geneid | 10407 |
---|---|
ensemblid | ENSG00000164871.18 |
hgncid | 14534 |
symbol | SPAG11B |
name | sperm associated antigen 11B |
refseq_nuc | NM_058201.4 |
refseq_prot | NP_478108.2 |
ensembl_nuc | ENST00000398462.7 |
ensembl_prot | ENSP00000381480.2 |
mane_status | MANE Select |
chr | chr8 |
start | 7450603 |
end | 7463542 |
strand | - |
ver | v1.2 |
region | chr8:7450603-7463542 |
region5000 | chr8:7445603-7468542 |
regionname0 | SPAG11B_chr8_7450603_7463542 |
regionname5000 | SPAG11B_chr8_7445603_7468542 |
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 | 0/0 | 133 | 97 | 12 | 16 | 54 | 6 | 9 | 37 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0002 | 0/1 | 133 | 82 | 17 | 11 | 39 | 2 | 12 | 33 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0003 | 0/0 | 133 | 13 | 2 | 3 | 8 | 0 | 0 | 5 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0004 | 0/0 | 133 | 5 | 0 | 2 | 2 | 0 | 1 | 2 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0005 | 0/0 | 133 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0006 | 0/0 | 133 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0007 | 0/0 | 133 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0008 | 0/0 | 133 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0009 | 0/0 | 133 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
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 | 0/0 | 402 | 95 | 12 | 16 | 52 | 6 | 9 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0002 | 0/1 | 402 | 82 | 17 | 11 | 39 | 2 | 12 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0003 | 0/0 | 402 | 13 | 2 | 3 | 8 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0004 | 0/0 | 402 | 5 | 0 | 2 | 2 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0005 | 0/0 | 402 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0006 | 0/0 | 402 | 2 | 1 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0007 | 0/0 | 402 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0008 | 0/0 | 402 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0009 | 0/0 | 402 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
c0010 | 0/0 | 402 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 150 | 190 | 32 | 30 | 101 | 8 | 18 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
t0002 | 0/0 | 150 | 11 | 2 | 4 | 5 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
t0003 | 0/0 | 150 | 4 | 0 | 0 | 0 | 0 | 4 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
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 | 13 | 1 | 1 | 11 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0002 | 0/0 | 9 | 0 | 1 | 4 | 1 | 3 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0005 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
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 | 0/0 | 402 | 95 | 12 | 16 | 52 | 6 | 9 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0001c0005 | 0/0 | 402 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0002c0002 | 0/1 | 402 | 82 | 17 | 11 | 39 | 2 | 12 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0003c0003 | 0/0 | 402 | 13 | 2 | 3 | 8 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0004c0004 | 0/0 | 402 | 5 | 0 | 2 | 2 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0005c0008 | 0/0 | 402 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0006c0006 | 0/0 | 402 | 2 | 1 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0007c0007 | 0/0 | 402 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0008c0009 | 0/0 | 402 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0009c0010 | 0/0 | 402 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 551 | 91 | 11 | 15 | 50 | 6 | 9 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0001c0001t0002 | 0/0 | 551 | 4 | 1 | 1 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0001c0005t0001 | 0/0 | 551 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0002c0002t0001 | 0/1 | 551 | 73 | 17 | 9 | 36 | 2 | 8 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0002c0002t0002 | 0/0 | 551 | 5 | 0 | 2 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0002c0002t0003 | 0/0 | 551 | 4 | 0 | 0 | 0 | 0 | 4 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0003c0003t0001 | 0/0 | 551 | 12 | 1 | 3 | 8 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0003c0003t0002 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0004c0004t0001 | 0/0 | 551 | 5 | 0 | 2 | 2 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0005c0008t0001 | 0/0 | 551 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0006c0006t0001 | 0/0 | 551 | 2 | 1 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0007c0007t0001 | 0/0 | 551 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0008c0009t0002 | 0/0 | 551 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
a0009c0010t0001 | 0/0 | 551 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | copy fasta | chr8 | 7445603 | 7468542 |
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 | 9 | 0 | 1 | 4 | 1 | 3 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0001 | 0/0 | 13 | 1 | 1 | 11 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0002c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0003c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0004c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0004c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0004c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0004c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0004c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0005c0008t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0005c0008t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0006c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0006c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0007c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0007c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0008c0009t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
a0009c0010t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0041 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0065 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0062 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01169 | hp2 | a0004 | c0004 | t0001 | g0063 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01243 | hp2 | a0008 | c0009 | t0002 | g0025 | AMR | PUR | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01496 | hp2 | a0009 | c0010 | t0001 | g0133 | AMR | CLM | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | IBS | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0124 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02040 | hp1 | a0006 | c0006 | t0001 | g0064 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02293 | hp2 | a0003 | c0003 | t0001 | g0012 | AMR | PEL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02976 | hp1 | a0005 | c0008 | t0001 | g0152 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0147 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03017 | hp2 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03041 | hp1 | a0006 | c0006 | t0001 | g0070 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0102 | AFR | GWD | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03130 | hp1 | a0005 | c0008 | t0001 | g0153 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0134 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0130 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | MSL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03654 | hp2 | a0004 | c0004 | t0001 | g0067 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0116 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0012 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18747 | hp1 | a0007 | c0007 | t0001 | g0069 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18962 | hp1 | a0001 | c0005 | t0001 | g0085 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18963 | hp2 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18965 | hp2 | a0007 | c0007 | t0001 | g0068 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18966 | hp2 | a0001 | c0005 | t0001 | g0105 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18973 | hp2 | a0004 | c0004 | t0001 | g0071 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18981 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18988 | hp2 | a0004 | c0004 | t0001 | g0066 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19002 | hp1 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19077 | hp1 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | GIH | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02109 | hp2 | a0003 | c0003 | t0002 | g0033 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | ACB | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | USA | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0106 | REF | REF | SPAG11B_chr8_7445603_7468542 | SPAG11B | chr8 | 7445603 | 7468542 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:7450864
|
T | C | 6 | a0001a0003a0004others(3): Show | 119 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(116): Show |
missense_variant | MODERATE | c.251A>G | p.His84Arg | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 290/551 | 251/402 | 84/133 | chr8 | 7450864 | ||
chr8:7450881
|
A | C | 3 | a0003a0004a0008 | 19 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(16): Show |
missense_variant | MODERATE | c.234T>G | p.Ile78Met | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 273/551 | 234/402 | 78/133 | chr8 | 7450881 | ||
chr8:7450888
|
G | A | 4 | a0003a0004a0008others(1): Show | 20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
missense_variant | MODERATE | c.227C>T | p.Pro76Leu | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 266/551 | 227/402 | 76/133 | chr8 | 7450888 | ||
chr8:7462743
|
G | A | 3 | a0004a0006a0007 | 9 | HG00639.hp2 HG01169.hp2 HG02040.hp1 others(6): Show |
missense_variant | MODERATE | c.178C>T | p.Arg60Trp | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/3 | 217/551 | 178/402 | 60/133 | chr8 | 7462743 | ||
chr8:7463479
|
C | A | 1 | a0005 | 2 | HG02976.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.25G>T | p.Val9Phe | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/3 | 64/551 | 25/402 | 9/133 | chr8 | 7463479 | ||
chr8:7463493
|
C | T | 1 | a0008 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.11G>A | p.Arg4Gln | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/3 | 50/551 | 11/402 | 4/133 | chr8 | 7463493 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:7450872
|
G | A | 1 | a0001c0005 | 2 | NA18962.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.243C>T | p.Thr81Thr | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 282/551 | 243/402 | 81/133 | chr8 | 7450872 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:7450609
|
G | A | 1 | a0002c0002t0003 | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*104C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 3/3 | 104 | chr8 | 7450609 | |||||
chr8:7463525
|
C | T | 4 | a0001c0001t0002a0002c0002t0002a0003c0003t0002others(1): Show | 11 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-22G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/3 | 22 | chr8 | 7463525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:7450962
|
C | A | 18 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(15): Show | 20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-62G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7450962 | ||||||
chr8:7450971
|
G | A | 18 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(15): Show | 20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-71C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7450971 | ||||||
chr8:7451007
|
C | T | 18 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(15): Show | 20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-107G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451007 | ||||||
chr8:7451031
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.215-131G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451031 | ||||||
chr8:7451148
|
T | C | 18 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(15): Show | 20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-248A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451148 | ||||||
chr8:7451153
|
A | G | 18 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(15): Show | 20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-253T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451153 | ||||||
chr8:7451160
|
C | T | 18 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(15): Show | 20 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.215-260G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451160 | ||||||
chr8:7451184
|
C | T | 17 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(14): Show | 19 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.215-284G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451184 | ||||||
chr8:7451207
|
G | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(54): Show | 80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.215-307C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451207 | ||||||
chr8:7451276
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 188 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(185): Show |
intron_variant | MODIFIER | c.215-376T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451276 | ||||||
chr8:7451399
|
T | G | 1 | a0002c0002t0001g0049 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.215-499A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451399 | ||||||
chr8:7451475
|
C | A | 1 | a0001c0001t0001g0024 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.215-575G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451475 | ||||||
chr8:7451476
|
T | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(55): Show | 81 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.215-576A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451476 | ||||||
chr8:7451512
|
G | GCAA | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(96): Show | 145 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.215-615_215-613dup others(3): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451512 | ||||||
chr8:7451701
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-801C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451701 | ||||||
chr8:7451709
|
AC | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(93): Show | 141 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.215-810delG | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451709 | ||||||
chr8:7451770
|
A | G | 4 | a0002c0002t0001g0023a0002c0002t0001g0134a0002c0002t0001g0142others(1): Show | 5 | HG02895.hp1 HG02897.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-870T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451770 | ||||||
chr8:7451809
|
C | T | 1 | a0006c0006t0001g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-909G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451809 | ||||||
chr8:7451857
|
C | T | 2 | a0002c0002t0001g0121a0002c0002t0001g0126 | 2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.215-957G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451857 | ||||||
chr8:7451998
|
C | T | 3 | a0002c0002t0003g0022a0002c0002t0003g0116a0002c0002t0003g0130 | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-1098G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7451998 | ||||||
chr8:7452051
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.215-1151G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452051 | ||||||
chr8:7452105
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.215-1205G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452105 | ||||||
chr8:7452179
|
T | C | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-1279A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452179 | ||||||
chr8:7452282
|
A | G | 1 | a0002c0002t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-1382T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452282 | ||||||
chr8:7452356
|
C | A | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-1456G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452356 | ||||||
chr8:7452357
|
A | G | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-1457T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452357 | ||||||
chr8:7452396
|
G | T | 1 | a0002c0002t0001g0048 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.215-1496C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452396 | ||||||
chr8:7452416
|
T | C | 1 | a0002c0002t0001g0056 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.215-1516A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452416 | ||||||
chr8:7452477
|
G | T | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-1577C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452477 | ||||||
chr8:7452581
|
G | A | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-1681C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452581 | ||||||
chr8:7452713
|
A | T | 16 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(13): Show | 18 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.215-1813T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452713 | ||||||
chr8:7452956
|
GAA | G | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-2058_215-2057d others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452956 | ||||||
chr8:7452969
|
A | T | 1 | a0002c0002t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-2069T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452969 | ||||||
chr8:7452974
|
C | T | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-2074G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452974 | ||||||
chr8:7452978
|
G | A | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-2078C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7452978 | ||||||
chr8:7453019
|
A | G | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-2119T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453019 | ||||||
chr8:7453082
|
G | T | 1 | a0001c0001t0001g0018 | 2 | NA18942.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.215-2182C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453082 | ||||||
chr8:7453095
|
G | C | 3 | a0002c0002t0003g0022a0002c0002t0003g0116a0002c0002t0003g0130 | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-2195C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453095 | ||||||
chr8:7453132
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-2232C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453132 | ||||||
chr8:7453280
|
T | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(53): Show | 78 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.215-2380A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453280 | ||||||
chr8:7453388
|
A | G | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-2488T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453388 | ||||||
chr8:7453478
|
C | A | 26 | a0001c0001t0001g0093a0002c0002t0001g0001a0002c0002t0001g0003others(23): Show | 47 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.215-2578G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453478 | ||||||
chr8:7453593
|
T | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(125): Show | 178 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.215-2693A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453593 | ||||||
chr8:7453682
|
T | C | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-2782A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453682 | ||||||
chr8:7453684
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.215-2784T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453684 | ||||||
chr8:7453744
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 73 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.215-2844C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453744 | ||||||
chr8:7453759
|
T | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(49): Show | 74 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.215-2859A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453759 | ||||||
chr8:7453771
|
C | T | 7 | a0002c0002t0001g0023a0002c0002t0001g0101a0002c0002t0001g0134others(4): Show | 8 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2871G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453771 | ||||||
chr8:7453854
|
T | C | 7 | a0002c0002t0001g0023a0002c0002t0001g0101a0002c0002t0001g0134others(4): Show | 8 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.215-2954A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453854 | ||||||
chr8:7453902
|
C | T | 1 | a0002c0002t0001g0084 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.215-3002G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7453902 | ||||||
chr8:7454084
|
A | T | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-3184T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454084 | ||||||
chr8:7454085
|
A | T | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-3185T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454085 | ||||||
chr8:7454097
|
AAAG | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0079others(5): Show | 9 | HG00408.hp2 HG01515.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.215-3200_215-3198d others(5): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454097 | ||||||
chr8:7454098
|
AAG | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(47): Show | 72 | HG00544.hp1 HG00558.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.215-3200_215-3199d others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454098 | ||||||
chr8:7454099
|
AG | A | 27 | a0001c0001t0001g0024a0001c0001t0001g0135a0002c0002t0001g0001others(24): Show | 49 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.215-3200delC | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454099 | ||||||
chr8:7454139
|
G | A | 1 | a0002c0002t0001g0052 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.215-3239C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454139 | ||||||
chr8:7454156
|
C | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 73 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.215-3256G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454156 | ||||||
chr8:7454237
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.215-3337G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454237 | ||||||
chr8:7454250
|
A | C | 1 | a0006c0006t0001g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-3350T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454250 | ||||||
chr8:7454412
|
T | G | 37 | a0001c0001t0001g0036a0001c0001t0002g0034a0002c0002t0001g0001others(34): Show | 60 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.215-3512A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454412 | ||||||
chr8:7454526
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0002g0034a0002c0002t0001g0023others(6): Show | 10 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.215-3626G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454526 | ||||||
chr8:7454560
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.215-3660A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454560 | ||||||
chr8:7454594
|
A | G | 1 | a0002c0002t0001g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.215-3694T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454594 | ||||||
chr8:7454597
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(70): Show | 98 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.215-3697A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454597 | ||||||
chr8:7454785
|
G | C | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-3885C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454785 | ||||||
chr8:7454831
|
GGAAAA | G | 12 | a0001c0001t0001g0036a0001c0001t0002g0034a0002c0002t0001g0023others(9): Show | 14 | HG01891.hp2 HG02895.hp1 HG02897.hp1 others(11): Show |
intron_variant | MODIFIER | c.215-3936_215-3932d others(7): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454831 | ||||||
chr8:7454893
|
T | C | 1 | a0002c0002t0001g0148 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.215-3993A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454893 | ||||||
chr8:7454920
|
A | T | 3 | a0003c0003t0001g0062a0003c0003t0001g0124a0008c0009t0002g0025 | 3 | HG01168.hp2 HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.215-4020T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454920 | ||||||
chr8:7454934
|
TCAA | T | 1 | a0002c0002t0001g0013 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.215-4037_215-4035d others(5): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7454934 | ||||||
chr8:7455026
|
A | G | 1 | a0002c0002t0002g0029 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.215-4126T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455026 | ||||||
chr8:7455031
|
A | G | 1 | a0002c0002t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-4131T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455031 | ||||||
chr8:7455060
|
C | A | 33 | a0001c0001t0001g0036a0001c0001t0002g0034a0002c0002t0001g0001others(30): Show | 56 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.215-4160G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455060 | ||||||
chr8:7455303
|
C | T | 1 | a0002c0002t0002g0027 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.215-4403G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455303 | ||||||
chr8:7455470
|
A | G | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-4570T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455470 | ||||||
chr8:7455583
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0134a0002c0002t0001g0142 | 4 | HG02895.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-4683A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455583 | ||||||
chr8:7455588
|
T | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(19): Show | 31 | HG00558.hp2 HG01168.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.215-4688A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455588 | ||||||
chr8:7455651
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-4751C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455651 | ||||||
chr8:7455661
|
G | A | 4 | a0002c0002t0001g0013a0002c0002t0001g0050a0002c0002t0001g0051others(1): Show | 5 | HG02735.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.215-4761C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455661 | ||||||
chr8:7455765
|
C | T | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-4865G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455765 | ||||||
chr8:7455800
|
G | A | 1 | a0002c0002t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.215-4900C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455800 | ||||||
chr8:7455849
|
A | G | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-4949T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455849 | ||||||
chr8:7455885
|
C | T | 1 | a0006c0006t0001g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.215-4985G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455885 | ||||||
chr8:7455966
|
T | TG | 25 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(22): Show | 46 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.215-5067dupC | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7455966 | ||||||
chr8:7456112
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.215-5212A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456112 | ||||||
chr8:7456129
|
G | A | 2 | a0002c0002t0001g0140a0002c0002t0001g0151 | 2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.215-5229C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456129 | ||||||
chr8:7456225
|
C | G | 15 | a0003c0003t0001g0012a0003c0003t0001g0015a0003c0003t0001g0041others(12): Show | 17 | HG00544.hp2 HG00639.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.215-5325G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456225 | ||||||
chr8:7456236
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.215-5336G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456236 | ||||||
chr8:7456300
|
G | A | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(26): Show | 43 | HG00408.hp2 HG00544.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.215-5400C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456300 | ||||||
chr8:7456338
|
A | G | 2 | a0003c0003t0001g0062a0008c0009t0002g0025 | 2 | HG01168.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.215-5438T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456338 | ||||||
chr8:7456395
|
G | C | 1 | a0003c0003t0002g0033 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.215-5495C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456395 | ||||||
chr8:7456478
|
G | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(48): Show | 73 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.215-5578C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456478 | ||||||
chr8:7456541
|
C | G | 3 | a0002c0002t0001g0023a0002c0002t0001g0134a0002c0002t0001g0142 | 4 | HG02895.hp1 HG02897.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-5641G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456541 | ||||||
chr8:7456632
|
GC | G | 3 | a0002c0002t0003g0022a0002c0002t0003g0116a0002c0002t0003g0130 | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.215-5733delG | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456632 | ||||||
chr8:7456701
|
G | C | 2 | a0002c0002t0001g0083a0002c0002t0001g0087 | 2 | HG01169.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.215-5801C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456701 | ||||||
chr8:7456865
|
C | G | 3 | a0001c0001t0001g0040a0002c0002t0001g0140a0002c0002t0001g0151 | 3 | HG02723.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.214+5842G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456865 | ||||||
chr8:7456925
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(96): Show | 145 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.214+5782T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7456925 | ||||||
chr8:7457028
|
T | G | 26 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(23): Show | 47 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+5679A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457028 | ||||||
chr8:7457054
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 151 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.214+5653C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457054 | ||||||
chr8:7457162
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(47): Show | 72 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.214+5545C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457162 | ||||||
chr8:7457166
|
C | T | 3 | a0002c0002t0001g0141a0002c0002t0001g0149a0005c0008t0001g0152 | 3 | HG02559.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.214+5541G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457166 | ||||||
chr8:7457304
|
T | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(45): Show | 69 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.214+5403A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457304 | ||||||
chr8:7457408
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.214+5299A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457408 | ||||||
chr8:7457556
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.214+5151G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457556 | ||||||
chr8:7457613
|
G | GT | 10 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0039others(7): Show | 12 | HG00544.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.214+5093dupA | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457613 | ||||||
chr8:7457726
|
T | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(26): Show | 34 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.214+4981A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457726 | ||||||
chr8:7457746
|
T | C | 1 | a0002c0002t0001g0053 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.214+4961A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457746 | ||||||
chr8:7457833
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(124): Show | 177 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.214+4874G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457833 | ||||||
chr8:7457885
|
C | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0120others(26): Show | 52 | HG00558.hp1 HG00597.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.214+4822G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457885 | ||||||
chr8:7457940
|
C | A | 19 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0005others(16): Show | 40 | HG00558.hp1 HG01069.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.214+4767G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457940 | ||||||
chr8:7457987
|
T | A | 1 | a0002c0002t0001g0054 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.214+4720A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7457987 | ||||||
chr8:7458078
|
A | T | 1 | a0003c0003t0001g0124 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.214+4629T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458078 | ||||||
chr8:7458237
|
G | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 23 | HG00558.hp2 HG01169.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.214+4470C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458237 | ||||||
chr8:7458284
|
T | G | 13 | a0001c0001t0001g0076a0001c0001t0001g0103a0002c0002t0001g0010others(10): Show | 15 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+4423A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458284 | ||||||
chr8:7458379
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0094 | 3 | HG02895.hp2 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.214+4328C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458379 | ||||||
chr8:7458410
|
CT | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(29): Show | 44 | HG00544.hp2 HG00738.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.214+4296delA | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458410 | ||||||
chr8:7458599
|
G | A | 3 | a0001c0001t0001g0135a0002c0002t0001g0134a0002c0002t0001g0151 | 3 | HG02145.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.214+4108C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458599 | ||||||
chr8:7458600
|
G | A | 5 | a0001c0001t0001g0036a0002c0002t0001g0148a0002c0002t0001g0149others(2): Show | 5 | HG00639.hp1 HG02109.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+4107C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458600 | ||||||
chr8:7458658
|
C | G | 34 | a0001c0001t0001g0036a0001c0001t0001g0055a0001c0001t0001g0122others(31): Show | 56 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.214+4049G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458658 | ||||||
chr8:7458674
|
TA | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0057others(40): Show | 68 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.214+4032delT | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458674 | ||||||
chr8:7458674
|
TAAA | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(24): Show | 39 | HG00408.hp2 HG00738.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.214+4030_214+4032d others(5): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458674 | ||||||
chr8:7458684
|
AAAAAAAA others(2): Show |
A | 10 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0103others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+4014_214+4022d others(11): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458684 | ||||||
chr8:7458693
|
T | A | 1 | a0002c0002t0001g0141 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+4014A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458693 | ||||||
chr8:7458694
|
A | T | 1 | a0002c0002t0001g0141 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+4013T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458694 | ||||||
chr8:7458695
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+4012C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458695 | ||||||
chr8:7458707
|
A | AGAAAGAG others(5): Show |
23 | a0001c0001t0001g0055a0001c0001t0001g0057a0002c0002t0001g0001others(20): Show | 44 | HG00558.hp1 HG00639.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.214+3999_214+4000i others(14): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458707 | ||||||
chr8:7458708
|
G | GAAAGAGA others(5): Show |
1 | a0005c0008t0001g0153 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.214+3998_214+3999i others(14): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458708 | ||||||
chr8:7458751
|
A | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0057others(25): Show | 37 | HG00738.hp2 HG01081.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.214+3956T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458751 | ||||||
chr8:7458766
|
G | A | 13 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0001g0076others(10): Show | 13 | HG00738.hp2 HG01168.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.214+3941C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458766 | ||||||
chr8:7458858
|
T | C | 1 | a0002c0002t0001g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.214+3849A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458858 | ||||||
chr8:7458860
|
T | C | 1 | a0005c0008t0001g0152 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.214+3847A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458860 | ||||||
chr8:7458893
|
T | C | 13 | a0001c0001t0001g0104a0001c0001t0001g0132a0001c0001t0001g0135others(10): Show | 14 | HG00544.hp1 HG01515.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.214+3814A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458893 | ||||||
chr8:7458904
|
A | T | 1 | a0002c0002t0001g0046 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.214+3803T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458904 | ||||||
chr8:7458926
|
CG | C | 22 | a0001c0001t0001g0055a0001c0001t0001g0057a0002c0002t0001g0001others(19): Show | 40 | HG01069.hp2 HG01074.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.214+3780delC | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458926 | ||||||
chr8:7458948
|
C | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(76): Show | 99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.214+3759G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458948 | ||||||
chr8:7458967
|
C | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(123): Show | 156 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.214+3740G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458967 | ||||||
chr8:7458969
|
C | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 50 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.214+3738G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458969 | ||||||
chr8:7458973
|
C | CCT | 34 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3733_214+3734i others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458973 | ||||||
chr8:7458974
|
A | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3733T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458974 | ||||||
chr8:7458975
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3732C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458975 | ||||||
chr8:7458977
|
T | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3730A>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458977 | ||||||
chr8:7458979
|
A | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 47 | HG00544.hp2 HG00738.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+3728T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7458979 | ||||||
chr8:7459023
|
A | G | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+3684T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459023 | ||||||
chr8:7459026
|
T | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(118): Show | 151 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.214+3681A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459026 | ||||||
chr8:7459055
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(117): Show | 150 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.214+3652C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459055 | ||||||
chr8:7459060
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.214+3647A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459060 | ||||||
chr8:7459067
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(118): Show | 151 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.214+3640T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459067 | ||||||
chr8:7459156
|
G | T | 1 | a0005c0008t0001g0153 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.214+3551C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459156 | ||||||
chr8:7459158
|
T | G | 1 | a0005c0008t0001g0153 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.214+3549A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459158 | ||||||
chr8:7459203
|
G | A | 32 | a0001c0001t0001g0055a0001c0001t0001g0057a0002c0002t0001g0001others(29): Show | 54 | HG00558.hp1 HG00639.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.214+3504C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459203 | ||||||
chr8:7459218
|
CA | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(140): Show | 195 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.214+3488delT | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459218 | ||||||
chr8:7459218
|
CAA | C | 10 | a0001c0001t0001g0072a0001c0001t0001g0103a0001c0001t0002g0031others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.214+3487_214+3488d others(4): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459218 | ||||||
chr8:7459230
|
A | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(150): Show | 205 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(202): Show |
intron_variant | MODIFIER | c.214+3477T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459230 | ||||||
chr8:7459234
|
A | T | 1 | a0003c0003t0001g0077 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.214+3473T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459234 | ||||||
chr8:7459298
|
A | C | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+3409T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459298 | ||||||
chr8:7459317
|
CA | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0108others(6): Show | 11 | HG00544.hp2 HG02040.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+3389delT | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459317 | ||||||
chr8:7459424
|
C | G | 8 | a0001c0001t0001g0072a0001c0001t0002g0031a0002c0002t0001g0099others(5): Show | 8 | HG01243.hp1 HG01243.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+3283G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459424 | ||||||
chr8:7459452
|
C | G | 33 | a0001c0001t0001g0039a0001c0001t0001g0055a0001c0001t0001g0057others(30): Show | 55 | HG00558.hp1 HG00639.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.214+3255G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459452 | ||||||
chr8:7459467
|
A | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.214+3240T>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459467 | ||||||
chr8:7459558
|
A | G | 40 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 54 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.214+3149T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459558 | ||||||
chr8:7459566
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.214+3141G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459566 | ||||||
chr8:7459691
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.214+3016G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459691 | ||||||
chr8:7459776
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0143a0001c0005t0001g0105 | 3 | HG00544.hp1 NA18966.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.214+2931G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459776 | ||||||
chr8:7459882
|
G | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0142 | 3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.214+2825C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459882 | ||||||
chr8:7459947
|
G | A | 1 | a0004c0004t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+2760C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459947 | ||||||
chr8:7459979
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.214+2728G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459979 | ||||||
chr8:7459980
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(142): Show | 196 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.214+2727T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459980 | ||||||
chr8:7459988
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.214+2719G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459988 | ||||||
chr8:7459998
|
G | A | 3 | a0001c0001t0001g0024a0002c0002t0001g0102a0002c0002t0001g0148 | 4 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2709C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7459998 | ||||||
chr8:7460077
|
G | A | 3 | a0001c0001t0001g0038a0002c0002t0001g0010a0002c0002t0002g0035 | 4 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2630C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460077 | ||||||
chr8:7460410
|
A | T | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+2297T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460410 | ||||||
chr8:7460422
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.214+2285C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460422 | ||||||
chr8:7460550
|
G | A | 3 | a0001c0001t0001g0024a0002c0002t0001g0102a0002c0002t0001g0148 | 4 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+2157C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460550 | ||||||
chr8:7460550
|
G | GA | 3 | a0001c0001t0001g0143a0003c0003t0001g0062a0008c0009t0002g0025 | 3 | HG01168.hp2 HG01243.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.214+2156dupT | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460550 | ||||||
chr8:7460569
|
C | T | 3 | a0001c0001t0001g0038a0002c0002t0001g0010a0002c0002t0002g0035 | 4 | HG00639.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+2138G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460569 | ||||||
chr8:7460744
|
G | T | 1 | a0002c0002t0001g0102 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.214+1963C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460744 | ||||||
chr8:7460857
|
G | C | 1 | a0004c0004t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.214+1850C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460857 | ||||||
chr8:7460900
|
G | C | 2 | a0001c0001t0001g0100a0002c0002t0001g0101 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+1807C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460900 | ||||||
chr8:7460968
|
ATGATGGG others(2): Show |
A | 2 | a0005c0008t0001g0152a0005c0008t0001g0153 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.214+1730_214+1738d others(11): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7460968 | ||||||
chr8:7461092
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0002g0026 | 3 | HG02056.hp2 NA18966.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.214+1615T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461092 | ||||||
chr8:7461226
|
G | C | 1 | a0002c0002t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.214+1481C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461226 | ||||||
chr8:7461347
|
A | G | 1 | a0003c0003t0001g0073 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.214+1360T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461347 | ||||||
chr8:7461356
|
C | T | 2 | a0001c0001t0001g0100a0002c0002t0001g0101 | 2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.214+1351G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461356 | ||||||
chr8:7461488
|
G | A | 1 | a0002c0002t0001g0005 | 3 | HG01074.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.214+1219C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461488 | ||||||
chr8:7461537
|
G | T | 142 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(139): Show | 192 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.214+1170C>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461537 | ||||||
chr8:7461549
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.214+1158C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461549 | ||||||
chr8:7461611
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 13 | HG00558.hp2 HG00597.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+1096C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461611 | ||||||
chr8:7461705
|
G | C | 2 | a0001c0001t0001g0038a0002c0002t0001g0010 | 3 | HG01257.hp1 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.214+1002C>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461705 | ||||||
chr8:7461747
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.214+960A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461747 | ||||||
chr8:7461877
|
T | G | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.214+830A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461877 | ||||||
chr8:7461879
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.214+828C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461879 | ||||||
chr8:7461888
|
G | A | 3 | a0001c0001t0001g0024a0002c0002t0001g0148a0002c0002t0001g0149 | 4 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+819C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461888 | ||||||
chr8:7461935
|
A | G | 2 | a0002c0002t0001g0011a0002c0002t0001g0042 | 3 | NA18975.hp2 NA19006.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.214+772T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7461935 | ||||||
chr8:7462266
|
T | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(149): Show | 204 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.214+441A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462266 | ||||||
chr8:7462404
|
T | G | 1 | a0001c0001t0001g0146 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.214+303A>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462404 | ||||||
chr8:7462449
|
T | C | 9 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 11 | HG01257.hp1 HG01258.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.214+258A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462449 | ||||||
chr8:7462468
|
C | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 47 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.214+239G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462468 | ||||||
chr8:7462484
|
T | C | 1 | a0002c0002t0001g0150 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.214+223A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 2/2 | chr8 | 7462484 | ||||||
chr8:7462935
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.62-76G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7462935 | ||||||
chr8:7462951
|
T | C | 1 | a0002c0002t0001g0151 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.62-92A>G | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7462951 | ||||||
chr8:7462997
|
C | G | 2 | a0001c0001t0001g0038a0002c0002t0001g0010 | 3 | HG01257.hp1 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.62-138G>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7462997 | ||||||
chr8:7463005
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.62-146C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463005 | ||||||
chr8:7463011
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(111): Show | 144 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.62-152C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463011 | ||||||
chr8:7463024
|
C | T | 1 | a0003c0003t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.62-165G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463024 | ||||||
chr8:7463081
|
C | CATGT | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-223_62-222insAC others(2): Show |
SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463081 | ||||||
chr8:7463085
|
A | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-226T>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463085 | ||||||
chr8:7463232
|
G | A | 11 | a0001c0001t0002g0026a0001c0001t0002g0031a0001c0001t0002g0032others(8): Show | 11 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+211C>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463232 | ||||||
chr8:7463271
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.61+172G>A | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463271 | ||||||
chr8:7463393
|
C | A | 2 | a0001c0001t0001g0038a0002c0002t0001g0010 | 3 | HG01257.hp1 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.61+50G>T | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463393 | ||||||
chr8:7463399
|
A | G | 17 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(14): Show | 18 | HG00639.hp1 HG01243.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.61+44T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463399 | ||||||
chr8:7463419
|
A | G | 2 | a0005c0008t0001g0152a0005c0008t0001g0153 | 2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.61+24T>C | SPAG11B | ENSG00000164871.18 | transcript | ENST00000398462.7 | protein_coding | 1/2 | chr8 | 7463419 |