geneid | 55812 |
---|---|
ensemblid | ENSG00000042317.17 |
hgncid | 20423 |
symbol | SPATA7 |
name | spermatogenesis associated 7 |
refseq_nuc | NM_018418.5 |
refseq_prot | NP_060888.2 |
ensembl_nuc | ENST00000393545.9 |
ensembl_prot | ENSP00000377176.4 |
mane_status | MANE Select |
chr | chr14 |
start | 88385657 |
end | 88438460 |
strand | + |
ver | v1.2 |
region | chr14:88385657-88438460 |
region5000 | chr14:88380657-88443460 |
regionname0 | SPATA7_chr14_88385657_88438460 |
regionname5000 | SPATA7_chr14_88380657_88443460 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 599 | 171 | 36 | 20 | 100 | 6 | 8 | 81 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0002 | 0/0 | 599 | 131 | 27 | 23 | 58 | 6 | 17 | 46 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0003 | 0/1 | 599 | 30 | 3 | 12 | 5 | 2 | 7 | 5 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0004 | 0/0 | 599 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0005 | 0/0 | 599 | 7 | 4 | 0 | 3 | 0 | 0 | 2 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0006 | 0/0 | 599 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0007 | 0/0 | 599 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0008 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0009 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0010 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0011 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1800 | 170 | 35 | 20 | 100 | 6 | 8 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0002 | 0/0 | 1800 | 130 | 27 | 23 | 57 | 6 | 17 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0003 | 0/1 | 1800 | 30 | 3 | 12 | 5 | 2 | 7 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0004 | 0/0 | 1800 | 14 | 13 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0005 | 0/0 | 1800 | 5 | 5 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0006 | 0/0 | 1800 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0007 | 0/0 | 1800 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0008 | 0/0 | 1800 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0009 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0010 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0011 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0012 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0013 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
c0014 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 201 | 349 | 78 | 56 | 168 | 14 | 32 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
t0002 | 1/0 | 201 | 11 | 10 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
t0003 | 0/0 | 201 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
t0004 | 0/0 | 201 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0002 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0007 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0286 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1800 | 170 | 35 | 20 | 100 | 6 | 8 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0001c0011 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0002c0002 | 0/0 | 1800 | 130 | 27 | 23 | 57 | 6 | 17 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0002c0010 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0003c0003 | 0/1 | 1800 | 30 | 3 | 12 | 5 | 2 | 7 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0004c0004 | 0/0 | 1800 | 14 | 13 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0005c0006 | 0/0 | 1800 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0005c0007 | 0/0 | 1800 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0006c0005 | 0/0 | 1800 | 5 | 5 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0007c0008 | 0/0 | 1800 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0008c0009 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0009c0012 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0010c0013 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0011c0014 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2000 | 160 | 26 | 20 | 100 | 6 | 8 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0001c0001t0002 | 1/0 | 2000 | 10 | 9 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0001c0011t0002 | 0/0 | 2000 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0002c0002t0001 | 0/0 | 2000 | 128 | 25 | 23 | 57 | 6 | 17 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0002c0002t0004 | 0/0 | 2000 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0002c0010t0001 | 0/0 | 2000 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0003c0003t0001 | 0/1 | 2000 | 30 | 3 | 12 | 5 | 2 | 7 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0004c0004t0001 | 0/0 | 2000 | 14 | 13 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0005c0006t0001 | 0/0 | 2000 | 4 | 4 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0005c0007t0001 | 0/0 | 2000 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0006c0005t0001 | 0/0 | 2000 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0006c0005t0003 | 0/0 | 2000 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0007c0008t0001 | 0/0 | 2000 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0008c0009t0001 | 0/0 | 2000 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0009c0012t0001 | 0/0 | 2000 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0010c0013t0001 | 0/0 | 2000 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
a0011c0014t0001 | 0/0 | 2000 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | copy fasta | chr14 | 88380657 | 88443460 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0001t0002g0286 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0001c0011t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0007 | 0/0 | 4 | 2 | 0 | 0 | 0 | 2 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0002c0010t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0004c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0005c0006t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0005c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0005c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0005c0007t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0005c0007t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0006c0005t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0006c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0006c0005t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0007c0008t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0007c0008t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0008c0009t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0009c0012t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0010c0013t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
a0011c0014t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0106 | EUR | GBR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0127 | EUR | FIN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0234 | EUR | FIN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0115 | EUR | FIN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00544 | hp2 | a0002 | c0010 | t0001 | g0125 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00639 | hp1 | a0003 | c0003 | t0001 | g0254 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0183 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00642 | hp2 | a0004 | c0004 | t0001 | g0038 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00733 | hp2 | a0003 | c0003 | t0001 | g0249 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0187 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0235 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01168 | hp1 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01169 | hp2 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0250 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0239 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01261 | hp1 | a0003 | c0003 | t0001 | g0206 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01358 | hp1 | a0003 | c0003 | t0001 | g0247 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0096 | EUR | IBS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0252 | EUR | IBS | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01884 | hp2 | a0005 | c0006 | t0001 | g0034 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0116 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01891 | hp2 | a0005 | c0006 | t0001 | g0273 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02040 | hp1 | a0005 | c0007 | t0001 | g0033 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02145 | hp2 | a0004 | c0004 | t0001 | g0013 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CDX | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CDX | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | CDX | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02280 | hp2 | a0005 | c0006 | t0001 | g0034 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0246 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PEL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02451 | hp1 | a0006 | c0005 | t0003 | g0015 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02572 | hp1 | a0003 | c0003 | t0001 | g0240 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02615 | hp1 | a0005 | c0006 | t0001 | g0274 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0149 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02630 | hp2 | a0004 | c0004 | t0001 | g0283 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02647 | hp1 | a0007 | c0008 | t0001 | g0276 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0241 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0243 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02723 | hp1 | a0004 | c0004 | t0001 | g0280 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0242 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02886 | hp1 | a0004 | c0004 | t0001 | g0279 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02895 | hp1 | a0004 | c0004 | t0001 | g0281 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02897 | hp2 | a0004 | c0004 | t0001 | g0282 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0136 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0238 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03098 | hp2 | a0008 | c0009 | t0001 | g0272 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03195 | hp1 | a0006 | c0005 | t0001 | g0014 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0186 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03209 | hp2 | a0004 | c0004 | t0001 | g0284 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03225 | hp1 | a0002 | c0002 | t0004 | g0117 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03486 | hp2 | a0007 | c0008 | t0001 | g0275 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0087 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0086 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03516 | hp2 | a0010 | c0013 | t0001 | g0266 | AFR | ESN | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03540 | hp1 | a0004 | c0004 | t0001 | g0012 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0245 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03704 | hp1 | a0003 | c0003 | t0001 | g0237 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | PJL | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0236 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0285 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | STU | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | STU | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0232 | SAS | BEB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | STU | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | STU | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | STU | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18522 | hp1 | a0006 | c0005 | t0001 | g0014 | AFR | YRI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | CHB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18906 | hp1 | a0004 | c0004 | t0001 | g0037 | AFR | YRI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | YRI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18947 | hp1 | a0009 | c0012 | t0001 | g0028 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0262 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18965 | hp1 | a0003 | c0003 | t0001 | g0251 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18966 | hp2 | a0003 | c0003 | t0001 | g0233 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18967 | hp1 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18980 | hp2 | a0005 | c0007 | t0001 | g0033 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19001 | hp2 | a0005 | c0007 | t0001 | g0271 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0248 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19030 | hp1 | a0004 | c0004 | t0001 | g0012 | AFR | LWK | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19030 | hp2 | a0001 | c0011 | t0002 | g0067 | AFR | LWK | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | LWK | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19056 | hp2 | a0011 | c0014 | t0001 | g0070 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19067 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19240 | hp1 | a0006 | c0005 | t0003 | g0015 | AFR | YRI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | YRI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ASW | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ASW | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0138 | EUR | TSI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0129 | EUR | TSI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02109 | hp1 | a0004 | c0004 | t0001 | g0278 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0092 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02559 | hp1 | a0006 | c0005 | t0001 | g0039 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG02559 | hp2 | a0004 | c0004 | t0001 | g0012 | AFR | ACB | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG06807 | hp1 | a0004 | c0004 | t0001 | g0013 | AFR | USA | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | USA | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0244 | REF | REF | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0286 | REF | REF | SPATA7_chr14_88380657_88443460 | SPATA7 | chr14 | 88380657 | 88443460 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88385822
|
G | A | 1 | a0003 | 30 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(27): Show |
missense_variant | MODERATE | c.4G>A | p.Asp2Asn | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/12 | 166/2000 | 4/1800 | 2/599 | chr14 | 88385822 | ||
chr14:88396185
|
G | A | 6 | a0002a0004a0005others(3): Show | 160 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(157): Show |
missense_variant | MODERATE | c.220G>A | p.Val74Met | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/12 | 382/2000 | 220/1800 | 74/599 | chr14 | 88396185 | ||
chr14:88416756
|
A | G | 2 | a0004a0006 | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
missense_variant | MODERATE | c.284A>G | p.Gln95Arg | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/12 | 446/2000 | 284/1800 | 95/599 | chr14 | 88416756 | ||
chr14:88416829
|
T | G | 2 | a0004a0006 | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
missense_variant | MODERATE | c.357T>G | p.Phe119Leu | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/12 | 519/2000 | 357/1800 | 119/599 | chr14 | 88416829 | ||
chr14:88416838
|
A | T | 1 | a0007 | 2 | HG02647.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.366A>T | p.Leu122Phe | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/12 | 528/2000 | 366/1800 | 122/599 | chr14 | 88416838 | ||
chr14:88426353
|
G | A | 2 | a0004a0006 | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
missense_variant | MODERATE | c.494G>A | p.Ser165Asn | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/12 | 656/2000 | 494/1800 | 165/599 | chr14 | 88426353 | ||
chr14:88426674
|
G | A | 1 | a0008 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.815G>A | p.Arg272Gln | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/12 | 977/2000 | 815/1800 | 272/599 | chr14 | 88426674 | ||
chr14:88429406
|
G | A | 2 | a0004a0006 | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
missense_variant | MODERATE | c.971G>A | p.Gly324Glu | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/12 | 1133/2000 | 971/1800 | 324/599 | chr14 | 88429406 | ||
chr14:88437566
|
G | A | 1 | a0009 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.1184G>A | p.Arg395Gln | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 11/12 | 1346/2000 | 1184/1800 | 395/599 | chr14 | 88437566 | ||
chr14:88437596
|
A | G | 1 | a0011 | 1 | NA19056.hp2 | missense_variant&splice_region_variant | MODERATE | c.1214A>G | p.Glu405Gly | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 11/12 | 1376/2000 | 1214/1800 | 405/599 | chr14 | 88437596 | ||
chr14:88438223
|
G | A | 4 | a0004a0005a0008others(1): Show | 23 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
missense_variant | MODERATE | c.1601G>A | p.Arg534Gln | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 12/12 | 1763/2000 | 1601/1800 | 534/599 | chr14 | 88438223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88426405
|
T | C | 2 | a0004c0004a0006c0005 | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
synonymous_variant | LOW | c.546T>C | p.Ser182Ser | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/12 | 708/2000 | 546/1800 | 182/599 | chr14 | 88426405 | ||
chr14:88426693
|
G | A | 1 | a0001c0011 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.834G>A | p.Gln278Gln | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/12 | 996/2000 | 834/1800 | 278/599 | chr14 | 88426693 | ||
chr14:88437579
|
A | G | 1 | a0002c0010 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1197A>G | p.Gln399Gln | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 11/12 | 1359/2000 | 1197/1800 | 399/599 | chr14 | 88437579 | ||
chr14:88437597
|
G | A | 1 | a0011c0014 | 1 | NA19056.hp2 | splice_region_variant&synonymous_variant | LOW | c.1215G>A | p.Glu405Glu | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 11/12 | 1377/2000 | 1215/1800 | 405/599 | chr14 | 88437597 | ||
chr14:88437877
|
T | C | 3 | a0005c0006a0007c0008a0008c0009 | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
synonymous_variant | LOW | c.1255T>C | p.Leu419Leu | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 12/12 | 1417/2000 | 1255/1800 | 419/599 | chr14 | 88437877 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88385687
|
A | G | 15 | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(12): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
5_prime_UTR_variant | MODIFIER | c.-132A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/12 | 132 | chr14 | 88385687 | |||||
chr14:88385724
|
C | T | 1 | a0002c0002t0004 | 2 | HG01891.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-95C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/12 | 95 | chr14 | 88385724 | |||||
chr14:88385768
|
G | A | 1 | a0006c0005t0003 | 2 | HG02451.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-51G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/12 | 51 | chr14 | 88385768 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:88385872
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19+35G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88385872 | ||||||
chr14:88385880
|
C | T | 4 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+43C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88385880 | ||||||
chr14:88385935
|
TG | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(290): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.19+102delG | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88385935 | |||||
chr14:88385954
|
G | A | 2 | a0001c0001t0002g0035a0001c0001t0002g0036 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.19+117G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88385954 | ||||||
chr14:88386069
|
A | G | 1 | a0002c0002t0001g0285 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.19+232A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386069 | ||||||
chr14:88386127
|
A | T | 7 | a0004c0004t0001g0012a0004c0004t0001g0279a0004c0004t0001g0280others(4): Show | 9 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+290A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386127 | ||||||
chr14:88386138
|
C | T | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.19+301C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386138 | ||||||
chr14:88386221
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+384T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386221 | ||||||
chr14:88386223
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | NA18956.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.19+386T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386223 | ||||||
chr14:88386315
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19+478G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386315 | ||||||
chr14:88386409
|
C | T | 1 | a0004c0004t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19+572C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386409 | ||||||
chr14:88386521
|
C | T | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.19+684C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386521 | ||||||
chr14:88386835
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.19+998T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386835 | ||||||
chr14:88386865
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+1028C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386865 | ||||||
chr14:88386956
|
G | T | 1 | a0001c0001t0001g0277 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.19+1119G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88386956 | ||||||
chr14:88387048
|
C | T | 22 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(19): Show | 29 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.19+1211C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387048 | ||||||
chr14:88387212
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.19+1375G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387212 | ||||||
chr14:88387221
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+1384A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387221 | ||||||
chr14:88387228
|
C | A | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.19+1391C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387228 | ||||||
chr14:88387233
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.19+1396A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387233 | ||||||
chr14:88387282
|
T | A | 1 | a0002c0002t0001g0045 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.19+1445T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387282 | ||||||
chr14:88387297
|
A | G | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+1460A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387297 | ||||||
chr14:88387393
|
T | TTTGAATT others(328): Show |
3 | a0004c0004t0001g0278a0006c0005t0001g0014a0006c0005t0001g0039 | 4 | HG02109.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1567_19+1568ins others(335): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88387393 | |||||
chr14:88387393
|
T | TTTGAATT others(326): Show |
2 | a0004c0004t0001g0012a0004c0004t0001g0279 | 4 | HG02559.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1567_19+1568ins others(333): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88387393 | |||||
chr14:88387393
|
T | TTTGAATT others(327): Show |
3 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038 | 4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+1567_19+1568ins others(334): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88387393 | |||||
chr14:88387393
|
T | TTTGAATT others(326): Show |
5 | a0004c0004t0001g0280a0004c0004t0001g0281a0004c0004t0001g0282others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+1567_19+1568ins others(333): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88387393 | |||||
chr14:88387393
|
T | TTTGAATT others(328): Show |
1 | a0006c0005t0003g0015 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19+1567_19+1568ins others(335): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88387393 | |||||
chr14:88387429
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+1592C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387429 | ||||||
chr14:88387430
|
A | G | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.19+1593A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387430 | ||||||
chr14:88387612
|
C | T | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.19+1775C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387612 | ||||||
chr14:88387681
|
G | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0047 | 6 | HG01106.hp2 HG01123.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+1844G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387681 | ||||||
chr14:88387737
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+1900T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88387737 | ||||||
chr14:88388056
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+2219G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388056 | ||||||
chr14:88388075
|
G | A | 1 | a0002c0002t0001g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19+2238G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388075 | ||||||
chr14:88388093
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+2256T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388093 | ||||||
chr14:88388094
|
C | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+2257C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388094 | ||||||
chr14:88388105
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+2268G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388105 | ||||||
chr14:88388128
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+2291G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388128 | ||||||
chr14:88388143
|
A | C | 1 | a0001c0001t0001g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.19+2306A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388143 | ||||||
chr14:88388381
|
G | A | 1 | a0006c0005t0003g0015 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19+2544G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388381 | ||||||
chr14:88388425
|
A | G | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.19+2588A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388425 | ||||||
chr14:88388543
|
ATT | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.19+2710_19+2711del others(2): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88388543 | |||||
chr14:88388577
|
A | G | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+2740A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388577 | ||||||
chr14:88388738
|
C | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-2643C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388738 | ||||||
chr14:88388754
|
T | TTAAAA | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-2626_20-2622dup others(5): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88388754 | |||||
chr14:88388780
|
G | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.20-2601G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388780 | ||||||
chr14:88388817
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.20-2564A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388817 | ||||||
chr14:88388883
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-2498T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88388883 | ||||||
chr14:88389040
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-2341T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389040 | ||||||
chr14:88389102
|
C | CA | 3 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038 | 4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-2272dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88389102 | |||||
chr14:88389143
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-2238G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389143 | ||||||
chr14:88389147
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-2234A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389147 | ||||||
chr14:88389210
|
G | GT | 12 | a0001c0001t0001g0265a0001c0001t0001g0287a0001c0001t0001g0288others(9): Show | 12 | HG02630.hp2 HG02723.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-2160dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88389210 | |||||
chr14:88389248
|
G | A | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.20-2133G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389248 | ||||||
chr14:88389286
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-2095T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389286 | ||||||
chr14:88389305
|
A | G | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.20-2076A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389305 | ||||||
chr14:88389362
|
C | A | 1 | a0004c0004t0001g0280 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20-2019C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389362 | ||||||
chr14:88389377
|
A | AT | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1997dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88389377 | |||||
chr14:88389450
|
C | T | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.20-1931C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389450 | ||||||
chr14:88389457
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1924A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389457 | ||||||
chr14:88389487
|
G | A | 3 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0051 | 3 | HG01243.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.20-1894G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389487 | ||||||
chr14:88389702
|
C | G | 1 | a0001c0001t0001g0263 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.20-1679C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389702 | ||||||
chr14:88389772
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1609G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389772 | ||||||
chr14:88389943
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1438A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88389943 | ||||||
chr14:88390129
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1252A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390129 | ||||||
chr14:88390255
|
A | AT | 11 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(8): Show | 12 | HG01192.hp2 HG01258.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-1111dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88390255 | |||||
chr14:88390255
|
ATT | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1112_20-1111del others(2): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 88390255 | |||||
chr14:88390298
|
G | A | 10 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(7): Show | 13 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.20-1083G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390298 | ||||||
chr14:88390354
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1027G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390354 | ||||||
chr14:88390361
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-1020A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390361 | ||||||
chr14:88390403
|
G | A | 1 | a0006c0005t0003g0015 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.20-978G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390403 | ||||||
chr14:88390414
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-967A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390414 | ||||||
chr14:88390432
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-949A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390432 | ||||||
chr14:88390580
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20-801C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390580 | ||||||
chr14:88390590
|
C | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-791C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390590 | ||||||
chr14:88390609
|
A | AAAAC | 2 | a0006c0005t0001g0014a0006c0005t0001g0039 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.20-772_20-771insAA others(2): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390609 | ||||||
chr14:88390712
|
G | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0053others(1): Show | 4 | HG00597.hp2 NA18948.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-669G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390712 | ||||||
chr14:88390731
|
A | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-650A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88390731 | ||||||
chr14:88391007
|
C | T | 1 | a0002c0002t0001g0255 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.20-374C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391007 | ||||||
chr14:88391035
|
C | T | 1 | a0003c0003t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.20-346C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391035 | ||||||
chr14:88391081
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-300T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391081 | ||||||
chr14:88391137
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG01081.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.20-244C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391137 | ||||||
chr14:88391138
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(93): Show | 113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.20-243A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391138 | ||||||
chr14:88391208
|
A | G | 1 | a0005c0006t0001g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.20-173A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391208 | ||||||
chr14:88391212
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-169T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391212 | ||||||
chr14:88391362
|
T | G | 1 | a0003c0003t0001g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.20-19T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391362 | ||||||
chr14:88391369
|
T | C | 1 | a0002c0002t0001g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.20-12T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 1/11 | chr14 | 88391369 | ||||||
chr14:88391475
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+20C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88391475 | ||||||
chr14:88391640
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+185C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88391640 | ||||||
chr14:88391650
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+195G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88391650 | ||||||
chr14:88391741
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+286A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88391741 | ||||||
chr14:88391886
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.94+431A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88391886 | ||||||
chr14:88391960
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.94+505A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88391960 | ||||||
chr14:88392112
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.94+657G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392112 | ||||||
chr14:88392144
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+689G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392144 | ||||||
chr14:88392246
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+791A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392246 | ||||||
chr14:88392306
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+851A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392306 | ||||||
chr14:88392355
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(253): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.94+900A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392355 | ||||||
chr14:88392504
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.95-889T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392504 | ||||||
chr14:88392582
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-811C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392582 | ||||||
chr14:88392624
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.95-769G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392624 | ||||||
chr14:88392657
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.95-736A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392657 | ||||||
chr14:88392675
|
A | G | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.95-718A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392675 | ||||||
chr14:88392715
|
G | A | 15 | a0001c0001t0001g0257a0004c0004t0001g0012a0004c0004t0001g0013others(12): Show | 20 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-678G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392715 | ||||||
chr14:88392749
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0253 | 3 | HG00099.hp1 HG01071.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.95-644A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392749 | ||||||
chr14:88392862
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-531T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392862 | ||||||
chr14:88392867
|
G | GCGATTAC others(297): Show |
1 | a0006c0005t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.95-512_95-511insTT others(302): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 88392867 | |||||
chr14:88392867
|
G | GCGATTAC others(313): Show |
2 | a0006c0005t0001g0014a0006c0005t0003g0015 | 4 | HG02451.hp1 HG03195.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-512_95-511insTT others(318): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 88392867 | |||||
chr14:88392912
|
G | C | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-481G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392912 | ||||||
chr14:88392995
|
T | G | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.95-398T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88392995 | ||||||
chr14:88393036
|
A | G | 9 | a0002c0002t0001g0024a0002c0002t0001g0049a0002c0002t0001g0050others(6): Show | 10 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-357A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88393036 | ||||||
chr14:88393044
|
A | C | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.95-349A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88393044 | ||||||
chr14:88393140
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-253A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88393140 | ||||||
chr14:88393299
|
A | T | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-94A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88393299 | ||||||
chr14:88393320
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-73T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 2/11 | chr14 | 88393320 | ||||||
chr14:88393504
|
T | C | 1 | a0003c0003t0001g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.190+16T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393504 | ||||||
chr14:88393562
|
A | G | 1 | a0003c0003t0001g0252 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.190+74A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393562 | ||||||
chr14:88393586
|
A | G | 1 | a0002c0002t0001g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.190+98A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393586 | ||||||
chr14:88393586
|
ATATG | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.190+99_190+102delT others(3): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393586 | ||||||
chr14:88393641
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.190+153G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393641 | ||||||
chr14:88393709
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.190+221G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393709 | ||||||
chr14:88393735
|
T | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | HG02717.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.190+247T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393735 | ||||||
chr14:88393747
|
T | C | 2 | a0002c0002t0001g0083a0002c0002t0001g0084 | 2 | NA18945.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.190+259T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393747 | ||||||
chr14:88393783
|
G | T | 1 | a0002c0002t0001g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.190+295G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393783 | ||||||
chr14:88393795
|
A | G | 3 | a0003c0003t0001g0251a0003c0003t0001g0261a0003c0003t0001g0262 | 3 | NA18959.hp1 NA18965.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.190+307A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393795 | ||||||
chr14:88393820
|
A | G | 5 | a0004c0004t0001g0280a0004c0004t0001g0281a0004c0004t0001g0282others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+332A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393820 | ||||||
chr14:88393987
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.190+499C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88393987 | ||||||
chr14:88394072
|
A | T | 2 | a0002c0002t0001g0153a0004c0004t0001g0013 | 3 | HG01943.hp2 HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.190+584A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394072 | ||||||
chr14:88394128
|
C | T | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.190+640C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394128 | ||||||
chr14:88394129
|
A | G | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.190+641A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394129 | ||||||
chr14:88394230
|
G | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(249): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.190+742G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394230 | ||||||
chr14:88394365
|
G | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0085 | 3 | HG00609.hp2 NA18972.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.190+877G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394365 | ||||||
chr14:88394558
|
G | A | 1 | a0003c0003t0001g0187 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.190+1070G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394558 | ||||||
chr14:88394578
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.190+1090T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394578 | ||||||
chr14:88394636
|
C | T | 1 | a0002c0002t0001g0152 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.190+1148C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394636 | ||||||
chr14:88394648
|
C | T | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.190+1160C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394648 | ||||||
chr14:88394654
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.190+1166A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394654 | ||||||
chr14:88394758
|
A | C | 4 | a0003c0003t0001g0261a0003c0003t0001g0262a0005c0007t0001g0033others(1): Show | 5 | HG02040.hp1 NA18959.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+1270A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394758 | ||||||
chr14:88394790
|
C | G | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+1302C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394790 | ||||||
chr14:88394795
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.190+1307C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394795 | ||||||
chr14:88394849
|
A | T | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.191-1307A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394849 | ||||||
chr14:88394886
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-1270G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394886 | ||||||
chr14:88394921
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0291 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.191-1235G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88394921 | ||||||
chr14:88395160
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-996G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395160 | ||||||
chr14:88395212
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-944C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395212 | ||||||
chr14:88395278
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-878T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395278 | ||||||
chr14:88395284
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-872C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395284 | ||||||
chr14:88395287
|
T | C | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.191-869T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395287 | ||||||
chr14:88395294
|
T | TTTA | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-859_191-857dup others(3): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 88395294 | |||||
chr14:88395367
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-789A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395367 | ||||||
chr14:88395398
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-758C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395398 | ||||||
chr14:88395416
|
G | A | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-740G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395416 | ||||||
chr14:88395506
|
AAT | A | 27 | a0003c0003t0001g0183a0003c0003t0001g0186a0003c0003t0001g0187others(24): Show | 27 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.191-647_191-646del others(2): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 88395506 | |||||
chr14:88395625
|
G | GT | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-524dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 88395625 | |||||
chr14:88395653
|
C | G | 13 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(10): Show | 18 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.191-503C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395653 | ||||||
chr14:88395775
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-381A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395775 | ||||||
chr14:88395800
|
C | T | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.191-356C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395800 | ||||||
chr14:88395851
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.191-305G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395851 | ||||||
chr14:88395893
|
G | A | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.191-263G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88395893 | ||||||
chr14:88396020
|
C | T | 3 | a0003c0003t0001g0251a0003c0003t0001g0261a0003c0003t0001g0262 | 3 | NA18959.hp1 NA18965.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.191-136C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88396020 | ||||||
chr14:88396041
|
C | T | 1 | a0003c0003t0001g0250 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.191-115C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88396041 | ||||||
chr14:88396090
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.191-66C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88396090 | ||||||
chr14:88396142
|
C | A | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.191-14C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 3/11 | chr14 | 88396142 | ||||||
chr14:88396235
|
A | T | 1 | a0002c0002t0001g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.238+32A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396235 | ||||||
chr14:88396242
|
A | C | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.238+39A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396242 | ||||||
chr14:88396271
|
T | G | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.238+68T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396271 | ||||||
chr14:88396361
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+158T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396361 | ||||||
chr14:88396504
|
C | G | 3 | a0002c0002t0001g0149a0002c0002t0001g0150a0002c0002t0001g0151 | 3 | HG02622.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.238+301C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396504 | ||||||
chr14:88396571
|
T | C | 22 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(19): Show | 29 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.238+368T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396571 | ||||||
chr14:88396579
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.238+376T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396579 | ||||||
chr14:88396731
|
A | G | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.238+528A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396731 | ||||||
chr14:88396874
|
TC | T | 3 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038 | 4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+672delC | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396874 | ||||||
chr14:88396875
|
C | CTTT | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.238+683_238+685dup others(3): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88396875 | |||||
chr14:88396875
|
C | T | 11 | a0004c0004t0001g0012a0004c0004t0001g0278a0004c0004t0001g0279others(8): Show | 15 | HG02109.hp1 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+672C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396875 | ||||||
chr14:88396943
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.238+740C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396943 | ||||||
chr14:88396950
|
G | T | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.238+747G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88396950 | ||||||
chr14:88397137
|
G | A | 1 | a0008c0009t0001g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+934G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397137 | ||||||
chr14:88397139
|
C | A | 1 | a0008c0009t0001g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+936C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397139 | ||||||
chr14:88397187
|
G | A | 1 | a0003c0003t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.238+984G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397187 | ||||||
chr14:88397219
|
A | G | 1 | a0002c0002t0001g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.238+1016A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397219 | ||||||
chr14:88397288
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+1085C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397288 | ||||||
chr14:88397313
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.238+1110T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397313 | ||||||
chr14:88397399
|
A | ATAATCAG others(5): Show |
14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+1197_238+1198i others(14): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88397399 | |||||
chr14:88397419
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+1216G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397419 | ||||||
chr14:88397436
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238+1233C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397436 | ||||||
chr14:88397582
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.238+1379G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397582 | ||||||
chr14:88397643
|
GA | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 9 | HG00733.hp2 HG01106.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+1455delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88397643 | |||||
chr14:88397859
|
G | A | 69 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(66): Show | 94 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.238+1656G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397859 | ||||||
chr14:88397910
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.238+1707C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88397910 | ||||||
chr14:88398060
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238+1857C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398060 | ||||||
chr14:88398081
|
C | CA | 71 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(68): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.238+1890dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88398081 | |||||
chr14:88398081
|
CA | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+1890delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88398081 | |||||
chr14:88398180
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+1977G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398180 | ||||||
chr14:88398302
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+2099A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398302 | ||||||
chr14:88398335
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+2132G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398335 | ||||||
chr14:88398417
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+2214A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398417 | ||||||
chr14:88398451
|
G | A | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.238+2248G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398451 | ||||||
chr14:88398491
|
A | G | 1 | a0002c0002t0001g0085 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.238+2288A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398491 | ||||||
chr14:88398496
|
G | A | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+2293G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398496 | ||||||
chr14:88398508
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.238+2305T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398508 | ||||||
chr14:88398639
|
T | TA | 30 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0024others(27): Show | 35 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.238+2436_238+2437i others(3): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398639 | ||||||
chr14:88398640
|
T | A | 30 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0024others(27): Show | 35 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.238+2437T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398640 | ||||||
chr14:88398640
|
T | TA | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.238+2444dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88398640 | |||||
chr14:88398682
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+2479T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398682 | ||||||
chr14:88398778
|
T | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.238+2575T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398778 | ||||||
chr14:88398823
|
C | T | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+2620C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398823 | ||||||
chr14:88398827
|
C | T | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.238+2624C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398827 | ||||||
chr14:88398869
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+2666G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398869 | ||||||
chr14:88398941
|
G | A | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.238+2738G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398941 | ||||||
chr14:88398945
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.238+2742G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398945 | ||||||
chr14:88398989
|
T | G | 1 | a0001c0001t0001g0059 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.238+2786T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88398989 | ||||||
chr14:88399046
|
C | T | 5 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | HG02809.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+2843C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399046 | ||||||
chr14:88399051
|
C | CA | 9 | a0001c0001t0001g0191a0001c0001t0001g0231a0002c0002t0001g0082others(6): Show | 9 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+2863dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88399051 | |||||
chr14:88399068
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.238+2865A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399068 | ||||||
chr14:88399097
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+2894A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399097 | ||||||
chr14:88399223
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+3020T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399223 | ||||||
chr14:88399254
|
A | G | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+3051A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399254 | ||||||
chr14:88399352
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.238+3149G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399352 | ||||||
chr14:88399430
|
T | C | 1 | a0002c0002t0001g0156 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238+3227T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399430 | ||||||
chr14:88399463
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.238+3260G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399463 | ||||||
chr14:88399557
|
C | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+3354C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399557 | ||||||
chr14:88399601
|
G | A | 1 | a0002c0002t0001g0285 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.238+3398G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399601 | ||||||
chr14:88399709
|
C | T | 1 | a0002c0002t0001g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.238+3506C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399709 | ||||||
chr14:88399825
|
A | G | 9 | a0002c0002t0001g0024a0002c0002t0001g0049a0002c0002t0001g0050others(6): Show | 10 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+3622A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399825 | ||||||
chr14:88399910
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+3707G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399910 | ||||||
chr14:88399951
|
C | T | 3 | a0002c0002t0001g0050a0002c0002t0001g0160a0002c0002t0001g0161 | 3 | HG01109.hp1 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.238+3748C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88399951 | ||||||
chr14:88400028
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+3825C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400028 | ||||||
chr14:88400054
|
C | T | 72 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(69): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.238+3851C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400054 | ||||||
chr14:88400187
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+3984T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400187 | ||||||
chr14:88400227
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+4024G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400227 | ||||||
chr14:88400294
|
A | G | 4 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(1): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+4091A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400294 | ||||||
chr14:88400560
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+4357G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400560 | ||||||
chr14:88400649
|
A | G | 1 | a0002c0002t0001g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.238+4446A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400649 | ||||||
chr14:88400679
|
C | T | 30 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0024others(27): Show | 35 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.238+4476C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400679 | ||||||
chr14:88400783
|
T | G | 4 | a0004c0004t0001g0280a0004c0004t0001g0281a0004c0004t0001g0282others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+4580T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400783 | ||||||
chr14:88400855
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.238+4652T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88400855 | ||||||
chr14:88401038
|
A | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+4835A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401038 | ||||||
chr14:88401076
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+4873G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401076 | ||||||
chr14:88401139
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+4936G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401139 | ||||||
chr14:88401473
|
A | T | 69 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0011others(66): Show | 94 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.238+5270A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401473 | ||||||
chr14:88401495
|
C | T | 2 | a0006c0005t0001g0014a0006c0005t0001g0039 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.238+5292C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401495 | ||||||
chr14:88401547
|
G | A | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.238+5344G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401547 | ||||||
chr14:88401553
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+5350G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401553 | ||||||
chr14:88401666
|
T | C | 2 | a0004c0004t0001g0012a0004c0004t0001g0279 | 4 | HG02559.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+5463T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401666 | ||||||
chr14:88401836
|
C | CA | 77 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(74): Show | 101 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.238+5659dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88401836 | |||||
chr14:88401836
|
C | CAA | 8 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0048others(5): Show | 10 | HG00673.hp1 HG02615.hp2 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+5658_238+5659d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88401836 | |||||
chr14:88401836
|
CA | C | 30 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0225others(27): Show | 35 | HG00408.hp2 HG00642.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.238+5659delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88401836 | |||||
chr14:88401836
|
CAA | C | 10 | a0002c0002t0001g0051a0002c0002t0001g0087a0004c0004t0001g0012others(7): Show | 12 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+5658_238+5659d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88401836 | |||||
chr14:88401964
|
C | G | 1 | a0002c0002t0001g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.238+5761C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88401964 | ||||||
chr14:88402250
|
C | T | 1 | a0003c0003t0001g0248 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.238+6047C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402250 | ||||||
chr14:88402253
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.238+6050A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402253 | ||||||
chr14:88402308
|
T | C | 1 | a0006c0005t0003g0015 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.238+6105T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402308 | ||||||
chr14:88402331
|
A | G | 1 | a0003c0003t0001g0249 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.238+6128A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402331 | ||||||
chr14:88402337
|
CAATCTT | C | 68 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0011others(65): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.238+6135_238+6140d others(8): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402337 | ||||||
chr14:88402433
|
CA | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.238+6239delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402433 | |||||
chr14:88402433
|
CAA | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6238_238+6239d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402433 | |||||
chr14:88402449
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6246C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402449 | ||||||
chr14:88402457
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6254A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402457 | ||||||
chr14:88402494
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6291G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402494 | ||||||
chr14:88402533
|
C | T | 3 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038 | 4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+6330C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402533 | ||||||
chr14:88402537
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6334G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402537 | ||||||
chr14:88402550
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+6347A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402550 | ||||||
chr14:88402603
|
G | C | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+6400G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402603 | ||||||
chr14:88402611
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6408A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402611 | ||||||
chr14:88402719
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.238+6516A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402719 | ||||||
chr14:88402746
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6543G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402746 | ||||||
chr14:88402800
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6597A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402800 | ||||||
chr14:88402854
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6651C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402854 | ||||||
chr14:88402944
|
A | C | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+6741A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88402944 | ||||||
chr14:88402959
|
C | CA | 71 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0025others(68): Show | 82 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.238+6780dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402959 | |||||
chr14:88402959
|
C | CAA | 70 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(67): Show | 89 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.238+6779_238+6780d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402959 | |||||
chr14:88402959
|
C | CAAA | 13 | a0001c0001t0001g0008a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 16 | HG00438.hp1 HG00741.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+6778_238+6780d others(5): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402959 | |||||
chr14:88402959
|
CA | C | 47 | a0001c0001t0001g0077a0002c0002t0001g0001a0002c0002t0001g0011others(44): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.238+6780delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402959 | |||||
chr14:88402959
|
CAAA | C | 13 | a0001c0001t0001g0044a0001c0001t0001g0191a0001c0001t0001g0218others(10): Show | 13 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.238+6778_238+6780d others(5): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402959 | |||||
chr14:88402959
|
CAAAAAAA others(5): Show |
C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+6769_238+6780d others(14): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88402959 | |||||
chr14:88403297
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.238+7094G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88403297 | ||||||
chr14:88403614
|
T | G | 2 | a0002c0002t0001g0094a0002c0002t0001g0105 | 2 | NA18947.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.238+7411T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88403614 | ||||||
chr14:88403771
|
T | C | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.238+7568T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88403771 | ||||||
chr14:88403904
|
C | CA | 7 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0001g0108others(4): Show | 8 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+7709dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88403904 | |||||
chr14:88404013
|
T | C | 2 | a0002c0002t0001g0021a0002c0002t0001g0110 | 3 | HG02040.hp2 HG02165.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.238+7810T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404013 | ||||||
chr14:88404017
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+7814G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404017 | ||||||
chr14:88404019
|
TTGTC | T | 4 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(1): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+7819_238+7822d others(6): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88404019 | |||||
chr14:88404299
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+8096C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404299 | ||||||
chr14:88404313
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+8110C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404313 | ||||||
chr14:88404329
|
G | T | 1 | a0002c0002t0001g0128 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.238+8126G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404329 | ||||||
chr14:88404443
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+8240G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404443 | ||||||
chr14:88404514
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.238+8311C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404514 | ||||||
chr14:88404545
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+8342G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404545 | ||||||
chr14:88404641
|
C | T | 3 | a0002c0002t0001g0150a0007c0008t0001g0275a0007c0008t0001g0276 | 3 | HG02647.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.238+8438C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404641 | ||||||
chr14:88404642
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+8439G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404642 | ||||||
chr14:88404650
|
G | A | 10 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(7): Show | 13 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.238+8447G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404650 | ||||||
chr14:88404951
|
A | G | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.238+8748A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88404951 | ||||||
chr14:88405011
|
A | G | 1 | a0002c0002t0001g0011 | 3 | HG00438.hp2 NA18973.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.238+8808A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88405011 | ||||||
chr14:88405060
|
T | C | 2 | a0004c0004t0001g0278a0004c0004t0001g0279 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.238+8857T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88405060 | ||||||
chr14:88405478
|
C | T | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.238+9275C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88405478 | ||||||
chr14:88405876
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+9673G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88405876 | ||||||
chr14:88405954
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.238+9751A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88405954 | ||||||
chr14:88406034
|
G | C | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.238+9831G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406034 | ||||||
chr14:88406144
|
C | T | 1 | a0002c0002t0001g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.238+9941C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406144 | ||||||
chr14:88406173
|
T | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+9970T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406173 | ||||||
chr14:88406201
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.238+9998T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406201 | ||||||
chr14:88406316
|
G | A | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.238+10113G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406316 | ||||||
chr14:88406337
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.238+10134A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406337 | ||||||
chr14:88406415
|
C | T | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.238+10212C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406415 | ||||||
chr14:88406434
|
C | CTT | 13 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(10): Show | 18 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+10245_238+1024 others(6): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88406434 | |||||
chr14:88406614
|
T | TTTA | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-10095_239-1009 others(7): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88406614 | |||||
chr14:88406614
|
T | TTTATTA | 11 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(8): Show | 14 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-10095_239-1009 others(10): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88406614 | |||||
chr14:88406617
|
T | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-10094T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406617 | ||||||
chr14:88406663
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-10048C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406663 | ||||||
chr14:88406693
|
G | A | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-10018G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406693 | ||||||
chr14:88406829
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-9882G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406829 | ||||||
chr14:88406933
|
T | C | 1 | a0002c0002t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.239-9778T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88406933 | ||||||
chr14:88407194
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.239-9517G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88407194 | ||||||
chr14:88407267
|
G | C | 2 | a0004c0004t0001g0012a0004c0004t0001g0279 | 4 | HG02559.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-9444G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88407267 | ||||||
chr14:88407357
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.239-9354C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88407357 | ||||||
chr14:88407492
|
G | A | 1 | a0002c0002t0001g0159 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.239-9219G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88407492 | ||||||
chr14:88407577
|
G | A | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.239-9134G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88407577 | ||||||
chr14:88407768
|
T | C | 5 | a0004c0004t0001g0280a0004c0004t0001g0281a0004c0004t0001g0282others(2): Show | 5 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-8943T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88407768 | ||||||
chr14:88407856
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.239-8855A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88407856 | ||||||
chr14:88408181
|
G | A | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.239-8530G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408181 | ||||||
chr14:88408333
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-8378T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408333 | ||||||
chr14:88408404
|
G | A | 3 | a0002c0002t0001g0024a0002c0002t0001g0157a0002c0002t0001g0158 | 4 | HG00741.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-8307G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408404 | ||||||
chr14:88408464
|
T | A | 1 | a0006c0005t0003g0015 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.239-8247T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408464 | ||||||
chr14:88408487
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.239-8224T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408487 | ||||||
chr14:88408549
|
GCAAA | G | 4 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(1): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-8159_239-8156d others(6): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88408549 | |||||
chr14:88408571
|
T | C | 125 | a0001c0001t0001g0057a0001c0001t0001g0200a0002c0002t0001g0001others(122): Show | 162 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.239-8140T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408571 | ||||||
chr14:88408682
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-8029G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408682 | ||||||
chr14:88408694
|
A | AAGGGAAT others(6): Show |
14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-8014_239-8002d others(15): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88408694 | |||||
chr14:88408778
|
T | C | 1 | a0003c0003t0001g0252 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.239-7933T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408778 | ||||||
chr14:88408778
|
T | G | 4 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(1): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-7933T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408778 | ||||||
chr14:88408835
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-7876C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408835 | ||||||
chr14:88408836
|
A | G | 92 | a0001c0001t0001g0057a0001c0001t0001g0200a0002c0002t0001g0001others(89): Show | 124 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.239-7875A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408836 | ||||||
chr14:88408840
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-7871G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408840 | ||||||
chr14:88408868
|
T | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0201 | 2 | HG01175.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.239-7843T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408868 | ||||||
chr14:88408911
|
T | G | 1 | a0002c0002t0001g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.239-7800T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88408911 | ||||||
chr14:88409091
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-7620G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409091 | ||||||
chr14:88409190
|
C | A | 1 | a0002c0002t0001g0113 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.239-7521C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409190 | ||||||
chr14:88409251
|
T | C | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.239-7460T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409251 | ||||||
chr14:88409281
|
A | T | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.239-7430A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409281 | ||||||
chr14:88409319
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-7392A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409319 | ||||||
chr14:88409320
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-7391G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409320 | ||||||
chr14:88409396
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.239-7315T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409396 | ||||||
chr14:88409436
|
A | T | 3 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038 | 4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-7275A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409436 | ||||||
chr14:88409443
|
C | T | 2 | a0004c0004t0001g0012a0004c0004t0001g0279 | 4 | HG02559.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-7268C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409443 | ||||||
chr14:88409530
|
CA | C | 8 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(5): Show | 10 | HG01884.hp2 HG01891.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-7174delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88409530 | |||||
chr14:88409532
|
A | G | 1 | a0001c0001t0001g0030 | 2 | NA18986.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.239-7179A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409532 | ||||||
chr14:88409588
|
C | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-7123C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409588 | ||||||
chr14:88409621
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.239-7090T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409621 | ||||||
chr14:88409689
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-7022C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88409689 | ||||||
chr14:88410120
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-6591A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410120 | ||||||
chr14:88410312
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-6399C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410312 | ||||||
chr14:88410525
|
G | A | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-6186G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410525 | ||||||
chr14:88410620
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.239-6091T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410620 | ||||||
chr14:88410681
|
G | T | 1 | a0002c0002t0001g0112 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.239-6030G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410681 | ||||||
chr14:88410805
|
G | A | 18 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0082others(15): Show | 22 | HG02055.hp1 HG02451.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.239-5906G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410805 | ||||||
chr14:88410896
|
G | C | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-5815G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410896 | ||||||
chr14:88410920
|
G | A | 6 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-5791G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410920 | ||||||
chr14:88410950
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5761C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88410950 | ||||||
chr14:88411009
|
G | GGGAGACA | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5698_239-5697i others(9): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88411009 | |||||
chr14:88411109
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5602G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411109 | ||||||
chr14:88411118
|
C | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5593C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411118 | ||||||
chr14:88411149
|
C | A | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-5562C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411149 | ||||||
chr14:88411155
|
G | A | 3 | a0002c0002t0001g0149a0002c0002t0001g0150a0002c0002t0001g0151 | 3 | HG02622.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-5556G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411155 | ||||||
chr14:88411221
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5490C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411221 | ||||||
chr14:88411255
|
C | G | 1 | a0002c0002t0001g0093 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.239-5456C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411255 | ||||||
chr14:88411357
|
A | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5354A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411357 | ||||||
chr14:88411559
|
A | G | 1 | a0002c0002t0001g0145 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.239-5152A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411559 | ||||||
chr14:88411573
|
GCA | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5134_239-5133d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88411573 | |||||
chr14:88411640
|
C | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5071C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411640 | ||||||
chr14:88411683
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5028C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411683 | ||||||
chr14:88411684
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-5027A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411684 | ||||||
chr14:88411690
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(91): Show | 111 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.239-5021C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411690 | ||||||
chr14:88411691
|
G | A | 68 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0011others(65): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.239-5020G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411691 | ||||||
chr14:88411775
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-4936G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411775 | ||||||
chr14:88411844
|
A | AT | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-4861dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88411844 | |||||
chr14:88411851
|
G | T | 15 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(12): Show | 20 | HG00642.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.239-4860G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88411851 | ||||||
chr14:88412001
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-4710C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412001 | ||||||
chr14:88412021
|
C | CA | 22 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(19): Show | 29 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.239-4689dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88412021 | |||||
chr14:88412031
|
A | G | 6 | a0002c0002t0001g0024a0002c0002t0001g0155a0002c0002t0001g0156others(3): Show | 7 | HG00741.hp1 HG01192.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-4680A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412031 | ||||||
chr14:88412222
|
CT | C | 8 | a0001c0001t0001g0062a0002c0002t0001g0089a0002c0002t0001g0090others(5): Show | 8 | HG02622.hp2 HG02818.hp1 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-4473delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88412222 | |||||
chr14:88412222
|
CTTTTT | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-4477_239-4473d others(7): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88412222 | |||||
chr14:88412226
|
T | A | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.239-4485T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412226 | ||||||
chr14:88412228
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.239-4483T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412228 | ||||||
chr14:88412419
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.239-4292C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412419 | ||||||
chr14:88412481
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-4230G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412481 | ||||||
chr14:88412515
|
G | A | 3 | a0002c0002t0001g0149a0002c0002t0001g0150a0002c0002t0001g0151 | 3 | HG02622.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.239-4196G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412515 | ||||||
chr14:88412524
|
C | A | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG01192.hp2 HG01258.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.239-4187C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412524 | ||||||
chr14:88412525
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239-4186A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412525 | ||||||
chr14:88412599
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-4112T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412599 | ||||||
chr14:88412911
|
C | T | 1 | a0004c0004t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.239-3800C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88412911 | ||||||
chr14:88413093
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.239-3618G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413093 | ||||||
chr14:88413311
|
TG | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0229 | 3 | HG02970.hp1 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.239-3399delG | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413311 | ||||||
chr14:88413384
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-3327T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413384 | ||||||
chr14:88413400
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-3311G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413400 | ||||||
chr14:88413435
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-3276A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413435 | ||||||
chr14:88413548
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-3163A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413548 | ||||||
chr14:88413607
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0291 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.239-3104A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413607 | ||||||
chr14:88413614
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-3097T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413614 | ||||||
chr14:88413723
|
A | T | 6 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-2988A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413723 | ||||||
chr14:88413741
|
GT | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-2959delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88413741 | |||||
chr14:88413750
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239-2961T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413750 | ||||||
chr14:88413784
|
G | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.239-2927G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413784 | ||||||
chr14:88413846
|
A | G | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.239-2865A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413846 | ||||||
chr14:88413900
|
G | A | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.239-2811G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413900 | ||||||
chr14:88413904
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.239-2807A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88413904 | ||||||
chr14:88414066
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-2645G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414066 | ||||||
chr14:88414286
|
G | A | 4 | a0004c0004t0001g0280a0004c0004t0001g0281a0004c0004t0001g0282others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-2425G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414286 | ||||||
chr14:88414347
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-2364A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414347 | ||||||
chr14:88414407
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-2304G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414407 | ||||||
chr14:88414548
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.239-2163A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414548 | ||||||
chr14:88414554
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-2157A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414554 | ||||||
chr14:88414612
|
A | G | 1 | a0002c0002t0001g0126 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.239-2099A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414612 | ||||||
chr14:88414622
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239-2089C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414622 | ||||||
chr14:88414773
|
TTTG | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-1935_239-1933d others(5): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88414773 | |||||
chr14:88414878
|
G | A | 15 | a0001c0001t0001g0204a0004c0004t0001g0012a0004c0004t0001g0013others(12): Show | 20 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.239-1833G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414878 | ||||||
chr14:88414904
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 169 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.239-1807C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414904 | ||||||
chr14:88414905
|
G | A | 1 | a0002c0002t0001g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.239-1806G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414905 | ||||||
chr14:88414926
|
C | T | 72 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(69): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.239-1785C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414926 | ||||||
chr14:88414970
|
C | T | 1 | a0002c0002t0001g0145 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.239-1741C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88414970 | ||||||
chr14:88415061
|
G | T | 1 | a0001c0001t0001g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.239-1650G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415061 | ||||||
chr14:88415152
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-1559G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415152 | ||||||
chr14:88415205
|
G | T | 2 | a0004c0004t0001g0037a0004c0004t0001g0038 | 2 | HG00642.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.239-1506G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415205 | ||||||
chr14:88415216
|
C | CTTG | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-1493_239-1491d others(5): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88415216 | |||||
chr14:88415229
|
G | A | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.239-1482G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415229 | ||||||
chr14:88415230
|
G | A | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-1481G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415230 | ||||||
chr14:88415231
|
G | T | 10 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(7): Show | 13 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-1480G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415231 | ||||||
chr14:88415494
|
T | TTTTTTTA others(20): Show |
2 | a0004c0004t0001g0012a0004c0004t0001g0279 | 4 | HG02559.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-1211_239-1210i others(29): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88415494 | |||||
chr14:88415501
|
T | TA | 12 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-1210_239-1209i others(3): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415501 | ||||||
chr14:88415502
|
T | A | 12 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-1209T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415502 | ||||||
chr14:88415502
|
T | TAA | 2 | a0004c0004t0001g0012a0004c0004t0001g0279 | 4 | HG02559.hp2 HG02886.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-1207_239-1206d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88415502 | |||||
chr14:88415538
|
T | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.239-1173T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415538 | ||||||
chr14:88415571
|
A | C | 72 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(69): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.239-1140A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415571 | ||||||
chr14:88415651
|
T | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-1060T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415651 | ||||||
chr14:88415658
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-1053T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415658 | ||||||
chr14:88415779
|
T | G | 1 | a0010c0013t0001g0266 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.239-932T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415779 | ||||||
chr14:88415858
|
G | A | 66 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0011others(63): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.239-853G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88415858 | ||||||
chr14:88416004
|
G | A | 22 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(19): Show | 29 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.239-707G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416004 | ||||||
chr14:88416022
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.239-689G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416022 | ||||||
chr14:88416191
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-520T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416191 | ||||||
chr14:88416356
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-355G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416356 | ||||||
chr14:88416409
|
C | CT | 14 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0164others(11): Show | 15 | HG00408.hp2 HG01358.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-281dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88416409 | |||||
chr14:88416409
|
CT | C | 92 | a0001c0001t0001g0027a0001c0001t0001g0054a0001c0001t0001g0063others(89): Show | 121 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.239-281delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88416409 | |||||
chr14:88416409
|
CTT | C | 12 | a0002c0002t0001g0096a0002c0002t0001g0106a0002c0002t0001g0115others(9): Show | 15 | HG00099.hp2 HG00323.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-282_239-281del others(2): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 88416409 | |||||
chr14:88416451
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-260T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416451 | ||||||
chr14:88416542
|
A | G | 1 | a0003c0003t0001g0245 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.239-169A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416542 | ||||||
chr14:88416568
|
C | G | 1 | a0001c0001t0001g0224 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.239-143C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416568 | ||||||
chr14:88416673
|
T | G | 1 | a0001c0001t0001g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.239-38T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 4/11 | chr14 | 88416673 | ||||||
chr14:88417023
|
A | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.372+179A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417023 | ||||||
chr14:88417026
|
C | T | 1 | a0002c0002t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.372+182C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417026 | ||||||
chr14:88417049
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+205A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417049 | ||||||
chr14:88417157
|
G | A | 30 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0024others(27): Show | 35 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.372+313G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417157 | ||||||
chr14:88417196
|
GT | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.372+362delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88417196 | |||||
chr14:88417303
|
G | GT | 5 | a0004c0004t0001g0012a0004c0004t0001g0279a0004c0004t0001g0280others(2): Show | 7 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.372+459_372+460ins others(1): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417303 | ||||||
chr14:88417304
|
G | T | 22 | a0002c0002t0001g0123a0002c0002t0001g0134a0004c0004t0001g0012others(19): Show | 28 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.372+460G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417304 | ||||||
chr14:88417304
|
GT | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.372+473delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88417304 | |||||
chr14:88417314
|
T | A | 1 | a0002c0002t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.372+470T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417314 | ||||||
chr14:88417314
|
T | TA | 4 | a0002c0002t0001g0106a0002c0002t0001g0108a0002c0002t0001g0109others(1): Show | 4 | HG00099.hp2 HG01168.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+470_372+471ins others(1): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417314 | ||||||
chr14:88417316
|
T | A | 8 | a0001c0001t0001g0173a0002c0002t0001g0097a0002c0002t0001g0106others(5): Show | 8 | HG00099.hp2 HG01123.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.372+472T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417316 | ||||||
chr14:88417316
|
T | TA | 25 | a0001c0001t0001g0043a0001c0001t0001g0058a0001c0001t0001g0059others(22): Show | 30 | HG02451.hp1 HG02451.hp2 HG02486.hp1 others(27): Show |
intron_variant | MODIFIER | c.372+472_372+473ins others(1): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417316 | ||||||
chr14:88417316
|
T | TTA | 16 | a0002c0002t0001g0159a0004c0004t0001g0012a0004c0004t0001g0013others(13): Show | 20 | HG00642.hp2 HG01192.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.372+487_372+488dup others(2): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88417316 | |||||
chr14:88417327
|
T | G | 2 | a0003c0003t0001g0232a0003c0003t0001g0242 | 2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.372+483T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417327 | ||||||
chr14:88417367
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+523C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417367 | ||||||
chr14:88417444
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+600T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417444 | ||||||
chr14:88417461
|
G | A | 8 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(5): Show | 10 | HG01884.hp2 HG01891.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.372+617G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417461 | ||||||
chr14:88417480
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+636G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417480 | ||||||
chr14:88417534
|
G | T | 1 | a0003c0003t0001g0240 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.372+690G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417534 | ||||||
chr14:88417585
|
A | G | 68 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0011others(65): Show | 93 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.372+741A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417585 | ||||||
chr14:88417684
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+840C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417684 | ||||||
chr14:88417817
|
G | C | 2 | a0003c0003t0001g0261a0003c0003t0001g0262 | 2 | NA18959.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.372+973G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417817 | ||||||
chr14:88417840
|
A | T | 1 | a0002c0002t0001g0096 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.372+996A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88417840 | ||||||
chr14:88418006
|
A | G | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.372+1162A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418006 | ||||||
chr14:88418078
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1234A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418078 | ||||||
chr14:88418140
|
ATTC | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1306_372+1308d others(5): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88418140 | |||||
chr14:88418150
|
T | G | 6 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1306T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418150 | ||||||
chr14:88418242
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.372+1398G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418242 | ||||||
chr14:88418272
|
C | CTTTGACT others(1): Show |
14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1429_372+1430i others(10): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88418272 | |||||
chr14:88418330
|
CCTTA | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1490_372+1493d others(6): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88418330 | |||||
chr14:88418342
|
G | GC | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1499dupC | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88418342 | |||||
chr14:88418404
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.372+1560C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418404 | ||||||
chr14:88418442
|
C | T | 2 | a0002c0002t0001g0122a0002c0002t0001g0184 | 2 | NA19062.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.372+1598C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418442 | ||||||
chr14:88418463
|
T | TTTTG | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1631_372+1634d others(6): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88418463 | |||||
chr14:88418535
|
T | C | 1 | a0002c0002t0001g0145 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.372+1691T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418535 | ||||||
chr14:88418561
|
G | A | 15 | a0002c0002t0001g0133a0004c0004t0001g0012a0004c0004t0001g0013others(12): Show | 20 | HG00642.hp2 HG00673.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.372+1717G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418561 | ||||||
chr14:88418584
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1740C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418584 | ||||||
chr14:88418649
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1805G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418649 | ||||||
chr14:88418769
|
C | T | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.372+1925C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418769 | ||||||
chr14:88418824
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+1980A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418824 | ||||||
chr14:88418883
|
T | G | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.372+2039T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418883 | ||||||
chr14:88418891
|
C | T | 22 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(19): Show | 29 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.372+2047C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418891 | ||||||
chr14:88418999
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.372+2155T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88418999 | ||||||
chr14:88419068
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.372+2224G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419068 | ||||||
chr14:88419171
|
A | G | 1 | a0002c0002t0001g0096 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.372+2327A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419171 | ||||||
chr14:88419478
|
A | G | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.372+2634A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419478 | ||||||
chr14:88419531
|
C | CT | 23 | a0001c0001t0001g0194a0001c0001t0001g0256a0002c0002t0001g0007others(20): Show | 28 | HG02040.hp1 HG02055.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.372+2700dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88419531 | |||||
chr14:88419531
|
CT | C | 13 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(10): Show | 18 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.372+2700delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88419531 | |||||
chr14:88419578
|
C | G | 1 | a0010c0013t0001g0266 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.372+2734C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419578 | ||||||
chr14:88419587
|
C | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0229 | 3 | HG02970.hp1 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.372+2743C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419587 | ||||||
chr14:88419771
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+2927T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419771 | ||||||
chr14:88419839
|
T | C | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.372+2995T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419839 | ||||||
chr14:88419841
|
T | C | 6 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+2997T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419841 | ||||||
chr14:88419963
|
A | T | 3 | a0002c0002t0001g0119a0002c0002t0001g0120a0002c0002t0001g0121 | 3 | NA18942.hp2 NA18988.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.372+3119A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88419963 | ||||||
chr14:88420195
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.372+3351C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420195 | ||||||
chr14:88420256
|
G | A | 15 | a0002c0002t0001g0105a0004c0004t0001g0012a0004c0004t0001g0013others(12): Show | 20 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.372+3412G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420256 | ||||||
chr14:88420351
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+3507G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420351 | ||||||
chr14:88420525
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+3681C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420525 | ||||||
chr14:88420527
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.372+3683C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420527 | ||||||
chr14:88420652
|
G | C | 1 | a0001c0001t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.372+3808G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420652 | ||||||
chr14:88420678
|
A | C | 1 | a0010c0013t0001g0266 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.372+3834A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420678 | ||||||
chr14:88420867
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.372+4023G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420867 | ||||||
chr14:88420890
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+4046T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420890 | ||||||
chr14:88420988
|
G | A | 4 | a0003c0003t0001g0235a0003c0003t0001g0237a0003c0003t0001g0238others(1): Show | 4 | HG00741.hp2 HG02572.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+4144G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88420988 | ||||||
chr14:88421060
|
G | A | 1 | a0002c0002t0004g0116 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.372+4216G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421060 | ||||||
chr14:88421099
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+4255C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421099 | ||||||
chr14:88421121
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+4277A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421121 | ||||||
chr14:88421137
|
A | C | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.372+4293A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421137 | ||||||
chr14:88421201
|
A | G | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.372+4357A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421201 | ||||||
chr14:88421238
|
C | T | 6 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+4394C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421238 | ||||||
chr14:88421258
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.372+4414G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421258 | ||||||
chr14:88421387
|
G | A | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.372+4543G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421387 | ||||||
chr14:88421484
|
A | G | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.372+4640A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421484 | ||||||
chr14:88421541
|
C | T | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.373-4691C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421541 | ||||||
chr14:88421559
|
A | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.373-4673A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421559 | ||||||
chr14:88421615
|
C | T | 8 | a0002c0002t0001g0024a0002c0002t0001g0049a0002c0002t0001g0050others(5): Show | 9 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-4617C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421615 | ||||||
chr14:88421664
|
A | G | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.373-4568A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421664 | ||||||
chr14:88421669
|
G | A | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.373-4563G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421669 | ||||||
chr14:88421710
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-4522G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421710 | ||||||
chr14:88421835
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-4397G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421835 | ||||||
chr14:88421847
|
G | A | 2 | a0006c0005t0001g0014a0006c0005t0001g0039 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.373-4385G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421847 | ||||||
chr14:88421859
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-4373G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421859 | ||||||
chr14:88421881
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0173a0001c0001t0001g0182others(1): Show | 5 | HG00544.hp1 HG02523.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-4351G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421881 | ||||||
chr14:88421943
|
A | G | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.373-4289A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421943 | ||||||
chr14:88421964
|
A | AG | 13 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(10): Show | 18 | HG00642.hp2 HG02145.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.373-4267dupG | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88421964 | |||||
chr14:88421964
|
A | G | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.373-4268A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88421964 | ||||||
chr14:88422009
|
TAAG | T | 8 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(5): Show | 10 | HG01884.hp2 HG01891.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.373-4219_373-4217d others(5): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88422009 | |||||
chr14:88422113
|
G | A | 3 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038 | 4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-4119G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88422113 | ||||||
chr14:88422288
|
A | C | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.373-3944A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88422288 | ||||||
chr14:88422580
|
CTATT | C | 25 | a0002c0002t0001g0011a0002c0002t0001g0095a0002c0002t0001g0112others(22): Show | 33 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.373-3648_373-3645d others(6): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88422580 | |||||
chr14:88422743
|
T | C | 4 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(1): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-3489T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88422743 | ||||||
chr14:88422836
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-3396T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88422836 | ||||||
chr14:88422854
|
G | T | 6 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-3378G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88422854 | ||||||
chr14:88423193
|
T | C | 30 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0024others(27): Show | 35 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.373-3039T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423193 | ||||||
chr14:88423245
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-2987A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423245 | ||||||
chr14:88423273
|
C | T | 1 | a0002c0002t0001g0122 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.373-2959C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423273 | ||||||
chr14:88423374
|
C | CA | 7 | a0001c0001t0001g0041a0002c0002t0001g0091a0002c0002t0001g0144others(4): Show | 7 | HG01175.hp1 HG02647.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.373-2841dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88423374 | |||||
chr14:88423374
|
C | CAA | 13 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(10): Show | 18 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.373-2842_373-2841d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88423374 | |||||
chr14:88423397
|
GA | G | 8 | a0001c0001t0001g0056a0002c0002t0001g0104a0005c0006t0001g0034others(5): Show | 9 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.373-2823delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88423397 | |||||
chr14:88423465
|
C | A | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-2767C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423465 | ||||||
chr14:88423497
|
A | G | 2 | a0006c0005t0001g0014a0006c0005t0001g0039 | 3 | HG02559.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.373-2735A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423497 | ||||||
chr14:88423542
|
T | C | 22 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0082others(19): Show | 26 | HG02055.hp1 HG02451.hp2 HG02486.hp1 others(23): Show |
intron_variant | MODIFIER | c.373-2690T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423542 | ||||||
chr14:88423548
|
T | TA | 13 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(10): Show | 17 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.373-2672dupA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88423548 | |||||
chr14:88423671
|
A | AT | 17 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0056others(14): Show | 21 | HG00408.hp1 HG00597.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.373-2533dupT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88423671 | |||||
chr14:88423671
|
A | ATTTTTTT others(3): Show |
1 | a0010c0013t0001g0266 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.373-2542_373-2533d others(12): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88423671 | |||||
chr14:88423674
|
TTTTTTTT others(150): Show |
T | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.373-2557_373-2401d others(2): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423674 | ||||||
chr14:88423832
|
C | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.373-2400C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423832 | ||||||
chr14:88423904
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-2328G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88423904 | ||||||
chr14:88424115
|
C | T | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-2117C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424115 | ||||||
chr14:88424240
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-1992C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424240 | ||||||
chr14:88424277
|
G | A | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-1955G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424277 | ||||||
chr14:88424293
|
T | C | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.373-1939T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424293 | ||||||
chr14:88424304
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.373-1928A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424304 | ||||||
chr14:88424384
|
A | G | 69 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(66): Show | 94 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.373-1848A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424384 | ||||||
chr14:88424498
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-1734C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424498 | ||||||
chr14:88424561
|
C | T | 30 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0024others(27): Show | 35 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.373-1671C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424561 | ||||||
chr14:88424583
|
T | A | 1 | a0004c0004t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.373-1649T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424583 | ||||||
chr14:88424634
|
A | C | 4 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-1598A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424634 | ||||||
chr14:88424635
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-1597C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424635 | ||||||
chr14:88424644
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-1588G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424644 | ||||||
chr14:88424727
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-1505A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88424727 | ||||||
chr14:88425016
|
T | G | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.373-1216T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425016 | ||||||
chr14:88425054
|
C | A | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.373-1178C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425054 | ||||||
chr14:88425077
|
G | A | 6 | a0001c0001t0001g0044a0001c0001t0001g0205a0001c0001t0001g0218others(3): Show | 6 | HG01081.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-1155G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425077 | ||||||
chr14:88425082
|
A | G | 9 | a0002c0002t0001g0024a0002c0002t0001g0049a0002c0002t0001g0050others(6): Show | 10 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-1150A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425082 | ||||||
chr14:88425094
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-1138A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425094 | ||||||
chr14:88425216
|
A | G | 1 | a0003c0003t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.373-1016A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425216 | ||||||
chr14:88425549
|
CTATCTGT others(5): Show |
C | 1 | a0011c0014t0001g0070 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.373-680_373-669del others(12): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 88425549 | |||||
chr14:88425635
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.373-597C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425635 | ||||||
chr14:88425647
|
T | A | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.373-585T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425647 | ||||||
chr14:88425990
|
T | A | 1 | a0011c0014t0001g0070 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.373-242T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88425990 | ||||||
chr14:88426003
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0002g0035a0001c0001t0002g0036 | 3 | HG02735.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.373-229C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88426003 | ||||||
chr14:88426031
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-201T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88426031 | ||||||
chr14:88426090
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.373-142G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 5/11 | chr14 | 88426090 | ||||||
chr14:88426728
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.845+24G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88426728 | ||||||
chr14:88426777
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.845+73T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88426777 | ||||||
chr14:88426863
|
A | G | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.845+159A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88426863 | ||||||
chr14:88426875
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.845+171A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88426875 | ||||||
chr14:88426948
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.845+244G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88426948 | ||||||
chr14:88426973
|
T | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.845+269T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88426973 | ||||||
chr14:88427027
|
G | A | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.845+323G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427027 | ||||||
chr14:88427047
|
T | G | 1 | a0003c0003t0001g0251 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.845+343T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427047 | ||||||
chr14:88427059
|
C | T | 7 | a0004c0004t0001g0012a0004c0004t0001g0279a0004c0004t0001g0280others(4): Show | 9 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.845+355C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427059 | ||||||
chr14:88427074
|
T | C | 1 | a0002c0002t0001g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.845+370T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427074 | ||||||
chr14:88427136
|
C | A | 16 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(13): Show | 22 | HG00642.hp2 HG02040.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.845+432C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427136 | ||||||
chr14:88427298
|
T | G | 1 | a0003c0003t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.846-332T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427298 | ||||||
chr14:88427402
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.846-228A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427402 | ||||||
chr14:88427440
|
A | G | 3 | a0002c0002t0001g0092a0002c0002t0001g0103a0002c0002t0001g0154 | 3 | HG02109.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.846-190A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427440 | ||||||
chr14:88427441
|
T | TAAG | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.846-188_846-186dup others(3): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 88427441 | |||||
chr14:88427529
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.846-101G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 6/11 | chr14 | 88427529 | ||||||
chr14:88427751
|
A | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.912+55A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88427751 | ||||||
chr14:88427778
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.912+82G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88427778 | ||||||
chr14:88427812
|
A | G | 2 | a0007c0008t0001g0275a0007c0008t0001g0276 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.912+116A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88427812 | ||||||
chr14:88427866
|
T | G | 70 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(67): Show | 95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.912+170T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88427866 | ||||||
chr14:88428057
|
CT | C | 11 | a0001c0001t0001g0181a0001c0001t0001g0190a0001c0001t0001g0218others(8): Show | 13 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.912+373delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 88428057 | |||||
chr14:88428120
|
A | G | 1 | a0001c0001t0001g0026 | 2 | NA19011.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.912+424A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88428120 | ||||||
chr14:88428186
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.912+490G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88428186 | ||||||
chr14:88428568
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01884.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.913-780A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88428568 | ||||||
chr14:88428665
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.913-683C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88428665 | ||||||
chr14:88428846
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.913-502T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88428846 | ||||||
chr14:88428890
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.913-458T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88428890 | ||||||
chr14:88429104
|
G | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.913-244G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88429104 | ||||||
chr14:88429124
|
T | G | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.913-224T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88429124 | ||||||
chr14:88429250
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.913-98G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88429250 | ||||||
chr14:88429268
|
C | T | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.913-80C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88429268 | ||||||
chr14:88429282
|
T | C | 3 | a0005c0006t0001g0034a0005c0006t0001g0274a0008c0009t0001g0272 | 4 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.913-66T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88429282 | ||||||
chr14:88429325
|
T | G | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(290): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.913-23T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88429325 | ||||||
chr14:88429334
|
T | A | 1 | a0001c0001t0001g0064 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.913-14T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 7/11 | chr14 | 88429334 | ||||||
chr14:88429474
|
C | G | 1 | a0002c0002t0001g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1028+11C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429474 | ||||||
chr14:88429539
|
G | A | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1028+76G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429539 | ||||||
chr14:88429566
|
C | T | 20 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(17): Show | 27 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1028+103C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429566 | ||||||
chr14:88429584
|
T | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1028+121T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429584 | ||||||
chr14:88429597
|
C | G | 61 | a0001c0001t0001g0057a0002c0002t0001g0001a0002c0002t0001g0006others(58): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1028+134C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429597 | ||||||
chr14:88429666
|
G | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1028+203G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429666 | ||||||
chr14:88429769
|
G | A | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1028+306G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429769 | ||||||
chr14:88429882
|
T | A | 1 | a0001c0001t0001g0190 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1028+419T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429882 | ||||||
chr14:88429890
|
C | CTATT | 10 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077others(7): Show | 10 | HG01109.hp1 HG02109.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1028+459_1028+462d others(6): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 88429890 | |||||
chr14:88429890
|
C | CTATTTAT others(1): Show |
131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(128): Show | 155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1028+455_1028+462d others(10): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 88429890 | |||||
chr14:88429890
|
C | CTATTTAT others(5): Show |
98 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(95): Show | 137 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1028+451_1028+462d others(14): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 88429890 | |||||
chr14:88429890
|
C | CTATTTAT others(9): Show |
18 | a0001c0001t0001g0180a0001c0001t0001g0268a0001c0001t0001g0269others(15): Show | 20 | HG00280.hp1 HG00544.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1028+447_1028+462d others(18): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 88429890 | |||||
chr14:88429890
|
C | CTATTTAT others(13): Show |
1 | a0001c0001t0001g0169 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1028+443_1028+462d others(22): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 88429890 | |||||
chr14:88429903
|
T | A | 1 | a0011c0014t0001g0070 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1028+440T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88429903 | ||||||
chr14:88430274
|
A | G | 1 | a0005c0006t0001g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1028+811A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430274 | ||||||
chr14:88430287
|
A | G | 1 | a0002c0002t0001g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1028+824A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430287 | ||||||
chr14:88430329
|
A | G | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1029-843A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430329 | ||||||
chr14:88430410
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1029-762G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430410 | ||||||
chr14:88430476
|
T | C | 2 | a0002c0002t0001g0099a0002c0002t0001g0129 | 2 | NA20129.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1029-696T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430476 | ||||||
chr14:88430478
|
C | G | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1029-694C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430478 | ||||||
chr14:88430662
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1029-510A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430662 | ||||||
chr14:88430920
|
C | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1029-252C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88430920 | ||||||
chr14:88431021
|
G | A | 4 | a0005c0006t0001g0034a0005c0006t0001g0273a0005c0006t0001g0274others(1): Show | 5 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029-151G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88431021 | ||||||
chr14:88431117
|
A | T | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1029-55A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 8/11 | chr14 | 88431117 | ||||||
chr14:88431372
|
T | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165 | 3 | HG02717.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1082+147T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431372 | ||||||
chr14:88431455
|
G | T | 1 | a0003c0003t0001g0248 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1082+230G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431455 | ||||||
chr14:88431456
|
T | C | 3 | a0006c0005t0001g0014a0006c0005t0001g0039a0006c0005t0003g0015 | 5 | HG02451.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1082+231T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431456 | ||||||
chr14:88431600
|
C | T | 1 | a0003c0003t0001g0250 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1082+375C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431600 | ||||||
chr14:88431636
|
A | G | 2 | a0002c0002t0001g0122a0002c0002t0001g0184 | 2 | NA19062.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1082+411A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431636 | ||||||
chr14:88431708
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1082+483C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431708 | ||||||
chr14:88431756
|
G | A | 30 | a0002c0002t0001g0007a0002c0002t0001g0023a0002c0002t0001g0024others(27): Show | 35 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1082+531G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431756 | ||||||
chr14:88431862
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1082+637T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431862 | ||||||
chr14:88431887
|
G | C | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1082+662G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431887 | ||||||
chr14:88431896
|
C | T | 1 | a0002c0002t0001g0143 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1082+671C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431896 | ||||||
chr14:88431949
|
T | A | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1082+724T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431949 | ||||||
chr14:88431983
|
A | T | 1 | a0004c0004t0001g0280 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1082+758A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88431983 | ||||||
chr14:88432166
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1082+941C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88432166 | ||||||
chr14:88432454
|
C | T | 1 | a0004c0004t0001g0278 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1083-681C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88432454 | ||||||
chr14:88432578
|
C | T | 14 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(11): Show | 19 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1083-557C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88432578 | ||||||
chr14:88432589
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG02895.hp2 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1083-546G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88432589 | ||||||
chr14:88432652
|
G | C | 3 | a0004c0004t0001g0013a0004c0004t0001g0037a0004c0004t0001g0038 | 4 | HG00642.hp2 HG02145.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083-483G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88432652 | ||||||
chr14:88432682
|
A | T | 2 | a0003c0003t0001g0187a0003c0003t0001g0247 | 2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1083-453A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88432682 | ||||||
chr14:88433097
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0025others(24): Show | 38 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1083-38G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 9/11 | chr14 | 88433097 | ||||||
chr14:88433300
|
A | T | 1 | a0011c0014t0001g0070 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1160+88A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433300 | ||||||
chr14:88433481
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1160+269T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433481 | ||||||
chr14:88433633
|
C | T | 1 | a0010c0013t0001g0266 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1160+421C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433633 | ||||||
chr14:88433634
|
G | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0058a0001c0001t0001g0059others(9): Show | 12 | HG00408.hp1 HG02155.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1160+422G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433634 | ||||||
chr14:88433679
|
A | G | 11 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(8): Show | 14 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1160+467A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433679 | ||||||
chr14:88433710
|
T | A | 11 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(8): Show | 14 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1160+498T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433710 | ||||||
chr14:88433746
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(92): Show | 112 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1160+534C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433746 | ||||||
chr14:88433760
|
G | A | 11 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(8): Show | 14 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1160+548G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433760 | ||||||
chr14:88433921
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1160+709A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433921 | ||||||
chr14:88433943
|
A | T | 2 | a0005c0007t0001g0033a0005c0007t0001g0271 | 3 | HG02040.hp1 NA18980.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1160+731A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433943 | ||||||
chr14:88433989
|
T | C | 1 | a0002c0002t0001g0156 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1160+777T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88433989 | ||||||
chr14:88434097
|
T | C | 11 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(8): Show | 14 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1160+885T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434097 | ||||||
chr14:88434221
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0178 | 3 | NA19005.hp1 NA19011.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1160+1009T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434221 | ||||||
chr14:88434228
|
A | C | 1 | a0003c0003t0001g0187 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1160+1016A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434228 | ||||||
chr14:88434512
|
T | C | 27 | a0001c0001t0001g0163a0001c0001t0001g0165a0002c0002t0001g0049others(24): Show | 30 | HG00741.hp1 HG01192.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1160+1300T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434512 | ||||||
chr14:88434546
|
G | A | 13 | a0001c0001t0001g0028a0001c0001t0001g0167a0001c0001t0001g0168others(10): Show | 13 | HG00408.hp2 HG02165.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160+1334G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434546 | ||||||
chr14:88434555
|
C | T | 3 | a0001c0001t0001g0205a0006c0005t0001g0014a0006c0005t0001g0039 | 4 | HG01081.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+1343C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434555 | ||||||
chr14:88434556
|
G | A | 19 | a0001c0001t0001g0052a0002c0002t0001g0097a0002c0002t0001g0108others(16): Show | 19 | HG00323.hp1 HG00733.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1160+1344G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434556 | ||||||
chr14:88434572
|
C | A | 3 | a0001c0001t0001g0205a0006c0005t0001g0014a0006c0005t0001g0039 | 4 | HG01081.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+1360C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434572 | ||||||
chr14:88434600
|
G | A | 7 | a0001c0001t0001g0205a0002c0002t0001g0149a0002c0002t0001g0150others(4): Show | 9 | HG01081.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1160+1388G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434600 | ||||||
chr14:88434611
|
G | A | 22 | a0001c0001t0001g0163a0001c0001t0001g0165a0002c0002t0001g0024others(19): Show | 26 | HG00642.hp2 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.1160+1399G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434611 | ||||||
chr14:88434627
|
A | G | 1 | a0006c0005t0003g0015 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1160+1415A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434627 | ||||||
chr14:88434641
|
G | A | 1 | a0002c0002t0001g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1160+1429G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434641 | ||||||
chr14:88434642
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 146 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1160+1430C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434642 | ||||||
chr14:88434649
|
G | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1160+1437G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434649 | ||||||
chr14:88434687
|
GA | G | 9 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 10 | HG01361.hp1 HG01891.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160+1490delA | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 88434687 | |||||
chr14:88434688
|
A | G | 1 | a0002c0002t0001g0083 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1160+1476A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434688 | ||||||
chr14:88434742
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1160+1530G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434742 | ||||||
chr14:88434867
|
T | A | 290 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(287): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1160+1655T>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434867 | ||||||
chr14:88434908
|
TG | T | 5 | a0002c0002t0001g0024a0002c0002t0001g0155a0002c0002t0001g0156others(2): Show | 6 | HG00741.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160+1698delG | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 88434908 | |||||
chr14:88434914
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1160+1702A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434914 | ||||||
chr14:88434985
|
C | A | 1 | a0002c0002t0001g0135 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1160+1773C>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88434985 | ||||||
chr14:88435283
|
A | T | 15 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(12): Show | 20 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1160+2071A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435283 | ||||||
chr14:88435390
|
G | A | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-2153G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435390 | ||||||
chr14:88435434
|
C | T | 1 | a0002c0002t0001g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1161-2109C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435434 | ||||||
chr14:88435468
|
T | C | 1 | a0002c0002t0001g0124 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1161-2075T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435468 | ||||||
chr14:88435486
|
G | A | 3 | a0002c0002t0001g0049a0002c0002t0001g0050a0002c0002t0001g0051 | 3 | HG01243.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1161-2057G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435486 | ||||||
chr14:88435701
|
C | G | 1 | a0004c0004t0001g0013 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1161-1842C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435701 | ||||||
chr14:88435816
|
A | G | 1 | a0002c0002t0001g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1161-1727A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435816 | ||||||
chr14:88435879
|
C | T | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-1664C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435879 | ||||||
chr14:88435909
|
G | A | 1 | a0002c0002t0001g0155 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1161-1634G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88435909 | ||||||
chr14:88436273
|
T | C | 1 | a0004c0004t0001g0284 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1161-1270T>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88436273 | ||||||
chr14:88436467
|
C | G | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1161-1076C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88436467 | ||||||
chr14:88436801
|
C | T | 11 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(8): Show | 14 | HG00642.hp2 HG02145.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161-742C>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88436801 | ||||||
chr14:88436918
|
A | G | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-625A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88436918 | ||||||
chr14:88436938
|
AT | A | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-596delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 88436938 | |||||
chr14:88437073
|
CT | C | 13 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(10): Show | 16 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1161-458delT | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 88437073 | |||||
chr14:88437143
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1161-400A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437143 | ||||||
chr14:88437149
|
A | T | 1 | a0011c0014t0001g0070 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1161-394A>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437149 | ||||||
chr14:88437203
|
T | TTG | 5 | a0001c0001t0001g0163a0001c0001t0001g0177a0002c0002t0001g0048others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161-320_1161-319d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 88437203 | |||||
chr14:88437203
|
TTG | T | 6 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(3): Show | 7 | HG02040.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161-320_1161-319d others(4): Show |
SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 88437203 | |||||
chr14:88437256
|
G | T | 1 | a0002c0010t0001g0125 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1161-287G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437256 | ||||||
chr14:88437287
|
G | C | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-256G>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437287 | ||||||
chr14:88437344
|
C | G | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-199C>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437344 | ||||||
chr14:88437375
|
A | C | 1 | a0011c0014t0001g0070 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1161-168A>C | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437375 | ||||||
chr14:88437476
|
G | A | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-67G>A | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437476 | ||||||
chr14:88437478
|
A | G | 12 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(9): Show | 15 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1161-65A>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 10/11 | chr14 | 88437478 | ||||||
chr14:88437621
|
T | G | 1 | a0002c0002t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1215+24T>G | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 11/11 | chr14 | 88437621 | ||||||
chr14:88437649
|
G | T | 18 | a0004c0004t0001g0012a0004c0004t0001g0013a0004c0004t0001g0037others(15): Show | 23 | HG00642.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1215+52G>T | SPATA7 | ENSG00000042317.17 | transcript | ENST00000393545.9 | protein_coding | 11/11 | chr14 | 88437649 |