 | AFR | LWK | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0158 | REF | REF | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
homoSapiens_grch38 | hp1 | a0022 | c0034 | t0009 | g0326 | REF | REF | SAMD11_chr1_918923_949574 | SAMD11 | chr1 | 918923 | 949574 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:924568
|
T | A | 2 | a0005a0016 | 9 | HG01884.hp1 HG02109.hp1 HG02886.hp2 others(6): Show |
missense_variant | MODERATE | c.137T>A | p.Leu46His | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 646/3465 | 137/2535 | 46/844 | chr1 | 924568 | ||
chr1:924574
|
C | T | 1 | a0017 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.143C>T | p.Pro48Leu | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 652/3465 | 143/2535 | 48/844 | chr1 | 924574 | ||
chr1:930165
|
G | A | 1 | a0008 | 4 | NA18747.hp1 NA18971.hp1 NA18975.hp2 others(1): Show |
missense_variant | MODERATE | c.620G>A | p.Arg207Gln | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/14 | 1129/3465 | 620/2535 | 207/844 | chr1 | 930165 | ||
chr1:930204
|
G | A | 1 | a0009 | 4 | HG01243.hp1 HG02280.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.659G>A | p.Arg220Gln | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/14 | 1168/3465 | 659/2535 | 220/844 | chr1 | 930204 | ||
chr1:930248
|
G | A | 1 | a0015 | 2 | HG01175.hp1 HG02004.hp2 |
missense_variant | MODERATE | c.703G>A | p.Gly235Ser | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/14 | 1212/3465 | 703/2535 | 235/844 | chr1 | 930248 | ||
chr1:930282
|
G | A | 1 | a0018 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.737G>A | p.Arg246Gln | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/14 | 1246/3465 | 737/2535 | 246/844 | chr1 | 930282 | ||
chr1:930314
|
C | T | 5 | a0002a0008a0014others(2): Show | 48 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(45): Show |
missense_variant | MODERATE | c.769C>T | p.His257Tyr | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/14 | 1278/3465 | 769/2535 | 257/844 | chr1 | 930314 | ||
chr1:930323
|
A | G | 1 | a0027 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.778A>G | p.Ile260Val | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/14 | 1287/3465 | 778/2535 | 260/844 | chr1 | 930323 | ||
chr1:935813
|
G | C | 1 | a0028 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.884G>C | p.Arg295Pro | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/14 | 1393/3465 | 884/2535 | 295/844 | chr1 | 935813 | ||
chr1:939075
|
C | T | 1 | a0012 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.1003C>T | p.Arg335Cys | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 6/14 | 1512/3465 | 1003/2535 | 335/844 | chr1 | 939075 | ||
chr1:939317
|
C | G | 1 | a0026 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.1100C>G | p.Pro367Arg | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/14 | 1609/3465 | 1100/2535 | 367/844 | chr1 | 939317 | ||
chr1:939337
|
C | G | 1 | a0025 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1120C>G | p.Leu374Val | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/14 | 1629/3465 | 1120/2535 | 374/844 | chr1 | 939337 | ||
chr1:939382
|
C | T | 1 | a0014 | 2 | NA19010.hp2 NA19057.hp2 |
missense_variant | MODERATE | c.1165C>T | p.Arg389Cys | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/14 | 1674/3465 | 1165/2535 | 389/844 | chr1 | 939382 | ||
chr1:942427
|
C | T | 1 | a0023 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.1492C>T | p.Pro498Ser | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 10/14 | 2001/3465 | 1492/2535 | 498/844 | chr1 | 942427 | ||
chr1:942451
|
T | C | 28 | a0001a0002a0003others(25): Show | 433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
missense_variant | MODERATE | c.1516T>C | p.Trp506Arg | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 10/14 | 2025/3465 | 1516/2535 | 506/844 | chr1 | 942451 | ||
chr1:942945
|
C | T | 1 | a0009 | 4 | HG01243.hp1 HG02280.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.1940C>T | p.Pro647Leu | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/14 | 2449/3465 | 1940/2535 | 647/844 | chr1 | 942945 | ||
chr1:942951
|
C | T | 1 | a0019 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1946C>T | p.Pro649Leu | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/14 | 2455/3465 | 1946/2535 | 649/844 | chr1 | 942951 | ||
chr1:943364
|
G | C | 1 | a0020 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.2165G>C | p.Gly722Ala | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/14 | 2674/3465 | 2165/2535 | 722/844 | chr1 | 943364 | ||
chr1:943996
|
G | A | 1 | a0021 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.2378G>A | p.Arg793Gln | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2887/3465 | 2378/2535 | 793/844 | chr1 | 943996 | ||
chr1:944001
|
C | T | 1 | a0007 | 5 | HG01891.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.2383C>T | p.Leu795Phe | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2892/3465 | 2383/2535 | 795/844 | chr1 | 944001 | ||
chr1:944004
|
G | A | 1 | a0010 | 3 | HG02074.hp2 HG02129.hp1 HG02132.hp1 |
missense_variant | MODERATE | c.2386G>A | p.Gly796Ser | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2895/3465 | 2386/2535 | 796/844 | chr1 | 944004 | ||
chr1:944076
|
C | A | 1 | a0029 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2458C>A | p.Gln820Lys | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2967/3465 | 2458/2535 | 820/844 | chr1 | 944076 | ||
chr1:944101
|
G | C | 2 | a0003a0006 | 6 | HG02976.hp2 HG03098.hp2 HG03130.hp2 others(3): Show |
missense_variant | MODERATE | c.2483G>C | p.Gly828Ala | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2992/3465 | 2483/2535 | 828/844 | chr1 | 944101 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:924533
|
A | G | 29 | a0001c0001a0001c0004a0001c0005others(26): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
synonymous_variant | LOW | c.102A>G | p.Pro34Pro | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 611/3465 | 102/2535 | 34/844 | chr1 | 924533 | ||
chr1:925935
|
G | A | 1 | a0001c0029 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.531G>A | p.Lys177Lys | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/14 | 1040/3465 | 531/2535 | 177/844 | chr1 | 925935 | ||
chr1:935835
|
C | G | 9 | a0001c0009a0001c0021a0001c0046others(6): Show | 55 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(52): Show |
synonymous_variant | LOW | c.906C>G | p.Pro302Pro | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/14 | 1415/3465 | 906/2535 | 302/844 | chr1 | 935835 | ||
chr1:939285
|
G | A | 1 | a0001c0010 | 6 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(3): Show |
synonymous_variant | LOW | c.1068G>A | p.Leu356Leu | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/14 | 1577/3465 | 1068/2535 | 356/844 | chr1 | 939285 | ||
chr1:942628
|
C | T | 1 | a0002c0018 | 3 | NA18995.hp1 NA19056.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.1623C>T | p.Pro541Pro | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/14 | 2132/3465 | 1623/2535 | 541/844 | chr1 | 942628 | ||
chr1:942874
|
C | T | 1 | a0001c0033 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1869C>T | p.Gly623Gly | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/14 | 2378/3465 | 1869/2535 | 623/844 | chr1 | 942874 | ||
chr1:942916
|
C | G | 1 | a0011c0044 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.1911C>G | p.Pro637Pro | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/14 | 2420/3465 | 1911/2535 | 637/844 | chr1 | 942916 | ||
chr1:942934
|
G | C | 1 | a0001c0005 | 14 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(11): Show |
synonymous_variant | LOW | c.1929G>C | p.Gly643Gly | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/14 | 2438/3465 | 1929/2535 | 643/844 | chr1 | 942934 | ||
chr1:943365
|
A | C | 1 | a0011c0044 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.2166A>C | p.Gly722Gly | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/14 | 2675/3465 | 2166/2535 | 722/844 | chr1 | 943365 | ||
chr1:943937
|
C | T | 8 | a0001c0004a0001c0011a0001c0017others(5): Show | 42 | HG00673.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
synonymous_variant | LOW | c.2319C>T | p.Tyr773Tyr | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2828/3465 | 2319/2535 | 773/844 | chr1 | 943937 | ||
chr1:943991
|
G | A | 1 | a0001c0046 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2373G>A | p.Pro791Pro | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2882/3465 | 2373/2535 | 791/844 | chr1 | 943991 | ||
chr1:944033
|
G | A | 2 | a0001c0019a0001c0023 | 4 | HG02723.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.2415G>A | p.Thr805Thr | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2924/3465 | 2415/2535 | 805/844 | chr1 | 944033 | ||
chr1:944051
|
T | C | 1 | a0001c0032 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2433T>C | p.Tyr811Tyr | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2942/3465 | 2433/2535 | 811/844 | chr1 | 944051 | ||
chr1:944102
|
G | C | 1 | a0001c0017 | 3 | HG01257.hp1 HG01258.hp1 HG01261.hp2 |
synonymous_variant | LOW | c.2484G>C | p.Gly828Gly | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 2993/3465 | 2484/2535 | 828/844 | chr1 | 944102 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:923952
|
G | A | 1 | a0001c0001t0019 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-480G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 480 | chr1 | 923952 | |||||
chr1:923955
|
G | A | 12 | a0001c0002t0011a0001c0002t0020a0001c0011t0006others(9): Show | 24 | HG00642.hp2 HG01884.hp1 HG02109.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-477G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 477 | chr1 | 923955 | |||||
chr1:923990
|
C | A | 2 | a0001c0002t0016a0006c0016t0015 | 4 | HG02965.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-442C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 442 | chr1 | 923990 | |||||
chr1:924024
|
C | G | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(31): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
5_prime_UTR_variant | MODIFIER | c.-408C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 408 | chr1 | 924024 | |||||
chr1:924064
|
C | T | 1 | a0001c0011t0028 | 1 | HG02723.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-368C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | chr1 | 924064 | ||||||
chr1:924092
|
G | A | 1 | a0001c0002t0023 | 1 | NA18984.hp1 | 5_prime_UTR_variant | MODIFIER | c.-340G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 340 | chr1 | 924092 | |||||
chr1:924131
|
C | T | 1 | a0001c0011t0028 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-301C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 301 | chr1 | 924131 | |||||
chr1:924305
|
G | A | 14 | a0001c0001t0003a0001c0001t0013a0001c0001t0019others(11): Show | 73 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(70): Show |
5_prime_UTR_variant | MODIFIER | c.-127G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 127 | chr1 | 924305 | |||||
chr1:924310
|
C | G | 36 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(33): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
5_prime_UTR_variant | MODIFIER | c.-122C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 122 | chr1 | 924310 | |||||
chr1:924321
|
C | G | 36 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(33): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
5_prime_UTR_variant | MODIFIER | c.-111C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/14 | 111 | chr1 | 924321 | |||||
chr1:944161
|
G | A | 1 | a0002c0003t0024 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 8 | chr1 | 944161 | |||||
chr1:944196
|
C | T | 4 | a0004c0008t0017a0005c0007t0008a0005c0007t0022others(1): Show | 11 | HG01099.hp2 HG01884.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*43C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 43 | chr1 | 944196 | |||||
chr1:944199
|
C | T | 2 | a0001c0002t0016a0011c0035t0021 | 3 | HG02965.hp2 HG03195.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 46 | chr1 | 944199 | |||||
chr1:944215
|
C | T | 1 | a0001c0002t0026 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 62 | chr1 | 944215 | |||||
chr1:944238
|
C | T | 1 | a0001c0001t0018 | 2 | HG03209.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*85C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 85 | chr1 | 944238 | |||||
chr1:944293
|
A | G | 1 | a0005c0007t0022 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 140 | chr1 | 944293 | |||||
chr1:944296
|
G | A | 76 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(73): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 143 | chr1 | 944296 | |||||
chr1:944307
|
T | C | 80 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(77): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
3_prime_UTR_variant | MODIFIER | c.*154T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 154 | chr1 | 944307 | |||||
chr1:944394
|
G | T | 1 | a0001c0001t0030 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 241 | chr1 | 944394 | |||||
chr1:944409
|
CCTGGAA | C | 13 | a0001c0001t0014a0001c0002t0004a0001c0002t0020others(10): Show | 51 | HG00423.hp2 HG00609.hp1 HG01123.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*261_*266delAACTGG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 261 | INFO_REALIGN_3_PRIME | chr1 | 944409 | ||||
chr1:944413
|
G | T | 1 | a0001c0001t0029 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*260G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 260 | chr1 | 944413 | |||||
chr1:944505
|
C | T | 1 | a0001c0001t0033 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 352 | chr1 | 944505 | |||||
chr1:944531
|
G | A | 2 | a0001c0001t0032a0001c0002t0025 | 2 | HG01169.hp1 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*378G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 14/14 | 378 | chr1 | 944531 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:925036
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(141): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.517+88G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925036 | ||||||
chr1:925081
|
G | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(212): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.517+133G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925081 | ||||||
chr1:925124
|
G | A | 43 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0222others(40): Show | 47 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.517+176G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925124 | ||||||
chr1:925141
|
C | A | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(213): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.517+193C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925141 | ||||||
chr1:925224
|
G | A | 1 | a0001c0004t0003g0153 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.517+276G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925224 | ||||||
chr1:925286
|
G | A | 1 | a0001c0046t0014g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.517+338G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925286 | ||||||
chr1:925308
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(138): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.517+360G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925308 | ||||||
chr1:925358
|
C | CG | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00597.hp1 HG00597.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+415dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 925358 | |||||
chr1:925387
|
C | T | 1 | a0001c0004t0001g0145 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.517+439C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925387 | ||||||
chr1:925398
|
A | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(216): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.517+450A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925398 | ||||||
chr1:925408
|
TTGGCGCC others(3): Show |
T | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(216): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.517+461_517+470del others(10): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925408 | ||||||
chr1:925419
|
G | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(216): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.517+471G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925419 | ||||||
chr1:925474
|
T | C | 325 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(322): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.518-448T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925474 | ||||||
chr1:925477
|
G | A | 4 | a0001c0002t0016g0265a0001c0002t0016g0266a0006c0016t0015g0263others(1): Show | 4 | HG02965.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-445G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925477 | ||||||
chr1:925576
|
C | G | 6 | a0001c0002t0002g0319a0001c0002t0002g0320a0001c0002t0009g0321others(3): Show | 6 | HG01099.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-346C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925576 | ||||||
chr1:925577
|
G | A | 6 | a0001c0002t0002g0319a0001c0002t0002g0320a0001c0002t0009g0321others(3): Show | 6 | HG01099.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-345G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925577 | ||||||
chr1:925628
|
G | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.518-294G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925628 | ||||||
chr1:925702
|
G | C | 1 | a0011c0035t0021g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.518-220G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925702 | ||||||
chr1:925761
|
C | T | 1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.518-161C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925761 | ||||||
chr1:925875
|
A | G | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.518-47A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 1/13 | chr1 | 925875 | ||||||
chr1:926137
|
C | T | 1 | a0004c0008t0017g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.609+124C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926137 | ||||||
chr1:926150
|
G | A | 1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.609+137G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926150 | ||||||
chr1:926152
|
G | A | 1 | a0001c0011t0002g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.609+139G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926152 | ||||||
chr1:926250
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(138): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.609+237G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926250 | ||||||
chr1:926322
|
C | T | 1 | a0001c0001t0012g0365 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.609+309C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926322 | ||||||
chr1:926345
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.609+332G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926345 | ||||||
chr1:926348
|
C | T | 6 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0217others(3): Show | 6 | HG03688.hp1 NA18974.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+335C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926348 | ||||||
chr1:926374
|
G | T | 1 | a0001c0001t0003g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.609+361G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926374 | ||||||
chr1:926428
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.609+415A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926428 | ||||||
chr1:926519
|
C | T | 1 | a0003c0006t0003g0213 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.609+506C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926519 | ||||||
chr1:926567
|
C | T | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.609+554C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926567 | ||||||
chr1:926692
|
C | T | 6 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(3): Show | 6 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.609+679C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926692 | ||||||
chr1:926713
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.609+700T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926713 | ||||||
chr1:926721
|
C | T | 1 | a0024c0037t0006g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.609+708C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926721 | ||||||
chr1:926744
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.609+731A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926744 | ||||||
chr1:926793
|
T | A | 1 | a0001c0001t0003g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.609+780T>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926793 | ||||||
chr1:926806
|
A | G | 45 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0222others(42): Show | 49 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.609+793A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926806 | ||||||
chr1:926922
|
G | A | 1 | a0001c0011t0002g0314 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.609+909G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 926922 | ||||||
chr1:927003
|
C | T | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.609+990C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927003 | ||||||
chr1:927009
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.609+996A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927009 | ||||||
chr1:927016
|
C | T | 4 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218others(1): Show | 4 | NA18974.hp1 NA18992.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+1003C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927016 | ||||||
chr1:927073
|
A | G | 1 | a0001c0001t0005g0144 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.609+1060A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927073 | ||||||
chr1:927102
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.609+1089C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927102 | ||||||
chr1:927127
|
G | T | 1 | a0001c0001t0001g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.609+1114G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927127 | ||||||
chr1:927135
|
C | T | 6 | a0001c0002t0020g0304a0001c0011t0006g0025a0004c0008t0006g0303others(3): Show | 7 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+1122C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927135 | ||||||
chr1:927173
|
C | A | 1 | a0001c0002t0009g0325 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.609+1160C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927173 | ||||||
chr1:927189
|
C | T | 1 | a0024c0037t0006g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.609+1176C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927189 | ||||||
chr1:927288
|
C | T | 6 | a0001c0002t0016g0265a0001c0002t0016g0266a0003c0031t0002g0299others(3): Show | 6 | HG02965.hp2 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+1275C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927288 | ||||||
chr1:927290
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.609+1277C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927290 | ||||||
chr1:927303
|
G | A | 28 | a0001c0002t0011g0272a0001c0002t0011g0273a0001c0002t0011g0274others(25): Show | 29 | HG00642.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.609+1290G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927303 | ||||||
chr1:927392
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG00639.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.609+1379A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927392 | ||||||
chr1:927422
|
C | T | 1 | a0001c0001t0003g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.609+1409C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927422 | ||||||
chr1:927442
|
G | GC | 14 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(11): Show | 15 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.609+1436dupC | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 927442 | |||||
chr1:927486
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(118): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.609+1473C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927486 | ||||||
chr1:927543
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.609+1530C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927543 | ||||||
chr1:927744
|
G | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(212): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.609+1731G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927744 | ||||||
chr1:927750
|
A | G | 4 | a0008c0014t0004g0257a0008c0014t0004g0258a0008c0014t0004g0259others(1): Show | 4 | NA18747.hp1 NA18971.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+1737A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927750 | ||||||
chr1:927758
|
A | C | 48 | a0001c0001t0001g0051a0001c0002t0002g0001a0001c0002t0002g0004others(45): Show | 67 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.609+1745A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927758 | ||||||
chr1:927904
|
C | T | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.609+1891C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927904 | ||||||
chr1:927935
|
C | T | 2 | a0009c0013t0002g0287a0009c0013t0002g0288 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.609+1922C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 927935 | ||||||
chr1:928119
|
T | C | 25 | a0001c0002t0002g0319a0001c0002t0002g0320a0001c0002t0009g0321others(22): Show | 28 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.610-2036T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928119 | ||||||
chr1:928121
|
T | C | 28 | a0001c0001t0001g0068a0001c0002t0002g0319a0001c0002t0002g0320others(25): Show | 31 | HG00733.hp2 HG00741.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.610-2034T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928121 | ||||||
chr1:928127
|
C | T | 1 | a0001c0002t0007g0298 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.610-2028C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928127 | ||||||
chr1:928128
|
G | T | 107 | a0001c0001t0001g0010a0001c0001t0001g0137a0001c0001t0001g0138others(104): Show | 116 | HG00099.hp1 HG00609.hp1 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.610-2027G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928128 | ||||||
chr1:928131
|
T | C | 116 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0072others(113): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.610-2024T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928131 | ||||||
chr1:928141
|
C | G | 2 | a0001c0001t0001g0140a0003c0006t0003g0213 | 2 | HG00735.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.610-2014C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928141 | ||||||
chr1:928160
|
G | A | 3 | a0001c0001t0013g0157a0001c0001t0030g0205a0011c0044t0031g0156 | 3 | HG03471.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.610-1995G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928160 | ||||||
chr1:928165
|
G | A | 1 | a0001c0001t0014g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.610-1990G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928165 | ||||||
chr1:928167
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.610-1988G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928167 | ||||||
chr1:928168
|
C | T | 7 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(4): Show | 7 | HG02145.hp1 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.610-1987C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928168 | ||||||
chr1:928176
|
G | A | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(338): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.610-1979G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928176 | ||||||
chr1:928182
|
A | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(310): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.610-1973A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928182 | ||||||
chr1:928182
|
A | G | 4 | a0001c0001t0001g0048a0001c0001t0003g0202a0001c0001t0003g0203others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-1973A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928182 | ||||||
chr1:928183
|
G | A | 1 | a0001c0002t0004g0327 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.610-1972G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928183 | ||||||
chr1:928189
|
C | A | 9 | a0001c0002t0002g0004a0001c0002t0002g0026a0001c0002t0002g0329others(6): Show | 14 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.610-1966C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928189 | ||||||
chr1:928190
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.610-1965G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928190 | ||||||
chr1:928190
|
G | C | 4 | a0001c0001t0001g0048a0001c0001t0003g0202a0001c0001t0003g0203others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-1965G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928190 | ||||||
chr1:928191
|
A | G | 3 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365 | 3 | HG02145.hp1 HG02258.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.610-1964A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928191 | ||||||
chr1:928194
|
C | T | 9 | a0001c0002t0002g0004a0001c0002t0002g0026a0001c0002t0002g0329others(6): Show | 14 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.610-1961C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928194 | ||||||
chr1:928196
|
A | G | 4 | a0001c0001t0001g0048a0001c0001t0003g0202a0001c0001t0003g0203others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-1959A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928196 | ||||||
chr1:928201
|
G | A | 9 | a0001c0019t0006g0269a0004c0008t0002g0270a0004c0008t0002g0271others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.610-1954G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928201 | ||||||
chr1:928202
|
A | G | 39 | a0001c0001t0001g0029a0001c0001t0001g0149a0001c0001t0003g0201others(36): Show | 45 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.610-1953A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928202 | ||||||
chr1:928208
|
A | T | 9 | a0001c0019t0006g0269a0004c0008t0002g0270a0004c0008t0002g0271others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.610-1947A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928208 | ||||||
chr1:928209
|
C | T | 11 | a0001c0001t0001g0129a0001c0002t0002g0004a0001c0002t0002g0026others(8): Show | 16 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.610-1946C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928209 | ||||||
chr1:928210
|
G | A | 28 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(25): Show | 29 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.610-1945G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928210 | ||||||
chr1:928216
|
A | AC | 53 | a0001c0001t0001g0030a0001c0001t0001g0079a0001c0001t0001g0082others(50): Show | 72 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.610-1936dupC | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 928216 | |||||
chr1:928216
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.610-1939A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928216 | ||||||
chr1:928220
|
G | A | 3 | a0001c0001t0001g0084a0001c0001t0005g0144a0006c0016t0002g0289 | 3 | HG04228.hp1 NA18906.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.610-1935G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928220 | ||||||
chr1:928223
|
T | A | 16 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(13): Show | 17 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.610-1932T>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928223 | ||||||
chr1:928252
|
C | T | 132 | a0001c0001t0001g0010a0001c0001t0001g0119a0001c0001t0001g0120others(129): Show | 139 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(136): Show |
intron_variant | MODIFIER | c.610-1903C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928252 | ||||||
chr1:928261
|
G | A | 134 | a0001c0001t0001g0086a0001c0001t0001g0119a0001c0001t0001g0120others(131): Show | 144 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(141): Show |
intron_variant | MODIFIER | c.610-1894G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928261 | ||||||
chr1:928264
|
T | C | 144 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0032others(141): Show | 156 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(153): Show |
intron_variant | MODIFIER | c.610-1891T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928264 | ||||||
chr1:928265
|
G | A | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.610-1890G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928265 | ||||||
chr1:928266
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.610-1889C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928266 | ||||||
chr1:928278
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.610-1877G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928278 | ||||||
chr1:928309
|
A | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(262): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.610-1846A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928309 | ||||||
chr1:928316
|
C | T | 46 | a0001c0001t0003g0219a0002c0003t0004g0011a0002c0003t0004g0022others(43): Show | 50 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.610-1839C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928316 | ||||||
chr1:928341
|
C | G | 1 | a0001c0002t0002g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.610-1814C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928341 | ||||||
chr1:928346
|
T | C | 1 | a0001c0002t0002g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.610-1809T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928346 | ||||||
chr1:928347
|
G | A | 1 | a0001c0002t0002g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.610-1808G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928347 | ||||||
chr1:928348
|
T | C | 1 | a0001c0002t0002g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.610-1807T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928348 | ||||||
chr1:928354
|
C | T | 1 | a0001c0002t0002g0341 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.610-1801C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928354 | ||||||
chr1:928365
|
C | G | 1 | a0001c0002t0002g0340 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.610-1790C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928365 | ||||||
chr1:928370
|
C | G | 1 | a0004c0008t0002g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.610-1785C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928370 | ||||||
chr1:928371
|
A | G | 1 | a0004c0008t0002g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.610-1784A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928371 | ||||||
chr1:928387
|
G | A | 5 | a0001c0002t0011g0272a0001c0002t0011g0273a0001c0002t0011g0274others(2): Show | 5 | HG00642.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-1768G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928387 | ||||||
chr1:928396
|
A | C | 96 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(93): Show | 102 | HG00609.hp1 HG01069.hp2 HG01123.hp1 others(99): Show |
intron_variant | MODIFIER | c.610-1759A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928396 | ||||||
chr1:928463
|
C | T | 122 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(119): Show | 146 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.610-1692C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928463 | ||||||
chr1:928483
|
G | A | 134 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(131): Show | 159 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.610-1672G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928483 | ||||||
chr1:928598
|
G | A | 65 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(62): Show | 70 | HG00609.hp1 HG01069.hp2 HG01123.hp1 others(67): Show |
intron_variant | MODIFIER | c.610-1557G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928598 | ||||||
chr1:928622
|
G | C | 66 | a0001c0001t0001g0018a0001c0001t0001g0082a0001c0001t0001g0088others(63): Show | 69 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.610-1533G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928622 | ||||||
chr1:928711
|
G | A | 1 | a0003c0006t0001g0089 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.610-1444G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928711 | ||||||
chr1:928735
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.610-1420C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928735 | ||||||
chr1:928858
|
G | A | 2 | a0001c0002t0004g0327a0001c0002t0025g0344 | 2 | NA18612.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.610-1297G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928858 | ||||||
chr1:928861
|
C | T | 14 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(11): Show | 15 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.610-1294C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928861 | ||||||
chr1:928967
|
T | G | 1 | a0001c0002t0007g0298 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.610-1188T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 928967 | ||||||
chr1:929007
|
A | G | 1 | a0005c0007t0022g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.610-1148A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929007 | ||||||
chr1:929102
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.610-1053C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929102 | ||||||
chr1:929109
|
C | T | 4 | a0002c0003t0004g0241a0002c0003t0004g0242a0002c0003t0004g0243others(1): Show | 4 | HG02132.hp2 NA18940.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-1046C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929109 | ||||||
chr1:929110
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG01255.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.610-1045C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929110 | ||||||
chr1:929182
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.610-973T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929182 | ||||||
chr1:929235
|
G | A | 39 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0222others(36): Show | 43 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(40): Show |
intron_variant | MODIFIER | c.610-920G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929235 | ||||||
chr1:929241
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0088 | 3 | NA18951.hp2 NA19001.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.610-914G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929241 | ||||||
chr1:929321
|
A | G | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-834A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929321 | ||||||
chr1:929346
|
T | A | 361 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(358): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.610-809T>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929346 | ||||||
chr1:929375
|
A | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(262): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.610-780A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929375 | ||||||
chr1:929377
|
G | A | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(262): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.610-778G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929377 | ||||||
chr1:929515
|
C | T | 1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.610-640C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929515 | ||||||
chr1:929518
|
A | G | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-637A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929518 | ||||||
chr1:929558
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(148): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.610-597G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929558 | ||||||
chr1:929774
|
G | A | 1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.610-381G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929774 | ||||||
chr1:929839
|
G | A | 64 | a0001c0001t0001g0082a0001c0001t0001g0147a0001c0001t0003g0020others(61): Show | 66 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.610-316G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929839 | ||||||
chr1:929861
|
T | G | 1 | a0001c0002t0002g0319 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610-294T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929861 | ||||||
chr1:929881
|
G | A | 5 | a0001c0001t0012g0363a0001c0001t0012g0365a0001c0002t0002g0315others(2): Show | 5 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-274G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929881 | ||||||
chr1:929886
|
GGGATGCC others(7): Show |
G | 1 | a0001c0001t0001g0068 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.610-266_610-253del others(14): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 929886 | |||||
chr1:929905
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.610-250C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929905 | ||||||
chr1:929962
|
C | T | 1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.610-193C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929962 | ||||||
chr1:929987
|
G | T | 44 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0222others(41): Show | 48 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.610-168G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 929987 | ||||||
chr1:930014
|
C | T | 1 | a0002c0003t0004g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.610-141C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 930014 | ||||||
chr1:930015
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.610-140G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 930015 | ||||||
chr1:930055
|
C | G | 2 | a0001c0002t0002g0345a0001c0002t0009g0325 | 2 | HG02735.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.610-100C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 930055 | ||||||
chr1:930055
|
C | T | 1 | a0003c0031t0002g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.610-100C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 930055 | ||||||
chr1:930058
|
C | T | 8 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(5): Show | 8 | NA18906.hp1 NA18942.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.610-97C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | chr1 | 930058 | ||||||
chr1:930081
|
A | AGCCCCAC others(14): Show |
3 | a0001c0002t0002g0338a0001c0002t0002g0339a0001c0002t0002g0352 | 3 | NA18945.hp1 NA18960.hp1 NA18998.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.610-23_610-3dupTTC others(18): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 930081 | |||||
chr1:930081
|
AGCCCCAC others(14): Show |
A | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.610-23_610-3delTTC others(18): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 930081 | |||||
chr1:930631
|
C | G | 1 | a0002c0003t0004g0245 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.791+295C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/13 | chr1 | 930631 | ||||||
chr1:930632
|
G | C | 1 | a0002c0003t0004g0245 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.791+296G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/13 | chr1 | 930632 | ||||||
chr1:930873
|
A | G | 1 | a0001c0002t0009g0323 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.792-166A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/13 | chr1 | 930873 | ||||||
chr1:930939
|
G | A | 361 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(358): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.792-100G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 3/13 | chr1 | 930939 | ||||||
chr1:931108
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.842+19G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931108 | ||||||
chr1:931131
|
C | CCCCT | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(150): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.842+54_842+57dupTC others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 931131 | |||||
chr1:931137
|
C | G | 2 | a0001c0002t0020g0304a0001c0011t0006g0025 | 3 | HG02257.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.842+48C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931137 | ||||||
chr1:931196
|
G | A | 1 | a0005c0007t0008g0277 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.842+107G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931196 | ||||||
chr1:931351
|
G | C | 6 | a0001c0002t0020g0304a0001c0011t0006g0025a0013c0020t0002g0318others(3): Show | 7 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+262G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931351 | ||||||
chr1:931442
|
A | T | 3 | a0001c0004t0001g0063a0001c0004t0001g0064a0001c0004t0001g0065 | 3 | HG02886.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.842+353A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931442 | ||||||
chr1:931513
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.842+424T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931513 | ||||||
chr1:931526
|
G | A | 28 | a0001c0002t0020g0304a0001c0011t0006g0025a0001c0019t0006g0269others(25): Show | 29 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.842+437G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931526 | ||||||
chr1:931540
|
A | G | 372 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(369): Show | 433 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(430): Show |
intron_variant | MODIFIER | c.842+451A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931540 | ||||||
chr1:931558
|
G | A | 115 | a0001c0001t0001g0082a0001c0001t0001g0147a0001c0001t0003g0020others(112): Show | 136 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.842+469G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931558 | ||||||
chr1:931771
|
G | A | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.842+682G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931771 | ||||||
chr1:931785
|
G | A | 5 | a0001c0002t0002g0319a0001c0002t0002g0320a0001c0002t0009g0321others(2): Show | 5 | HG01099.hp1 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.842+696G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931785 | ||||||
chr1:931859
|
T | A | 1 | a0001c0004t0012g0055 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.842+770T>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931859 | ||||||
chr1:931867
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.842+778G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931867 | ||||||
chr1:931869
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.842+780A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931869 | ||||||
chr1:931877
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.842+788G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931877 | ||||||
chr1:931918
|
G | A | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.842+829G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931918 | ||||||
chr1:931990
|
T | C | 28 | a0001c0002t0020g0304a0001c0011t0006g0025a0001c0019t0006g0269others(25): Show | 29 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.842+901T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 931990 | ||||||
chr1:932002
|
C | T | 1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.842+913C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932002 | ||||||
chr1:932023
|
C | T | 1 | a0020c0039t0005g0111 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.842+934C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932023 | ||||||
chr1:932024
|
G | A | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.842+935G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932024 | ||||||
chr1:932038
|
C | T | 28 | a0001c0002t0020g0304a0001c0011t0006g0025a0001c0019t0006g0269others(25): Show | 29 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.842+949C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932038 | ||||||
chr1:932062
|
C | T | 2 | a0001c0010t0007g0294a0001c0010t0007g0295 | 2 | HG01069.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.842+973C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932062 | ||||||
chr1:932099
|
A | T | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.842+1010A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932099 | ||||||
chr1:932172
|
T | G | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.842+1083T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932172 | ||||||
chr1:932203
|
C | T | 1 | a0006c0016t0015g0264 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.842+1114C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932203 | ||||||
chr1:932204
|
A | T | 359 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(356): Show | 420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.842+1115A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932204 | ||||||
chr1:932206
|
G | T | 1 | a0001c0001t0001g0030 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.842+1117G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932206 | ||||||
chr1:932255
|
C | T | 63 | a0001c0001t0001g0082a0001c0001t0001g0147a0001c0001t0003g0020others(60): Show | 65 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.842+1166C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932255 | ||||||
chr1:932312
|
C | T | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.842+1223C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932312 | ||||||
chr1:932340
|
C | T | 2 | a0001c0001t0003g0214a0001c0001t0003g0220 | 2 | NA18967.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.842+1251C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932340 | ||||||
chr1:932477
|
G | A | 1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.842+1388G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932477 | ||||||
chr1:932512
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.842+1423G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932512 | ||||||
chr1:932599
|
C | A | 1 | a0001c0004t0012g0055 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.842+1510C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932599 | ||||||
chr1:932613
|
GTTTC | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(306): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.842+1529_842+1532d others(6): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 932613 | |||||
chr1:932716
|
T | C | 50 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(47): Show | 52 | HG01069.hp2 HG01123.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.842+1627T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932716 | ||||||
chr1:932732
|
C | T | 7 | a0001c0001t0005g0127a0001c0001t0012g0363a0001c0001t0012g0364others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+1643C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932732 | ||||||
chr1:932733
|
G | A | 42 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0026others(39): Show | 61 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.842+1644G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932733 | ||||||
chr1:932814
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.842+1725C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932814 | ||||||
chr1:932949
|
A | C | 363 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(360): Show | 424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.842+1860A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932949 | ||||||
chr1:932963
|
C | T | 4 | a0001c0019t0006g0269a0001c0019t0006g0282a0001c0023t0001g0091others(1): Show | 4 | HG02723.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.842+1874C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932963 | ||||||
chr1:932975
|
GCGTGGGC others(32): Show |
G | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.842+1888_842+1926d others(41): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 932975 | |||||
chr1:932976
|
C | T | 10 | a0001c0001t0013g0200a0001c0002t0007g0296a0001c0002t0007g0297others(7): Show | 11 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+1887C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 932976 | ||||||
chr1:933018
|
C | G | 1 | a0001c0001t0003g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.842+1929C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933018 | ||||||
chr1:933022
|
CCCT | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0110others(2): Show | 6 | NA18949.hp2 NA18971.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.842+1935_842+1937d others(5): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933022 | |||||
chr1:933024
|
C | T | 347 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(344): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.842+1935C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933024 | ||||||
chr1:933028
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0051a0001c0001t0001g0110others(2): Show | 6 | NA18949.hp2 NA18971.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.842+1939C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933028 | ||||||
chr1:933036
|
C | T | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.842+1947C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933036 | ||||||
chr1:933038
|
C | T | 74 | a0001c0001t0001g0082a0001c0001t0001g0147a0001c0001t0003g0020others(71): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.842+1949C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933038 | ||||||
chr1:933142
|
A | AG | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.842+2056dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933142 | |||||
chr1:933303
|
C | T | 1 | a0003c0006t0003g0213 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.842+2214C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933303 | ||||||
chr1:933355
|
C | T | 1 | a0001c0005t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.842+2266C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933355 | ||||||
chr1:933401
|
A | C | 8 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0010t0007g0024others(5): Show | 9 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+2312A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933401 | ||||||
chr1:933411
|
C | T | 331 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(328): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.842+2322C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933411 | ||||||
chr1:933434
|
A | G | 2 | a0001c0004t0027g0362a0011c0035t0021g0267 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.843-2338A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933434 | ||||||
chr1:933460
|
C | T | 44 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0224others(41): Show | 48 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.843-2312C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933460 | ||||||
chr1:933481
|
C | T | 16 | a0001c0002t0002g0319a0001c0002t0002g0320a0001c0002t0009g0321others(13): Show | 16 | HG00642.hp2 HG01099.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.843-2291C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933481 | ||||||
chr1:933491
|
A | G | 1 | a0001c0002t0002g0367 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.843-2281A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933491 | ||||||
chr1:933511
|
A | G | 358 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(355): Show | 419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.843-2261A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933511 | ||||||
chr1:933548
|
A | AG | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.843-2218dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933548 | |||||
chr1:933601
|
C | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(211): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.843-2171C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933601 | ||||||
chr1:933653
|
C | T | 12 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(9): Show | 12 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.843-2119C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933653 | ||||||
chr1:933691
|
G | A | 7 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(4): Show | 7 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-2081G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933691 | ||||||
chr1:933727
|
C | T | 1 | a0001c0046t0014g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.843-2045C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933727 | ||||||
chr1:933741
|
T | TG | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(190): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.843-2023dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933741 | |||||
chr1:933742
|
G | GC | 2 | a0001c0001t0001g0018a0001c0001t0001g0088 | 3 | NA18951.hp2 NA19001.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.843-2030_843-2029i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933742 | ||||||
chr1:933771
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.843-2001G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933771 | ||||||
chr1:933775
|
G | A | 1 | a0001c0001t0003g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.843-1997G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933775 | ||||||
chr1:933864
|
C | CAG | 29 | a0001c0001t0018g0151a0001c0001t0018g0152a0001c0019t0006g0269others(26): Show | 29 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.843-1907_843-1906d others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933864 | |||||
chr1:933869
|
T | C | 29 | a0001c0001t0018g0151a0001c0001t0018g0152a0001c0019t0006g0269others(26): Show | 29 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.843-1903T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933869 | ||||||
chr1:933923
|
C | T | 68 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(65): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.843-1849C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933923 | ||||||
chr1:933943
|
T | C | 362 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(359): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.843-1829T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933943 | ||||||
chr1:933954
|
G | A | 2 | a0001c0001t0001g0093a0003c0006t0001g0089 | 2 | HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.843-1818G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933954 | ||||||
chr1:933959
|
A | ACTGCTCC others(21): Show |
2 | a0001c0019t0006g0269a0004c0008t0017g0361 | 2 | HG01099.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.843-1811_843-1784d others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933959 | |||||
chr1:933961
|
T | TGCTCCGT others(49): Show |
1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1784_843-1783i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933961 | |||||
chr1:933961
|
TGCTCCGT others(133): Show |
T | 1 | a0001c0001t0003g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.843-1695_843-1556d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933961 | |||||
chr1:933961
|
TGCTCCGT others(245): Show |
T | 3 | a0005c0007t0008g0280a0005c0007t0022g0283a0016c0028t0008g0268 | 3 | HG02886.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.843-1779_843-1528d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933961 | |||||
chr1:933965
|
C | CCGTTACA others(189): Show |
1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.843-1784_843-1783i others(198): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933965 | |||||
chr1:933965
|
CCGTTACA others(77): Show |
C | 2 | a0004c0008t0002g0271a0011c0035t0021g0267 | 2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.843-1751_843-1668d others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933965 | |||||
chr1:933967
|
G | A | 1 | a0001c0004t0001g0063 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843-1805G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933967 | ||||||
chr1:933975
|
T | A | 1 | a0001c0002t0002g0347 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.843-1797T>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933975 | ||||||
chr1:933980
|
A | AGGGGAGG others(21): Show |
1 | a0018c0030t0006g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.843-1784_843-1783i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933980 | |||||
chr1:933980
|
A | AGGGGAGG others(309): Show |
1 | a0001c0001t0012g0363 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.843-1784_843-1783i others(318): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933980 | |||||
chr1:933980
|
A | AGGGGAGG others(2622): Show |
1 | a0001c0011t0002g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.843-1784_843-1783i others(2631): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933980 | |||||
chr1:933980
|
AGGGGAGG others(693): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.843-1779_843-1080d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933980 | |||||
chr1:933980
|
AGGGGAGG others(749): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.843-1708_843-953de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933980 | |||||
chr1:933980
|
AGGGGAGG others(833): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.843-1779_843-940de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933980 | |||||
chr1:933985
|
A | AGGCTGCT others(107): Show |
3 | a0013c0020t0002g0318a0013c0020t0006g0302a0024c0037t0006g0307 | 3 | HG02922.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.843-1784_843-1783i others(116): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 933985 | |||||
chr1:933988
|
C | CTGCTCCG others(18): Show |
1 | a0001c0009t0010g0308 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.843-1784_843-1783i others(27): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933988 | ||||||
chr1:933989
|
G | T | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(338): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.843-1783G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933989 | ||||||
chr1:933993
|
G | C | 343 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(340): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.843-1779G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 933993 | ||||||
chr1:934005
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1767G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934005 | ||||||
chr1:934008
|
A | G | 7 | a0001c0001t0012g0363a0001c0001t0012g0365a0001c0011t0002g0291others(4): Show | 7 | HG02258.hp2 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-1764A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934008 | ||||||
chr1:934008
|
AGGGGAGG others(301): Show |
A | 1 | a0001c0004t0027g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.843-1736_843-1429d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934008 | |||||
chr1:934008
|
AGGGGAGG others(721): Show |
A | 1 | a0001c0001t0001g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.843-1680_843-953de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934008 | |||||
chr1:934013
|
A | AGGCGGCT others(50): Show |
1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.843-1737_843-1736i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934013 | |||||
chr1:934013
|
AGGCGGCT others(357): Show |
A | 1 | a0005c0007t0008g0300 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.843-1736_843-1373d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934013 | |||||
chr1:934016
|
C | T | 1 | a0001c0001t0012g0365 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.843-1756C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934016 | ||||||
chr1:934017
|
G | GGCTGCGT others(49): Show |
1 | a0001c0002t0011g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843-1700_843-1699i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934017 | |||||
chr1:934017
|
G | T | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-1755G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934017 | ||||||
chr1:934021
|
G | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(279): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.843-1751G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934021 | ||||||
chr1:934021
|
G | GCGTTACA others(21): Show |
3 | a0005c0007t0008g0277a0005c0007t0008g0278a0005c0007t0008g0279 | 3 | HG02109.hp1 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.843-1737_843-1736i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934021 | |||||
chr1:934033
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.843-1739G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934033 | ||||||
chr1:934035
|
C | CGGGGGAG others(81): Show |
1 | a0006c0016t0015g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843-1737_843-1736i others(90): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934035 | ||||||
chr1:934036
|
A | AGGGGAGG others(49): Show |
1 | a0006c0016t0002g0289 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.843-1724_843-1723i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934036 | |||||
chr1:934036
|
A | G | 24 | a0001c0001t0001g0018a0001c0001t0001g0088a0001c0001t0001g0097others(21): Show | 25 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.843-1736A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934036 | ||||||
chr1:934036
|
AGGGGAGG others(693): Show |
A | 8 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0085others(5): Show | 8 | HG00673.hp2 HG02135.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-1667_843-968de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934036 | |||||
chr1:934036
|
AGGGGAGG others(861): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.843-1708_843-841de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934036 | |||||
chr1:934041
|
A | AGGCGGCT others(22): Show |
2 | a0013c0020t0002g0318a0013c0020t0006g0302 | 2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.843-1709_843-1708i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934041 | |||||
chr1:934041
|
A | AGGCTGCT others(499): Show |
1 | a0001c0009t0010g0313 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.843-1728_843-1727i others(508): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934041 | |||||
chr1:934041
|
A | G | 2 | a0001c0011t0028g0316a0018c0030t0006g0301 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.843-1731A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934041 | ||||||
chr1:934044
|
C | T | 5 | a0001c0002t0002g0315a0001c0002t0016g0265a0001c0002t0016g0266others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1728C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934044 | ||||||
chr1:934045
|
G | T | 9 | a0001c0009t0010g0309a0001c0009t0010g0310a0001c0009t0010g0311others(6): Show | 9 | HG02280.hp1 HG02896.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-1727G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934045 | ||||||
chr1:934045
|
G | TGCTCCGT others(21): Show |
1 | a0009c0013t0002g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.843-1728_843-1727i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934045 | ||||||
chr1:934049
|
G | C | 25 | a0001c0001t0003g0201a0001c0001t0012g0364a0001c0001t0012g0365others(22): Show | 26 | HG01069.hp2 HG01099.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.843-1723G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934049 | ||||||
chr1:934049
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0029g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.843-1709_843-1708i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934049 | |||||
chr1:934049
|
GCGTTACA others(161): Show |
G | 1 | a0001c0001t0003g0178 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.843-1695_843-1528d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934049 | |||||
chr1:934061
|
G | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(209): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.843-1711G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934061 | ||||||
chr1:934063
|
C | CG | 3 | a0006c0016t0002g0289a0006c0016t0015g0263a0024c0037t0006g0307 | 3 | HG02922.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.843-1709_843-1708i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934063 | ||||||
chr1:934063
|
CAGGGGAG others(804): Show |
C | 1 | a0001c0002t0002g0315 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.843-1708_843-898de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934063 | ||||||
chr1:934064
|
A | AGGGGAGG others(279): Show |
1 | a0001c0001t0012g0364 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.843-1700_843-1699i others(288): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934064
|
A | AGGGGGGG others(597): Show |
1 | a0002c0018t0004g0226 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.843-1704_843-1703i others(606): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934064
|
A | G | 18 | a0001c0001t0012g0363a0001c0001t0012g0365a0001c0002t0016g0265others(15): Show | 18 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.843-1708A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934064 | ||||||
chr1:934064
|
AGGGGAGG others(637): Show |
A | 1 | a0001c0001t0001g0106 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.843-1680_843-1037d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934064
|
AGGGGAGG others(749): Show |
A | 2 | a0001c0001t0001g0018a0001c0001t0001g0088 | 3 | NA18951.hp2 NA19001.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.843-1695_843-940de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934064
|
AGGGGAGG others(777): Show |
A | 1 | a0001c0002t0002g0337 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.843-1680_843-897de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934064
|
AGGGGAGG others(805): Show |
A | 1 | a0001c0004t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.843-1680_843-869de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934064
|
AGGGGAGG others(833): Show |
A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(101): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.843-1680_843-841de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934064
|
AGGGGAGG others(834): Show |
A | 1 | a0001c0004t0012g0055 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.843-1704_843-864de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934064 | |||||
chr1:934069
|
A | AGGCTGCT others(21): Show |
3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG02083.hp1 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.843-1700_843-1699i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934069 | |||||
chr1:934069
|
A | G | 10 | a0001c0001t0012g0363a0001c0001t0029g0170a0001c0009t0010g0308others(7): Show | 10 | HG00438.hp1 HG02258.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.843-1703A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934069 | ||||||
chr1:934069
|
AGGCGGCT others(861): Show |
A | 1 | a0001c0005t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.843-1680_843-813de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934069 | |||||
chr1:934073
|
G | T | 66 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(63): Show | 69 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.843-1699G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934073 | ||||||
chr1:934077
|
G | C | 95 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(92): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.843-1695G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934077 | ||||||
chr1:934077
|
GCGTTACA others(21): Show |
G | 4 | a0001c0001t0001g0142a0001c0002t0002g0358a0002c0003t0004g0224others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1667_843-1640d others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934077 | |||||
chr1:934077
|
GCGTTACA others(133): Show |
G | 1 | a0001c0002t0002g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.843-1596_843-1457d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934077 | |||||
chr1:934077
|
GCGTTACA others(609): Show |
G | 2 | a0001c0004t0001g0061a0001c0004t0001g0062 | 2 | HG01358.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.843-1680_843-1065d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934077 | |||||
chr1:934089
|
G | T | 5 | a0001c0001t0005g0050a0001c0001t0005g0122a0001c0001t0005g0127others(2): Show | 5 | NA18612.hp2 NA18939.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1683G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934089 | ||||||
chr1:934092
|
A | AGGGGAGG others(189): Show |
1 | a0001c0023t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843-1668_843-1667i others(198): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934092 | |||||
chr1:934092
|
A | AGGGGGGG others(21): Show |
1 | a0002c0003t0004g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.843-1676_843-1675i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934092 | |||||
chr1:934092
|
A | AGGGGGGG others(964): Show |
1 | a0002c0003t0004g0256 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.843-1676_843-1675i others(973): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934092 | |||||
chr1:934092
|
A | G | 29 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0098others(26): Show | 29 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.843-1680A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934092 | ||||||
chr1:934092
|
AGGGGAGG others(217): Show |
A | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.843-1667_843-1444d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934092 | |||||
chr1:934092
|
AGGGGAGG others(412): Show |
A | 1 | a0005c0007t0008g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.843-1675_843-1257d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934092 | |||||
chr1:934092
|
AGGGGAGG others(749): Show |
A | 2 | a0001c0002t0004g0327a0001c0002t0025g0344 | 2 | NA18612.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.843-1667_843-912de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934092 | |||||
chr1:934092
|
AGGGGAGG others(805): Show |
A | 47 | a0001c0001t0001g0010a0001c0001t0001g0138a0001c0001t0005g0007others(44): Show | 69 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.843-1667_843-856de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934092 | |||||
chr1:934097
|
A | AGGCGGCT others(217): Show |
1 | a0001c0019t0006g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.843-1668_843-1667i others(226): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934097 | |||||
chr1:934097
|
A | G | 53 | a0001c0001t0003g0171a0001c0001t0003g0197a0001c0001t0003g0198others(50): Show | 56 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(53): Show |
intron_variant | MODIFIER | c.843-1675A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934097 | ||||||
chr1:934101
|
G | T | 5 | a0001c0001t0012g0365a0001c0004t0001g0060a0001c0004t0001g0145others(2): Show | 5 | HG02895.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1671G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934101 | ||||||
chr1:934105
|
C | CCGTTACA others(46): Show |
4 | a0008c0014t0004g0258a0008c0014t0004g0259a0008c0014t0004g0260others(1): Show | 4 | NA18971.hp1 NA18975.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-1653_843-1652i others(55): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934105 | |||||
chr1:934105
|
C | G | 39 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0098others(36): Show | 39 | HG01074.hp2 HG01884.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.843-1667C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934105 | ||||||
chr1:934105
|
CCGTTACA others(637): Show |
C | 2 | a0001c0001t0003g0176a0021c0040t0003g0174 | 2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.843-1596_843-953de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934105 | |||||
chr1:934117
|
G | T | 6 | a0001c0002t0002g0359a0001c0011t0002g0324a0002c0003t0004g0224others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-1655G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934117 | ||||||
chr1:934119
|
C | CG | 13 | a0001c0001t0012g0363a0001c0002t0007g0296a0001c0002t0007g0297others(10): Show | 14 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.843-1653_843-1652i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934119 | ||||||
chr1:934119
|
C | CGG | 3 | a0001c0002t0016g0265a0001c0002t0016g0266a0006c0016t0015g0264 | 3 | HG02965.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.843-1653_843-1652i others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934119 | ||||||
chr1:934120
|
A | AGGGGAGC others(104): Show |
1 | a0002c0003t0004g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.843-1646_843-1645i others(113): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934120 | |||||
chr1:934120
|
A | AGGGGCGG others(127): Show |
1 | a0002c0018t0004g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.843-1648_843-1647i others(136): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934120 | |||||
chr1:934120
|
A | AGGGGGGG others(21): Show |
2 | a0002c0003t0004g0235a0002c0003t0004g0236 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.843-1648_843-1647i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934120 | |||||
chr1:934120
|
A | G | 69 | a0001c0001t0001g0086a0001c0001t0001g0105a0001c0001t0003g0177others(66): Show | 70 | HG00609.hp1 HG01069.hp2 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.843-1652A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934120 | ||||||
chr1:934122
|
GGGAGGCG others(159): Show |
G | 1 | a0003c0031t0002g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.843-1647_843-1482d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934122 | |||||
chr1:934123
|
G | GGCGGCTG others(264): Show |
1 | a0002c0018t0004g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.843-1648_843-1647i others(273): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934123 | |||||
chr1:934123
|
G | GGGGGCGG others(619): Show |
1 | a0002c0003t0004g0239 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.843-1648_843-1647i others(628): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934123 | |||||
chr1:934125
|
A | AGGCGGCT others(274): Show |
1 | a0004c0008t0002g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.843-1640_843-1639i others(283): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934125 | |||||
chr1:934125
|
A | AGGCGGCT others(18): Show |
3 | a0002c0003t0004g0253a0002c0003t0004g0254a0002c0003t0004g0255 | 3 | HG00609.hp1 HG02523.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.843-1644_843-1620d others(27): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934125 | |||||
chr1:934125
|
A | AGGCGGCT others(186): Show |
1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1625_843-1624i others(195): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934125 | |||||
chr1:934125
|
A | G | 29 | a0001c0001t0001g0142a0001c0001t0003g0171a0001c0001t0003g0214others(26): Show | 30 | HG01069.hp2 HG01123.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.843-1647A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934125 | ||||||
chr1:934127
|
G | GCGGCTGC others(432): Show |
1 | a0008c0014t0004g0259 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.843-1625_843-1624i others(441): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934127 | |||||
chr1:934128
|
C | T | 1 | a0001c0011t0002g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.843-1644C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934128 | ||||||
chr1:934129
|
G | T | 1 | a0001c0001t0003g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.843-1643G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934129 | ||||||
chr1:934133
|
G | C | 18 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0003g0197others(15): Show | 18 | HG00642.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.843-1639G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934133 | ||||||
chr1:934133
|
G | GCGTTACA others(74): Show |
1 | a0001c0009t0010g0309 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.843-1621_843-1620i others(83): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934133 | |||||
chr1:934133
|
G | GCGTTACA others(21): Show |
1 | a0001c0009t0003g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.843-1625_843-1624i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934133 | |||||
chr1:934133
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.843-1625_843-1624i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934133 | |||||
chr1:934133
|
GCGTTACA others(105): Show |
G | 3 | a0001c0002t0002g0358a0002c0003t0004g0224a0002c0049t0004g0223 | 3 | HG02451.hp2 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.843-1568_843-1457d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934133 | |||||
chr1:934133
|
GCGTTACA others(693): Show |
G | 1 | a0001c0001t0003g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.843-1624_843-925de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934133 | |||||
chr1:934145
|
G | T | 3 | a0001c0004t0001g0071a0007c0012t0001g0009a0007c0012t0001g0115 | 5 | HG01891.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-1627G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934145 | ||||||
chr1:934147
|
C | CG | 5 | a0001c0001t0012g0365a0001c0002t0007g0296a0001c0002t0007g0297others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1625_843-1624i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934147 | ||||||
chr1:934148
|
A | AGGGGAGG others(1736): Show |
1 | a0001c0009t0010g0308 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.843-1616_843-1615i others(1745): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934148
|
A | AGGGGCGG others(348): Show |
1 | a0008c0014t0004g0257 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.843-1620_843-1619i others(357): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934148
|
A | AGGGGCGG others(741): Show |
1 | a0002c0003t0004g0251 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.843-1620_843-1619i others(750): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934148
|
A | AGGGGCGG others(1522): Show |
1 | a0002c0003t0004g0245 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.843-1620_843-1619i others(1531): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934148
|
A | AGGGGCGG others(675): Show |
1 | a0002c0003t0004g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.843-1620_843-1619i others(684): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934148
|
A | AGGGGCGG others(986): Show |
1 | a0001c0046t0014g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.843-1620_843-1619i others(995): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934148
|
A | G | 120 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(117): Show | 126 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.843-1624A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934148 | ||||||
chr1:934148
|
AGGGGAGG others(721): Show |
A | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.843-1596_843-869de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934148
|
AGGGGAGG others(749): Show |
A | 1 | a0004c0036t0002g0346 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.843-1596_843-841de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934148 | |||||
chr1:934150
|
G | GGGCGGCT others(43): Show |
1 | a0002c0003t0004g0238 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.843-1620_843-1619i others(52): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934150 | |||||
chr1:934150
|
GGGA | G | 5 | a0002c0003t0004g0236a0002c0003t0004g0241a0002c0003t0004g0242others(2): Show | 5 | HG02071.hp2 HG02132.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1619_843-1617d others(5): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934150 | |||||
chr1:934150
|
GGGAGGCG others(332): Show |
G | 1 | a0002c0003t0004g0250 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.843-1619_843-1281d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934150 | |||||
chr1:934151
|
G | GGCGGCTG others(127): Show |
1 | a0002c0003t0004g0305 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.843-1620_843-1619i others(136): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934151 | |||||
chr1:934151
|
G | GGCGGCTG others(264): Show |
3 | a0002c0003t0004g0246a0002c0003t0004g0252a0002c0003t0004g0306 | 3 | NA18952.hp1 NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.843-1620_843-1619i others(273): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934151 | |||||
chr1:934151
|
G | GGCGGCTG others(286): Show |
1 | a0002c0003t0004g0237 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.843-1620_843-1619i others(295): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934151 | |||||
chr1:934153
|
A | AGGCGGCT others(77): Show |
1 | a0001c0011t0002g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.843-1597_843-1596i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934153 | |||||
chr1:934153
|
A | AGGCGGCT others(850): Show |
1 | a0008c0014t0004g0260 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.843-1597_843-1596i others(859): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934153 | |||||
chr1:934153
|
A | G | 24 | a0001c0001t0003g0171a0001c0001t0003g0214a0001c0001t0012g0365others(21): Show | 24 | HG01099.hp2 HG01891.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.843-1619A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934153 | ||||||
chr1:934153
|
AGGCGGCT others(217): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.843-1596_843-1373d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934153 | |||||
chr1:934155
|
G | T | 2 | a0002c0003t0004g0256a0002c0018t0004g0227 | 2 | NA18993.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.843-1617G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934155 | ||||||
chr1:934157
|
G | T | 4 | a0001c0019t0006g0269a0004c0008t0002g0317a0009c0013t0002g0288others(1): Show | 4 | HG01106.hp2 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-1615G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934157 | ||||||
chr1:934161
|
G | C | 24 | a0001c0001t0001g0097a0001c0001t0001g0142a0001c0001t0003g0173others(21): Show | 24 | HG01099.hp1 HG01106.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.843-1611G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934161 | ||||||
chr1:934161
|
G | GCGTTACA others(246): Show |
1 | a0006c0024t0003g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.843-1597_843-1596i others(255): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934161 | |||||
chr1:934161
|
G | GCGTTACA others(386): Show |
1 | a0001c0001t0003g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.843-1597_843-1596i others(395): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934161 | |||||
chr1:934161
|
GCGTTACA others(77): Show |
G | 1 | a0001c0002t0002g0359 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.843-1555_843-1472d others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934161 | |||||
chr1:934161
|
GCGTTACA others(665): Show |
G | 2 | a0001c0001t0001g0086a0001c0001t0001g0105 | 2 | HG02735.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.843-1596_843-925de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934161 | |||||
chr1:934168
|
A | AGGTGGGC others(105): Show |
2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-1597_843-1596i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934168 | |||||
chr1:934168
|
A | T | 1 | a0001c0001t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.843-1604A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934168 | ||||||
chr1:934175
|
C | CG | 6 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-1597_843-1596i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934175 | ||||||
chr1:934176
|
A | AGGGGCGG others(18): Show |
1 | a0002c0003t0004g0230 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.843-1592_843-1591i others(27): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934176 | |||||
chr1:934176
|
A | G | 130 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(127): Show | 133 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.843-1596A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934176 | ||||||
chr1:934176
|
AGGGGAGG others(133): Show |
A | 1 | a0002c0003t0004g0248 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.843-1568_843-1429d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934176 | |||||
chr1:934176
|
AGGGGAGG others(637): Show |
A | 1 | a0001c0004t0001g0060 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.843-1583_843-940de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934176 | |||||
chr1:934178
|
GGGAGGCG others(80): Show |
G | 4 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0024g0233others(1): Show | 7 | HG01255.hp2 HG01358.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-1591_843-1505d others(89): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934178 | |||||
chr1:934178
|
GGGAGGCG others(248): Show |
G | 1 | a0014c0027t0004g0231 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.843-1591_843-1337d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934178 | |||||
chr1:934179
|
G | GGCGGCTC others(15): Show |
1 | a0002c0003t0004g0229 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.843-1592_843-1591i others(24): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934179 | |||||
chr1:934179
|
G | GGGGGCGG others(961): Show |
1 | a0008c0014t0004g0258 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.843-1592_843-1591i others(970): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934179 | |||||
chr1:934181
|
A | AGGCGGCT others(133): Show |
1 | a0001c0001t0003g0159 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.843-1569_843-1568i others(142): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934181 | |||||
chr1:934181
|
A | AGGCGGCT others(245): Show |
1 | a0001c0001t0003g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.843-1569_843-1568i others(254): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934181 | |||||
chr1:934181
|
A | G | 32 | a0001c0001t0003g0172a0001c0001t0003g0203a0001c0001t0003g0204others(29): Show | 32 | HG01123.hp2 HG01167.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.843-1591A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934181 | ||||||
chr1:934183
|
G | GCGGCTGC others(687): Show |
1 | a0002c0003t0004g0255 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.843-1570_843-1569i others(696): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934183 | |||||
chr1:934183
|
G | T | 3 | a0002c0003t0004g0235a0002c0018t0004g0225a0008c0014t0004g0257 | 3 | HG02165.hp2 NA18747.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.843-1589G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934183 | ||||||
chr1:934185
|
G | T | 3 | a0001c0001t0012g0364a0001c0009t0010g0310a0001c0009t0010g0311 | 3 | HG02145.hp1 NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.843-1587G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934185 | ||||||
chr1:934189
|
G | C | 26 | a0001c0001t0003g0172a0001c0001t0012g0364a0001c0001t0013g0200others(23): Show | 28 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.843-1583G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934189 | ||||||
chr1:934189
|
G | GCGTTACA others(49): Show |
1 | a0001c0021t0002g0342 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.843-1560_843-1559i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934189 | |||||
chr1:934189
|
G | GCGTTACA others(105): Show |
1 | a0001c0001t0003g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.843-1569_843-1568i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934189 | |||||
chr1:934189
|
G | GCGTTACA others(582): Show |
1 | a0001c0001t0003g0020 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.843-1569_843-1568i others(591): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934189 | |||||
chr1:934189
|
G | GCGTTACA others(385): Show |
1 | a0001c0001t0003g0168 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.843-1569_843-1568i others(394): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934189 | |||||
chr1:934189
|
G | GCGTTACA others(527): Show |
1 | a0001c0001t0003g0169 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.843-1569_843-1568i others(536): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934189 | |||||
chr1:934189
|
G | GCGTTACA others(78): Show |
1 | a0004c0008t0017g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.843-1569_843-1568i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934189 | |||||
chr1:934189
|
GCGTTACA others(49): Show |
G | 1 | a0001c0001t0003g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.843-1555_843-1500d others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934189 | |||||
chr1:934201
|
G | T | 1 | a0002c0003t0004g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.843-1571G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934201 | ||||||
chr1:934204
|
A | AGGGGCGG others(576): Show |
1 | a0028c0048t0004g0244 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.843-1564_843-1563i others(585): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934204 | |||||
chr1:934204
|
A | G | 130 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(127): Show | 132 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.843-1568A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934204 | ||||||
chr1:934209
|
A | AGGCGGCT others(385): Show |
1 | a0002c0003t0004g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.843-1556_843-1555i others(394): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934209 | |||||
chr1:934209
|
A | AGGCGGCT others(357): Show |
1 | a0006c0024t0003g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(366): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934209 | |||||
chr1:934209
|
A | AGGCGGCT others(105): Show |
1 | a0003c0006t0003g0183 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.843-1556_843-1555i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934209 | |||||
chr1:934209
|
A | AGGCGGCT others(413): Show |
1 | a0001c0001t0003g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.843-1556_843-1555i others(422): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934209 | |||||
chr1:934209
|
A | AGGCGGCT others(553): Show |
1 | a0001c0001t0003g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(562): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934209 | |||||
chr1:934209
|
A | G | 25 | a0001c0001t0003g0168a0001c0001t0003g0209a0001c0001t0012g0363others(22): Show | 25 | HG00733.hp1 HG02258.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.843-1563A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934209 | ||||||
chr1:934211
|
G | T | 7 | a0001c0046t0014g0028a0002c0003t0004g0246a0002c0003t0004g0252others(4): Show | 7 | HG03579.hp2 NA18952.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-1561G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934211 | ||||||
chr1:934213
|
G | GGCTGCGT others(302): Show |
1 | a0001c0001t0003g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(311): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(219): Show |
1 | a0019c0041t0003g0160 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(228): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(556): Show |
1 | a0001c0001t0003g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.843-1556_843-1555i others(565): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(78): Show |
1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(78): Show |
1 | a0001c0009t0003g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.843-1556_843-1555i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(582): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(591): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(357): Show |
2 | a0001c0001t0003g0162a0001c0001t0003g0163 | 2 | HG00738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.843-1556_843-1555i others(366): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(331): Show |
1 | a0001c0001t0001g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(340): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(359): Show |
2 | a0012c0025t0003g0195a0012c0025t0003g0196 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.843-1556_843-1555i others(368): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | GGCTGCGT others(667): Show |
1 | a0001c0001t0003g0189 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.843-1556_843-1555i others(676): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934213 | |||||
chr1:934213
|
G | T | 4 | a0001c0001t0003g0168a0001c0001t0012g0365a0001c0009t0010g0310others(1): Show | 4 | HG00733.hp1 HG02895.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-1559G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934213 | ||||||
chr1:934217
|
C | CCGTTACA others(21): Show |
2 | a0001c0002t0007g0296a0001c0002t0007g0298 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.843-1541_843-1540i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934217 | |||||
chr1:934217
|
C | G | 105 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(102): Show | 107 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.843-1555C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934217 | ||||||
chr1:934217
|
CCGTTACA others(49): Show |
C | 1 | a0011c0035t0021g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.843-1527_843-1472d others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934217 | |||||
chr1:934217
|
CCGTTACA others(77): Show |
C | 1 | a0001c0010t0007g0024 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.843-1540_843-1457d others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934217 | |||||
chr1:934217
|
CCGTTACA others(525): Show |
C | 4 | a0001c0001t0001g0142a0001c0004t0001g0145a0007c0012t0001g0009others(1): Show | 6 | HG01891.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-1527_843-996de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934217 | |||||
chr1:934224
|
A | T | 16 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0003g0021others(13): Show | 17 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.843-1548A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934224 | ||||||
chr1:934232
|
A | AGGGGCGG others(239): Show |
2 | a0002c0003t0004g0253a0002c0003t0004g0254 | 2 | HG02523.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.843-1536_843-1535i others(248): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934232 | |||||
chr1:934232
|
A | G | 129 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(126): Show | 131 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.843-1540A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934232 | ||||||
chr1:934232
|
AGGGGAGG others(497): Show |
A | 1 | a0001c0004t0001g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.843-1527_843-1024d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934232 | |||||
chr1:934237
|
A | AGGCGGCT others(1430): Show |
1 | a0001c0002t0002g0319 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.843-1528_843-1527i others(1439): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934237 | |||||
chr1:934237
|
A | AGGCGGCT others(99): Show |
1 | a0029c0050t0004g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.843-1528_843-1527i others(108): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934237 | |||||
chr1:934237
|
A | AGGCGGCT others(948): Show |
1 | a0001c0001t0003g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.843-1528_843-1527i others(957): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934237 | |||||
chr1:934237
|
A | G | 31 | a0001c0001t0001g0123a0001c0001t0003g0159a0001c0001t0003g0179others(28): Show | 31 | HG00639.hp2 HG01074.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.843-1535A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934237 | ||||||
chr1:934239
|
G | T | 1 | a0008c0014t0004g0258 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.843-1533G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934239 | ||||||
chr1:934241
|
G | GGCTGCGT others(722): Show |
1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.843-1528_843-1527i others(731): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934241 | |||||
chr1:934241
|
G | GGCTGCGT others(49): Show |
1 | a0001c0002t0011g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.843-1528_843-1527i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934241 | |||||
chr1:934241
|
G | GGCTGCGT others(359): Show |
1 | a0001c0001t0003g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.843-1528_843-1527i others(368): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934241 | |||||
chr1:934241
|
G | GGCTGCGT others(358): Show |
1 | a0001c0001t0003g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.843-1528_843-1527i others(367): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934241 | |||||
chr1:934241
|
G | GGCTGCGT others(272): Show |
1 | a0001c0001t0013g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.843-1528_843-1527i others(281): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934241 | |||||
chr1:934241
|
G | GGCTGCGT others(442): Show |
1 | a0001c0001t0003g0220 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.843-1528_843-1527i others(451): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934241 | |||||
chr1:934241
|
G | T | 8 | a0001c0001t0003g0179a0001c0001t0003g0209a0001c0001t0003g0212others(5): Show | 8 | HG01074.hp2 HG01099.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-1531G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934241 | ||||||
chr1:934245
|
C | CCGTTACA others(133): Show |
1 | a0024c0037t0006g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.843-1513_843-1512i others(142): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934245 | |||||
chr1:934245
|
C | G | 92 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(89): Show | 94 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.843-1527C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934245 | ||||||
chr1:934252
|
A | T | 4 | a0001c0001t0003g0171a0001c0001t0003g0197a0001c0001t0003g0198others(1): Show | 4 | NA18944.hp1 NA18948.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-1520A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934252 | ||||||
chr1:934254
|
G | GTGGGCGG others(162): Show |
1 | a0013c0020t0006g0302 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843-1513_843-1512i others(171): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934254 | |||||
chr1:934257
|
G | T | 3 | a0001c0002t0002g0262a0001c0002t0002g0358a0004c0008t0002g0270 | 3 | HG02451.hp2 HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.843-1515G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934257 | ||||||
chr1:934259
|
C | CGGGGGAG others(23): Show |
1 | a0001c0001t0012g0364 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.843-1513_843-1512i others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934259 | ||||||
chr1:934260
|
A | AGGGGAGG others(502): Show |
1 | a0001c0002t0009g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.843-1500_843-1499i others(511): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934260 | |||||
chr1:934260
|
A | AGGGGGGG others(278): Show |
1 | a0001c0009t0010g0309 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.843-1508_843-1507i others(287): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934260 | |||||
chr1:934260
|
A | G | 121 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(118): Show | 123 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.843-1512A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934260 | ||||||
chr1:934261
|
GGGGAGGC others(20): Show |
G | 1 | a0004c0008t0002g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.843-1507_843-1481d others(29): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934261 | |||||
chr1:934262
|
GGGA | G | 8 | a0002c0003t0004g0229a0002c0003t0004g0230a0002c0003t0004g0237others(5): Show | 8 | HG01361.hp2 HG02132.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-1507_843-1505d others(5): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934262 | |||||
chr1:934263
|
G | GGCGGCTG others(395): Show |
1 | a0002c0003t0004g0236 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.843-1508_843-1507i others(404): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934263 | |||||
chr1:934265
|
A | AGGCGGCT others(161): Show |
2 | a0001c0001t0003g0021a0001c0001t0003g0186 | 3 | NA18948.hp1 NA18969.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.843-1485_843-1484i others(170): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934265 | |||||
chr1:934265
|
A | AGGCGGCT others(217): Show |
1 | a0001c0001t0003g0210 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.843-1485_843-1484i others(226): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934265 | |||||
chr1:934265
|
A | AGGCTGCT others(105): Show |
1 | a0001c0021t0002g0342 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.843-1504_843-1503i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934265 | |||||
chr1:934265
|
A | G | 34 | a0001c0001t0001g0113a0001c0001t0003g0159a0001c0001t0003g0177others(31): Show | 34 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.843-1507A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934265 | ||||||
chr1:934267
|
G | T | 1 | a0002c0018t0004g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.843-1505G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934267 | ||||||
chr1:934269
|
G | T | 5 | a0001c0002t0002g0320a0001c0002t0009g0323a0001c0011t0028g0316others(2): Show | 5 | HG01099.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-1503G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934269 | ||||||
chr1:934273
|
G | C | 15 | a0001c0001t0003g0220a0001c0001t0013g0200a0001c0002t0002g0320others(12): Show | 15 | HG01099.hp1 HG02258.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.843-1499G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934273 | ||||||
chr1:934273
|
G | GCGTTACA others(237): Show |
1 | a0002c0003t0004g0238 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.843-1485_843-1484i others(246): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934273 | |||||
chr1:934273
|
G | GCGTTACA others(21): Show |
2 | a0001c0001t0003g0211a0001c0019t0006g0282 | 2 | HG02922.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.843-1485_843-1484i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934273 | |||||
chr1:934273
|
G | GCGTTACA others(386): Show |
1 | a0001c0001t0029g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.843-1485_843-1484i others(395): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934273 | |||||
chr1:934273
|
G | GCGTTACA others(498): Show |
1 | a0001c0001t0003g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.843-1485_843-1484i others(507): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934273 | |||||
chr1:934273
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0003g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.843-1485_843-1484i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934273 | |||||
chr1:934280
|
A | AGGTGGGC others(77): Show |
1 | a0001c0001t0003g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.843-1485_843-1484i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934280 | |||||
chr1:934280
|
A | T | 2 | a0001c0001t0003g0167a0001c0001t0003g0191 | 2 | HG01074.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.843-1492A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934280 | ||||||
chr1:934285
|
G | T | 2 | a0001c0009t0003g0180a0001c0046t0014g0028 | 2 | HG03579.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.843-1487G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934285 | ||||||
chr1:934287
|
C | CGGGGGGG others(106): Show |
1 | a0013c0020t0002g0318 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843-1485_843-1484i others(115): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934287 | ||||||
chr1:934287
|
C | CGGGGGGG others(76): Show |
1 | a0004c0008t0002g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.843-1485_843-1484i others(85): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934287 | ||||||
chr1:934287
|
C | CGGGGGGG others(107): Show |
1 | a0024c0037t0006g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.843-1485_843-1484i others(116): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934287 | ||||||
chr1:934288
|
A | AGGGGAGG others(273): Show |
1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.843-1472_843-1471i others(282): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934288 | |||||
chr1:934288
|
A | C | 1 | a0004c0008t0002g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.843-1484A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934288 | ||||||
chr1:934288
|
A | G | 146 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(143): Show | 151 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.843-1484A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934288 | ||||||
chr1:934291
|
G | GGCGGCTG others(155): Show |
1 | a0002c0003t0009g0228 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.843-1480_843-1479i others(164): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934291 | |||||
chr1:934291
|
G | GGCGGCTG others(264): Show |
1 | a0002c0003t0004g0238 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.843-1480_843-1479i others(273): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934291 | |||||
chr1:934293
|
A | AGGCGGCT others(217): Show |
1 | a0004c0008t0006g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.843-1472_843-1471i others(226): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934293 | |||||
chr1:934293
|
A | AGGCGGCT others(1086): Show |
1 | a0001c0001t0003g0171 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.843-1452_843-1451i others(1095): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934293 | |||||
chr1:934293
|
A | AGGCGGCT others(51): Show |
1 | a0018c0030t0006g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.843-1452_843-1451i others(60): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934293 | |||||
chr1:934293
|
A | AGGCTGCT others(105): Show |
1 | a0001c0009t0010g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.843-1476_843-1475i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934293 | |||||
chr1:934293
|
A | AGGCTGCT others(77): Show |
1 | a0001c0009t0010g0311 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.843-1476_843-1475i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934293 | |||||
chr1:934293
|
A | AGTCGGCT others(239): Show |
1 | a0002c0003t0004g0237 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.843-1478_843-1477i others(248): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934293 | |||||
chr1:934293
|
A | G | 47 | a0001c0001t0003g0021a0001c0001t0003g0154a0001c0001t0003g0155others(44): Show | 48 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.843-1479A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934293 | ||||||
chr1:934295
|
G | T | 8 | a0002c0003t0004g0246a0002c0003t0004g0251a0002c0003t0004g0252others(5): Show | 8 | HG02523.hp2 NA18952.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-1477G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934295 | ||||||
chr1:934296
|
C | T | 2 | a0001c0011t0002g0291a0006c0016t0015g0264 | 2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.843-1476C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934296 | ||||||
chr1:934297
|
G | GGCTCCGT others(303): Show |
1 | a0001c0001t0003g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.843-1472_843-1471i others(312): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934297 | |||||
chr1:934297
|
G | T | 8 | a0001c0001t0030g0205a0001c0002t0011g0272a0001c0002t0016g0265others(5): Show | 8 | HG01243.hp1 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-1475G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934297 | ||||||
chr1:934301
|
G | C | 27 | a0001c0001t0003g0154a0001c0001t0003g0187a0001c0001t0003g0201others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.843-1471G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934301 | ||||||
chr1:934301
|
G | GCGTTACA others(49): Show |
1 | a0009c0013t0002g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.843-1448_843-1447i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934301 | |||||
chr1:934301
|
G | GCGTTACA others(21): Show |
1 | a0003c0006t0003g0181 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.843-1452_843-1451i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934301 | |||||
chr1:934308
|
A | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0123others(1): Show | 4 | HG01109.hp1 HG01346.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1464A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934308 | ||||||
chr1:934310
|
G | A | 1 | a0013c0020t0002g0318 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843-1462G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934310 | ||||||
chr1:934313
|
G | T | 1 | a0004c0008t0006g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.843-1459G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934313 | ||||||
chr1:934315
|
C | CGGGGGAG others(78): Show |
1 | a0008c0014t0004g0258 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.843-1450_843-1449i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934315 | |||||
chr1:934316
|
G | A | 4 | a0001c0002t0011g0272a0001c0002t0011g0275a0001c0019t0006g0269others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-1456G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934316 | ||||||
chr1:934319
|
G | GGGGGCGG others(130): Show |
1 | a0001c0023t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843-1452_843-1451i others(139): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934319 | |||||
chr1:934321
|
A | AGGCTGCT others(78): Show |
1 | a0009c0013t0002g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.843-1448_843-1447i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934321 | |||||
chr1:934321
|
A | AGGCTGCT others(106): Show |
1 | a0009c0013t0002g0288 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.843-1448_843-1447i others(115): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934321 | |||||
chr1:934321
|
A | AGTCGGCT others(579): Show |
1 | a0002c0003t0004g0242 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.843-1450_843-1449i others(588): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934321 | |||||
chr1:934321
|
A | G | 54 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0113others(51): Show | 54 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.843-1451A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934321 | ||||||
chr1:934323
|
G | T | 5 | a0001c0001t0003g0171a0002c0003t0004g0241a0002c0003t0004g0243others(2): Show | 5 | HG02132.hp2 NA18940.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-1449G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934323 | ||||||
chr1:934325
|
G | GGCTCCGT others(105): Show |
1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.843-1444_843-1443i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934325 | |||||
chr1:934325
|
G | T | 6 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0003g0220others(3): Show | 6 | HG00642.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-1447G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934325 | ||||||
chr1:934329
|
G | C | 26 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0003g0169others(23): Show | 26 | HG00642.hp1 HG00642.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.843-1443G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934329 | ||||||
chr1:934329
|
G | GCGTTACA others(246): Show |
1 | a0001c0001t0013g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.843-1420_843-1419i others(255): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934329 | |||||
chr1:934329
|
G | GCGTTACA others(106): Show |
1 | a0006c0016t0015g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843-1424_843-1423i others(115): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934329 | |||||
chr1:934329
|
G | GCGTTACA others(610): Show |
1 | a0001c0001t0001g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.843-1424_843-1423i others(619): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934329 | |||||
chr1:934329
|
G | GCGTTACA others(50): Show |
1 | a0001c0001t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.843-1424_843-1423i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934329 | |||||
chr1:934336
|
A | T | 2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-1436A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934336 | ||||||
chr1:934341
|
G | T | 1 | a0002c0049t0004g0223 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.843-1431G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934341 | ||||||
chr1:934343
|
C | CGGGGGAG others(897): Show |
1 | a0001c0002t0009g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-1401_843-1400i others(906): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934343 | |||||
chr1:934344
|
G | A | 4 | a0001c0001t0003g0167a0001c0011t0002g0291a0002c0003t0004g0249others(1): Show | 4 | HG01074.hp1 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1428G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934344 | ||||||
chr1:934349
|
A | AGGCGGCT others(444): Show |
1 | a0001c0002t0002g0320 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.843-1395_843-1394i others(453): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934349 | |||||
chr1:934349
|
A | AGGCGGCT others(102): Show |
1 | a0002c0003t0004g0240 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.843-1401_843-1400i others(111): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934349 | |||||
chr1:934349
|
A | AGGCGGCT others(21): Show |
2 | a0001c0009t0010g0310a0001c0009t0010g0311 | 2 | NA19002.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.843-1401_843-1400i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934349 | |||||
chr1:934349
|
A | G | 53 | a0001c0001t0001g0079a0001c0001t0001g0113a0001c0001t0003g0159others(50): Show | 56 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.843-1423A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934349 | ||||||
chr1:934349
|
AGGCGGCT others(21): Show |
A | 2 | a0001c0001t0003g0178a0001c0002t0002g0359 | 2 | HG03239.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.843-1400_843-1373d others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934349 | |||||
chr1:934351
|
G | T | 2 | a0001c0046t0014g0028a0002c0003t0009g0228 | 2 | HG03579.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.843-1421G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934351 | ||||||
chr1:934352
|
C | T | 1 | a0006c0016t0015g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843-1420C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934352 | ||||||
chr1:934353
|
G | T | 3 | a0001c0001t0003g0169a0001c0002t0011g0273a0009c0013t0002g0286 | 3 | HG00642.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.843-1419G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934353 | ||||||
chr1:934357
|
G | C | 21 | a0001c0001t0001g0082a0001c0001t0003g0020a0001c0001t0003g0162others(18): Show | 25 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.843-1415G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934357 | ||||||
chr1:934357
|
G | GCGTTACA others(106): Show |
1 | a0001c0009t0010g0313 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.843-1401_843-1400i others(115): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934357 | |||||
chr1:934364
|
A | T | 3 | a0001c0001t0003g0182a0001c0001t0003g0184a0001c0009t0010g0312 | 3 | HG01975.hp2 HG01981.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.843-1408A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934364 | ||||||
chr1:934369
|
G | T | 1 | a0004c0008t0002g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.843-1403G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934369 | ||||||
chr1:934371
|
C | CG | 8 | a0001c0001t0003g0179a0001c0001t0003g0191a0002c0003t0004g0239others(5): Show | 8 | HG01074.hp2 HG02559.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-1401_843-1400i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934371 | ||||||
chr1:934371
|
C | CGGGGGAG others(162): Show |
1 | a0004c0008t0006g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.843-1401_843-1400i others(171): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934371 | ||||||
chr1:934372
|
A | AGGGGAGG others(133): Show |
1 | a0004c0008t0006g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.843-1396_843-1395i others(142): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934372 | |||||
chr1:934372
|
A | G | 143 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(140): Show | 146 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.843-1400A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934372 | ||||||
chr1:934372
|
AGGG | A | 6 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0229others(3): Show | 9 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-1395_843-1393d others(5): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934372 | |||||
chr1:934375
|
G | GGAGGCGG others(46): Show |
1 | a0002c0003t0004g0243 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.843-1396_843-1395i others(55): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934375 | |||||
chr1:934375
|
G | GGAGGCGG others(264): Show |
1 | a0029c0050t0004g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.843-1396_843-1395i others(273): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934375 | |||||
chr1:934377
|
G | A | 78 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(75): Show | 80 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.843-1395G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934377 | ||||||
chr1:934377
|
G | GA | 13 | a0001c0001t0013g0200a0001c0002t0009g0321a0001c0002t0009g0323others(10): Show | 13 | HG02523.hp2 HG02572.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.843-1395_843-1394i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934377 | ||||||
chr1:934377
|
G | GAGGCGGC others(22): Show |
1 | a0001c0002t0002g0320 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.843-1395_843-1394i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934377 | ||||||
chr1:934377
|
G | GGGCGGCT others(158): Show |
1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1388_843-1387i others(167): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934377 | |||||
chr1:934377
|
G | GGGCGGCT others(722): Show |
1 | a0001c0001t0003g0204 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.843-1388_843-1387i others(731): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934377 | |||||
chr1:934377
|
G | GGGCGGCT others(77): Show |
3 | a0001c0001t0001g0082a0001c0001t0003g0162a0001c0001t0003g0163 | 3 | HG00738.hp2 HG01192.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.843-1368_843-1367i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934377 | |||||
chr1:934377
|
G | GGGGCTGC others(51): Show |
2 | a0012c0025t0003g0195a0012c0025t0003g0196 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.843-1393_843-1392i others(60): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934377 | |||||
chr1:934379
|
G | GCGGCTCC others(74): Show |
1 | a0002c0003t0004g0235 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.843-1388_843-1387i others(83): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934379 | |||||
chr1:934379
|
G | T | 2 | a0002c0003t0004g0242a0002c0003t0004g0251 | 2 | NA18962.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.843-1393G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934379 | ||||||
chr1:934381
|
G | T | 10 | a0001c0001t0003g0020a0001c0001t0003g0168a0001c0001t0003g0203others(7): Show | 11 | HG00733.hp1 HG01106.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-1391G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934381 | ||||||
chr1:934385
|
G | C | 27 | a0001c0001t0001g0112a0001c0001t0003g0020a0001c0001t0003g0168others(24): Show | 28 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.843-1387G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934385 | ||||||
chr1:934385
|
G | GCGTTACA others(105): Show |
1 | a0004c0008t0017g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.843-1340_843-1339i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934385 | |||||
chr1:934385
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0029g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.843-1364_843-1363i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934385 | |||||
chr1:934385
|
G | GCGTTACA others(106): Show |
1 | a0001c0001t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.843-1368_843-1367i others(115): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934385 | |||||
chr1:934385
|
G | GCGTTACA others(247): Show |
1 | a0001c0001t0003g0187 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.843-1368_843-1367i others(256): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934385 | |||||
chr1:934392
|
A | AGGTGGGC others(21): Show |
1 | a0001c0001t0003g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.843-1353_843-1352i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934392 | |||||
chr1:934392
|
A | T | 1 | a0001c0001t0003g0178 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.843-1380A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934392 | ||||||
chr1:934399
|
C | CAGGGGGA others(137): Show |
1 | a0001c0002t0011g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.843-1373_843-1372i others(146): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934399 | ||||||
chr1:934399
|
C | CG | 8 | a0001c0001t0019g0190a0001c0023t0001g0150a0003c0031t0002g0299others(5): Show | 8 | HG02559.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-1368dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934399 | |||||
chr1:934400
|
G | A | 4 | a0001c0001t0001g0097a0001c0011t0002g0324a0009c0013t0002g0287others(1): Show | 4 | HG01243.hp1 HG02559.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1372G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934400 | ||||||
chr1:934400
|
G | GGGGGAGG others(525): Show |
1 | a0001c0002t0011g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843-1364_843-1363i others(534): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934400 | |||||
chr1:934400
|
G | GGGGGGGG others(920): Show |
1 | a0001c0019t0006g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.843-1368_843-1367i others(929): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934400 | |||||
chr1:934405
|
A | AGGCGGCT others(50): Show |
1 | a0001c0001t0001g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.843-1332_843-1331i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934405 | |||||
chr1:934405
|
A | G | 43 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0123others(40): Show | 43 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.843-1367A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934405 | ||||||
chr1:934407
|
G | T | 3 | a0002c0003t0004g0230a0002c0003t0004g0241a0002c0018t0004g0227 | 3 | HG02300.hp1 NA18940.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.843-1365G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934407 | ||||||
chr1:934408
|
C | CTGCTCCG others(74): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.843-1364_843-1363i others(83): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934408 | ||||||
chr1:934409
|
G | GGCTCCGT others(22): Show |
3 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0164 | 3 | HG00738.hp2 HG01346.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.843-1360_843-1359i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934409 | |||||
chr1:934409
|
G | T | 5 | a0001c0001t0001g0112a0001c0001t0018g0151a0001c0001t0018g0152others(2): Show | 5 | HG00323.hp1 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-1363G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934409 | ||||||
chr1:934413
|
G | C | 23 | a0001c0001t0001g0082a0001c0001t0001g0112a0001c0001t0003g0162others(20): Show | 23 | HG00323.hp1 HG00733.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.843-1359G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934413 | ||||||
chr1:934413
|
G | GCGTTACA others(21): Show |
2 | a0001c0002t0007g0296a0001c0002t0007g0298 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.843-1331_843-1304d others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934413 | |||||
chr1:934413
|
G | GCGTTACA others(78): Show |
1 | a0001c0001t0003g0220 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.843-1340_843-1339i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934413 | |||||
chr1:934420
|
A | T | 1 | a0001c0009t0010g0312 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.843-1352A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934420 | ||||||
chr1:934420
|
A | TGGTGGGC others(332): Show |
1 | a0001c0009t0010g0313 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.843-1353_843-1352i others(341): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934420 | ||||||
chr1:934425
|
G | GGCGGGGG others(49): Show |
1 | a0004c0008t0002g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.843-1332_843-1331i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934425 | |||||
chr1:934425
|
G | T | 2 | a0001c0046t0014g0028a0004c0008t0002g0271 | 2 | HG02145.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.843-1347G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934425 | ||||||
chr1:934427
|
C | CA | 3 | a0001c0002t0011g0274a0002c0003t0004g0256a0009c0013t0002g0286 | 3 | HG00642.hp2 HG02896.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.843-1345_843-1344i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934427 | ||||||
chr1:934427
|
C | CG | 6 | a0001c0001t0001g0082a0001c0001t0003g0209a0001c0001t0003g0211others(3): Show | 6 | HG01192.hp2 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-1340dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934427 | |||||
chr1:934428
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0003g0020a0001c0009t0003g0180others(2): Show | 6 | HG01256.hp2 HG01258.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-1344G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934428 | ||||||
chr1:934433
|
A | AGGCGGCT others(134): Show |
1 | a0009c0013t0002g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.843-1332_843-1331i others(143): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934433 | |||||
chr1:934433
|
A | AGGCTGCT others(504): Show |
1 | a0002c0003t0004g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.843-1336_843-1335i others(513): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934433 | |||||
chr1:934433
|
A | G | 37 | a0001c0001t0001g0082a0001c0001t0001g0112a0001c0001t0003g0177others(34): Show | 37 | HG00323.hp1 HG00735.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.843-1339A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934433 | ||||||
chr1:934435
|
G | T | 9 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0229others(6): Show | 12 | HG01123.hp2 HG01255.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.843-1337G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934435 | ||||||
chr1:934437
|
G | GGCTGCGT others(78): Show |
1 | a0001c0002t0009g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-1332_843-1331i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934437 | |||||
chr1:934437
|
G | GGCTGCGT others(49): Show |
1 | a0001c0001t0003g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.843-1332_843-1331i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934437 | |||||
chr1:934437
|
G | GGCTGCGT others(779): Show |
1 | a0003c0006t0003g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.843-1332_843-1331i others(788): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934437 | |||||
chr1:934437
|
G | GGCTGCGT others(780): Show |
1 | a0001c0001t0003g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.843-1332_843-1331i others(789): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934437 | |||||
chr1:934437
|
G | GGCTGCGT others(780): Show |
1 | a0003c0006t0003g0193 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.843-1332_843-1331i others(789): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934437 | |||||
chr1:934437
|
G | T | 17 | a0001c0001t0001g0082a0001c0001t0003g0198a0001c0001t0003g0199others(14): Show | 17 | HG01099.hp1 HG01106.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.843-1335G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934437 | ||||||
chr1:934441
|
C | CCGTTACA others(105): Show |
1 | a0001c0021t0002g0342 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.843-1256_843-1255i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934441 | |||||
chr1:934441
|
C | CCGTTACA others(49): Show |
1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.843-1308_843-1307i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934441 | |||||
chr1:934441
|
C | CCGTTACA others(21): Show |
2 | a0001c0001t0003g0159a0006c0024t0003g0207 | 2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.843-1312_843-1311i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934441 | |||||
chr1:934441
|
C | CCGTTACA others(105): Show |
1 | a0001c0001t0003g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.843-1312_843-1311i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934441 | |||||
chr1:934441
|
C | G | 103 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0112others(100): Show | 107 | HG00323.hp1 HG00609.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.843-1331C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934441 | ||||||
chr1:934441
|
C | GCGTTACA others(161): Show |
1 | a0001c0002t0007g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.843-1332_843-1331i others(170): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934441 | ||||||
chr1:934448
|
A | T | 3 | a0001c0001t0003g0167a0001c0001t0003g0178a0001c0001t0003g0184 | 3 | HG01074.hp1 HG01975.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.843-1324A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934448 | ||||||
chr1:934453
|
G | GGCGGGGG others(50): Show |
1 | a0004c0008t0002g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.843-1312_843-1311i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934453 | |||||
chr1:934453
|
G | T | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.843-1319G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934453 | ||||||
chr1:934455
|
C | CA | 4 | a0001c0002t0009g0323a0001c0002t0011g0272a0002c0003t0004g0242others(1): Show | 4 | HG02572.hp1 HG02630.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1317_843-1316i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934455 | ||||||
chr1:934455
|
C | CAGGGGGG others(51): Show |
1 | a0001c0023t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843-1317_843-1316i others(60): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934455 | ||||||
chr1:934455
|
C | CG | 11 | a0001c0002t0016g0265a0001c0002t0016g0266a0001c0009t0003g0180others(8): Show | 11 | HG02559.hp2 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-1312dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934455 | |||||
chr1:934455
|
C | CGGGGGGG others(163): Show |
2 | a0005c0007t0008g0277a0005c0007t0008g0278 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.843-1312_843-1311i others(172): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934455 | |||||
chr1:934455
|
C | CGGGGGGG others(139): Show |
1 | a0013c0020t0006g0302 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843-1312_843-1311i others(148): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934455 | |||||
chr1:934456
|
G | A | 4 | a0001c0001t0003g0020a0001c0002t0002g0358a0002c0003t0004g0249others(1): Show | 5 | HG01256.hp2 HG01258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1316G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934456 | ||||||
chr1:934456
|
G | GGGGGAGG others(21): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.843-1292_843-1291i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934456 | |||||
chr1:934456
|
G | GGGGGGGA others(79): Show |
1 | a0001c0001t0012g0364 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.843-1312_843-1311i others(88): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934456 | |||||
chr1:934458
|
G | GGGGGGCG others(102): Show |
1 | a0028c0048t0004g0244 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.843-1312_843-1311i others(111): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934458 | |||||
chr1:934461
|
A | AGGCGGCT others(21): Show |
2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-1284_843-1283i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934461 | |||||
chr1:934461
|
A | AGGCTGCT others(610): Show |
1 | a0001c0001t0001g0083 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.843-1308_843-1307i others(619): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934461 | |||||
chr1:934461
|
A | G | 50 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0114others(47): Show | 50 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.843-1311A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934461 | ||||||
chr1:934463
|
G | GCGGCTGC others(270): Show |
1 | a0002c0003t0004g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.843-1284_843-1283i others(279): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934463 | |||||
chr1:934463
|
G | T | 6 | a0002c0003t0004g0235a0002c0003t0004g0236a0002c0003t0004g0237others(3): Show | 6 | HG02071.hp2 HG02165.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-1309G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934463 | ||||||
chr1:934464
|
C | CTGCTCCG others(74): Show |
1 | a0001c0001t0003g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.843-1308_843-1307i others(83): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934464 | ||||||
chr1:934464
|
C | CTGCTCCG others(130): Show |
1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.843-1308_843-1307i others(139): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934464 | ||||||
chr1:934464
|
C | T | 1 | a0001c0011t0002g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.843-1308C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934464 | ||||||
chr1:934465
|
G | T | 8 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0003g0171others(5): Show | 8 | HG00438.hp1 HG02895.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-1307G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934465 | ||||||
chr1:934465
|
GGCTGCGT others(77): Show |
G | 1 | a0001c0002t0002g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.843-1303_843-1220d others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934465 | |||||
chr1:934469
|
G | C | 24 | a0001c0001t0001g0082a0001c0001t0001g0092a0001c0001t0001g0114others(21): Show | 24 | HG00438.hp1 HG01192.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.843-1303G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934469 | ||||||
chr1:934476
|
A | AGGTGGGC others(133): Show |
1 | a0001c0010t0007g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.843-1276_843-1275i others(142): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934476 | |||||
chr1:934476
|
A | T | 2 | a0001c0001t0013g0175a0002c0018t0004g0225 | 2 | HG03710.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.843-1296A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934476 | ||||||
chr1:934481
|
G | T | 3 | a0001c0001t0018g0151a0001c0001t0018g0152a0004c0008t0006g0303 | 3 | HG03209.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.843-1291G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934481 | ||||||
chr1:934483
|
C | CA | 5 | a0001c0002t0009g0323a0001c0002t0011g0272a0001c0002t0011g0274others(2): Show | 5 | HG00642.hp2 HG02300.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-1289_843-1288i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934483 | ||||||
chr1:934483
|
C | CGGGGGAG others(592): Show |
1 | a0001c0002t0011g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.843-1261_843-1260i others(601): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934483 | |||||
chr1:934484
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0012g0364a0002c0003t0004g0249 | 3 | HG02145.hp1 NA18961.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.843-1288G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934484 | ||||||
chr1:934489
|
A | AGGCGGCT others(105): Show |
2 | a0001c0001t0003g0021a0001c0001t0003g0154 | 3 | HG01978.hp1 NA18948.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.843-1276_843-1275i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934489 | |||||
chr1:934489
|
A | AGGCGGCT others(21): Show |
1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.843-1255_843-1228d others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934489 | |||||
chr1:934489
|
A | AGGCGGCT others(807): Show |
1 | a0001c0001t0003g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.843-1248_843-1247i others(816): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934489 | |||||
chr1:934489
|
A | AGTCGGCT others(21): Show |
1 | a0001c0001t0003g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.843-1282_843-1281i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934489 | |||||
chr1:934489
|
A | G | 35 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0003g0155others(32): Show | 35 | HG00323.hp1 HG00642.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.843-1283A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934489 | ||||||
chr1:934491
|
G | T | 1 | a0001c0001t0003g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.843-1281G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934491 | ||||||
chr1:934493
|
G | T | 2 | a0001c0002t0011g0275a0001c0011t0028g0316 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.843-1279G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934493 | ||||||
chr1:934497
|
G | C | 26 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0003g0172others(23): Show | 26 | HG00438.hp1 HG01074.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.843-1275G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934497 | ||||||
chr1:934497
|
G | CCGTTACA others(77): Show |
1 | a0001c0010t0007g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.843-1276_843-1275i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934497 | ||||||
chr1:934497
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0003g0186 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.843-1256_843-1255i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934497 | |||||
chr1:934497
|
G | GCGTTACA others(161): Show |
1 | a0001c0001t0003g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.843-1256_843-1255i others(170): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934497 | |||||
chr1:934509
|
G | T | 3 | a0001c0001t0018g0151a0001c0001t0018g0152a0004c0008t0002g0270 | 3 | HG02896.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.843-1263G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934509 | ||||||
chr1:934511
|
C | CA | 3 | a0001c0002t0011g0274a0001c0009t0010g0313a0002c0003t0004g0222 | 3 | HG00642.hp2 HG02976.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.843-1261_843-1260i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934511 | ||||||
chr1:934511
|
C | CAGGGGAG others(22): Show |
1 | a0006c0016t0015g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843-1261_843-1260i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934511 | ||||||
chr1:934511
|
C | CGGGGGAG others(107): Show |
1 | a0001c0009t0010g0312 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.843-1256_843-1255i others(116): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934511 | |||||
chr1:934511
|
C | CGGGGGAG others(191): Show |
1 | a0001c0001t0013g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.843-1256_843-1255i others(200): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934511 | |||||
chr1:934511
|
C | CGGGGGAG others(107): Show |
2 | a0005c0007t0008g0277a0005c0007t0008g0278 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.843-1256_843-1255i others(116): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934511 | |||||
chr1:934511
|
C | CGGGGGGG others(23): Show |
1 | a0013c0020t0002g0318 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843-1253_843-1252i others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934511 | |||||
chr1:934511
|
C | CGGGGGGG others(53): Show |
1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.843-1253_843-1252i others(62): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934511 | |||||
chr1:934512
|
G | A | 5 | a0001c0002t0009g0321a0001c0002t0009g0322a0001c0002t0011g0275others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-1260G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934512 | ||||||
chr1:934513
|
G | GGGGAGGC others(1098): Show |
1 | a0001c0002t0011g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.843-1256_843-1255i others(1107): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934513 | |||||
chr1:934515
|
G | A | 3 | a0002c0003t0004g0224a0002c0018t0004g0226a0002c0018t0004g0227 | 3 | NA18995.hp1 NA19065.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.843-1257G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934515 | ||||||
chr1:934515
|
G | GGGGGCGG others(18): Show |
1 | a0029c0050t0004g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.843-1248_843-1247i others(27): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934515 | |||||
chr1:934517
|
G | A | 69 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0123others(66): Show | 70 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.843-1255G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934517 | ||||||
chr1:934517
|
G | GGCGGCTG others(21): Show |
1 | a0001c0002t0009g0323 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.843-1254_843-1253i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934517 | |||||
chr1:934517
|
G | GGCGGCTG others(20): Show |
1 | a0001c0001t0003g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.843-1254_843-1253i others(29): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934517 | |||||
chr1:934517
|
G | GGGCGGCT others(23): Show |
1 | a0009c0013t0002g0288 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.843-1228_843-1227i others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934517 | |||||
chr1:934517
|
G | GGGCTGCT others(360): Show |
1 | a0001c0046t0014g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.843-1252_843-1251i others(369): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934517 | |||||
chr1:934517
|
G | GGGGCTGC others(50): Show |
1 | a0002c0003t0004g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.843-1253_843-1252i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934517 | |||||
chr1:934517
|
GGGCGGCT others(273): Show |
G | 1 | a0001c0001t0003g0178 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.843-1223_843-944de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934517 | |||||
chr1:934519
|
G | GGCGGCTG others(605): Show |
1 | a0008c0014t0004g0260 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.843-1253_843-1252i others(614): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934519 | ||||||
chr1:934519
|
G | T | 2 | a0002c0003t0004g0243a0014c0027t0004g0232 | 2 | HG02132.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.843-1253G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934519 | ||||||
chr1:934520
|
C | T | 1 | a0001c0011t0002g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.843-1252C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934520 | ||||||
chr1:934521
|
G | T | 11 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0003g0172others(8): Show | 11 | HG01106.hp2 HG01167.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-1251G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934521 | ||||||
chr1:934525
|
G | C | 27 | a0001c0001t0001g0092a0001c0001t0001g0114a0001c0001t0003g0172others(24): Show | 30 | HG01069.hp2 HG01074.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.843-1247G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934525 | ||||||
chr1:934525
|
G | GCGTTACA others(359): Show |
1 | a0001c0001t0001g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.843-1224_843-1223i others(368): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934525 | |||||
chr1:934525
|
G | GCGTTACA others(243): Show |
1 | a0001c0001t0003g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.843-1226_843-1225i others(252): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934525 | |||||
chr1:934525
|
G | GCGTTACA others(1115): Show |
1 | a0003c0006t0003g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.843-1228_843-1227i others(1124): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934525 | |||||
chr1:934525
|
G | GCGTTACA others(752): Show |
1 | a0025c0045t0003g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.843-1228_843-1227i others(761): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934525 | |||||
chr1:934532
|
A | T | 5 | a0001c0002t0007g0296a0001c0002t0007g0298a0001c0009t0010g0309others(2): Show | 5 | HG01243.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-1240A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934532 | ||||||
chr1:934537
|
G | T | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.843-1235G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934537 | ||||||
chr1:934539
|
C | CA | 4 | a0001c0002t0009g0323a0001c0009t0010g0313a0001c0011t0002g0291others(1): Show | 4 | HG02165.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1233_843-1232i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934539 | ||||||
chr1:934539
|
C | CG | 9 | a0001c0001t0003g0179a0001c0001t0003g0220a0001c0001t0012g0364others(6): Show | 9 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-1228dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934539 | |||||
chr1:934539
|
C | CGGGGGGG others(286): Show |
1 | a0006c0016t0002g0289 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.843-1228_843-1227i others(295): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934539 | |||||
chr1:934540
|
G | A | 10 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0229others(7): Show | 13 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.843-1232G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934540 | ||||||
chr1:934540
|
GGGGGAGG others(48): Show |
G | 1 | a0003c0031t0002g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.843-1227_843-1173d others(57): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934540 | |||||
chr1:934540
|
GGGGGAGG others(104): Show |
G | 2 | a0001c0002t0016g0265a0001c0002t0016g0266 | 2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.843-1227_843-1117d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934540 | |||||
chr1:934541
|
GGGGAGGC others(19): Show |
G | 1 | a0001c0004t0027g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.843-1227_843-1202d others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934541 | |||||
chr1:934542
|
GGGAGGCT others(136): Show |
G | 1 | a0002c0003t0024g0233 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.843-1227_843-1085d others(2): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934542 | |||||
chr1:934542
|
GGGAGGCT others(276): Show |
G | 1 | a0002c0003t0004g0248 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.843-1227_843-945de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934542 | |||||
chr1:934545
|
A | AGGCGGCT others(22): Show |
1 | a0001c0001t0003g0159 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.843-1224_843-1223i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934545 | |||||
chr1:934545
|
A | AGGCGGCT others(134): Show |
1 | a0001c0019t0006g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.843-1224_843-1223i others(143): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934545 | |||||
chr1:934545
|
A | AGTCGGCT others(218): Show |
1 | a0002c0003t0004g0243 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.843-1226_843-1225i others(227): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934545 | |||||
chr1:934545
|
A | C | 6 | a0002c0003t0004g0011a0002c0003t0004g0022a0002c0003t0004g0229others(3): Show | 9 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-1227A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934545 | ||||||
chr1:934545
|
A | G | 62 | a0001c0001t0001g0079a0001c0001t0001g0112a0001c0001t0001g0113others(59): Show | 63 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.843-1227A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934545 | ||||||
chr1:934545
|
AGGCTGCT others(49): Show |
A | 1 | a0005c0007t0008g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.843-1223_843-1168d others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934545 | |||||
chr1:934547
|
G | A | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.843-1225G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934547 | ||||||
chr1:934547
|
G | GCGGCTGC others(186): Show |
1 | a0002c0003t0004g0253 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.843-1224_843-1223i others(195): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934547 | |||||
chr1:934547
|
G | T | 1 | a0002c0003t0004g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.843-1225G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934547 | ||||||
chr1:934548
|
C | T | 1 | a0005c0007t0008g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843-1224C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934548 | ||||||
chr1:934549
|
T | G | 142 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0092others(139): Show | 145 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.843-1223T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934549 | ||||||
chr1:934550
|
GCTC | G | 5 | a0002c0003t0004g0011a0002c0003t0004g0229a0002c0003t0004g0239others(2): Show | 7 | HG01361.hp2 HG01981.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-1220_843-1218d others(5): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934550 | |||||
chr1:934550
|
GCTCCGTT others(24): Show |
G | 1 | a0002c0003t0004g0022 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.843-1220_843-1190d others(33): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934550 | |||||
chr1:934553
|
C | CCGTTACA others(21): Show |
2 | a0001c0002t0009g0321a0001c0002t0009g0322 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.843-1205_843-1204i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934553 | |||||
chr1:934553
|
C | CCGTTACA others(21): Show |
1 | a0001c0019t0006g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.843-1200_843-1199i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934553 | |||||
chr1:934553
|
C | CCGTTACA others(49): Show |
1 | a0006c0024t0003g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.843-1200_843-1199i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934553 | |||||
chr1:934553
|
C | G | 96 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0097others(93): Show | 99 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.843-1219C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934553 | ||||||
chr1:934560
|
A | T | 3 | a0001c0001t0003g0167a0001c0001t0003g0173a0001c0009t0010g0312 | 3 | HG01074.hp1 NA18948.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.843-1212A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934560 | ||||||
chr1:934565
|
G | T | 3 | a0001c0001t0018g0151a0001c0001t0018g0152a0009c0013t0002g0288 | 3 | HG03209.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.843-1207G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934565 | ||||||
chr1:934567
|
C | CG | 6 | a0001c0001t0003g0162a0001c0001t0003g0163a0005c0007t0008g0300others(3): Show | 6 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-1200dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934567 | |||||
chr1:934567
|
C | CGGGGGGG others(420): Show |
1 | a0005c0007t0008g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.843-1200_843-1199i others(429): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934567 | |||||
chr1:934567
|
C | CGGGGGGG others(80): Show |
1 | a0001c0001t0012g0363 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.843-1200_843-1199i others(89): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934567 | |||||
chr1:934567
|
C | CGGGGGGG others(23): Show |
2 | a0018c0030t0006g0301a0024c0037t0006g0307 | 2 | HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.843-1200_843-1199i others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934567 | |||||
chr1:934568
|
G | A | 9 | a0001c0011t0002g0291a0001c0011t0002g0324a0002c0003t0004g0236others(6): Show | 9 | HG00609.hp1 HG02071.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.843-1204G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934568 | ||||||
chr1:934573
|
A | AGGCGGCT others(49): Show |
1 | a0001c0001t0003g0214 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.843-1196_843-1195i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934573 | |||||
chr1:934573
|
A | AGGCGGCT others(553): Show |
1 | a0001c0001t0003g0187 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.843-1196_843-1195i others(562): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934573 | |||||
chr1:934573
|
A | AGGCGGCT others(134): Show |
1 | a0001c0001t0003g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.843-1196_843-1195i others(143): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934573 | |||||
chr1:934573
|
A | AGTCGGCT others(77): Show |
1 | a0001c0001t0003g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.843-1198_843-1197i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934573 | |||||
chr1:934573
|
A | C | 6 | a0002c0003t0004g0236a0002c0003t0004g0237a0002c0003t0004g0238others(3): Show | 6 | HG00609.hp1 HG02071.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-1199A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934573 | ||||||
chr1:934573
|
A | G | 65 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0097others(62): Show | 67 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.843-1199A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934573 | ||||||
chr1:934573
|
AGGCTGCT others(21): Show |
A | 2 | a0002c0003t0004g0224a0014c0027t0004g0232 | 2 | NA19010.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.843-1195_843-1168d others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934573 | |||||
chr1:934575
|
G | T | 1 | a0029c0050t0004g0234 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.843-1197G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934575 | ||||||
chr1:934576
|
C | T | 1 | a0001c0011t0002g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.843-1196C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934576 | ||||||
chr1:934577
|
T | G | 134 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(131): Show | 139 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.843-1195T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934577 | ||||||
chr1:934578
|
GCTC | G | 6 | a0002c0003t0004g0236a0002c0003t0004g0237a0002c0003t0004g0238others(3): Show | 6 | HG00609.hp1 HG02071.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.843-1192_843-1190d others(5): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934578 | |||||
chr1:934581
|
C | CCGTTACA others(581): Show |
1 | a0001c0001t0003g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.843-1172_843-1171i others(590): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934581 | |||||
chr1:934581
|
C | CCGTTACA others(581): Show |
1 | a0001c0001t0003g0186 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.843-1172_843-1171i others(590): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934581 | |||||
chr1:934581
|
C | CCGTTACA others(553): Show |
1 | a0019c0041t0003g0160 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.843-1172_843-1171i others(562): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934581 | |||||
chr1:934581
|
C | CCGTTACA others(49): Show |
1 | a0004c0008t0006g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.843-1164_843-1163i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934581 | |||||
chr1:934581
|
C | G | 109 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(106): Show | 113 | HG00323.hp1 HG00438.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.843-1191C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934581 | ||||||
chr1:934588
|
A | T | 2 | a0001c0009t0010g0309a0001c0009t0010g0313 | 2 | NA18953.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.843-1184A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934588 | ||||||
chr1:934593
|
G | T | 2 | a0001c0001t0018g0152a0004c0008t0002g0270 | 2 | HG02896.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.843-1179G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934593 | ||||||
chr1:934595
|
C | CAGGGGAG others(78): Show |
1 | a0004c0008t0002g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.843-1177_843-1176i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934595 | ||||||
chr1:934595
|
C | CGGGGGGG others(23): Show |
1 | a0001c0019t0006g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.843-1169_843-1168i others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934595 | |||||
chr1:934596
|
G | A | 1 | a0002c0003t0004g0250 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.843-1176G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934596 | ||||||
chr1:934599
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1173G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934599 | ||||||
chr1:934601
|
G | A | 80 | a0001c0001t0001g0113a0001c0001t0003g0162a0001c0001t0003g0163others(77): Show | 84 | HG00323.hp2 HG00609.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.843-1171G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934601 | ||||||
chr1:934601
|
G | GGGCGGCT others(520): Show |
1 | a0008c0014t0004g0258 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.843-1164_843-1163i others(529): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934601 | |||||
chr1:934601
|
G | GGGCGGCT others(1090): Show |
1 | a0001c0002t0002g0320 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.843-1149_843-1148i others(1099): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934601 | |||||
chr1:934603
|
G | T | 6 | a0002c0003t0004g0011a0002c0003t0004g0229a0002c0003t0004g0239others(3): Show | 8 | HG01361.hp2 HG01981.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-1169G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934603 | ||||||
chr1:934605
|
G | T | 5 | a0001c0001t0003g0184a0002c0003t0004g0242a0002c0003t0004g0243others(2): Show | 5 | HG01099.hp2 HG01975.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1167G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934605 | ||||||
chr1:934609
|
G | C | 21 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0179others(18): Show | 22 | HG00738.hp2 HG01074.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.843-1163G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934609 | ||||||
chr1:934616
|
A | T | 1 | a0001c0010t0007g0294 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.843-1156A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934616 | ||||||
chr1:934621
|
G | T | 2 | a0004c0008t0002g0270a0009c0013t0002g0288 | 2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.843-1151G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934621 | ||||||
chr1:934623
|
C | CGGGGGAG others(22): Show |
1 | a0005c0007t0008g0284 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.843-1144_843-1143i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934623 | |||||
chr1:934623
|
C | CGGGGGGG others(80): Show |
1 | a0013c0020t0006g0302 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843-1141_843-1140i others(89): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934623 | |||||
chr1:934624
|
G | A | 3 | a0001c0023t0001g0091a0002c0003t0004g0250a0004c0008t0002g0270 | 3 | HG02896.hp2 NA18959.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.843-1148G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934624 | ||||||
chr1:934624
|
G | GGGGGGGC others(104): Show |
1 | a0001c0002t0011g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.843-1142_843-1141i others(113): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934624 | |||||
chr1:934626
|
G | GGGAGTCG others(155): Show |
1 | a0008c0014t0004g0259 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.843-1144_843-1143i others(164): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934626 | |||||
chr1:934627
|
G | GGAGGCGG others(75): Show |
1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-1144_843-1143i others(84): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934627 | |||||
chr1:934629
|
G | A | 79 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0003g0020others(76): Show | 85 | HG00609.hp1 HG00735.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.843-1143G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934629 | ||||||
chr1:934629
|
G | GGGCGGCT others(162): Show |
1 | a0001c0001t0003g0168 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.843-1080_843-1079i others(171): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934629 | |||||
chr1:934629
|
G | GGGGCTGC others(22): Show |
1 | a0001c0001t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.843-1141_843-1140i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934629 | |||||
chr1:934631
|
G | GCGGCTGC others(130): Show |
3 | a0002c0003t0004g0252a0002c0003t0004g0305a0002c0003t0004g0306 | 3 | NA18952.hp1 NA18983.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.843-1088_843-1087i others(139): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934631 | |||||
chr1:934631
|
G | T | 9 | a0002c0003t0004g0022a0002c0003t0004g0236a0002c0003t0004g0237others(6): Show | 10 | HG00609.hp1 HG01255.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-1141G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934631 | ||||||
chr1:934633
|
G | T | 4 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0004t0027g0362others(1): Show | 4 | HG00738.hp2 HG02622.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1139G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934633 | ||||||
chr1:934637
|
G | C | 14 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0173others(11): Show | 15 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.843-1135G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934637 | ||||||
chr1:934637
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0013g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.843-1116_843-1115i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934637 | |||||
chr1:934637
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0003g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.843-1116_843-1115i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934637 | |||||
chr1:934644
|
A | T | 1 | a0001c0009t0010g0313 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.843-1128A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934644 | ||||||
chr1:934649
|
G | GGCGGGGG others(21): Show |
1 | a0009c0013t0002g0286 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.843-1116_843-1115i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934649 | |||||
chr1:934649
|
G | T | 1 | a0009c0013t0002g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.843-1123G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934649 | ||||||
chr1:934651
|
C | CG | 14 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0023t0001g0150others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.843-1116dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934651 | |||||
chr1:934652
|
G | A | 2 | a0002c0003t0004g0224a0002c0049t0004g0223 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.843-1120G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934652 | ||||||
chr1:934657
|
A | AGGCGGCT others(527): Show |
1 | a0001c0001t0003g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.843-1108_843-1107i others(536): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934657 | |||||
chr1:934657
|
A | AGGCGGCT others(50): Show |
1 | a0001c0001t0012g0365 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.843-1080_843-1079i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934657 | |||||
chr1:934657
|
A | AGGCGGCT others(23): Show |
1 | a0013c0020t0002g0318 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.843-1088_843-1087i others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934657 | |||||
chr1:934657
|
A | AGGCGGCT others(74): Show |
1 | a0002c0003t0004g0249 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.843-1088_843-1087i others(83): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934657 | |||||
chr1:934657
|
A | AGGCTGCT others(753): Show |
1 | a0001c0001t0003g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.843-1112_843-1111i others(762): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934657 | |||||
chr1:934657
|
A | G | 48 | a0001c0001t0001g0083a0001c0001t0001g0092a0001c0001t0001g0114others(45): Show | 48 | HG00438.hp1 HG01167.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.843-1115A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934657 | ||||||
chr1:934659
|
G | T | 2 | a0002c0003t0004g0254a0029c0050t0004g0234 | 2 | HG01123.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.843-1113G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934659 | ||||||
chr1:934661
|
G | GGCTCCGT others(22): Show |
1 | a0001c0001t0003g0020 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.843-1108_843-1107i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934661 | |||||
chr1:934661
|
G | T | 7 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0210others(4): Show | 7 | HG01928.hp1 HG01978.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-1111G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934661 | ||||||
chr1:934665
|
G | C | 19 | a0001c0001t0001g0112a0001c0001t0003g0020a0001c0001t0003g0171others(16): Show | 20 | HG00323.hp1 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.843-1107G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934665 | ||||||
chr1:934665
|
G | GCGTTACA others(161): Show |
1 | a0001c0023t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843-1093_843-1092i others(170): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934665 | |||||
chr1:934665
|
G | GCGTTACA others(22): Show |
1 | a0001c0001t0003g0220 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.843-1088_843-1087i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934665 | |||||
chr1:934665
|
GCGTTACA others(21): Show |
G | 1 | a0001c0002t0002g0358 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.843-1079_843-1052d others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934665 | |||||
chr1:934672
|
A | T | 2 | a0001c0002t0007g0297a0001c0004t0027g0362 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.843-1100A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934672 | ||||||
chr1:934677
|
G | T | 1 | a0001c0002t0011g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.843-1095G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934677 | ||||||
chr1:934679
|
C | CG | 7 | a0001c0001t0003g0020a0001c0001t0003g0191a0003c0006t0003g0181others(4): Show | 7 | HG01099.hp2 HG01258.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-1088dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934679 | |||||
chr1:934679
|
C | CGGGGGAG others(23): Show |
1 | a0004c0008t0002g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.843-1080_843-1079i others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934679 | |||||
chr1:934680
|
G | A | 2 | a0001c0002t0011g0272a0002c0003t0004g0256 | 2 | HG02630.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.843-1092G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934680 | ||||||
chr1:934685
|
A | AGGCGGCT others(107): Show |
1 | a0001c0010t0007g0293 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.843-1080_843-1079i others(116): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934685 | |||||
chr1:934685
|
A | G | 37 | a0001c0001t0001g0083a0001c0001t0001g0097a0001c0001t0001g0113others(34): Show | 37 | HG00323.hp2 HG01099.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.843-1087A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934685 | ||||||
chr1:934687
|
G | T | 6 | a0002c0003t0004g0011a0002c0003t0004g0229a0002c0003t0004g0239others(3): Show | 8 | HG01361.hp2 HG01981.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-1085G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934687 | ||||||
chr1:934689
|
G | GGCTCCGT others(161): Show |
1 | a0001c0001t0001g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.843-1060_843-1059i others(170): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934689 | |||||
chr1:934689
|
G | GGCTCCGT others(22): Show |
1 | a0001c0001t0003g0169 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.843-1060_843-1059i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934689 | |||||
chr1:934689
|
G | GGCTGCGT others(79): Show |
2 | a0012c0025t0003g0195a0012c0025t0003g0196 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.843-1080_843-1079i others(88): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934689 | |||||
chr1:934689
|
G | GGCTGCGT others(107): Show |
1 | a0001c0009t0003g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.843-1080_843-1079i others(116): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934689 | |||||
chr1:934689
|
G | GGCTGCGT others(528): Show |
1 | a0001c0001t0003g0159 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.843-1080_843-1079i others(537): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934689 | |||||
chr1:934689
|
G | GGCTGCGT others(22): Show |
1 | a0001c0001t0003g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.843-1080_843-1079i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934689 | |||||
chr1:934689
|
G | T | 14 | a0001c0001t0001g0079a0001c0001t0001g0092a0001c0001t0001g0108others(11): Show | 14 | HG00438.hp1 HG01109.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.843-1083G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934689 | ||||||
chr1:934693
|
C | CCGTTACA others(49): Show |
1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.843-1056_843-1055i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934693 | |||||
chr1:934693
|
C | CCGTTACA others(348): Show |
1 | a0028c0048t0004g0244 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.843-1060_843-1059i others(357): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934693 | |||||
chr1:934693
|
C | CCGTTACA others(245): Show |
1 | a0001c0001t0003g0220 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.843-1060_843-1059i others(254): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934693 | |||||
chr1:934693
|
C | CCGTTACA others(105): Show |
1 | a0001c0001t0003g0162 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.843-1060_843-1059i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934693 | |||||
chr1:934693
|
C | CCGTTACA others(133): Show |
1 | a0001c0001t0003g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.843-1060_843-1059i others(142): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934693 | |||||
chr1:934693
|
C | G | 122 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0113others(119): Show | 126 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.843-1079C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934693 | ||||||
chr1:934700
|
A | T | 1 | a0001c0010t0007g0024 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.843-1072A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934700 | ||||||
chr1:934705
|
G | T | 2 | a0001c0001t0001g0123a0009c0013t0002g0285 | 2 | HG02109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.843-1067G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934705 | ||||||
chr1:934707
|
C | CA | 7 | a0001c0002t0011g0274a0001c0002t0011g0275a0001c0023t0001g0091others(4): Show | 7 | HG00642.hp2 HG01243.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-1065_843-1064i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934707 | ||||||
chr1:934707
|
C | CG | 10 | a0001c0019t0006g0269a0004c0008t0006g0281a0005c0007t0008g0276others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.843-1060dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934707 | |||||
chr1:934707
|
C | CGGGGGGG others(50): Show |
1 | a0006c0024t0003g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.843-1060_843-1059i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934707 | |||||
chr1:934708
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0123a0002c0003t0004g0245 | 3 | HG02109.hp2 NA18961.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.843-1064G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934708 | ||||||
chr1:934713
|
A | AGGCGGCT others(50): Show |
2 | a0001c0002t0009g0321a0001c0002t0009g0322 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.843-1052_843-1051i others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | AGGCGGCT others(77): Show |
1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.843-1052_843-1051i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | AGGCGGCT others(18): Show |
1 | a0002c0018t0004g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.843-1037_843-1036i others(27): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | AGGCGGCT others(667): Show |
2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-1024_843-1023i others(676): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | AGGCGGCT others(21): Show |
1 | a0001c0001t0001g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.843-1032_843-1031i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | AGGCGGCT others(134): Show |
1 | a0001c0019t0006g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.843-1032_843-1031i others(143): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | AGGCGGCT others(22): Show |
1 | a0004c0008t0006g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.843-1032_843-1031i others(31): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | AGGCGGCT others(79): Show |
1 | a0001c0010t0007g0295 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.843-1032_843-1031i others(88): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934713 | |||||
chr1:934713
|
A | G | 47 | a0001c0001t0001g0082a0001c0001t0001g0113a0001c0001t0003g0162others(44): Show | 47 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.843-1059A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934713 | ||||||
chr1:934713
|
A | GGGCGGCT others(79): Show |
1 | a0001c0010t0007g0292 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.843-1060_843-1059i others(88): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934713 | ||||||
chr1:934715
|
G | A | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.843-1057G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934715 | ||||||
chr1:934715
|
G | T | 12 | a0002c0003t0004g0022a0002c0003t0004g0236a0002c0003t0004g0237others(9): Show | 13 | HG00609.hp1 HG01255.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.843-1057G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934715 | ||||||
chr1:934717
|
G | T | 9 | a0001c0001t0001g0083a0001c0001t0001g0108a0001c0001t0001g0114others(6): Show | 9 | HG00733.hp1 HG01358.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.843-1055G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934717 | ||||||
chr1:934721
|
G | C | 19 | a0001c0001t0001g0083a0001c0001t0001g0108a0001c0001t0001g0114others(16): Show | 20 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.843-1051G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934721 | ||||||
chr1:934721
|
G | GCGTTACA others(529): Show |
1 | a0001c0021t0002g0342 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.843-1009_843-1008i others(538): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934721 | |||||
chr1:934721
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0001g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.843-1028_843-1027i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934721 | |||||
chr1:934721
|
G | GCGTTACA others(917): Show |
1 | a0001c0001t0003g0189 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.843-1032_843-1031i others(926): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934721 | |||||
chr1:934721
|
GCGTTACA others(105): Show |
G | 1 | a0001c0002t0002g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.843-1008_843-897de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934721 | |||||
chr1:934733
|
G | T | 1 | a0004c0008t0017g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.843-1039G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934733 | ||||||
chr1:934735
|
C | CAGGGGGA others(195): Show |
1 | a0001c0002t0011g0274 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.843-1037_843-1036i others(204): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934735 | ||||||
chr1:934735
|
C | CGGGGGGG others(79): Show |
1 | a0006c0024t0003g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.843-1032_843-1031i others(88): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934735 | |||||
chr1:934736
|
G | A | 5 | a0001c0011t0002g0324a0001c0011t0028g0316a0002c0003t0004g0246others(2): Show | 5 | HG02523.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.843-1036G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934736 | ||||||
chr1:934736
|
G | GGGGGAGG others(301): Show |
1 | a0001c0001t0003g0197 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.843-1024_843-1023i others(310): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934736 | |||||
chr1:934736
|
G | GGGGGAGG others(49): Show |
1 | a0001c0001t0003g0210 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.843-1028_843-1027i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934736 | |||||
chr1:934736
|
G | GGGGGGGG others(161): Show |
1 | a0001c0001t0003g0211 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.843-1032_843-1031i others(170): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934736 | |||||
chr1:934736
|
GGGGGAGG others(21): Show |
G | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.843-980_843-953del others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934736 | |||||
chr1:934736
|
GGGGGAGG others(49): Show |
G | 2 | a0001c0002t0002g0359a0001c0004t0027g0362 | 2 | HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.843-1008_843-953de others(57): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934736 | |||||
chr1:934741
|
A | AGGCGGCT others(831): Show |
1 | a0001c0001t0003g0021 | 2 | NA18948.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.843-1024_843-1023i others(840): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934741 | |||||
chr1:934741
|
A | AGGCGGCT others(107): Show |
1 | a0004c0008t0017g0361 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.843-1009_843-1008i others(116): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934741 | |||||
chr1:934741
|
A | G | 48 | a0001c0001t0001g0082a0001c0001t0001g0112a0001c0001t0003g0155others(45): Show | 48 | HG00323.hp1 HG00738.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.843-1031A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934741 | ||||||
chr1:934743
|
G | T | 2 | a0002c0003t0024g0233a0028c0048t0004g0244 | 2 | HG01496.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.843-1029G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934743 | ||||||
chr1:934744
|
C | T | 1 | a0006c0024t0003g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.843-1028C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934744 | ||||||
chr1:934745
|
G | T | 3 | a0001c0001t0001g0147a0001c0001t0003g0198a0001c0011t0028g0316 | 3 | HG02723.hp2 HG03927.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.843-1027G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934745 | ||||||
chr1:934749
|
G | C | 9 | a0001c0001t0001g0094a0001c0001t0001g0108a0001c0001t0001g0147others(6): Show | 9 | HG01361.hp1 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-1023G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934749 | ||||||
chr1:934749
|
G | GCGTTACA others(413): Show |
1 | a0003c0006t0003g0213 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.843-1009_843-1008i others(422): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934749 | |||||
chr1:934749
|
G | GCGTTACA others(49): Show |
1 | a0001c0001t0003g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.843-1009_843-1008i others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934749 | |||||
chr1:934749
|
G | GCGTTACA others(106): Show |
1 | a0003c0006t0003g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.843-1009_843-1008i others(115): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934749 | |||||
chr1:934749
|
G | GCGTTACA others(476): Show |
1 | a0004c0008t0006g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.843-1009_843-1008i others(485): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934749 | |||||
chr1:934749
|
GCGTTACA others(77): Show |
G | 1 | a0014c0027t0004g0232 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.843-1008_843-925de others(85): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934749 | |||||
chr1:934756
|
A | T | 2 | a0001c0010t0007g0292a0001c0010t0007g0293 | 2 | HG01123.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.843-1016A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934756 | ||||||
chr1:934761
|
G | GGCGGGGG others(21): Show |
1 | a0009c0013t0002g0287 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.843-1009_843-1008i others(30): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934761 | |||||
chr1:934761
|
G | T | 13 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0085others(10): Show | 13 | HG00673.hp2 HG02135.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.843-1011G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934761 | ||||||
chr1:934763
|
C | CG | 11 | a0001c0002t0016g0265a0001c0002t0016g0266a0001c0023t0001g0091others(8): Show | 11 | HG02109.hp1 HG02965.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-1009_843-1008i others(3): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934763 | ||||||
chr1:934763
|
C | CGGGGGGG others(328): Show |
1 | a0001c0002t0011g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.843-1009_843-1008i others(337): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934763 | ||||||
chr1:934763
|
CAGGGGAG others(103): Show |
C | 2 | a0005c0007t0022g0283a0016c0028t0008g0268 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.843-1008_843-899de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934763 | ||||||
chr1:934764
|
A | AG | 9 | a0001c0001t0013g0200a0001c0002t0011g0274a0001c0002t0011g0275others(6): Show | 11 | HG00642.hp2 HG01361.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-1004dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934764 | |||||
chr1:934764
|
A | AGGGGGGG others(77): Show |
1 | a0001c0009t0010g0312 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.843-1004_843-1003i others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934764 | |||||
chr1:934764
|
A | AGGGGGGG others(78): Show |
1 | a0009c0013t0002g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.843-1004_843-1003i others(87): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934764 | |||||
chr1:934764
|
A | G | 148 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(145): Show | 152 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.843-1008A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934764 | ||||||
chr1:934764
|
AGGGGAGG others(105): Show |
A | 1 | a0001c0001t0003g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.843-980_843-869del | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934764 | |||||
chr1:934765
|
GGGGAGGC others(20): Show |
G | 1 | a0014c0027t0004g0231 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.843-1003_843-977de others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934765 | |||||
chr1:934769
|
A | AGGCGGCT others(134): Show |
1 | a0001c0002t0009g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-981_843-980ins others(141): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934769 | |||||
chr1:934769
|
A | G | 52 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0003g0154others(49): Show | 52 | HG00438.hp1 HG00738.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.843-1003A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934769 | ||||||
chr1:934769
|
A | GGGCGGCT others(105): Show |
1 | a0001c0001t0001g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.843-1004_843-1003i others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934769 | ||||||
chr1:934773
|
G | T | 7 | a0001c0001t0001g0108a0001c0001t0003g0171a0001c0001t0003g0172others(4): Show | 7 | HG01346.hp2 HG01361.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.843-999G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934773 | ||||||
chr1:934777
|
G | C | 21 | a0001c0001t0001g0108a0001c0001t0001g0147a0001c0001t0003g0168others(18): Show | 21 | HG00733.hp1 HG01346.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.843-995G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934777 | ||||||
chr1:934777
|
G | GCGTTACA others(217): Show |
1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.843-981_843-980ins others(224): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934777 | |||||
chr1:934777
|
G | GCGTTACA others(1030): Show |
1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.843-981_843-980ins others(1037): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934777 | |||||
chr1:934784
|
A | AGGTGGGC others(163): Show |
1 | a0001c0010t0007g0294 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.843-981_843-980ins others(170): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934784 | |||||
chr1:934784
|
A | T | 1 | a0001c0010t0007g0295 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.843-988A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934784 | ||||||
chr1:934789
|
G | GGCGGGGG others(103): Show |
1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.843-981_843-980ins others(110): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934789 | |||||
chr1:934789
|
G | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0001g0147others(3): Show | 8 | HG01099.hp2 HG01891.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-983G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934789 | ||||||
chr1:934791
|
C | CGGGGGGG others(107): Show |
1 | a0006c0024t0003g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.843-981_843-980ins others(114): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934791 | ||||||
chr1:934791
|
CAGGGGAG others(104): Show |
C | 2 | a0002c0003t0004g0224a0002c0049t0004g0223 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.843-980_843-870del | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934791 | ||||||
chr1:934792
|
A | AG | 13 | a0001c0009t0010g0313a0002c0003t0004g0022a0002c0003t0004g0236others(10): Show | 14 | HG00609.hp1 HG01255.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.843-976dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934792 | |||||
chr1:934792
|
A | AGGGGGAG others(310): Show |
1 | a0001c0002t0011g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843-976_843-975ins others(317): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934792 | |||||
chr1:934792
|
A | AGGGGGGG others(248): Show |
1 | a0009c0013t0002g0288 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.843-976_843-975ins others(255): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934792 | |||||
chr1:934792
|
A | G | 156 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0082others(153): Show | 161 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.843-980A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934792 | ||||||
chr1:934792
|
AGGGGAGG others(49): Show |
A | 2 | a0001c0004t0001g0061a0001c0004t0001g0062 | 2 | HG01358.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.843-939_843-884del others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934792 | |||||
chr1:934792
|
AGGGGAGG others(77): Show |
A | 1 | a0004c0008t0002g0271 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.843-939_843-856del others(84): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934792 | |||||
chr1:934797
|
A | AGACTGCT others(105): Show |
1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.843-974_843-973ins others(112): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934797 | |||||
chr1:934797
|
A | AGGCGGCT others(413): Show |
1 | a0001c0001t0003g0020 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.843-968_843-967ins others(420): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934797 | |||||
chr1:934797
|
A | AGGCTGCT others(21): Show |
1 | a0001c0001t0003g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.843-972_843-971ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934797 | |||||
chr1:934797
|
A | AGGCTGCT others(133): Show |
1 | a0001c0001t0003g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.843-972_843-971ins others(140): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934797 | |||||
chr1:934797
|
A | AGGCTGCT others(134): Show |
1 | a0001c0001t0029g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.843-972_843-971ins others(141): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934797 | |||||
chr1:934797
|
A | G | 54 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(51): Show | 54 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.843-975A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934797 | ||||||
chr1:934801
|
G | T | 8 | a0001c0001t0001g0112a0001c0001t0003g0168a0001c0001t0003g0186others(5): Show | 8 | HG00323.hp1 HG00733.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.843-971G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934801 | ||||||
chr1:934805
|
G | C | 22 | a0001c0001t0001g0108a0001c0001t0001g0112a0001c0001t0003g0168others(19): Show | 22 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.843-967G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934805 | ||||||
chr1:934805
|
G | GCGTTACA others(106): Show |
1 | a0001c0001t0003g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.843-948_843-947ins others(113): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934805 | |||||
chr1:934805
|
GCGTTACA others(21): Show |
G | 2 | a0001c0001t0019g0190a0001c0004t0001g0145 | 2 | HG03831.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.843-939_843-912del others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934805 | |||||
chr1:934820
|
G | A | 15 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0001g0085others(12): Show | 15 | HG00323.hp1 HG00673.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.843-952G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934820 | ||||||
chr1:934825
|
A | AGGCGGCT others(592): Show |
1 | a0001c0023t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.843-940_843-939ins others(599): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934825 | |||||
chr1:934825
|
A | AGGCGGCT others(136): Show |
1 | a0001c0023t0001g0091 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843-940_843-939ins others(143): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934825 | |||||
chr1:934825
|
A | AGGCGGCT others(22): Show |
3 | a0001c0002t0011g0272a0009c0013t0002g0285a0009c0013t0002g0286 | 3 | HG02280.hp1 HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.843-940_843-939ins others(29): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934825 | |||||
chr1:934825
|
A | G | 43 | a0001c0001t0001g0082a0001c0001t0001g0123a0001c0001t0001g0147others(40): Show | 43 | HG00438.hp1 HG00639.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.843-947A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934825 | ||||||
chr1:934827
|
G | T | 1 | a0002c0003t0004g0253 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.843-945G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934827 | ||||||
chr1:934828
|
C | G | 1 | a0001c0001t0030g0205 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.843-944C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934828 | ||||||
chr1:934829
|
G | GGCTGCGT others(79): Show |
1 | a0004c0008t0002g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.843-940_843-939ins others(86): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934829 | |||||
chr1:934829
|
G | T | 24 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0092others(21): Show | 26 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.843-943G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934829 | ||||||
chr1:934833
|
C | CCGTTACA others(21): Show |
1 | a0001c0001t0003g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.843-863_843-836dup others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934833 | |||||
chr1:934833
|
C | CCGTTACA others(77): Show |
1 | a0001c0001t0003g0168 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.843-920_843-919ins others(84): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934833 | |||||
chr1:934833
|
C | CCGTTACA others(665): Show |
1 | a0003c0006t0003g0183 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.843-920_843-919ins others(672): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934833 | |||||
chr1:934833
|
C | CCGTTACA others(807): Show |
1 | a0003c0006t0003g0181 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.843-920_843-919ins others(814): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934833 | |||||
chr1:934833
|
C | CCGTTACA others(1170): Show |
1 | a0019c0041t0003g0160 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.843-920_843-919ins others(1177): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934833 | |||||
chr1:934833
|
C | CCGTTACA others(441): Show |
1 | a0001c0001t0003g0020 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.843-920_843-919ins others(448): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934833 | |||||
chr1:934833
|
C | G | 130 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0123others(127): Show | 134 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(131): Show |
intron_variant | MODIFIER | c.843-939C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934833 | ||||||
chr1:934840
|
A | T | 1 | a0006c0016t0002g0289 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.843-932A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934840 | ||||||
chr1:934845
|
G | T | 2 | a0001c0004t0001g0071a0001c0004t0001g0145 | 2 | NA18975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.843-927G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934845 | ||||||
chr1:934848
|
G | A | 18 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0112others(15): Show | 20 | HG00323.hp1 HG01361.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.843-924G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934848 | ||||||
chr1:934853
|
A | AGGCGGCT others(2039): Show |
1 | a0001c0001t0003g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.843-912_843-911ins others(2046): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934853 | |||||
chr1:934853
|
A | AGGCGGCT others(18): Show |
1 | a0001c0011t0002g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.843-897_843-896ins others(25): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934853 | |||||
chr1:934853
|
A | AGGCGGCT others(51): Show |
1 | a0001c0019t0006g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.843-892_843-891ins others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934853 | |||||
chr1:934853
|
A | G | 66 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(63): Show | 69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.843-919A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934853 | ||||||
chr1:934855
|
G | T | 1 | a0001c0001t0003g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.843-917G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934855 | ||||||
chr1:934856
|
C | CTGCTCCG others(74): Show |
1 | a0001c0001t0003g0198 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.843-916_843-915ins others(81): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934856 | ||||||
chr1:934856
|
C | CTGCTCCG others(103): Show |
1 | a0001c0001t0003g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.843-916_843-915ins others(110): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934856 | ||||||
chr1:934857
|
G | T | 14 | a0001c0001t0001g0082a0001c0001t0003g0171a0001c0001t0003g0172others(11): Show | 14 | HG01192.hp2 HG01346.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.843-915G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934857 | ||||||
chr1:934861
|
G | C | 28 | a0001c0001t0001g0082a0001c0001t0001g0107a0001c0001t0001g0142others(25): Show | 28 | HG00738.hp2 HG01099.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.843-911G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934861 | ||||||
chr1:934861
|
G | GCGTTACA others(749): Show |
2 | a0012c0025t0003g0195a0012c0025t0003g0196 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.843-884_843-883ins others(756): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(915): Show |
1 | a0001c0001t0003g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.843-884_843-883ins others(922): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(525): Show |
1 | a0001c0001t0003g0184 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.843-884_843-883ins others(532): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(551): Show |
1 | a0001c0001t0003g0021 | 2 | NA18948.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.843-884_843-883ins others(558): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(833): Show |
1 | a0001c0001t0003g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.843-884_843-883ins others(840): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(49): Show |
6 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0113others(3): Show | 6 | HG00323.hp2 HG01109.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.843-864_843-863ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(161): Show |
1 | a0001c0002t0007g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.843-892_843-891ins others(168): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(49): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.843-892_843-891ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(133): Show |
1 | a0001c0001t0003g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.843-892_843-891ins others(140): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934861
|
G | GCGTTACA others(21): Show |
4 | a0001c0001t0003g0177a0001c0001t0003g0186a0001c0001t0003g0187others(1): Show | 4 | HG01081.hp1 HG01943.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.843-892_843-891ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934861 | |||||
chr1:934868
|
A | T | 3 | a0001c0001t0003g0176a0004c0008t0006g0303a0021c0040t0003g0174 | 3 | HG02698.hp2 HG03453.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.843-904A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934868 | ||||||
chr1:934873
|
G | T | 5 | a0001c0001t0001g0108a0001c0002t0004g0327a0001c0002t0025g0344others(2): Show | 7 | HG01361.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-899G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934873 | ||||||
chr1:934875
|
C | CG | 7 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0019t0006g0269others(4): Show | 7 | HG02109.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-892dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934875 | |||||
chr1:934875
|
C | CGGGGGGG others(25): Show |
1 | a0006c0016t0015g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843-892_843-891ins others(32): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934875 | |||||
chr1:934875
|
C | CGGGGGGG others(614): Show |
1 | a0001c0002t0011g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.843-892_843-891ins others(621): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934875 | |||||
chr1:934875
|
C | G | 3 | a0001c0002t0002g0315a0005c0007t0022g0283a0016c0028t0008g0268 | 3 | HG02280.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.843-897C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934875 | ||||||
chr1:934876
|
G | A | 32 | a0001c0001t0001g0018a0001c0001t0001g0068a0001c0001t0001g0084others(29): Show | 35 | HG00673.hp2 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.843-896G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934876 | ||||||
chr1:934876
|
G | GGGGGGGG others(21): Show |
1 | a0001c0011t0002g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.843-892_843-891ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934876 | |||||
chr1:934881
|
A | AGGCGGCT others(106): Show |
1 | a0001c0001t0003g0169 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.843-884_843-883ins others(113): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934881 | |||||
chr1:934881
|
A | AGGCGGCT others(20): Show |
2 | a0001c0002t0011g0274a0004c0008t0006g0281 | 2 | HG00642.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.843-890_843-864dup others(27): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934881 | |||||
chr1:934881
|
A | AGGCGGCT others(52): Show |
2 | a0013c0020t0002g0318a0024c0037t0006g0307 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.843-864_843-863ins others(59): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934881 | |||||
chr1:934881
|
A | AGGCGGCT others(135): Show |
1 | a0006c0016t0002g0289 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.843-864_843-863ins others(142): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934881 | |||||
chr1:934881
|
A | G | 56 | a0001c0001t0001g0097a0001c0001t0001g0123a0001c0001t0003g0020others(53): Show | 60 | HG00609.hp1 HG00639.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.843-891A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934881 | ||||||
chr1:934885
|
G | T | 1 | a0025c0045t0003g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.843-887G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934885 | ||||||
chr1:934889
|
G | C | 13 | a0001c0002t0007g0297a0001c0009t0010g0308a0001c0009t0010g0310others(10): Show | 14 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.843-883G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934889 | ||||||
chr1:934889
|
G | GCGTTACA others(21): Show |
3 | a0001c0002t0007g0298a0001c0010t0007g0294a0001c0010t0007g0295 | 3 | HG01069.hp2 HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.843-856_843-855ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934889 | |||||
chr1:934889
|
G | GCGTTACA others(49): Show |
1 | a0001c0002t0007g0296 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.843-856_843-855ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934889 | |||||
chr1:934889
|
G | GCGTTACA others(49): Show |
1 | a0004c0008t0002g0270 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.843-841_843-840ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934889 | |||||
chr1:934896
|
A | T | 9 | a0001c0001t0012g0365a0001c0004t0027g0362a0001c0046t0014g0028others(6): Show | 9 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.843-876A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934896 | ||||||
chr1:934901
|
G | T | 5 | a0001c0001t0003g0197a0001c0001t0003g0210a0001c0001t0003g0211others(2): Show | 5 | HG01358.hp2 HG01943.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-871G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934901 | ||||||
chr1:934903
|
C | G | 2 | a0002c0003t0004g0224a0002c0049t0004g0223 | 2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.843-869C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934903 | ||||||
chr1:934904
|
G | A | 12 | a0001c0001t0001g0106a0001c0001t0001g0142a0001c0001t0003g0197others(9): Show | 12 | HG01358.hp2 HG01943.hp1 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.843-868G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934904 | ||||||
chr1:934904
|
G | GGGGGAGG others(106): Show |
1 | a0002c0003t0004g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.843-841_843-840ins others(113): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934904 | |||||
chr1:934904
|
G | GGGGGGGG others(413): Show |
1 | a0001c0001t0003g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.843-864_843-863ins others(420): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934904 | |||||
chr1:934904
|
G | GGGGGGGG others(49): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.843-864_843-863ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934904 | |||||
chr1:934909
|
A | AGGCGGCT others(49): Show |
1 | a0001c0002t0009g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.843-856_843-855ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934909 | |||||
chr1:934909
|
A | AGGCGGCT others(219): Show |
1 | a0001c0001t0013g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.843-836_843-835ins others(226): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934909 | |||||
chr1:934909
|
A | AGGCGGCT others(22): Show |
2 | a0001c0001t0003g0165a0001c0001t0003g0166 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-861_843-833dup others(29): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934909 | |||||
chr1:934909
|
A | G | 53 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0169others(50): Show | 56 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.843-863A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934909 | ||||||
chr1:934909
|
AGGCGGCT others(21): Show |
A | 23 | a0001c0001t0001g0018a0001c0001t0001g0068a0001c0001t0001g0084others(20): Show | 24 | HG00673.hp2 HG01361.hp1 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.843-837_843-810del others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934909 | |||||
chr1:934911
|
G | T | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-861G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934911 | ||||||
chr1:934917
|
G | C | 7 | a0001c0009t0010g0310a0001c0009t0010g0311a0001c0009t0010g0313others(4): Show | 7 | HG02132.hp2 HG02165.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.843-855G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934917 | ||||||
chr1:934924
|
A | T | 1 | a0001c0001t0003g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.843-848A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934924 | ||||||
chr1:934932
|
G | A | 16 | a0001c0002t0002g0315a0001c0004t0027g0362a0002c0003t0004g0230others(13): Show | 16 | HG01123.hp2 HG01496.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.843-840G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934932 | ||||||
chr1:934932
|
G | GGGGGAGG others(77): Show |
1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.843-836_843-835ins others(84): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934932 | |||||
chr1:934932
|
G | GGGGGAGG others(525): Show |
1 | a0002c0003t0004g0247 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.843-836_843-835ins others(532): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934932 | |||||
chr1:934937
|
G | A | 306 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(303): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.843-835G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934937 | ||||||
chr1:934937
|
G | GGGCGGCT others(21): Show |
1 | a0006c0016t0002g0289 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.843-828_843-827ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(21): Show |
1 | a0002c0003t0004g0011 | 3 | HG01981.hp2 HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.843-813_843-812ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(105): Show |
1 | a0008c0014t0004g0259 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.843-813_843-812ins others(112): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(21): Show |
1 | a0001c0001t0003g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(133): Show |
1 | a0002c0003t0004g0243 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(140): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(329): Show |
2 | a0002c0003t0004g0305a0002c0003t0004g0306 | 2 | NA18983.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.843-810_843-809ins others(336): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(523): Show |
1 | a0002c0003t0004g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(530): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(217): Show |
1 | a0001c0002t0009g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(224): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(189): Show |
1 | a0001c0001t0003g0203 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(196): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(105): Show |
1 | a0001c0001t0013g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(112): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(49): Show |
2 | a0002c0003t0004g0229a0002c0003t0004g0235 | 2 | HG01361.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.843-810_843-809ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(133): Show |
1 | a0002c0003t0004g0246 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(140): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(833): Show |
1 | a0002c0003t0004g0255 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(840): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(105): Show |
1 | a0008c0014t0004g0257 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(112): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(245): Show |
1 | a0002c0003t0004g0245 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(252): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(476): Show |
1 | a0002c0003t0004g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(483): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCGGCT others(77): Show |
1 | a0001c0001t0003g0169 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(84): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGCTGCT others(1681): Show |
1 | a0001c0002t0009g0323 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.843-832_843-831ins others(1688): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGGCGGC others(50): Show |
1 | a0013c0020t0006g0302 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.843-833_843-832ins others(57): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934937
|
G | GGGGGCGG others(51): Show |
1 | a0018c0030t0006g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.843-833_843-832ins others(58): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934937 | |||||
chr1:934941
|
G | GGCTGCGT others(49): Show |
1 | a0001c0019t0006g0269 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934941 | |||||
chr1:934941
|
G | T | 22 | a0001c0023t0001g0091a0001c0023t0001g0150a0004c0008t0002g0270others(19): Show | 22 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.843-831G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934941 | ||||||
chr1:934945
|
G | C | 2 | a0001c0001t0001g0082a0001c0021t0002g0342 | 2 | HG01192.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.843-827G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934945 | ||||||
chr1:934945
|
G | GCGTTACA others(21): Show |
1 | a0001c0001t0003g0162 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934945 | |||||
chr1:934945
|
G | GCGTTACA others(49): Show |
1 | a0001c0001t0003g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(56): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934945 | |||||
chr1:934945
|
G | GCGTTACA others(21): Show |
1 | a0002c0003t0004g0022 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.843-810_843-809ins others(28): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934945 | |||||
chr1:934946
|
C | CGTTACAG others(1710): Show |
1 | a0001c0009t0010g0309 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.843-818_843-817ins others(1717): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934946 | |||||
chr1:934946
|
C | T | 1 | a0001c0004t0027g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.843-826C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934946 | ||||||
chr1:934959
|
C | CAGGGGGG others(727): Show |
1 | a0001c0009t0010g0308 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.843-813_843-812ins others(734): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934959 | ||||||
chr1:934959
|
C | CGGGGGAG others(50): Show |
1 | a0001c0009t0010g0312 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(57): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGAG others(1121): Show |
1 | a0001c0021t0002g0342 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(1128): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGAG others(1291): Show |
1 | a0001c0009t0010g0313 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(1298): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGGG others(1738): Show |
1 | a0001c0009t0010g0311 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(1745): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGGG others(3427): Show |
1 | a0001c0009t0010g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.843-810_843-809ins others(3434): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGGG others(22): Show |
1 | a0001c0002t0011g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(29): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGGG others(190): Show |
1 | a0002c0018t0004g0226 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(197): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGGG others(388): Show |
1 | a0002c0018t0004g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(395): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934959
|
C | CGGGGGGG others(218): Show |
1 | a0002c0018t0004g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.843-810_843-809ins others(225): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 934959 | |||||
chr1:934962
|
G | GT | 3 | a0001c0001t0018g0151a0001c0001t0018g0152a0001c0011t0002g0291 | 3 | HG02630.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.843-810_843-809ins others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934962 | ||||||
chr1:934976
|
G | A | 2 | a0001c0032t0002g0353a0004c0008t0017g0354 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.843-796G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 934976 | ||||||
chr1:935063
|
C | T | 1 | a0001c0004t0001g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.843-709C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935063 | ||||||
chr1:935080
|
G | C | 3 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365 | 3 | HG02145.hp1 HG02258.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.843-692G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935080 | ||||||
chr1:935099
|
C | T | 1 | a0002c0003t0004g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.843-673C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935099 | ||||||
chr1:935260
|
T | G | 1 | a0001c0011t0002g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.843-512T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935260 | ||||||
chr1:935265
|
T | C | 71 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0081others(68): Show | 77 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.843-507T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935265 | ||||||
chr1:935271
|
C | T | 43 | a0001c0001t0005g0126a0001c0002t0002g0001a0001c0002t0002g0004others(40): Show | 62 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.843-501C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935271 | ||||||
chr1:935370
|
C | A | 1 | a0001c0001t0014g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.843-402C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935370 | ||||||
chr1:935374
|
C | T | 8 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(5): Show | 9 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.843-398C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935374 | ||||||
chr1:935386
|
C | T | 41 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0027others(38): Show | 60 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.843-386C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935386 | ||||||
chr1:935422
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.843-350C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935422 | ||||||
chr1:935426
|
C | CGGAGCTC others(4): Show |
111 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(108): Show | 115 | HG00609.hp1 HG01069.hp2 HG01099.hp2 others(112): Show |
intron_variant | MODIFIER | c.843-345_843-344ins others(11): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 935426 | |||||
chr1:935431
|
G | A | 30 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365others(27): Show | 31 | HG01069.hp2 HG01109.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.843-341G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935431 | ||||||
chr1:935481
|
C | T | 2 | a0002c0003t0004g0253a0002c0003t0004g0254 | 2 | HG02523.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.843-291C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935481 | ||||||
chr1:935523
|
T | C | 356 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(353): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.843-249T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935523 | ||||||
chr1:935546
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.843-226G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | chr1 | 935546 | ||||||
chr1:935954
|
G | A | 4 | a0013c0020t0002g0318a0013c0020t0006g0302a0018c0030t0006g0301others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+58G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 935954 | ||||||
chr1:935954
|
G | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(141): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.967+58G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 935954 | ||||||
chr1:935993
|
G | C | 1 | a0001c0004t0027g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.967+97G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 935993 | ||||||
chr1:935998
|
G | A | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.967+102G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 935998 | ||||||
chr1:936021
|
A | G | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+125A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936021 | ||||||
chr1:936026
|
C | T | 2 | a0001c0002t0002g0319a0001c0002t0002g0320 | 2 | HG01099.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.967+130C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936026 | ||||||
chr1:936053
|
C | T | 2 | a0002c0003t0004g0235a0002c0003t0004g0236 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.967+157C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936053 | ||||||
chr1:936084
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.967+188G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936084 | ||||||
chr1:936133
|
C | T | 10 | a0001c0002t0002g0315a0001c0002t0016g0265a0001c0002t0016g0266others(7): Show | 10 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.967+237C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936133 | ||||||
chr1:936141
|
C | A | 1 | a0001c0002t0009g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.967+245C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936141 | ||||||
chr1:936144
|
C | G | 1 | a0001c0004t0001g0145 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.967+248C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936144 | ||||||
chr1:936202
|
G | A | 2 | a0001c0001t0003g0168a0001c0001t0003g0169 | 2 | HG00642.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.967+306G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936202 | ||||||
chr1:936217
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0105 | 2 | HG02735.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.967+321C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936217 | ||||||
chr1:936234
|
T | TGGTCCCG others(32): Show |
6 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(3): Show | 6 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+368_967+406dup others(39): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936234 | |||||
chr1:936234
|
T | TGGTCCCG others(149): Show |
2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.967+406_967+407ins others(156): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936234 | |||||
chr1:936234
|
T | TGGTCCCG others(36): Show |
2 | a0006c0024t0003g0207a0006c0024t0003g0208 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.967+367_967+368ins others(43): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936234 | |||||
chr1:936234
|
T | TGGTCCCG others(75): Show |
7 | a0001c0002t0002g0315a0001c0002t0016g0265a0001c0002t0016g0266others(4): Show | 7 | HG02280.hp2 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.967+367_967+368ins others(82): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936234 | |||||
chr1:936234
|
T | TGGTCCCG others(32): Show |
1 | a0001c0009t0010g0311 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.967+355_967+356ins others(39): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936234 | |||||
chr1:936234
|
TGGTCCCG others(71): Show |
T | 44 | a0001c0001t0014g0080a0001c0004t0001g0096a0001c0021t0004g0328others(41): Show | 47 | HG00609.hp1 HG00673.hp2 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.967+407_967+484del others(78): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936234 | |||||
chr1:936264
|
A | AGGGGTCC others(110): Show |
5 | a0001c0002t0002g0319a0001c0002t0002g0320a0001c0002t0009g0321others(2): Show | 5 | HG01099.hp1 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.967+406_967+407ins others(117): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936264 | |||||
chr1:936264
|
A | G | 1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.967+368A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936264 | ||||||
chr1:936264
|
AGGGGTCC others(32): Show |
A | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(189): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.967+407_967+445del others(39): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936264 | |||||
chr1:936299
|
C | G | 9 | a0001c0002t0002g0315a0001c0002t0016g0265a0001c0002t0016g0266others(6): Show | 9 | HG02280.hp2 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.967+403C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936299 | ||||||
chr1:936303
|
G | A | 35 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(32): Show | 35 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.967+407G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936303 | ||||||
chr1:936303
|
G | GGGGGGTC others(37): Show |
1 | a0003c0006t0003g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.967+411_967+412ins others(44): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936303 | |||||
chr1:936303
|
G | GGGGGTCC others(36): Show |
64 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0082others(61): Show | 68 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.967+420_967+421ins others(43): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936303 | |||||
chr1:936303
|
GGGGGTCC others(32): Show |
G | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.967+485_967+523del others(39): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936303 | |||||
chr1:936311
|
C | CCGGT | 10 | a0001c0001t0003g0173a0001c0002t0002g0315a0001c0002t0016g0265others(7): Show | 10 | HG02280.hp2 HG02965.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.967+417_967+420dup others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936311 | |||||
chr1:936312
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0097 | 2 | NA18961.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.967+416C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936312 | ||||||
chr1:936313
|
G | GGTCA | 9 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(6): Show | 10 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.967+420_967+421ins others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936313 | |||||
chr1:936342
|
A | G | 14 | a0001c0001t0013g0200a0001c0001t0018g0151a0001c0001t0018g0152others(11): Show | 15 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.967+446A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936342 | ||||||
chr1:936350
|
C | CCGGT | 9 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(6): Show | 10 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.967+456_967+459dup others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936350 | |||||
chr1:936351
|
C | T | 1 | a0001c0011t0002g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.967+455C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936351 | ||||||
chr1:936354
|
TCCCGCCT others(28): Show |
T | 2 | a0005c0007t0008g0279a0016c0028t0008g0268 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.967+460_967+494del others(35): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936354 | |||||
chr1:936377
|
C | G | 1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.967+481C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936377 | ||||||
chr1:936381
|
A | G | 26 | a0001c0019t0006g0269a0001c0019t0006g0282a0001c0023t0001g0091others(23): Show | 26 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.967+485A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936381 | ||||||
chr1:936389
|
C | CCGGT | 26 | a0001c0019t0006g0269a0001c0019t0006g0282a0001c0023t0001g0091others(23): Show | 26 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.967+495_967+498dup others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936389 | |||||
chr1:936390
|
C | A | 1 | a0001c0005t0001g0069 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.967+494C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936390 | ||||||
chr1:936420
|
G | A | 38 | a0001c0001t0003g0173a0001c0002t0002g0315a0001c0002t0016g0265others(35): Show | 38 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.967+524G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936420 | ||||||
chr1:936424
|
G | A | 5 | a0001c0002t0002g0319a0001c0002t0002g0320a0001c0002t0009g0321others(2): Show | 5 | HG01099.hp1 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.967+528G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936424 | ||||||
chr1:936428
|
CCGGT | C | 36 | a0001c0002t0002g0315a0001c0002t0016g0265a0001c0002t0016g0266others(33): Show | 36 | HG01099.hp2 HG01243.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.967+538_967+541del others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936428 | |||||
chr1:936432
|
T | TCAGTCCC others(153): Show |
1 | a0005c0007t0008g0300 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.967+537_967+538ins others(160): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936432 | |||||
chr1:936432
|
T | TCAGTCCC others(153): Show |
8 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(5): Show | 9 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.967+537_967+538ins others(160): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936432 | |||||
chr1:936432
|
T | TCCCGCCT others(28): Show |
1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.967+537_967+538ins others(35): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 936432 | |||||
chr1:936444
|
T | C | 46 | a0001c0002t0002g0315a0001c0002t0007g0296a0001c0002t0007g0297others(43): Show | 47 | HG01069.hp2 HG01099.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.967+548T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936444 | ||||||
chr1:936456
|
G | T | 2 | a0014c0027t0004g0231a0014c0027t0004g0232 | 2 | NA19010.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.967+560G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936456 | ||||||
chr1:936473
|
G | A | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+577G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936473 | ||||||
chr1:936486
|
T | C | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.967+590T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936486 | ||||||
chr1:936492
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.967+596G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936492 | ||||||
chr1:936498
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.967+602G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936498 | ||||||
chr1:936513
|
C | T | 10 | a0001c0002t0002g0315a0001c0002t0016g0265a0001c0002t0016g0266others(7): Show | 10 | HG02258.hp1 HG02280.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.967+617C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936513 | ||||||
chr1:936588
|
C | T | 1 | a0002c0003t0004g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.967+692C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936588 | ||||||
chr1:936618
|
C | T | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.967+722C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936618 | ||||||
chr1:936623
|
C | T | 1 | a0001c0004t0001g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.967+727C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936623 | ||||||
chr1:936707
|
T | C | 58 | a0001c0001t0001g0106a0001c0001t0014g0080a0001c0002t0002g0315others(55): Show | 61 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.967+811T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936707 | ||||||
chr1:936711
|
T | G | 58 | a0001c0001t0001g0106a0001c0001t0014g0080a0001c0002t0002g0315others(55): Show | 61 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(58): Show |
intron_variant | MODIFIER | c.967+815T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936711 | ||||||
chr1:936735
|
C | T | 3 | a0001c0002t0002g0347a0001c0002t0002g0351a0026c0038t0002g0350 | 3 | NA18950.hp2 NA18974.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.967+839C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936735 | ||||||
chr1:936788
|
T | C | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+892T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936788 | ||||||
chr1:936846
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.967+950C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936846 | ||||||
chr1:936847
|
C | G | 1 | a0001c0004t0027g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.967+951C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936847 | ||||||
chr1:936902
|
C | T | 1 | a0002c0003t0004g0239 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.967+1006C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936902 | ||||||
chr1:936972
|
G | C | 169 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0082others(166): Show | 177 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.967+1076G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 936972 | ||||||
chr1:937010
|
G | T | 3 | a0001c0001t0012g0363a0001c0001t0012g0364a0001c0001t0012g0365 | 3 | HG02145.hp1 HG02258.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.967+1114G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937010 | ||||||
chr1:937044
|
C | T | 1 | a0001c0019t0006g0282 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.967+1148C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937044 | ||||||
chr1:937087
|
C | G | 2 | a0001c0002t0002g0315a0004c0008t0002g0317 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.967+1191C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937087 | ||||||
chr1:937088
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.967+1192C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937088 | ||||||
chr1:937154
|
A | AG | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+1262dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 937154 | |||||
chr1:937173
|
G | A | 1 | a0003c0006t0003g0183 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.967+1277G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937173 | ||||||
chr1:937236
|
G | A | 7 | a0001c0002t0009g0323a0003c0031t0002g0299a0006c0016t0002g0289others(4): Show | 7 | HG02572.hp1 HG02976.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.967+1340G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937236 | ||||||
chr1:937307
|
C | G | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+1411C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937307 | ||||||
chr1:937396
|
G | GC | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0029others(15): Show | 20 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.967+1511dupC | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 937396 | |||||
chr1:937396
|
GCC | G | 220 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0082others(217): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.967+1510_967+1511d others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 937396 | |||||
chr1:937404
|
C | A | 52 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0027others(49): Show | 70 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.967+1508C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937404 | ||||||
chr1:937477
|
G | A | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.968-1563G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937477 | ||||||
chr1:937572
|
C | T | 38 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0027others(35): Show | 56 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.968-1468C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937572 | ||||||
chr1:937703
|
G | A | 1 | a0005c0007t0008g0300 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.968-1337G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937703 | ||||||
chr1:937738
|
G | A | 2 | a0001c0002t0020g0304a0001c0011t0006g0025 | 3 | HG02257.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.968-1302G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937738 | ||||||
chr1:937788
|
G | A | 1 | a0001c0009t0010g0310 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.968-1252G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937788 | ||||||
chr1:937816
|
A | G | 1 | a0001c0005t0001g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.968-1224A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937816 | ||||||
chr1:937900
|
A | G | 1 | a0004c0008t0006g0281 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.968-1140A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937900 | ||||||
chr1:937962
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.968-1078G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 937962 | ||||||
chr1:938014
|
A | G | 143 | a0001c0001t0003g0214a0001c0001t0003g0220a0001c0001t0014g0080others(140): Show | 165 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.968-1026A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938014 | ||||||
chr1:938037
|
TAGAGCCC others(625): Show |
T | 2 | a0001c0002t0002g0348a0001c0029t0002g0349 | 2 | NA19012.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.968-1000_968-369de others(1): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 938037 | |||||
chr1:938082
|
G | T | 4 | a0001c0002t0016g0265a0001c0002t0016g0266a0006c0016t0015g0263others(1): Show | 4 | HG02965.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-958G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938082 | ||||||
chr1:938106
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.968-934G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938106 | ||||||
chr1:938178
|
G | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(142): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.968-862G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938178 | ||||||
chr1:938266
|
T | C | 4 | a0008c0014t0004g0257a0008c0014t0004g0258a0008c0014t0004g0259others(1): Show | 4 | NA18747.hp1 NA18971.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-774T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938266 | ||||||
chr1:938320
|
G | T | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.968-720G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938320 | ||||||
chr1:938321
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.968-719T>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938321 | ||||||
chr1:938324
|
G | T | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.968-716G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938324 | ||||||
chr1:938347
|
G | A | 1 | a0001c0002t0002g0332 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.968-693G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938347 | ||||||
chr1:938479
|
G | T | 37 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(34): Show | 38 | HG01069.hp2 HG01099.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.968-561G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938479 | ||||||
chr1:938503
|
G | A | 1 | a0011c0044t0031g0156 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.968-537G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938503 | ||||||
chr1:938555
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0146 | 3 | NA18943.hp1 NA18956.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.968-485G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938555 | ||||||
chr1:938603
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.968-437G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938603 | ||||||
chr1:938654
|
G | A | 48 | a0001c0001t0001g0034a0001c0001t0001g0110a0001c0002t0002g0001others(45): Show | 66 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.968-386G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938654 | ||||||
chr1:938693
|
C | G | 47 | a0001c0001t0014g0080a0001c0004t0001g0058a0001c0021t0004g0328others(44): Show | 50 | HG00609.hp1 HG01123.hp2 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.968-347C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938693 | ||||||
chr1:938741
|
G | A | 1 | a0005c0007t0008g0280 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.968-299G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938741 | ||||||
chr1:938771
|
TGGGGCAG others(4): Show |
T | 1 | a0001c0009t0010g0311 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.968-267_968-257del others(11): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 938771 | |||||
chr1:938840
|
T | C | 1 | a0001c0001t0013g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.968-200T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938840 | ||||||
chr1:938934
|
G | A | 3 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204 | 3 | HG01167.hp2 HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.968-106G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938934 | ||||||
chr1:938949
|
T | C | 7 | a0001c0009t0010g0308a0001c0009t0010g0309a0001c0009t0010g0310others(4): Show | 7 | NA18942.hp1 NA18948.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.968-91T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 938949 | ||||||
chr1:939033
|
C | G | 1 | a0001c0009t0010g0313 | 1 | NA18967.hp1 | splice_region_variant&intron_variant | LOW | c.968-7C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 5/13 | chr1 | 939033 | ||||||
chr1:939148
|
C | T | 1 | a0001c0001t0018g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1057+19C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 6/13 | chr1 | 939148 | ||||||
chr1:939170
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1057+41G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 6/13 | chr1 | 939170 | ||||||
chr1:939171
|
G | A | 1 | a0001c0005t0001g0066 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1057+42G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 6/13 | chr1 | 939171 | ||||||
chr1:939173
|
GGCAGTCC others(31): Show |
G | 1 | a0001c0001t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1057+45_1058-64del others(38): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 6/13 | chr1 | 939173 | ||||||
chr1:939208
|
C | T | 1 | a0001c0002t0023g0336 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1058-67C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 6/13 | chr1 | 939208 | ||||||
chr1:939221
|
C | T | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1058-54C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 6/13 | chr1 | 939221 | ||||||
chr1:939398
|
G | GCCTCCCC others(41): Show |
7 | a0007c0012t0001g0009a0007c0012t0001g0115a0007c0012t0001g0131others(4): Show | 9 | HG01192.hp1 HG01891.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195+25_1195+72dup others(48): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939398 | |||||
chr1:939398
|
G | GCCTCCCC others(89): Show |
17 | a0004c0008t0002g0270a0004c0008t0002g0271a0004c0008t0002g0290others(14): Show | 17 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1195+72_1195+73ins others(96): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939398 | |||||
chr1:939398
|
G | GCCTCCCC others(137): Show |
7 | a0009c0013t0002g0285a0009c0013t0002g0286a0009c0013t0002g0287others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195+72_1195+73ins others(144): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939398 | |||||
chr1:939398
|
G | GCCTCCCC others(186): Show |
1 | a0024c0037t0006g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1195+96_1195+97ins others(193): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939398 | |||||
chr1:939398
|
GCCTCCCC others(41): Show |
G | 11 | a0003c0006t0001g0089a0003c0006t0001g0102a0003c0006t0002g0261others(8): Show | 11 | HG00735.hp2 HG01081.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1195+25_1195+72del others(48): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939398 | |||||
chr1:939436
|
C | CCCCCTCA others(42): Show |
1 | a0006c0024t0003g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1195+48_1195+96dup others(49): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939436 | |||||
chr1:939436
|
CCCCCTCA others(42): Show |
C | 1 | a0001c0001t0001g0106 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1195+48_1195+96del others(49): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939436 | |||||
chr1:939500
|
C | T | 1 | a0001c0046t0014g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1195+88C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 939500 | ||||||
chr1:939547
|
A | G | 63 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0040others(60): Show | 69 | HG01099.hp1 HG01123.hp2 HG01255.hp2 others(66): Show |
intron_variant | MODIFIER | c.1195+135A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 939547 | ||||||
chr1:939553
|
G | A | 1 | a0021c0040t0003g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1195+141G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 939553 | ||||||
chr1:939570
|
T | TCCCTGGA others(5): Show |
301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(298): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1195+162_1195+163i others(14): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939570 | |||||
chr1:939663
|
T | A | 1 | a0001c0009t0010g0311 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1195+251T>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 939663 | ||||||
chr1:939779
|
AGCCAGTG others(11): Show |
A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(145): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1195+373_1195+390d others(20): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 939779 | |||||
chr1:939895
|
A | T | 1 | a0001c0001t0003g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1195+483A>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 939895 | ||||||
chr1:939984
|
C | T | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1195+572C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 939984 | ||||||
chr1:940000
|
C | T | 1 | a0001c0002t0002g0360 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1195+588C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940000 | ||||||
chr1:940066
|
G | C | 1 | a0001c0002t0025g0344 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1195+654G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940066 | ||||||
chr1:940091
|
G | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0033 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1195+679G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940091 | ||||||
chr1:940114
|
A | G | 1 | a0001c0002t0011g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1195+702A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940114 | ||||||
chr1:940115
|
C | G | 2 | a0001c0001t0018g0151a0001c0001t0018g0152 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1195+703C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940115 | ||||||
chr1:940147
|
C | G | 1 | a0004c0008t0006g0303 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1195+735C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940147 | ||||||
chr1:940189
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1195+777C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940189 | ||||||
chr1:940256
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1195+844C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940256 | ||||||
chr1:940260
|
C | G | 2 | a0009c0013t0002g0287a0009c0013t0002g0288 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1195+848C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940260 | ||||||
chr1:940263
|
C | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(251): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1195+851C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940263 | ||||||
chr1:940280
|
A | C | 1 | a0001c0004t0027g0362 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1196-864A>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940280 | ||||||
chr1:940296
|
G | C | 1 | a0002c0003t0009g0228 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1196-848G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940296 | ||||||
chr1:940296
|
G | GCCCCC | 15 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0092others(12): Show | 17 | HG01123.hp2 HG01978.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.1196-840_1196-836d others(7): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 940296 | |||||
chr1:940296
|
G | GCCCCCC | 44 | a0001c0001t0001g0032a0001c0001t0001g0113a0001c0001t0003g0020others(41): Show | 48 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1196-841_1196-836d others(8): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 940296 | |||||
chr1:940296
|
G | GCCCCCCC | 19 | a0001c0001t0001g0082a0001c0001t0001g0147a0001c0001t0003g0021others(16): Show | 20 | HG00140.hp1 HG01106.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1196-842_1196-836d others(9): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 940296 | |||||
chr1:940296
|
G | GCCCCCCC others(5): Show |
1 | a0002c0003t0004g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1196-847_1196-836d others(14): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 940296 | |||||
chr1:940296
|
GC | G | 33 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0035others(30): Show | 34 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1196-836delC | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 940296 | |||||
chr1:940296
|
GCC | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(192): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1196-837_1196-836d others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 940296 | |||||
chr1:940308
|
C | A | 1 | a0001c0002t0007g0298 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1196-836C>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940308 | ||||||
chr1:940346
|
T | A | 1 | a0001c0001t0003g0164 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1196-798T>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940346 | ||||||
chr1:940378
|
C | G | 1 | a0001c0001t0003g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1196-766C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940378 | ||||||
chr1:940390
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1196-754A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940390 | ||||||
chr1:940463
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1196-681G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940463 | ||||||
chr1:940605
|
T | C | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1196-539T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940605 | ||||||
chr1:940687
|
C | T | 6 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0108others(3): Show | 6 | HG00323.hp1 HG00738.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196-457C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940687 | ||||||
chr1:940758
|
C | T | 1 | a0001c0002t0002g0348 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1196-386C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940758 | ||||||
chr1:940792
|
C | T | 1 | a0001c0046t0014g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1196-352C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940792 | ||||||
chr1:940820
|
G | C | 1 | a0001c0001t0001g0016 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1196-324G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940820 | ||||||
chr1:940953
|
C | T | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1196-191C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 940953 | ||||||
chr1:941013
|
G | A | 5 | a0006c0016t0002g0289a0006c0016t0015g0263a0006c0016t0015g0264others(2): Show | 5 | HG02976.hp2 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196-131G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 941013 | ||||||
chr1:941104
|
C | T | 10 | a0001c0001t0003g0021a0001c0001t0003g0154a0001c0001t0003g0182others(7): Show | 11 | HG01167.hp1 HG01169.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1196-40C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 941104 | ||||||
chr1:941119
|
A | G | 341 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(338): Show | 400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.1196-25A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 7/13 | chr1 | 941119 | ||||||
chr1:941326
|
T | C | 2 | a0008c0014t0004g0258a0008c0014t0004g0260 | 2 | NA18975.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1358+20T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941326 | ||||||
chr1:941404
|
G | C | 1 | a0001c0004t0001g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1358+98G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941404 | ||||||
chr1:941498
|
A | AGGCTGGG others(30): Show |
1 | a0001c0001t0003g0179 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1358+197_1358+198i others(39): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 941498 | |||||
chr1:941528
|
G | A | 2 | a0001c0004t0027g0362a0001c0011t0028g0316 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1358+222G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941528 | ||||||
chr1:941569
|
G | C | 57 | a0001c0001t0003g0214a0001c0001t0003g0220a0001c0001t0014g0045others(54): Show | 61 | HG00423.hp2 HG00609.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1358+263G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941569 | ||||||
chr1:941585
|
G | A | 1 | a0001c0011t0028g0316 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1358+279G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941585 | ||||||
chr1:941757
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1359-379C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941757 | ||||||
chr1:941767
|
G | A | 63 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0082others(60): Show | 67 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1359-369G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941767 | ||||||
chr1:941771
|
C | T | 1 | a0003c0006t0003g0194 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1359-365C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941771 | ||||||
chr1:941884
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1359-252C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941884 | ||||||
chr1:941951
|
G | A | 1 | a0001c0001t0001g0014 | 2 | NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1359-185G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941951 | ||||||
chr1:941983
|
G | C | 8 | a0001c0001t0003g0179a0001c0002t0002g0315a0003c0031t0002g0299others(5): Show | 8 | HG01074.hp2 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1359-153G>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 941983 | ||||||
chr1:942068
|
G | A | 1 | a0001c0002t0002g0334 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1359-68G>A | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 942068 | ||||||
chr1:942127
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1359-9C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 8/13 | chr1 | 942127 | ||||||
chr1:942265
|
T | C | 1 | a0004c0008t0017g0354 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1474+14T>C | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 9/13 | chr1 | 942265 | ||||||
chr1:942294
|
C | G | 1 | a0020c0039t0005g0111 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1474+43C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 9/13 | chr1 | 942294 | ||||||
chr1:942335
|
C | G | 334 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(331): Show | 393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.1475-75C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 9/13 | chr1 | 942335 | ||||||
chr1:942402
|
C | G | 46 | a0001c0001t0014g0045a0001c0001t0014g0080a0001c0002t0004g0327others(43): Show | 49 | HG00423.hp2 HG00609.hp1 HG01123.hp2 others(46): Show |
splice_region_variant&intron_variant | LOW | c.1475-8C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 9/13 | chr1 | 942402 | ||||||
chr1:943128
|
G | T | 2 | a0002c0003t0004g0238a0002c0003t0004g0239 | 2 | NA18964.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.2053+70G>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/13 | chr1 | 943128 | ||||||
chr1:943136
|
GA | G | 9 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(6): Show | 10 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2053+83delA | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 943136 | |||||
chr1:943381
|
A | AG | 11 | a0001c0001t0001g0075a0001c0001t0001g0082a0001c0001t0001g0110others(8): Show | 11 | HG01169.hp2 HG01192.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2178+11dupG | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 943381 | |||||
chr1:943389
|
C | G | 1 | a0001c0002t0002g0315 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2178+12C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943389 | ||||||
chr1:943404
|
C | G | 3 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0003g0167 | 3 | HG01074.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2178+27C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943404 | ||||||
chr1:943429
|
C | T | 2 | a0001c0001t0001g0093a0003c0006t0001g0089 | 2 | HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2178+52C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943429 | ||||||
chr1:943520
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2178+143C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943520 | ||||||
chr1:943526
|
CT | C | 103 | a0001c0001t0001g0120a0001c0001t0003g0179a0001c0001t0003g0214others(100): Show | 113 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.2179-150delT | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 943526 | |||||
chr1:943526
|
CTT | C | 31 | a0001c0001t0001g0013a0001c0001t0001g0041a0001c0001t0001g0072others(28): Show | 34 | HG00738.hp2 HG01975.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.2179-151_2179-150d others(4): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 943526 | |||||
chr1:943526
|
CTTT | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(208): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2179-152_2179-150d others(5): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 943526 | |||||
chr1:943526
|
CTTTTT | C | 8 | a0001c0002t0007g0296a0001c0002t0007g0297a0001c0002t0007g0298others(5): Show | 9 | HG01069.hp2 HG01123.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2179-154_2179-150d others(7): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 943526 | |||||
chr1:943551
|
C | T | 1 | a0004c0008t0002g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2179-147C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943551 | ||||||
chr1:943552
|
A | G | 1 | a0016c0028t0008g0268 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2179-146A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943552 | ||||||
chr1:943635
|
C | T | 4 | a0013c0020t0002g0318a0013c0020t0006g0302a0018c0030t0006g0301others(1): Show | 4 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2179-63C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943635 | ||||||
chr1:943645
|
C | G | 2 | a0001c0001t0001g0093a0003c0006t0001g0089 | 2 | HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2179-53C>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943645 | ||||||
chr1:943658
|
C | T | 1 | a0002c0018t0004g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2179-40C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 12/13 | chr1 | 943658 | ||||||
chr1:943896
|
A | G | 5 | a0001c0004t0001g0071a0001c0011t0002g0291a0007c0012t0001g0009others(2): Show | 7 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2290-12A>G | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 13/13 | chr1 | 943896 | ||||||
chr1:943905
|
C | T | 1 | a0001c0001t0005g0124 | 1 | HG02074.hp1 | splice_region_variant&intron_variant | LOW | c.2290-3C>T | SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 13/13 | chr1 | 943905 |