geneid | 23353 |
---|---|
ensemblid | ENSG00000164828.18 |
hgncid | 18587 |
symbol | SUN1 |
name | Sad1 and UNC84 domain containing 1 |
refseq_nuc | NM_001130965.3 |
refseq_prot | NP_001124437.1 |
ensembl_nuc | ENST00000401592.6 |
ensembl_prot | ENSP00000384015.1 |
mane_status | MANE Select |
chr | chr7 |
start | 832476 |
end | 874934 |
strand | + |
ver | v1.2 |
region | chr7:832476-874934 |
region5000 | chr7:827476-879934 |
regionname0 | SUN1_chr7_832476_874934 |
regionname5000 | SUN1_chr7_827476_879934 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 785 | 191 | 48 | 34 | 85 | 5 | 19 | 67 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0002 | 1/1 | 785 | 123 | 25 | 24 | 50 | 6 | 16 | 36 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003 | 0/0 | 785 | 64 | 8 | 15 | 27 | 3 | 11 | 21 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0004 | 0/0 | 785 | 10 | 0 | 0 | 10 | 0 | 0 | 5 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0005 | 0/0 | 785 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0006 | 0/0 | 785 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0007 | 0/0 | 785 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0008 | 0/0 | 785 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0009 | 0/0 | 785 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0010 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0011 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0012 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0013 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0014 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0015 | 0/0 | 785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0016 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0017 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0018 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0019 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0020 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0021 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0022 | 0/0 | 785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2358 | 141 | 34 | 32 | 53 | 5 | 17 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0002 | 0/1 | 2358 | 94 | 22 | 17 | 48 | 2 | 4 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0003 | 0/0 | 2358 | 61 | 7 | 13 | 27 | 3 | 11 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0004 | 0/0 | 2358 | 33 | 0 | 0 | 32 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0005 | 1/0 | 2358 | 29 | 3 | 7 | 2 | 4 | 12 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0006 | 0/0 | 2358 | 13 | 12 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0007 | 0/0 | 2358 | 10 | 0 | 0 | 10 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0008 | 0/0 | 2358 | 6 | 5 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0009 | 0/0 | 2358 | 5 | 5 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0010 | 0/0 | 2358 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0011 | 0/0 | 2358 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0012 | 0/0 | 2358 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0013 | 0/0 | 2358 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0014 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0015 | 0/0 | 2339 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0016 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0017 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0018 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0019 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0020 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0021 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0022 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0023 | 0/0 | 2358 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0024 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0025 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0026 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0027 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0028 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0029 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0030 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
c0031 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1653 | 338 | 81 | 67 | 131 | 12 | 45 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0002 | 0/0 | 1653 | 31 | 0 | 0 | 30 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0003 | 0/0 | 1653 | 10 | 0 | 0 | 10 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0004 | 0/0 | 1653 | 6 | 0 | 0 | 6 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0005 | 0/0 | 1653 | 4 | 3 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0006 | 0/0 | 1653 | 3 | 3 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0007 | 0/0 | 1653 | 3 | 3 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0008 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0009 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0010 | 0/0 | 1653 | 2 | 0 | 1 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0011 | 0/0 | 1653 | 2 | 0 | 1 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0012 | 0/0 | 1653 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0013 | 0/0 | 1653 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0014 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0015 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0016 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0017 | 0/0 | 1653 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0018 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0019 | 0/0 | 1653 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0020 | 0/0 | 1653 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0021 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0022 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0023 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
t0024 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0004 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2358 | 141 | 34 | 32 | 53 | 5 | 17 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0004 | 0/0 | 2358 | 33 | 0 | 0 | 32 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0006 | 0/0 | 2358 | 13 | 12 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0022 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0023 | 0/0 | 2358 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0024 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0025 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0002c0002 | 0/1 | 2358 | 94 | 22 | 17 | 48 | 2 | 4 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0002c0005 | 1/0 | 2358 | 29 | 3 | 7 | 2 | 4 | 12 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0003 | 0/0 | 2358 | 61 | 7 | 13 | 27 | 3 | 11 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0012 | 0/0 | 2358 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0021 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0004c0007 | 0/0 | 2358 | 10 | 0 | 0 | 10 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0005c0008 | 0/0 | 2358 | 6 | 5 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0006c0009 | 0/0 | 2358 | 5 | 5 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0007c0010 | 0/0 | 2358 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0008c0011 | 0/0 | 2358 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0009c0013 | 0/0 | 2358 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0010c0014 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0011c0031 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0012c0016 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0013c0017 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0014c0018 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0015c0019 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0016c0020 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0017c0015 | 0/0 | 2339 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0018c0027 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0019c0028 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0020c0026 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0021c0029 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0022c0030 | 0/0 | 2358 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4010 | 131 | 31 | 27 | 52 | 4 | 17 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0011 | 0/0 | 4010 | 2 | 0 | 1 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0013 | 0/0 | 4010 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0015 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0016 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0017 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0019 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0021 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0001t0024 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0004t0002 | 0/0 | 4010 | 30 | 0 | 0 | 29 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0004t0008 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0004t0022 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0004t0023 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0006t0001 | 0/0 | 4010 | 10 | 10 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0006t0012 | 0/0 | 4010 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0006t0018 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0022t0001 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0023t0001 | 0/0 | 4010 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0024t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0001c0025t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0002c0002t0001 | 0/1 | 4010 | 82 | 20 | 17 | 38 | 2 | 4 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0002c0002t0003 | 0/0 | 4010 | 10 | 0 | 0 | 10 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0002c0002t0009 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0002c0005t0001 | 1/0 | 4010 | 29 | 3 | 7 | 2 | 4 | 12 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0003t0001 | 0/0 | 4010 | 54 | 2 | 12 | 27 | 2 | 11 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0003t0005 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0003t0007 | 0/0 | 4010 | 3 | 3 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0003t0010 | 0/0 | 4010 | 2 | 0 | 1 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0012t0005 | 0/0 | 4010 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0003c0021t0020 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0004c0007t0001 | 0/0 | 4010 | 4 | 0 | 0 | 4 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0004c0007t0004 | 0/0 | 4010 | 6 | 0 | 0 | 6 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0005c0008t0001 | 0/0 | 4010 | 6 | 5 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0006c0009t0001 | 0/0 | 4010 | 5 | 5 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0007c0010t0001 | 0/0 | 4010 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0008c0011t0006 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0009c0013t0001 | 0/0 | 4010 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0010c0014t0002 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0011c0031t0014 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0012c0016t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0013c0017t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0014c0018t0006 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0015c0019t0001 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0016c0020t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0017c0015t0008 | 0/0 | 3991 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0018c0027t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0019c0028t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0020c0026t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0021c0029t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
a0022c0030t0001 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | copy fasta | chr7 | 827476 | 879934 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0011g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0011g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0013g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0013g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0015g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0016g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0017g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0019g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0021g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0024g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0008g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0022g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0023g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0012g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0022t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0023t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0024t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0025t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0002 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0001 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0007g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0010g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0010g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0012t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0012t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0021t0020g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0005c0008t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0005c0008t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0005c0008t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0005c0008t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0007c0010t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0007c0010t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0008c0011t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0008c0011t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0009c0013t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0009c0013t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0010c0014t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0011c0031t0014g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0012c0016t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0013c0017t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0014c0018t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0015c0019t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0016c0020t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0017c0015t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0018c0027t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0019c0028t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0020c0026t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0021c0029t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0022c0030t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00099 | hp2 | a0002 | c0005 | t0001 | g0001 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0285 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00140 | hp2 | a0002 | c0005 | t0001 | g0046 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0373 | EUR | FIN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00323 | hp2 | a0003 | c0003 | t0010 | g0362 | EUR | FIN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00408 | hp2 | a0020 | c0026 | t0001 | g0222 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00423 | hp2 | a0004 | c0007 | t0004 | g0212 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00438 | hp1 | a0004 | c0007 | t0004 | g0007 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00438 | hp2 | a0004 | c0007 | t0001 | g0019 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00544 | hp2 | a0001 | c0004 | t0002 | g0008 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0364 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00621 | hp1 | a0001 | c0004 | t0002 | g0253 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0363 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00642 | hp1 | a0001 | c0001 | t0011 | g0188 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00642 | hp2 | a0003 | c0003 | t0010 | g0361 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00673 | hp2 | a0004 | c0007 | t0001 | g0158 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00735 | hp1 | a0001 | c0001 | t0019 | g0114 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00735 | hp2 | a0003 | c0003 | t0001 | g0029 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00738 | hp1 | a0002 | c0005 | t0001 | g0097 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01069 | hp1 | a0003 | c0003 | t0001 | g0352 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0312 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01074 | hp2 | a0015 | c0019 | t0001 | g0101 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01099 | hp2 | a0002 | c0005 | t0001 | g0100 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01106 | hp1 | a0003 | c0012 | t0005 | g0310 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0291 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01109 | hp2 | a0001 | c0022 | t0001 | g0174 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01167 | hp1 | a0002 | c0005 | t0001 | g0099 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01168 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01169 | hp1 | a0001 | c0001 | t0013 | g0192 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01169 | hp2 | a0002 | c0005 | t0001 | g0001 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01175 | hp2 | a0001 | c0001 | t0017 | g0180 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01243 | hp1 | a0005 | c0008 | t0001 | g0027 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01243 | hp2 | a0001 | c0006 | t0012 | g0038 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01255 | hp2 | a0002 | c0005 | t0001 | g0048 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01256 | hp1 | a0002 | c0005 | t0001 | g0010 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0292 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0288 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01346 | hp2 | a0002 | c0005 | t0001 | g0010 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01358 | hp1 | a0003 | c0021 | t0020 | g0337 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0320 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0349 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01496 | hp2 | a0022 | c0030 | t0001 | g0045 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01515 | hp1 | a0003 | c0003 | t0001 | g0360 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01515 | hp2 | a0002 | c0005 | t0001 | g0001 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0359 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01884 | hp1 | a0002 | c0005 | t0001 | g0095 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01884 | hp2 | a0005 | c0008 | t0001 | g0028 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01891 | hp1 | a0016 | c0020 | t0001 | g0282 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0351 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0350 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0333 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02040 | hp2 | a0003 | c0003 | t0001 | g0328 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02055 | hp2 | a0005 | c0008 | t0001 | g0300 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02056 | hp1 | a0001 | c0004 | t0002 | g0241 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0315 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02071 | hp2 | a0002 | c0005 | t0001 | g0018 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0317 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02080 | hp1 | a0012 | c0016 | t0001 | g0372 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02083 | hp1 | a0004 | c0007 | t0001 | g0019 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0334 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02129 | hp1 | a0002 | c0005 | t0001 | g0018 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02132 | hp2 | a0001 | c0004 | t0002 | g0245 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0322 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02145 | hp2 | a0001 | c0024 | t0001 | g0172 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0339 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02257 | hp1 | a0001 | c0025 | t0001 | g0225 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0055 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0316 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0029 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0276 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02572 | hp1 | a0006 | c0009 | t0001 | g0105 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02572 | hp2 | a0001 | c0001 | t0024 | g0237 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02602 | hp1 | a0002 | c0005 | t0001 | g0091 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0355 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02615 | hp1 | a0003 | c0012 | t0005 | g0309 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02615 | hp2 | a0001 | c0006 | t0018 | g0294 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02622 | hp2 | a0006 | c0009 | t0001 | g0107 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02630 | hp2 | a0006 | c0009 | t0001 | g0106 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02698 | hp2 | a0002 | c0005 | t0001 | g0092 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02717 | hp1 | a0001 | c0006 | t0012 | g0037 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02723 | hp2 | a0008 | c0011 | t0006 | g0304 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0356 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02735 | hp2 | a0002 | c0005 | t0001 | g0001 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0354 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0280 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02809 | hp2 | a0005 | c0008 | t0001 | g0027 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02895 | hp2 | a0003 | c0003 | t0005 | g0308 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02896 | hp1 | a0003 | c0003 | t0007 | g0347 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02897 | hp2 | a0003 | c0003 | t0007 | g0348 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02922 | hp1 | a0006 | c0009 | t0001 | g0032 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02965 | hp2 | a0001 | c0006 | t0001 | g0053 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02970 | hp1 | a0005 | c0008 | t0001 | g0301 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0050 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0330 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03041 | hp1 | a0001 | c0006 | t0001 | g0051 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03041 | hp2 | a0001 | c0001 | t0021 | g0136 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03098 | hp1 | a0014 | c0018 | t0006 | g0305 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03130 | hp1 | a0008 | c0011 | t0006 | g0306 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0274 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03195 | hp1 | a0001 | c0006 | t0001 | g0054 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0049 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0289 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03239 | hp2 | a0001 | c0023 | t0001 | g0022 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03453 | hp2 | a0011 | c0031 | t0014 | g0296 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03486 | hp1 | a0001 | c0006 | t0001 | g0108 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03490 | hp1 | a0002 | c0005 | t0001 | g0089 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0370 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03492 | hp1 | a0002 | c0005 | t0001 | g0088 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0369 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03516 | hp1 | a0018 | c0027 | t0001 | g0056 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03516 | hp2 | a0006 | c0009 | t0001 | g0031 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03579 | hp2 | a0003 | c0003 | t0007 | g0346 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03669 | hp1 | a0002 | c0005 | t0001 | g0096 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0335 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03688 | hp2 | a0002 | c0005 | t0001 | g0094 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03704 | hp1 | a0003 | c0003 | t0001 | g0336 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03927 | hp1 | a0001 | c0004 | t0002 | g0252 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04115 | hp1 | a0002 | c0005 | t0001 | g0104 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0357 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0340 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04199 | hp2 | a0002 | c0005 | t0001 | g0103 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04204 | hp1 | a0002 | c0005 | t0001 | g0093 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04204 | hp2 | a0002 | c0005 | t0001 | g0090 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04228 | hp1 | a0002 | c0005 | t0001 | g0102 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18522 | hp1 | a0003 | c0003 | t0001 | g0368 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0284 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18612 | hp1 | a0001 | c0004 | t0002 | g0265 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18747 | hp1 | a0013 | c0017 | t0001 | g0345 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18906 | hp1 | a0005 | c0008 | t0001 | g0028 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18939 | hp2 | a0001 | c0004 | t0002 | g0264 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18940 | hp2 | a0004 | c0007 | t0004 | g0007 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18941 | hp2 | a0001 | c0004 | t0002 | g0255 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18944 | hp1 | a0001 | c0001 | t0015 | g0130 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18944 | hp2 | a0002 | c0002 | t0003 | g0081 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18945 | hp2 | a0001 | c0004 | t0002 | g0250 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0338 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18947 | hp1 | a0001 | c0004 | t0002 | g0257 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18950 | hp1 | a0001 | c0004 | t0002 | g0263 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0323 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18951 | hp2 | a0009 | c0013 | t0001 | g0181 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18952 | hp2 | a0004 | c0007 | t0004 | g0135 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0353 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18957 | hp2 | a0001 | c0004 | t0002 | g0243 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0365 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18960 | hp1 | a0001 | c0004 | t0002 | g0261 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18961 | hp1 | a0002 | c0002 | t0003 | g0230 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18962 | hp1 | a0001 | c0004 | t0002 | g0242 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18963 | hp1 | a0004 | c0007 | t0004 | g0007 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18963 | hp2 | a0007 | c0010 | t0001 | g0147 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18965 | hp1 | a0003 | c0003 | t0001 | g0342 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18967 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0367 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18972 | hp1 | a0001 | c0004 | t0002 | g0268 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18973 | hp1 | a0003 | c0003 | t0001 | g0313 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18973 | hp2 | a0001 | c0004 | t0002 | g0026 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18977 | hp2 | a0007 | c0010 | t0001 | g0226 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18978 | hp1 | a0003 | c0003 | t0001 | g0324 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18978 | hp2 | a0001 | c0004 | t0023 | g0267 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18979 | hp1 | a0001 | c0004 | t0008 | g0270 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0329 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18982 | hp2 | a0001 | c0004 | t0002 | g0262 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18983 | hp1 | a0002 | c0002 | t0003 | g0082 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0326 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18999 | hp1 | a0001 | c0004 | t0002 | g0254 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19000 | hp1 | a0004 | c0007 | t0004 | g0162 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0321 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19005 | hp1 | a0001 | c0004 | t0002 | g0008 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19006 | hp2 | a0001 | c0004 | t0022 | g0246 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19007 | hp1 | a0001 | c0004 | t0002 | g0008 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19009 | hp1 | a0003 | c0003 | t0001 | g0318 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0343 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19012 | hp1 | a0001 | c0004 | t0002 | g0026 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19012 | hp2 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19030 | hp2 | a0002 | c0002 | t0009 | g0034 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0298 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19043 | hp2 | a0001 | c0006 | t0001 | g0040 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19055 | hp1 | a0003 | c0003 | t0001 | g0331 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19055 | hp2 | a0017 | c0015 | t0008 | g0259 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0371 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19056 | hp2 | a0010 | c0014 | t0002 | g0266 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19057 | hp1 | a0003 | c0003 | t0001 | g0327 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19057 | hp2 | a0009 | c0013 | t0001 | g0139 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0341 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19062 | hp1 | a0001 | c0004 | t0002 | g0249 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19064 | hp1 | a0001 | c0004 | t0002 | g0260 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19068 | hp2 | a0001 | c0004 | t0002 | g0256 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0325 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0366 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19077 | hp2 | a0021 | c0029 | t0001 | g0155 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19079 | hp1 | a0001 | c0004 | t0002 | g0247 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19080 | hp1 | a0004 | c0007 | t0001 | g0202 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19080 | hp2 | a0001 | c0004 | t0002 | g0269 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19081 | hp1 | a0001 | c0004 | t0002 | g0248 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0332 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19085 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19086 | hp2 | a0001 | c0004 | t0002 | g0258 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19088 | hp1 | a0001 | c0004 | t0002 | g0244 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0344 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19240 | hp1 | a0002 | c0002 | t0009 | g0033 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20129 | hp1 | a0001 | c0006 | t0001 | g0039 | AFR | ASW | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0062 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20805 | hp1 | a0002 | c0005 | t0001 | g0001 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0358 | SAS | GIH | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0319 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02486 | hp1 | a0002 | c0005 | t0001 | g0047 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0275 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02559 | hp1 | a0019 | c0028 | t0001 | g0057 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03471 | hp1 | a0001 | c0006 | t0001 | g0052 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18955 | hp1 | a0001 | c0004 | t0002 | g0251 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20300 | hp1 | a0002 | c0005 | t0001 | g0098 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA21309 | hp1 | a0003 | c0003 | t0005 | g0307 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0287 | REF | REF | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
homoSapiens_grch38 | hp1 | a0002 | c0005 | t0001 | g0036 | REF | REF | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:838923
|
G | A | 1 | a0010 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.203G>A | p.Gly68Asp | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 252/4010 | 203/2358 | 68/785 | chr7 | 838923 | ||
chr7:838946
|
G | T | 1 | a0011 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.226G>T | p.Gly76Cys | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 275/4010 | 226/2358 | 76/785 | chr7 | 838946 | ||
chr7:838947
|
G | C | 1 | a0007 | 2 | NA18963.hp2 NA18977.hp2 |
missense_variant | MODERATE | c.227G>C | p.Gly76Ala | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 276/4010 | 227/2358 | 76/785 | chr7 | 838947 | ||
chr7:838977
|
G | C | 1 | a0012 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.257G>C | p.Arg86Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 306/4010 | 257/2358 | 86/785 | chr7 | 838977 | ||
chr7:841957
|
A | C | 1 | a0006 | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.278A>C | p.Gln93Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 327/4010 | 278/2358 | 93/785 | chr7 | 841957 | ||
chr7:841960
|
G | A | 1 | a0013 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.281G>A | p.Arg94His | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 330/4010 | 281/2358 | 94/785 | chr7 | 841960 | ||
chr7:842031
|
C | T | 14 | a0001a0004a0005others(11): Show | 220 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(217): Show |
missense_variant | MODERATE | c.352C>T | p.His118Tyr | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 401/4010 | 352/2358 | 118/785 | chr7 | 842031 | ||
chr7:843451
|
G | A | 2 | a0008a0014 | 3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.589G>A | p.Val197Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/19 | 638/4010 | 589/2358 | 197/785 | chr7 | 843451 | ||
chr7:851470
|
G | A | 1 | a0009 | 2 | NA18951.hp2 NA19057.hp2 |
missense_variant | MODERATE | c.745G>A | p.Val249Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/19 | 794/4010 | 745/2358 | 249/785 | chr7 | 851470 | ||
chr7:852644
|
TCATCCCA others(12): Show |
T | 1 | a0017 | 1 | NA19055.hp2 | frameshift_variant | HIGH | c.889_907delATCCCACT others(11): Show |
p.Ile297fs | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/19 | 938/4010 | 889/2358 | 297/785 | INFO_REALIGN_3_PRIME | chr7 | 852644 | |
chr7:853488
|
A | G | 1 | a0022 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1133A>G | p.His378Arg | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/19 | 1182/4010 | 1133/2358 | 378/785 | chr7 | 853488 | ||
chr7:856386
|
A | T | 1 | a0021 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.1379A>T | p.Lys460Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/19 | 1428/4010 | 1379/2358 | 460/785 | chr7 | 856386 | ||
chr7:857859
|
G | A | 3 | a0003a0013a0020 | 66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
missense_variant | MODERATE | c.1426G>A | p.Glu476Lys | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/19 | 1475/4010 | 1426/2358 | 476/785 | chr7 | 857859 | ||
chr7:860183
|
G | T | 2 | a0004a0021 | 11 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(8): Show |
missense_variant | MODERATE | c.1580G>T | p.Gly527Val | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1629/4010 | 1580/2358 | 527/785 | chr7 | 860183 | ||
chr7:860249
|
C | T | 1 | a0005 | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
missense_variant | MODERATE | c.1646C>T | p.Thr549Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1695/4010 | 1646/2358 | 549/785 | chr7 | 860249 | ||
chr7:860279
|
T | C | 1 | a0016 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1676T>C | p.Leu559Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1725/4010 | 1676/2358 | 559/785 | chr7 | 860279 | ||
chr7:860363
|
C | T | 1 | a0019 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1760C>T | p.Ala587Val | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1809/4010 | 1760/2358 | 587/785 | chr7 | 860363 | ||
chr7:861461
|
G | A | 1 | a0014 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1861G>A | p.Gly621Ser | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/19 | 1910/4010 | 1861/2358 | 621/785 | chr7 | 861461 | ||
chr7:869482
|
A | G | 1 | a0018 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2114A>G | p.Asn705Ser | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/19 | 2163/4010 | 2114/2358 | 705/785 | chr7 | 869482 | ||
chr7:873317
|
G | A | 1 | a0015 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2344G>A | p.Glu782Lys | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 2393/4010 | 2344/2358 | 782/785 | chr7 | 873317 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:838834
|
G | A | 3 | a0001c0004a0010c0014a0017c0015 | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
synonymous_variant | LOW | c.114G>A | p.Thr38Thr | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 163/4010 | 114/2358 | 38/785 | chr7 | 838834 | ||
chr7:842045
|
C | T | 1 | a0003c0021 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.366C>T | p.Val122Val | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 415/4010 | 366/2358 | 122/785 | chr7 | 842045 | ||
chr7:843468
|
C | T | 3 | a0003c0012a0008c0011a0014c0018 | 5 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.606C>T | p.Pro202Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/19 | 655/4010 | 606/2358 | 202/785 | chr7 | 843468 | ||
chr7:857831
|
G | A | 1 | a0001c0022 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1398G>A | p.Ala466Ala | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/19 | 1447/4010 | 1398/2358 | 466/785 | chr7 | 857831 | ||
chr7:857855
|
A | G | 15 | a0001c0004a0001c0006a0002c0002others(12): Show | 217 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(214): Show |
synonymous_variant | LOW | c.1422A>G | p.Thr474Thr | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/19 | 1471/4010 | 1422/2358 | 474/785 | chr7 | 857855 | ||
chr7:869411
|
G | A | 3 | a0001c0004a0010c0014a0017c0015 | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
synonymous_variant | LOW | c.2043G>A | p.Arg681Arg | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/19 | 2092/4010 | 2043/2358 | 681/785 | chr7 | 869411 | ||
chr7:869435
|
C | T | 1 | a0001c0025 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.2067C>T | p.Ala689Ala | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/19 | 2116/4010 | 2067/2358 | 689/785 | chr7 | 869435 | ||
chr7:872560
|
C | T | 1 | a0001c0024 | 1 | HG02145.hp2 | splice_region_variant&synonymous_variant | LOW | c.2239C>T | p.Leu747Leu | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/19 | 2288/4010 | 2239/2358 | 747/785 | chr7 | 872560 | ||
chr7:873223
|
C | T | 1 | a0001c0023 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.2250C>T | p.Pro750Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 2299/4010 | 2250/2358 | 750/785 | chr7 | 873223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:873355
|
C | T | 1 | a0004c0007t0004 | 6 | HG00423.hp2 HG00438.hp1 NA18940.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 24 | chr7 | 873355 | |||||
chr7:873419
|
T | C | 2 | a0001c0004t0008a0017c0015t0008 | 2 | NA18979.hp1 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*88T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 88 | chr7 | 873419 | |||||
chr7:873483
|
C | T | 1 | a0003c0003t0007 | 3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*152C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 152 | chr7 | 873483 | |||||
chr7:873495
|
C | T | 1 | a0001c0001t0024 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 164 | chr7 | 873495 | |||||
chr7:873554
|
C | G | 1 | a0001c0001t0013 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*223C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 223 | chr7 | 873554 | |||||
chr7:873566
|
G | A | 1 | a0011c0031t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*235G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 235 | chr7 | 873566 | |||||
chr7:873580
|
C | T | 1 | a0001c0004t0023 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 249 | chr7 | 873580 | |||||
chr7:873592
|
A | T | 1 | a0001c0004t0022 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 261 | chr7 | 873592 | |||||
chr7:873594
|
C | T | 1 | a0001c0006t0012 | 2 | HG01243.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*263C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 263 | chr7 | 873594 | |||||
chr7:873595
|
G | T | 4 | a0003c0003t0005a0003c0012t0005a0008c0011t0006others(1): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 264 | chr7 | 873595 | |||||
chr7:873815
|
G | A | 6 | a0001c0004t0002a0001c0004t0008a0001c0004t0022others(3): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*484G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 484 | chr7 | 873815 | |||||
chr7:873844
|
T | G | 1 | a0001c0006t0012 | 2 | HG01243.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*513T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 513 | chr7 | 873844 | |||||
chr7:873874
|
A | G | 1 | a0001c0001t0011 | 2 | HG00323.hp1 HG00642.hp1 |
3_prime_UTR_variant | MODIFIER | c.*543A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 543 | chr7 | 873874 | |||||
chr7:873972
|
T | G | 2 | a0003c0003t0005a0003c0012t0005 | 4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*641T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 641 | chr7 | 873972 | |||||
chr7:874100
|
A | T | 1 | a0001c0001t0021 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*769A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 769 | chr7 | 874100 | |||||
chr7:874111
|
G | A | 1 | a0002c0002t0009 | 2 | NA19030.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*780G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 780 | chr7 | 874111 | |||||
chr7:874124
|
G | T | 1 | a0003c0021t0020 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 793 | chr7 | 874124 | |||||
chr7:874161
|
G | A | 1 | a0002c0002t0003 | 10 | NA18943.hp2 NA18944.hp2 NA18961.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*830G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 830 | chr7 | 874161 | |||||
chr7:874215
|
G | T | 1 | a0001c0001t0019 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*884G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 884 | chr7 | 874215 | |||||
chr7:874220
|
C | T | 1 | a0001c0006t0018 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 889 | chr7 | 874220 | |||||
chr7:874221
|
G | A | 1 | a0003c0003t0010 | 2 | HG00323.hp2 HG00642.hp2 |
3_prime_UTR_variant | MODIFIER | c.*890G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 890 | chr7 | 874221 | |||||
chr7:874370
|
C | T | 1 | a0001c0001t0017 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1039C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1039 | chr7 | 874370 | |||||
chr7:874849
|
A | G | 1 | a0001c0001t0016 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1518A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1518 | chr7 | 874849 | |||||
chr7:874899
|
A | C | 1 | a0001c0001t0015 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1568 | chr7 | 874899 | |||||
chr7:874916
|
C | T | 1 | a0011c0031t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1585C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1585 | chr7 | 874916 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:832618
|
A | T | 1 | a0001c0001t0011g0373 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.77+17A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832618 | ||||||
chr7:832657
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77+56G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832657 | ||||||
chr7:832661
|
G | A | 2 | a0006c0009t0001g0031a0006c0009t0001g0032 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.77+60G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832661 | ||||||
chr7:832694
|
C | T | 1 | a0012c0016t0001g0372 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.77+93C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832694 | ||||||
chr7:832750
|
T | G | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.77+149T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832750 | ||||||
chr7:832813
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+212G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832813 | ||||||
chr7:832875
|
G | T | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.77+274G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832875 | ||||||
chr7:832993
|
C | T | 1 | a0002c0002t0001g0371 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.77+392C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832993 | ||||||
chr7:833021
|
A | G | 68 | a0001c0001t0001g0314a0003c0003t0001g0029a0003c0003t0001g0311others(65): Show | 69 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.77+420A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833021 | ||||||
chr7:833140
|
A | G | 288 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(285): Show | 315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.77+539A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833140 | ||||||
chr7:833169
|
A | G | 1 | a0002c0002t0001g0016 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.77+568A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833169 | ||||||
chr7:833211
|
G | A | 147 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(144): Show | 159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.77+610G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833211 | ||||||
chr7:833306
|
C | CT | 149 | a0001c0001t0001g0314a0001c0006t0001g0039a0001c0006t0001g0040others(146): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.77+719dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 833306 | |||||
chr7:833306
|
CT | C | 216 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(213): Show | 242 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.77+719delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 833306 | |||||
chr7:833320
|
T | C | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.77+719T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833320 | ||||||
chr7:833321
|
C | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.77+720C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833321 | ||||||
chr7:833322
|
G | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.77+721G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833322 | ||||||
chr7:833386
|
C | A | 1 | a0001c0006t0001g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.77+785C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833386 | ||||||
chr7:833467
|
C | T | 220 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(217): Show | 246 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.77+866C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833467 | ||||||
chr7:833477
|
A | T | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.77+876A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833477 | ||||||
chr7:833483
|
G | A | 1 | a0001c0006t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.77+882G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833483 | ||||||
chr7:833515
|
G | T | 290 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(287): Show | 317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.77+914G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833515 | ||||||
chr7:833555
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.77+954C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833555 | ||||||
chr7:833758
|
C | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(186): Show | 212 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.77+1157C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833758 | ||||||
chr7:833776
|
C | T | 1 | a0001c0001t0024g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+1175C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833776 | ||||||
chr7:833783
|
C | T | 1 | a0002c0002t0001g0302 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.77+1182C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833783 | ||||||
chr7:833836
|
TGCTGCTT others(6): Show |
T | 68 | a0001c0001t0001g0314a0003c0003t0001g0029a0003c0003t0001g0311others(65): Show | 69 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.77+1237_77+1249del others(13): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 833836 | |||||
chr7:833887
|
T | C | 1 | a0002c0002t0001g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.77+1286T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833887 | ||||||
chr7:833973
|
A | G | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+1372A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833973 | ||||||
chr7:834012
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.77+1411C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834012 | ||||||
chr7:834070
|
T | TTGTAGGC others(46): Show |
139 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(136): Show | 152 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.77+1516_77+1568dup others(53): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834070 | |||||
chr7:834070
|
TTGTAGGC others(46): Show |
T | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.77+1516_77+1568del others(53): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834070 | |||||
chr7:834117
|
T | TGGATGGT others(46): Show |
17 | a0001c0001t0001g0017a0001c0001t0001g0109a0001c0001t0001g0110others(14): Show | 18 | HG00099.hp1 HG00735.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+1597_77+1649dup others(53): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834117 | |||||
chr7:834118
|
G | A | 2 | a0002c0002t0001g0042a0002c0002t0001g0043 | 2 | NA18984.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.77+1517G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834118 | ||||||
chr7:834150
|
C | T | 5 | a0006c0009t0001g0031a0006c0009t0001g0032a0006c0009t0001g0105others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+1549C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834150 | ||||||
chr7:834224
|
G | A | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+1623G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834224 | ||||||
chr7:834258
|
C | T | 291 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(288): Show | 318 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.77+1657C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834258 | ||||||
chr7:834557
|
A | C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+1956A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834557 | ||||||
chr7:834607
|
T | C | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+2006T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834607 | ||||||
chr7:834629
|
G | C | 220 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(217): Show | 246 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.77+2028G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834629 | ||||||
chr7:834639
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0234a0001c0001t0001g0235 | 4 | HG01192.hp1 HG02055.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+2038C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834639 | ||||||
chr7:834661
|
G | A | 4 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(1): Show | 4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+2060G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834661 | ||||||
chr7:834736
|
G | C | 1 | a0001c0001t0001g0025 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.77+2135G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834736 | ||||||
chr7:834775
|
A | AT | 31 | a0001c0006t0001g0108a0002c0002t0001g0002a0002c0002t0001g0005others(28): Show | 40 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.77+2182dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834775 | |||||
chr7:834839
|
G | C | 1 | a0002c0002t0009g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.77+2238G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834839 | ||||||
chr7:835002
|
A | G | 103 | a0001c0001t0001g0314a0001c0004t0002g0008a0001c0004t0002g0026others(100): Show | 107 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.77+2401A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835002 | ||||||
chr7:835095
|
A | T | 68 | a0001c0001t0001g0314a0003c0003t0001g0029a0003c0003t0001g0311others(65): Show | 69 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.77+2494A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835095 | ||||||
chr7:835101
|
T | G | 1 | a0002c0002t0001g0044 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.77+2500T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835101 | ||||||
chr7:835199
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.77+2598C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835199 | ||||||
chr7:835242
|
CACGGGTT others(6): Show |
C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2642_77+2654del others(13): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835242 | ||||||
chr7:835256
|
C | T | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2655C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835256 | ||||||
chr7:835257
|
C | G | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2656C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835257 | ||||||
chr7:835259
|
G | A | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2658G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835259 | ||||||
chr7:835551
|
T | C | 2 | a0001c0006t0018g0294a0022c0030t0001g0045 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.77+2950T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835551 | ||||||
chr7:835560
|
A | T | 1 | a0012c0016t0001g0372 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.77+2959A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835560 | ||||||
chr7:835579
|
C | G | 31 | a0001c0006t0001g0108a0002c0002t0001g0002a0002c0002t0001g0005others(28): Show | 40 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.77+2978C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835579 | ||||||
chr7:835748
|
C | T | 2 | a0003c0003t0001g0369a0003c0003t0001g0370 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.78-3050C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835748 | ||||||
chr7:835923
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.78-2875C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835923 | ||||||
chr7:835968
|
G | T | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-2830G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835968 | ||||||
chr7:836020
|
G | A | 33 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(30): Show | 36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-2778G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836020 | ||||||
chr7:836026
|
G | A | 4 | a0002c0005t0001g0010a0002c0005t0001g0046a0002c0005t0001g0047others(1): Show | 5 | HG00140.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-2772G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836026 | ||||||
chr7:836034
|
C | T | 1 | a0001c0004t0008g0270 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.78-2764C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836034 | ||||||
chr7:836147
|
G | A | 352 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(349): Show | 390 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(387): Show |
intron_variant | MODIFIER | c.78-2651G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836147 | ||||||
chr7:836240
|
G | T | 1 | a0001c0001t0001g0231 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.78-2558G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836240 | ||||||
chr7:836305
|
C | G | 46 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(43): Show | 56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-2493C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836305 | ||||||
chr7:836348
|
C | T | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78-2450C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836348 | ||||||
chr7:836363
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.78-2435A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836363 | ||||||
chr7:836478
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.78-2320A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836478 | ||||||
chr7:836590
|
C | T | 146 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(143): Show | 158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.78-2208C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836590 | ||||||
chr7:836888
|
C | T | 65 | a0001c0001t0001g0314a0003c0003t0001g0029a0003c0003t0001g0312others(62): Show | 66 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.78-1910C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836888 | ||||||
chr7:836902
|
C | T | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-1896C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836902 | ||||||
chr7:837033
|
G | A | 1 | a0003c0003t0001g0312 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.78-1765G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837033 | ||||||
chr7:837041
|
T | C | 46 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(43): Show | 56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-1757T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837041 | ||||||
chr7:837256
|
T | C | 1 | a0002c0005t0001g0018 | 2 | HG02071.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.78-1542T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837256 | ||||||
chr7:837275
|
G | A | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78-1523G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837275 | ||||||
chr7:837342
|
G | A | 1 | a0003c0003t0001g0313 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.78-1456G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837342 | ||||||
chr7:837437
|
TCAATTTT others(16): Show |
T | 1 | a0002c0002t0009g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-1357_78-1335del others(23): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 837437 | |||||
chr7:837444
|
T | C | 61 | a0001c0001t0001g0314a0003c0003t0001g0029a0003c0003t0001g0311others(58): Show | 62 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.78-1354T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837444 | ||||||
chr7:837474
|
A | T | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-1324A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837474 | ||||||
chr7:837501
|
A | T | 1 | a0001c0001t0001g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.78-1297A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837501 | ||||||
chr7:837519
|
A | G | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-1279A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837519 | ||||||
chr7:837638
|
A | G | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-1160A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837638 | ||||||
chr7:837848
|
A | G | 2 | a0002c0002t0001g0016a0002c0002t0001g0058 | 3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.78-950A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837848 | ||||||
chr7:837885
|
C | G | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.78-913C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837885 | ||||||
chr7:838178
|
T | A | 33 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(30): Show | 36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-620T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838178 | ||||||
chr7:838206
|
C | G | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.78-592C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838206 | ||||||
chr7:838212
|
C | G | 2 | a0002c0002t0001g0009a0002c0002t0001g0293 | 4 | HG02258.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-586C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838212 | ||||||
chr7:838394
|
A | C | 6 | a0002c0005t0001g0010a0002c0005t0001g0046a0002c0005t0001g0047others(3): Show | 7 | HG00140.hp2 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-404A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838394 | ||||||
chr7:838401
|
G | A | 1 | a0022c0030t0001g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.78-397G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838401 | ||||||
chr7:838431
|
G | T | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-367G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838431 | ||||||
chr7:838483
|
G | A | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78-315G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838483 | ||||||
chr7:838624
|
A | G | 2 | a0002c0002t0001g0016a0002c0002t0001g0058 | 3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.78-174A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838624 | ||||||
chr7:838652
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.78-146G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838652 | ||||||
chr7:838795
|
T | C | 9 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG02040.hp1 HG02698.hp1 NA18944.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.78-3T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838795 | ||||||
chr7:839109
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+123G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839109 | ||||||
chr7:839130
|
T | C | 289 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(286): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.266+144T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839130 | ||||||
chr7:839161
|
G | A | 1 | a0001c0006t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266+175G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839161 | ||||||
chr7:839341
|
A | C | 2 | a0001c0006t0018g0294a0022c0030t0001g0045 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.266+355A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839341 | ||||||
chr7:839366
|
G | A | 1 | a0004c0007t0004g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.266+380G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839366 | ||||||
chr7:839436
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.266+450A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839436 | ||||||
chr7:839478
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+492G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839478 | ||||||
chr7:839515
|
AGCTGGGA others(296): Show |
A | 191 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(188): Show | 208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.266+534_266+836del | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 839515 | |||||
chr7:839558
|
C | CT | 7 | a0001c0006t0018g0294a0002c0002t0001g0041a0002c0002t0001g0044others(4): Show | 7 | HG02027.hp1 HG02132.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+581dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 839558 | |||||
chr7:839585
|
C | T | 1 | a0003c0003t0001g0368 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.266+599C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839585 | ||||||
chr7:839601
|
G | T | 2 | a0003c0003t0001g0366a0003c0003t0001g0367 | 2 | NA18968.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.266+615G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839601 | ||||||
chr7:839664
|
T | C | 67 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(64): Show | 68 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.266+678T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839664 | ||||||
chr7:839744
|
G | A | 1 | a0003c0003t0001g0368 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.266+758G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839744 | ||||||
chr7:839899
|
C | G | 1 | a0001c0001t0001g0228 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.266+913C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839899 | ||||||
chr7:839936
|
G | A | 191 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(188): Show | 208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.266+950G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839936 | ||||||
chr7:839957
|
T | C | 1 | a0001c0004t0002g0241 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.266+971T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839957 | ||||||
chr7:839977
|
A | G | 1 | a0002c0002t0001g0016 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.266+991A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839977 | ||||||
chr7:840137
|
T | C | 2 | a0001c0006t0001g0049a0001c0006t0001g0050 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.266+1151T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840137 | ||||||
chr7:840228
|
C | T | 374 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(371): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.266+1242C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840228 | ||||||
chr7:840262
|
G | A | 1 | a0001c0001t0021g0136 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.266+1276G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840262 | ||||||
chr7:840270
|
G | A | 290 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(287): Show | 317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.266+1284G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840270 | ||||||
chr7:840306
|
C | A | 1 | a0003c0003t0001g0315 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.266+1320C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840306 | ||||||
chr7:840358
|
C | T | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+1372C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840358 | ||||||
chr7:840426
|
G | A | 1 | a0002c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.266+1440G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840426 | ||||||
chr7:840535
|
C | G | 46 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(43): Show | 56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.267-1411C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840535 | ||||||
chr7:840574
|
T | G | 46 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(43): Show | 56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.267-1372T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840574 | ||||||
chr7:840583
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.267-1363T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840583 | ||||||
chr7:840639
|
C | CT | 102 | a0001c0001t0001g0227a0001c0004t0002g0008a0001c0004t0002g0026others(99): Show | 107 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.267-1287dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | |||||
chr7:840639
|
C | CTT | 53 | a0001c0001t0016g0298a0001c0004t0002g0268a0001c0004t0002g0269others(50): Show | 64 | HG00558.hp1 HG00558.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.267-1288_267-1287d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | |||||
chr7:840639
|
CT | C | 7 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0273others(4): Show | 7 | HG00140.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.267-1287delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | |||||
chr7:840639
|
CTTTTT | C | 153 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(150): Show | 166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.267-1291_267-1287d others(7): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | |||||
chr7:840694
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(189): Show | 209 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.267-1252T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840694 | ||||||
chr7:840766
|
C | T | 5 | a0001c0001t0001g0224a0002c0002t0001g0061a0002c0002t0003g0081others(2): Show | 5 | NA18944.hp2 NA18967.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.267-1180C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840766 | ||||||
chr7:840861
|
C | T | 290 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(287): Show | 317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.267-1085C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840861 | ||||||
chr7:840912
|
A | T | 1 | a0002c0002t0001g0292 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.267-1034A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840912 | ||||||
chr7:840986
|
T | G | 60 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(57): Show | 61 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.267-960T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840986 | ||||||
chr7:840994
|
C | CG | 33 | a0001c0001t0001g0227a0001c0004t0002g0008a0001c0004t0002g0026others(30): Show | 36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.267-951dupG | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840994 | |||||
chr7:841011
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.267-935G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841011 | ||||||
chr7:841133
|
A | G | 7 | a0001c0001t0001g0123a0001c0001t0001g0218a0001c0001t0001g0219others(4): Show | 7 | HG00408.hp2 HG02015.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.267-813A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841133 | ||||||
chr7:841143
|
G | A | 2 | a0002c0005t0001g0088a0002c0005t0001g0089 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.267-803G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841143 | ||||||
chr7:841161
|
G | A | 1 | a0007c0010t0001g0226 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.267-785G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841161 | ||||||
chr7:841219
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.267-727C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841219 | ||||||
chr7:841244
|
A | AT | 156 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(153): Show | 168 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.267-685dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 841244 | |||||
chr7:841244
|
A | ATT | 39 | a0001c0001t0001g0214a0001c0001t0001g0227a0001c0004t0002g0008others(36): Show | 44 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.267-686_267-685dup others(2): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 841244 | |||||
chr7:841244
|
A | ATTT | 66 | a0001c0001t0001g0215a0001c0001t0001g0216a0003c0003t0001g0029others(63): Show | 67 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.267-687_267-685dup others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 841244 | |||||
chr7:841346
|
C | G | 67 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(64): Show | 68 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.267-600C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841346 | ||||||
chr7:841366
|
C | T | 1 | a0003c0003t0001g0365 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.267-580C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841366 | ||||||
chr7:841444
|
G | A | 289 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(286): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.267-502G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841444 | ||||||
chr7:841537
|
T | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.267-409T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841537 | ||||||
chr7:841643
|
G | T | 352 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(349): Show | 390 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(387): Show |
intron_variant | MODIFIER | c.267-303G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841643 | ||||||
chr7:841752
|
G | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG01106.hp2 HG01433.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.267-194G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841752 | ||||||
chr7:841858
|
C | G | 1 | a0001c0001t0001g0223 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.267-88C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841858 | ||||||
chr7:841884
|
A | G | 1 | a0002c0002t0001g0078 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.267-62A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841884 | ||||||
chr7:842207
|
G | T | 1 | a0003c0003t0001g0363 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.451+77G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842207 | ||||||
chr7:842221
|
C | T | 190 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(187): Show | 206 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.451+91C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842221 | ||||||
chr7:842327
|
A | T | 31 | a0001c0001t0001g0227a0001c0004t0002g0008a0001c0004t0002g0026others(28): Show | 34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.451+197A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842327 | ||||||
chr7:842398
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.451+268G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842398 | ||||||
chr7:842575
|
G | T | 4 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(1): Show | 4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+445G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842575 | ||||||
chr7:842581
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451+451G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842581 | ||||||
chr7:842613
|
G | A | 7 | a0001c0001t0001g0137a0001c0001t0001g0143a0001c0001t0001g0144others(4): Show | 7 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.451+483G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842613 | ||||||
chr7:842710
|
G | A | 8 | a0002c0002t0001g0274a0002c0002t0001g0275a0002c0002t0001g0276others(5): Show | 8 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-496G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842710 | ||||||
chr7:842810
|
G | C | 1 | a0001c0001t0016g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.452-396G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842810 | ||||||
chr7:842906
|
G | A | 61 | a0002c0002t0001g0281a0003c0003t0001g0029a0003c0003t0001g0311others(58): Show | 62 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-300G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842906 | ||||||
chr7:842989
|
G | A | 1 | a0002c0002t0001g0371 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.452-217G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842989 | ||||||
chr7:843122
|
T | C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.452-84T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 843122 | ||||||
chr7:843191
|
TG | T | 33 | a0001c0001t0001g0227a0001c0004t0002g0008a0001c0004t0002g0026others(30): Show | 36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.452-14delG | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 843191 | ||||||
chr7:843192
|
GT | G | 110 | a0001c0001t0001g0035a0001c0001t0001g0295a0001c0001t0001g0297others(107): Show | 122 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(119): Show |
splice_region_variant&intron_variant | LOW | c.452-3delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 843192 | |||||
chr7:843194
|
T | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0007c0010t0001g0147others(1): Show | 4 | NA18963.hp2 NA18968.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-12T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 843194 | ||||||
chr7:843255
|
C | G | 4 | a0003c0003t0001g0359a0003c0003t0001g0360a0003c0003t0010g0361others(1): Show | 4 | HG00323.hp2 HG00642.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+23C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 4/18 | chr7 | 843255 | ||||||
chr7:843258
|
C | G | 193 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.478+26C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 4/18 | chr7 | 843258 | ||||||
chr7:843641
|
A | G | 7 | a0003c0003t0001g0354a0003c0003t0001g0355a0003c0003t0001g0356others(4): Show | 7 | HG02602.hp2 HG02735.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.658+121A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843641 | ||||||
chr7:843685
|
C | A | 3 | a0008c0011t0006g0304a0008c0011t0006g0306a0014c0018t0006g0305 | 3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.658+165C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843685 | ||||||
chr7:843697
|
T | A | 5 | a0001c0001t0001g0227a0001c0004t0002g0247a0001c0004t0002g0248others(2): Show | 5 | NA19006.hp1 NA19006.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.658+177T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843697 | ||||||
chr7:843706
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.658+186T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843706 | ||||||
chr7:843865
|
G | C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+345G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843865 | ||||||
chr7:843943
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.658+423G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843943 | ||||||
chr7:844060
|
C | T | 2 | a0008c0011t0006g0304a0008c0011t0006g0306 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.658+540C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844060 | ||||||
chr7:844062
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0297a0001c0006t0018g0294others(1): Show | 4 | HG01496.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.658+542C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844062 | ||||||
chr7:844123
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.658+603G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844123 | ||||||
chr7:844306
|
C | G | 32 | a0001c0001t0001g0227a0001c0004t0002g0008a0001c0004t0002g0026others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.658+786C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844306 | ||||||
chr7:844333
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.658+813C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844333 | ||||||
chr7:844404
|
G | A | 3 | a0002c0005t0001g0090a0002c0005t0001g0091a0002c0005t0001g0092 | 3 | HG02602.hp1 HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.658+884G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844404 | ||||||
chr7:844420
|
G | A | 28 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.658+900G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844420 | ||||||
chr7:844517
|
G | A | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+997G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844517 | ||||||
chr7:844580
|
C | T | 5 | a0006c0009t0001g0031a0006c0009t0001g0032a0006c0009t0001g0105others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.658+1060C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844580 | ||||||
chr7:844642
|
G | A | 59 | a0001c0001t0001g0151a0003c0003t0001g0029a0003c0003t0001g0311others(56): Show | 60 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.658+1122G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844642 | ||||||
chr7:844668
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.658+1148G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844668 | ||||||
chr7:844685
|
T | A | 2 | a0002c0002t0001g0009a0002c0002t0001g0293 | 4 | HG02258.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.658+1165T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844685 | ||||||
chr7:844810
|
G | C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+1290G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844810 | ||||||
chr7:844925
|
C | A | 1 | a0003c0003t0001g0315 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.658+1405C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844925 | ||||||
chr7:844938
|
G | A | 1 | a0002c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.658+1418G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844938 | ||||||
chr7:844961
|
G | A | 1 | a0003c0003t0001g0318 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.658+1441G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844961 | ||||||
chr7:845028
|
A | G | 131 | a0001c0001t0001g0227a0001c0004t0002g0008a0001c0004t0002g0026others(128): Show | 145 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.658+1508A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845028 | ||||||
chr7:845067
|
A | G | 163 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(160): Show | 179 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.658+1547A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845067 | ||||||
chr7:845092
|
T | C | 1 | a0001c0025t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.658+1572T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845092 | ||||||
chr7:845106
|
C | T | 161 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(158): Show | 176 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.658+1586C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845106 | ||||||
chr7:845149
|
T | G | 1 | a0002c0005t0001g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.658+1629T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845149 | ||||||
chr7:845178
|
A | G | 2 | a0002c0002t0001g0016a0002c0002t0001g0058 | 3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.658+1658A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845178 | ||||||
chr7:845306
|
G | A | 3 | a0002c0002t0001g0274a0002c0002t0001g0275a0002c0002t0001g0276 | 3 | HG02451.hp2 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.658+1786G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845306 | ||||||
chr7:845332
|
T | G | 3 | a0002c0002t0001g0011a0002c0002t0001g0064a0002c0002t0001g0065 | 4 | NA18946.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.658+1812T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845332 | ||||||
chr7:845364
|
C | G | 1 | a0005c0008t0001g0028 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.658+1844C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845364 | ||||||
chr7:845402
|
C | G | 2 | a0002c0005t0001g0103a0002c0005t0001g0104 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.658+1882C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845402 | ||||||
chr7:845444
|
T | C | 1 | a0005c0008t0001g0028 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.658+1924T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845444 | ||||||
chr7:845765
|
A | G | 47 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(44): Show | 57 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(54): Show |
intron_variant | MODIFIER | c.658+2245A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845765 | ||||||
chr7:845907
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.658+2387G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845907 | ||||||
chr7:845926
|
C | T | 2 | a0001c0006t0018g0294a0022c0030t0001g0045 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.658+2406C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845926 | ||||||
chr7:845947
|
G | A | 1 | a0001c0006t0012g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.658+2427G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845947 | ||||||
chr7:845960
|
G | C | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.658+2440G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845960 | ||||||
chr7:846059
|
A | G | 21 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(18): Show | 30 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.658+2539A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846059 | ||||||
chr7:846202
|
G | A | 1 | a0003c0003t0005g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.658+2682G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846202 | ||||||
chr7:846211
|
C | T | 1 | a0004c0007t0004g0212 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.658+2691C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846211 | ||||||
chr7:846253
|
C | T | 67 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(64): Show | 68 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.658+2733C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846253 | ||||||
chr7:846265
|
T | C | 1 | a0003c0003t0001g0319 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.658+2745T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846265 | ||||||
chr7:846289
|
C | A | 287 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(284): Show | 314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.658+2769C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846289 | ||||||
chr7:846527
|
A | T | 31 | a0001c0001t0001g0227a0001c0004t0002g0008a0001c0004t0002g0026others(28): Show | 34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.658+3007A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846527 | ||||||
chr7:846602
|
C | T | 28 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.658+3082C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846602 | ||||||
chr7:846746
|
A | G | 223 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(220): Show | 249 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.658+3226A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846746 | ||||||
chr7:846905
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.658+3385T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846905 | ||||||
chr7:846930
|
C | T | 1 | a0001c0025t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.658+3410C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846930 | ||||||
chr7:846962
|
A | G | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0207others(3): Show | 8 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.658+3442A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846962 | ||||||
chr7:847004
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3492_658+3493i others(12): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847004 | |||||
chr7:847013
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3493T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847013 | ||||||
chr7:847014
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3494T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847014 | ||||||
chr7:847015
|
A | T | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+3495A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847015 | ||||||
chr7:847020
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3500T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847020 | ||||||
chr7:847206
|
G | A | 1 | a0002c0002t0001g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.658+3686G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847206 | ||||||
chr7:847215
|
G | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0203a0001c0001t0001g0204others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.658+3695G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847215 | ||||||
chr7:847254
|
G | A | 1 | a0001c0006t0012g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.658+3734G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847254 | ||||||
chr7:847255
|
G | GTCCCCTG others(137): Show |
1 | a0003c0003t0001g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.658+3759_658+3902d others(146): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847255 | |||||
chr7:847282
|
G | A | 30 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(27): Show | 39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.658+3762G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847282 | ||||||
chr7:847351
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.658+3831G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847351 | ||||||
chr7:847373
|
G | T | 2 | a0008c0011t0006g0304a0008c0011t0006g0306 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.658+3853G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847373 | ||||||
chr7:847382
|
G | A | 2 | a0003c0003t0001g0319a0003c0003t0001g0320 | 2 | HG01123.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.658+3862G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847382 | ||||||
chr7:847396
|
G | A | 58 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(55): Show | 59 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.658+3876G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847396 | ||||||
chr7:847423
|
A | G | 290 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(287): Show | 317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.658+3903A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847423 | ||||||
chr7:847483
|
T | C | 2 | a0002c0005t0001g0088a0002c0005t0001g0089 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.659-3901T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847483 | ||||||
chr7:847489
|
C | T | 1 | a0004c0007t0001g0202 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.659-3895C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847489 | ||||||
chr7:847490
|
A | G | 193 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.659-3894A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847490 | ||||||
chr7:847517
|
GGCCTTCC others(79): Show |
G | 3 | a0001c0001t0001g0201a0001c0006t0012g0037a0001c0006t0012g0038 | 3 | HG01243.hp2 HG02717.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.659-3781_659-3696d others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847517 | |||||
chr7:847541
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.659-3843C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847541 | ||||||
chr7:847544
|
T | C | 1 | a0021c0029t0001g0155 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.659-3840T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847544 | ||||||
chr7:847573
|
C | T | 3 | a0001c0004t0002g0264a0001c0004t0002g0265a0010c0014t0002g0266 | 3 | NA18612.hp1 NA18939.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.659-3811C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847573 | ||||||
chr7:847603
|
A | G | 105 | a0001c0001t0001g0024a0001c0001t0001g0120a0001c0001t0001g0121others(102): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.659-3781A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847603 | ||||||
chr7:847625
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.659-3759C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847625 | ||||||
chr7:847681
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0297 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.659-3703G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847681 | ||||||
chr7:847686
|
G | A | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3698G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847686 | ||||||
chr7:847712
|
G | A | 1 | a0001c0001t0001g0221 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.659-3672G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847712 | ||||||
chr7:847739
|
G | A | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-3645G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847739 | ||||||
chr7:847748
|
G | A | 258 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(255): Show | 292 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.659-3636G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847748 | ||||||
chr7:847748
|
G | GCAGCGCC others(79): Show |
1 | a0022c0030t0001g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.659-3551_659-3550i others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847748 | |||||
chr7:847766
|
G | A | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3618G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847766 | ||||||
chr7:847766
|
G | GGAGTTGG others(79): Show |
59 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(56): Show | 60 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.659-3551_659-3550i others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847766 | |||||
chr7:847766
|
G | GGAGTTGG others(79): Show |
1 | a0003c0003t0001g0353 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.659-3533_659-3532i others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847766 | |||||
chr7:847834
|
G | A | 9 | a0001c0006t0001g0049a0001c0006t0001g0050a0001c0006t0001g0052others(6): Show | 9 | HG01515.hp1 HG01517.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.659-3550G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847834 | ||||||
chr7:847841
|
C | T | 1 | a0003c0003t0001g0368 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.659-3543C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847841 | ||||||
chr7:847845
|
C | T | 7 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0273others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3539C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847845 | ||||||
chr7:847852
|
G | A | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3532G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847852 | ||||||
chr7:847859
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.659-3525G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847859 | ||||||
chr7:847861
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.659-3523G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847861 | ||||||
chr7:847874
|
G | T | 30 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(27): Show | 39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.659-3510G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847874 | ||||||
chr7:847884
|
G | C | 1 | a0021c0029t0001g0155 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.659-3500G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847884 | ||||||
chr7:847933
|
C | T | 6 | a0003c0003t0001g0029a0003c0003t0001g0349a0003c0003t0001g0350others(3): Show | 7 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.659-3451C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847933 | ||||||
chr7:847934
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.659-3450G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847934 | ||||||
chr7:847976
|
T | TCCTGGGG others(29): Show |
13 | a0001c0006t0001g0039a0001c0006t0001g0040a0001c0006t0001g0049others(10): Show | 13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.659-3393_659-3358d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847976 | |||||
chr7:847991
|
C | T | 147 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(144): Show | 159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.659-3393C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847991 | ||||||
chr7:848012
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.659-3372C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848012 | ||||||
chr7:848017
|
G | A | 5 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(2): Show | 5 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.659-3367G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848017 | ||||||
chr7:848064
|
G | A | 3 | a0002c0005t0001g0090a0002c0005t0001g0091a0002c0005t0001g0092 | 3 | HG02602.hp1 HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.659-3320G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848064 | ||||||
chr7:848068
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.659-3316C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848068 | ||||||
chr7:848069
|
G | A | 1 | a0001c0004t0023g0267 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.659-3315G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848069 | ||||||
chr7:848074
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.659-3310C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848074 | ||||||
chr7:848084
|
T | TCCTGGGG others(29): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.659-3285_659-3284i others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 848084 | |||||
chr7:848084
|
T | TCCTGGGG others(29): Show |
154 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(151): Show | 168 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.659-3279_659-3244d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 848084 | |||||
chr7:848135
|
C | T | 1 | a0002c0002t0009g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.659-3249C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848135 | ||||||
chr7:848185
|
C | A | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.659-3199C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848185 | ||||||
chr7:848198
|
G | GA | 146 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(143): Show | 158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.659-3186_659-3185i others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848198 | ||||||
chr7:848360
|
A | G | 1 | a0001c0006t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.659-3024A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848360 | ||||||
chr7:848368
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.659-3016G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848368 | ||||||
chr7:848559
|
A | G | 7 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0273others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-2825A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848559 | ||||||
chr7:848653
|
A | T | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.659-2731A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848653 | ||||||
chr7:848739
|
C | G | 3 | a0003c0003t0007g0346a0003c0003t0007g0347a0003c0003t0007g0348 | 3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.659-2645C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848739 | ||||||
chr7:848799
|
C | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01261.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.659-2585C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848799 | ||||||
chr7:848811
|
T | C | 290 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(287): Show | 317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.659-2573T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848811 | ||||||
chr7:848855
|
T | C | 1 | a0002c0002t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.659-2529T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848855 | ||||||
chr7:848973
|
C | G | 1 | a0001c0001t0001g0198 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.659-2411C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848973 | ||||||
chr7:848973
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.659-2411C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848973 | ||||||
chr7:849003
|
G | C | 1 | a0001c0001t0001g0025 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.659-2381G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849003 | ||||||
chr7:849028
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.659-2356C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849028 | ||||||
chr7:849077
|
A | G | 352 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(349): Show | 390 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(387): Show |
intron_variant | MODIFIER | c.659-2307A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849077 | ||||||
chr7:849113
|
G | A | 1 | a0001c0004t0002g0251 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.659-2271G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849113 | ||||||
chr7:849180
|
A | G | 1 | a0001c0004t0002g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.659-2204A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849180 | ||||||
chr7:849197
|
C | T | 2 | a0008c0011t0006g0304a0008c0011t0006g0306 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.659-2187C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849197 | ||||||
chr7:849245
|
C | T | 1 | a0001c0004t0002g0249 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.659-2139C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849245 | ||||||
chr7:849246
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(156): Show | 173 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.659-2138G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849246 | ||||||
chr7:849248
|
C | A | 61 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.659-2136C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849248 | ||||||
chr7:849282
|
G | A | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-2102G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849282 | ||||||
chr7:849334
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.659-2050G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849334 | ||||||
chr7:849389
|
A | G | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.659-1995A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849389 | ||||||
chr7:849532
|
A | G | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.659-1852A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849532 | ||||||
chr7:849672
|
A | T | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.659-1712A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849672 | ||||||
chr7:849696
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.659-1688C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849696 | ||||||
chr7:849721
|
T | C | 45 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(42): Show | 46 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.659-1663T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849721 | ||||||
chr7:849955
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.659-1429G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849955 | ||||||
chr7:850049
|
G | A | 1 | a0002c0002t0001g0067 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.659-1335G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850049 | ||||||
chr7:850174
|
A | G | 46 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(43): Show | 56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.659-1210A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850174 | ||||||
chr7:850221
|
C | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0024others(53): Show | 60 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.659-1163C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850221 | ||||||
chr7:850255
|
G | A | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.659-1129G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850255 | ||||||
chr7:850279
|
GCCTCCA | G | 13 | a0001c0006t0001g0039a0001c0006t0001g0040a0001c0006t0001g0049others(10): Show | 13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.659-1098_659-1093d others(8): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850279 | |||||
chr7:850356
|
AC | A | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-1025delC | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850356 | |||||
chr7:850414
|
T | C | 223 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(220): Show | 249 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.659-970T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850414 | ||||||
chr7:850456
|
C | T | 8 | a0002c0002t0001g0274a0002c0002t0001g0275a0002c0002t0001g0276others(5): Show | 8 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.659-928C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850456 | ||||||
chr7:850647
|
T | C | 190 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(187): Show | 207 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.659-737T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850647 | ||||||
chr7:850767
|
T | TA | 24 | a0002c0002t0001g0041a0002c0002t0001g0058a0002c0002t0001g0060others(21): Show | 25 | HG00140.hp2 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.659-602dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | |||||
chr7:850767
|
T | TAA | 43 | a0001c0001t0001g0035a0001c0001t0001g0297a0001c0001t0001g0299others(40): Show | 48 | HG00544.hp2 HG01243.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.659-603_659-602dup others(2): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | |||||
chr7:850767
|
T | TAAA | 8 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(5): Show | 8 | HG00621.hp1 HG01070.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.659-604_659-602dup others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | |||||
chr7:850767
|
T | TAAAA | 126 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(123): Show | 138 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.659-605_659-602dup others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | |||||
chr7:850767
|
T | TAAAAA | 12 | a0001c0001t0001g0113a0001c0001t0001g0156a0001c0001t0001g0160others(9): Show | 12 | HG00544.hp1 HG00673.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.659-606_659-602dup others(5): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | |||||
chr7:850782
|
A | C | 2 | a0003c0003t0005g0307a0003c0003t0005g0308 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.659-602A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850782 | ||||||
chr7:850782
|
AC | A | 30 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(27): Show | 39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.659-601delC | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850782 | ||||||
chr7:850783
|
C | A | 22 | a0001c0001t0001g0159a0001c0001t0001g0229a0001c0001t0001g0299others(19): Show | 24 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.659-601C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850783 | ||||||
chr7:850864
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.659-520G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850864 | ||||||
chr7:850959
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.659-425A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850959 | ||||||
chr7:850980
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.659-404A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850980 | ||||||
chr7:851009
|
A | C | 1 | a0001c0004t0002g0262 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.659-375A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851009 | ||||||
chr7:851055
|
G | A | 8 | a0002c0002t0001g0274a0002c0002t0001g0275a0002c0002t0001g0276others(5): Show | 8 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.659-329G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851055 | ||||||
chr7:851069
|
A | G | 1 | a0001c0001t0016g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.659-315A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851069 | ||||||
chr7:851276
|
C | T | 11 | a0003c0003t0001g0315a0003c0003t0001g0317a0003c0003t0001g0339others(8): Show | 11 | HG02056.hp2 HG02074.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.659-108C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851276 | ||||||
chr7:851341
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(189): Show | 209 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.659-43T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851341 | ||||||
chr7:851547
|
C | CGAT | 291 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(288): Show | 318 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.757+66_757+68dupGA others(1): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 851547 | |||||
chr7:851701
|
G | A | 46 | a0001c0001t0001g0035a0001c0001t0001g0123a0001c0001t0001g0227others(43): Show | 51 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.757+219G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | chr7 | 851701 | ||||||
chr7:851841
|
C | T | 3 | a0008c0011t0006g0304a0008c0011t0006g0306a0014c0018t0006g0305 | 3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.758-109C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | chr7 | 851841 | ||||||
chr7:851946
|
G | A | 1 | a0002c0002t0003g0081 | 1 | NA18944.hp2 | splice_region_variant&intron_variant | LOW | c.758-4G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | chr7 | 851946 | ||||||
chr7:852109
|
C | T | 1 | a0001c0004t0002g0269 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.851+66C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 7/18 | chr7 | 852109 | ||||||
chr7:852143
|
T | C | 1 | a0003c0003t0001g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851+100T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 7/18 | chr7 | 852143 | ||||||
chr7:852409
|
G | T | 2 | a0003c0003t0001g0357a0003c0003t0001g0358 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.852-200G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 7/18 | chr7 | 852409 | ||||||
chr7:852699
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.910+32G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852699 | ||||||
chr7:852706
|
C | G | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+39C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852706 | ||||||
chr7:852707
|
G | T | 3 | a0003c0003t0007g0346a0003c0003t0007g0347a0003c0003t0007g0348 | 3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.910+40G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852707 | ||||||
chr7:852770
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.911-40G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852770 | ||||||
chr7:852779
|
C | A | 5 | a0001c0006t0001g0049a0001c0006t0001g0050a0001c0006t0001g0052others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.911-31C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852779 | ||||||
chr7:853002
|
C | A | 1 | a0003c0003t0001g0349 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1053+50C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853002 | ||||||
chr7:853144
|
A | G | 48 | a0001c0004t0002g0261a0002c0002t0001g0003a0002c0002t0001g0011others(45): Show | 58 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(55): Show |
intron_variant | MODIFIER | c.1053+192A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853144 | ||||||
chr7:853252
|
A | G | 5 | a0001c0006t0001g0049a0001c0006t0001g0050a0001c0006t0001g0052others(2): Show | 5 | HG02965.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-157A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853252 | ||||||
chr7:853265
|
C | T | 65 | a0001c0001t0001g0199a0002c0002t0009g0034a0003c0003t0001g0029others(62): Show | 66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1054-144C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853265 | ||||||
chr7:853268
|
C | T | 1 | a0001c0004t0002g0260 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1054-141C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853268 | ||||||
chr7:853660
|
G | C | 191 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(188): Show | 208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1263+42G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853660 | ||||||
chr7:853687
|
T | C | 1 | a0002c0002t0001g0016 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1263+69T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853687 | ||||||
chr7:853770
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(141): Show | 156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1263+152G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853770 | ||||||
chr7:853828
|
G | A | 1 | a0002c0002t0001g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1263+210G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853828 | ||||||
chr7:853879
|
C | T | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1263+261C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853879 | ||||||
chr7:853880
|
A | G | 259 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(256): Show | 277 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.1263+262A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853880 | ||||||
chr7:853960
|
T | C | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1263+342T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853960 | ||||||
chr7:854000
|
G | A | 352 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(349): Show | 390 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(387): Show |
intron_variant | MODIFIER | c.1263+382G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854000 | ||||||
chr7:854018
|
C | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0297 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1263+400C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854018 | ||||||
chr7:854062
|
G | A | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1263+444G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854062 | ||||||
chr7:854169
|
T | G | 1 | a0002c0005t0001g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1263+551T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854169 | ||||||
chr7:854259
|
G | A | 1 | a0002c0002t0001g0016 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1263+641G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854259 | ||||||
chr7:854301
|
G | A | 1 | a0001c0001t0017g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1264-619G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854301 | ||||||
chr7:854315
|
G | A | 28 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1264-605G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854315 | ||||||
chr7:854343
|
T | C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1264-577T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854343 | ||||||
chr7:854390
|
G | A | 61 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1264-530G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854390 | ||||||
chr7:854443
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1264-477C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854443 | ||||||
chr7:854534
|
C | T | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1264-386C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854534 | ||||||
chr7:854551
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1264-369C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854551 | ||||||
chr7:854714
|
A | AAT | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264-196_1264-195d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 854714 | |||||
chr7:854734
|
C | T | 1 | a0002c0005t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1264-186C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854734 | ||||||
chr7:854785
|
T | C | 30 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(27): Show | 39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1264-135T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854785 | ||||||
chr7:854822
|
G | GATTGTCG others(15): Show |
1 | a0002c0002t0001g0080 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1264-96_1264-75dup others(22): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 854822 | |||||
chr7:854876
|
G | A | 1 | a0002c0002t0001g0062 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1264-44G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854876 | ||||||
chr7:854897
|
G | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1264-23G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854897 | ||||||
chr7:854914
|
C | A | 1 | a0003c0003t0001g0330 | 1 | HG03017.hp2 | splice_region_variant&intron_variant | LOW | c.1264-6C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854914 | ||||||
chr7:855021
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1350+15C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855021 | ||||||
chr7:855027
|
G | A | 1 | a0002c0002t0009g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1350+21G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855027 | ||||||
chr7:855035
|
A | T | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1350+29A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855035 | ||||||
chr7:855039
|
T | A | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1350+33T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855039 | ||||||
chr7:855040
|
A | T | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1350+34A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855040 | ||||||
chr7:855096
|
T | C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1350+90T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855096 | ||||||
chr7:855163
|
G | T | 1 | a0002c0002t0001g0016 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1350+157G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855163 | ||||||
chr7:855165
|
G | A | 1 | a0001c0004t0002g0241 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1350+159G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855165 | ||||||
chr7:855193
|
T | C | 289 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(286): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1350+187T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855193 | ||||||
chr7:855204
|
C | T | 158 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(155): Show | 172 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1350+198C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855204 | ||||||
chr7:855250
|
A | C | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1350+244A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855250 | ||||||
chr7:855261
|
C | T | 2 | a0002c0002t0001g0016a0002c0002t0001g0058 | 3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1350+255C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855261 | ||||||
chr7:855300
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1350+294T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855300 | ||||||
chr7:855305
|
G | A | 1 | a0002c0005t0001g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1350+299G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855305 | ||||||
chr7:855357
|
G | A | 1 | a0001c0001t0016g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1350+351G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855357 | ||||||
chr7:855389
|
C | T | 146 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(143): Show | 158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1350+383C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855389 | ||||||
chr7:855463
|
C | T | 1 | a0001c0006t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1350+457C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855463 | ||||||
chr7:855485
|
G | A | 1 | a0003c0003t0001g0368 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1350+479G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855485 | ||||||
chr7:855648
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(110): Show | 123 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1350+642G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855648 | ||||||
chr7:855746
|
C | T | 1 | a0002c0005t0001g0100 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1351-612C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855746 | ||||||
chr7:855787
|
T | G | 1 | a0002c0002t0001g0285 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1351-571T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855787 | ||||||
chr7:855807
|
A | G | 59 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(56): Show | 60 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1351-551A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855807 | ||||||
chr7:855824
|
T | G | 5 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0198others(2): Show | 5 | NA18963.hp2 NA18968.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351-534T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855824 | ||||||
chr7:855837
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1351-521G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855837 | ||||||
chr7:855868
|
G | C | 41 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(38): Show | 51 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(48): Show |
intron_variant | MODIFIER | c.1351-490G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855868 | ||||||
chr7:855900
|
C | T | 4 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(1): Show | 4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351-458C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855900 | ||||||
chr7:855925
|
G | A | 1 | a0002c0002t0001g0064 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1351-433G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855925 | ||||||
chr7:855964
|
C | T | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1351-394C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855964 | ||||||
chr7:856171
|
C | T | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1351-187C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 856171 | ||||||
chr7:856291
|
A | G | 28 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1351-67A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 856291 | ||||||
chr7:856440
|
G | C | 1 | a0003c0003t0001g0311 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1394+39G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856440 | ||||||
chr7:856448
|
G | A | 1 | a0016c0020t0001g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1394+47G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856448 | ||||||
chr7:856505
|
C | T | 28 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1394+104C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856505 | ||||||
chr7:856537
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1394+136C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856537 | ||||||
chr7:856561
|
G | A | 2 | a0009c0013t0001g0139a0009c0013t0001g0181 | 2 | NA18951.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1394+160G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856561 | ||||||
chr7:856606
|
G | A | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1394+205G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856606 | ||||||
chr7:856649
|
G | T | 1 | a0002c0002t0001g0290 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1394+248G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856649 | ||||||
chr7:856656
|
T | C | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1394+255T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856656 | ||||||
chr7:856657
|
G | C | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1394+256G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856657 | ||||||
chr7:856671
|
G | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0201a0001c0001t0001g0240 | 3 | NA18939.hp1 NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1394+270G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856671 | ||||||
chr7:856749
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0295a0001c0001t0001g0297others(1): Show | 4 | HG02647.hp1 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394+348G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856749 | ||||||
chr7:856808
|
G | A | 191 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(188): Show | 208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1394+407G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856808 | ||||||
chr7:856816
|
C | G | 1 | a0003c0003t0001g0339 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1394+415C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856816 | ||||||
chr7:856888
|
G | A | 1 | a0003c0003t0001g0339 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1394+487G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856888 | ||||||
chr7:856923
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1394+522G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856923 | ||||||
chr7:856947
|
T | G | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1394+546T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856947 | ||||||
chr7:856966
|
C | T | 6 | a0002c0002t0001g0275a0002c0002t0001g0276a0002c0002t0001g0277others(3): Show | 6 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1394+565C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856966 | ||||||
chr7:856983
|
C | G | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1394+582C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856983 | ||||||
chr7:857010
|
A | G | 1 | a0002c0005t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1394+609A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857010 | ||||||
chr7:857014
|
A | C | 288 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(285): Show | 315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1394+613A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857014 | ||||||
chr7:857015
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1394+614G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857015 | ||||||
chr7:857015
|
G | C | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1394+614G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857015 | ||||||
chr7:857038
|
A | G | 259 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(256): Show | 277 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.1394+637A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857038 | ||||||
chr7:857061
|
G | T | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1394+660G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857061 | ||||||
chr7:857105
|
GTCTT | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | NA18957.hp1 NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1394+709_1394+712d others(6): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 857105 | |||||
chr7:857129
|
C | A | 1 | a0002c0002t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395-699C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857129 | ||||||
chr7:857137
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1395-691G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857137 | ||||||
chr7:857338
|
T | G | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1395-490T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857338 | ||||||
chr7:857360
|
T | G | 1 | a0002c0002t0001g0069 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1395-468T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857360 | ||||||
chr7:857504
|
A | C | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1395-324A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857504 | ||||||
chr7:857736
|
G | A | 31 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(28): Show | 34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.1395-92G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857736 | ||||||
chr7:858074
|
C | T | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+117C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858074 | ||||||
chr7:858113
|
C | T | 1 | a0001c0001t0016g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1524+156C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858113 | ||||||
chr7:858147
|
C | T | 32 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(29): Show | 43 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1524+190C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858147 | ||||||
chr7:858158
|
G | A | 7 | a0002c0002t0001g0274a0002c0002t0001g0275a0002c0002t0001g0276others(4): Show | 7 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+201G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858158 | ||||||
chr7:858180
|
G | C | 1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1524+223G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858180 | ||||||
chr7:858195
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1524+238C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858195 | ||||||
chr7:858210
|
A | G | 67 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(64): Show | 68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+253A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858210 | ||||||
chr7:858283
|
G | T | 1 | a0002c0002t0001g0281 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1524+326G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858283 | ||||||
chr7:858365
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1524+408G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858365 | ||||||
chr7:858390
|
CT | C | 265 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(262): Show | 292 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.1524+446delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 858390 | |||||
chr7:858390
|
CTT | C | 20 | a0003c0003t0001g0315a0003c0003t0001g0316a0003c0003t0001g0317others(17): Show | 20 | HG01106.hp1 HG02056.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1524+445_1524+446d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 858390 | |||||
chr7:858500
|
G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02015.hp2 NA18943.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1524+543G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858500 | ||||||
chr7:858526
|
C | T | 1 | a0003c0003t0001g0339 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1524+569C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858526 | ||||||
chr7:858555
|
A | G | 1 | a0002c0005t0001g0093 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1524+598A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858555 | ||||||
chr7:858753
|
A | G | 1 | a0002c0002t0001g0076 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1524+796A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858753 | ||||||
chr7:858789
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1524+832G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858789 | ||||||
chr7:858868
|
C | T | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1524+911C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858868 | ||||||
chr7:858871
|
T | C | 67 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(64): Show | 68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+914T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858871 | ||||||
chr7:858875
|
C | T | 2 | a0001c0004t0002g0258a0001c0004t0023g0267 | 2 | NA18978.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1524+918C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858875 | ||||||
chr7:858919
|
C | T | 1 | a0013c0017t0001g0345 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1524+962C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858919 | ||||||
chr7:858928
|
C | T | 67 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(64): Show | 68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+971C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858928 | ||||||
chr7:858983
|
G | A | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1524+1026G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858983 | ||||||
chr7:859010
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1524+1053G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859010 | ||||||
chr7:859018
|
T | G | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1524+1061T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859018 | ||||||
chr7:859107
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-1021C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859107 | ||||||
chr7:859108
|
G | A | 11 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0001g0156others(8): Show | 12 | HG00423.hp1 HG00673.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1525-1020G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859108 | ||||||
chr7:859152
|
C | CA | 14 | a0001c0001t0001g0109a0001c0001t0001g0145a0001c0001t0001g0183others(11): Show | 14 | HG02257.hp2 HG02559.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1525-960dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 859152 | |||||
chr7:859152
|
CA | C | 7 | a0001c0001t0001g0196a0001c0022t0001g0174a0002c0002t0001g0293others(4): Show | 7 | HG01109.hp2 HG01975.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1525-960delA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 859152 | |||||
chr7:859265
|
C | CACGAGG | 46 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(43): Show | 56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.1525-858_1525-853d others(8): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 859265 | |||||
chr7:859289
|
C | T | 30 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(27): Show | 39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1525-839C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859289 | ||||||
chr7:859309
|
T | C | 1 | a0001c0006t0001g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-819T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859309 | ||||||
chr7:859418
|
G | A | 2 | a0003c0003t0001g0331a0003c0003t0001g0332 | 2 | NA19055.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1525-710G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859418 | ||||||
chr7:859478
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1525-650C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859478 | ||||||
chr7:859603
|
G | A | 1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1525-525G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859603 | ||||||
chr7:859727
|
A | G | 1 | a0001c0006t0001g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1525-401A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859727 | ||||||
chr7:859806
|
C | T | 191 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(188): Show | 208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1525-322C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859806 | ||||||
chr7:859826
|
G | C | 3 | a0008c0011t0006g0304a0008c0011t0006g0306a0014c0018t0006g0305 | 3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1525-302G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859826 | ||||||
chr7:859844
|
G | A | 1 | a0003c0003t0001g0368 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1525-284G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859844 | ||||||
chr7:859850
|
G | A | 1 | a0001c0006t0001g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1525-278G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859850 | ||||||
chr7:859909
|
G | A | 1 | a0002c0005t0001g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1525-219G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859909 | ||||||
chr7:859950
|
A | G | 259 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(256): Show | 277 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.1525-178A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859950 | ||||||
chr7:860073
|
A | C | 194 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 211 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1525-55A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 860073 | ||||||
chr7:860398
|
G | A | 30 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(27): Show | 39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.1779+16G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860398 | ||||||
chr7:860528
|
G | A | 8 | a0001c0006t0001g0049a0001c0006t0001g0050a0001c0006t0001g0052others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1779+146G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860528 | ||||||
chr7:860839
|
A | T | 1 | a0002c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1779+457A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860839 | ||||||
chr7:860855
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1779+473G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860855 | ||||||
chr7:860941
|
C | G | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1780-439C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860941 | ||||||
chr7:860947
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1780-433C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860947 | ||||||
chr7:861049
|
G | A | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1780-331G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861049 | ||||||
chr7:861051
|
A | T | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1780-329A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861051 | ||||||
chr7:861109
|
T | G | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1780-271T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861109 | ||||||
chr7:861172
|
C | T | 46 | a0002c0002t0001g0003a0002c0002t0001g0011a0002c0002t0001g0013others(43): Show | 56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.1780-208C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861172 | ||||||
chr7:861212
|
C | T | 1 | a0020c0026t0001g0222 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1780-168C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861212 | ||||||
chr7:861268
|
C | G | 61 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1780-112C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861268 | ||||||
chr7:861322
|
C | T | 3 | a0003c0003t0001g0319a0003c0003t0001g0320a0003c0021t0020g0337 | 3 | HG01123.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1780-58C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861322 | ||||||
chr7:861341
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1780-39G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861341 | ||||||
chr7:861633
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1864+169G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861633 | ||||||
chr7:861642
|
T | C | 1 | a0022c0030t0001g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1864+178T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861642 | ||||||
chr7:861745
|
C | T | 28 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1864+281C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861745 | ||||||
chr7:861746
|
T | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0023others(79): Show | 90 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1864+282T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861746 | ||||||
chr7:861937
|
C | T | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1864+473C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861937 | ||||||
chr7:861998
|
C | T | 1 | a0002c0002t0009g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1864+534C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861998 | ||||||
chr7:861999
|
G | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0207others(3): Show | 9 | HG00639.hp1 HG01099.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1864+535G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861999 | ||||||
chr7:862089
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1864+625C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862089 | ||||||
chr7:862117
|
C | T | 5 | a0006c0009t0001g0031a0006c0009t0001g0032a0006c0009t0001g0105others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864+653C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862117 | ||||||
chr7:862138
|
C | T | 3 | a0003c0003t0007g0346a0003c0003t0007g0347a0003c0003t0007g0348 | 3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1864+674C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862138 | ||||||
chr7:862156
|
A | G | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1864+692A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862156 | ||||||
chr7:862339
|
A | G | 1 | a0002c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1864+875A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862339 | ||||||
chr7:862398
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1864+934C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862398 | ||||||
chr7:862445
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1864+981C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862445 | ||||||
chr7:862542
|
A | C | 1 | a0001c0004t0002g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1864+1078A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862542 | ||||||
chr7:862718
|
T | A | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1864+1254T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862718 | ||||||
chr7:862722
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1864+1258G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862722 | ||||||
chr7:862757
|
A | G | 260 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(257): Show | 278 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1864+1293A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862757 | ||||||
chr7:862771
|
T | A | 1 | a0001c0006t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1864+1307T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862771 | ||||||
chr7:862813
|
C | G | 289 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(286): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1864+1349C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862813 | ||||||
chr7:862874
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0299 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1864+1410G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862874 | ||||||
chr7:862878
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1864+1414G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862878 | ||||||
chr7:862890
|
G | A | 1 | a0001c0006t0001g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1864+1426G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862890 | ||||||
chr7:862912
|
G | A | 1 | a0002c0002t0001g0065 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1864+1448G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862912 | ||||||
chr7:862933
|
C | G | 1 | a0003c0003t0001g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1864+1469C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862933 | ||||||
chr7:862947
|
C | G | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1864+1483C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862947 | ||||||
chr7:862950
|
G | A | 160 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(157): Show | 174 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1864+1486G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862950 | ||||||
chr7:863108
|
C | G | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1864+1644C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863108 | ||||||
chr7:863123
|
C | A | 3 | a0008c0011t0006g0304a0008c0011t0006g0306a0014c0018t0006g0305 | 3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1864+1659C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863123 | ||||||
chr7:863129
|
G | A | 148 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(145): Show | 160 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1864+1665G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863129 | ||||||
chr7:863235
|
C | T | 1 | a0001c0004t0002g0243 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1864+1771C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863235 | ||||||
chr7:863252
|
A | ATTCACCA others(53): Show |
109 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(106): Show | 119 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1864+1829_1864+183 others(64): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863252 | |||||
chr7:863252
|
A | ATTCACCA others(113): Show |
65 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(62): Show | 66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1864+1906_1864+190 others(124): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863252 | |||||
chr7:863290
|
G | A | 28 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1864+1826G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863290 | ||||||
chr7:863294
|
T | G | 146 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(143): Show | 158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1864+1830T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863294 | ||||||
chr7:863342
|
G | GCCCTCCC others(113): Show |
2 | a0008c0011t0006g0306a0014c0018t0006g0305 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1864+1906_1864+190 others(124): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863342 | |||||
chr7:863342
|
G | GCCCTCCC others(113): Show |
1 | a0008c0011t0006g0304 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1864+1906_1864+190 others(124): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863342 | |||||
chr7:863513
|
A | G | 1 | a0001c0001t0017g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1864+2049A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863513 | ||||||
chr7:863550
|
C | T | 1 | a0006c0009t0001g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1864+2086C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863550 | ||||||
chr7:863648
|
C | A | 12 | a0001c0006t0001g0039a0001c0006t0001g0040a0001c0006t0001g0049others(9): Show | 12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1864+2184C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863648 | ||||||
chr7:863660
|
C | A | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1864+2196C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863660 | ||||||
chr7:863754
|
C | T | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865-2198C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863754 | ||||||
chr7:863785
|
A | G | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1865-2167A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863785 | ||||||
chr7:863955
|
G | C | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1865-1997G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863955 | ||||||
chr7:864001
|
C | A | 61 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1865-1951C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864001 | ||||||
chr7:864065
|
T | C | 1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1865-1887T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864065 | ||||||
chr7:864125
|
A | G | 1 | a0018c0027t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1865-1827A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864125 | ||||||
chr7:864266
|
G | A | 4 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(1): Show | 4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1865-1686G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864266 | ||||||
chr7:864318
|
C | T | 160 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(157): Show | 174 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1865-1634C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864318 | ||||||
chr7:864336
|
T | C | 1 | a0002c0005t0001g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1865-1616T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864336 | ||||||
chr7:864340
|
G | A | 5 | a0001c0001t0001g0129a0003c0003t0001g0359a0003c0003t0001g0360others(2): Show | 5 | HG00323.hp2 HG00642.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1865-1612G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864340 | ||||||
chr7:864411
|
G | A | 1 | a0014c0018t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1865-1541G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864411 | ||||||
chr7:864490
|
G | A | 4 | a0002c0005t0001g0010a0002c0005t0001g0046a0002c0005t0001g0047others(1): Show | 5 | HG00140.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1865-1462G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864490 | ||||||
chr7:864509
|
G | A | 1 | a0003c0003t0005g0307 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1865-1443G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864509 | ||||||
chr7:864514
|
A | G | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1865-1438A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864514 | ||||||
chr7:864554
|
C | CA | 96 | a0001c0001t0001g0035a0001c0001t0001g0164a0001c0001t0001g0184others(93): Show | 105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1865-1379dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | |||||
chr7:864554
|
C | CAAA | 29 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(26): Show | 32 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1865-1381_1865-137 others(7): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | |||||
chr7:864554
|
CA | C | 10 | a0001c0001t0001g0152a0001c0001t0001g0195a0002c0002t0001g0073others(7): Show | 12 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1865-1379delA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | |||||
chr7:864554
|
CAAAAA | C | 29 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0125others(26): Show | 31 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1865-1383_1865-137 others(9): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | |||||
chr7:864573
|
A | G | 6 | a0002c0002t0001g0014a0002c0002t0001g0061a0002c0002t0001g0063others(3): Show | 7 | HG02015.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1865-1379A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864573 | ||||||
chr7:864620
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1865-1332A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864620 | ||||||
chr7:864647
|
GACAAAGA others(29): Show |
G | 1 | a0002c0002t0001g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1865-1303_1865-126 others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864647 | |||||
chr7:864668
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0187 | 3 | HG02155.hp2 HG03654.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1865-1284G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864668 | ||||||
chr7:864693
|
ATCTCGGC others(49): Show |
A | 228 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(225): Show | 243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.1865-1253_1865-119 others(60): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864693 | |||||
chr7:864770
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0297 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1865-1182A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864770 | ||||||
chr7:864778
|
G | A | 31 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(28): Show | 34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.1865-1174G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864778 | ||||||
chr7:864789
|
C | T | 35 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(32): Show | 38 | HG00544.hp2 HG00621.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1865-1163C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864789 | ||||||
chr7:864942
|
C | T | 289 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(286): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.1865-1010C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864942 | ||||||
chr7:864982
|
A | C | 1 | a0001c0004t0002g0257 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1865-970A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864982 | ||||||
chr7:865005
|
C | A | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1865-947C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865005 | ||||||
chr7:865120
|
G | T | 113 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(110): Show | 123 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1865-832G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865120 | ||||||
chr7:865177
|
A | G | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1865-775A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865177 | ||||||
chr7:865356
|
C | T | 1 | a0002c0002t0001g0077 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1865-596C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865356 | ||||||
chr7:865592
|
C | T | 26 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(23): Show | 35 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1865-360C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865592 | ||||||
chr7:865593
|
G | A | 1 | a0003c0003t0001g0330 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1865-359G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865593 | ||||||
chr7:865628
|
T | C | 166 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(163): Show | 180 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1865-324T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865628 | ||||||
chr7:865736
|
C | T | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1865-216C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865736 | ||||||
chr7:865781
|
T | C | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1865-171T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865781 | ||||||
chr7:865920
|
G | A | 1 | a0001c0006t0001g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1865-32G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865920 | ||||||
chr7:866081
|
G | A | 1 | a0001c0025t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1980+14G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866081 | ||||||
chr7:866107
|
A | G | 1 | a0022c0030t0001g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1980+40A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866107 | ||||||
chr7:866118
|
T | C | 4 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0273others(1): Show | 4 | HG02723.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+51T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866118 | ||||||
chr7:866149
|
A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.1980+82A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866149 | ||||||
chr7:866159
|
G | A | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1980+92G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866159 | ||||||
chr7:866185
|
G | C | 3 | a0001c0001t0001g0233a0001c0001t0011g0188a0001c0001t0011g0373 | 3 | HG00323.hp1 HG00642.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1980+118G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866185 | ||||||
chr7:866227
|
G | C | 65 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(62): Show | 66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1980+160G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866227 | ||||||
chr7:866249
|
G | A | 1 | a0001c0004t0002g0251 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1980+182G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866249 | ||||||
chr7:866333
|
T | C | 5 | a0006c0009t0001g0031a0006c0009t0001g0032a0006c0009t0001g0105others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1980+266T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866333 | ||||||
chr7:866399
|
G | A | 1 | a0001c0001t0016g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1980+332G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866399 | ||||||
chr7:866440
|
C | T | 1 | a0003c0003t0001g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1980+373C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866440 | ||||||
chr7:866523
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1980+456C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866523 | ||||||
chr7:866532
|
T | G | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0179others(2): Show | 5 | HG01433.hp1 HG01517.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980+465T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866532 | ||||||
chr7:866532
|
T | TCCCCCAC others(29): Show |
10 | a0003c0003t0001g0335a0003c0003t0001g0336a0003c0003t0001g0368others(7): Show | 10 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1980+493_1980+494i others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866532 | |||||
chr7:866561
|
T | G | 260 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(257): Show | 278 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1980+494T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866561 | ||||||
chr7:866562
|
A | ACCTTCGC others(29): Show |
11 | a0002c0002t0001g0074a0002c0002t0003g0006a0002c0002t0003g0012others(8): Show | 14 | HG02071.hp1 HG02622.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1980+599_1980+634d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866562 | |||||
chr7:866562
|
A | ACCTTCGC others(65): Show |
9 | a0002c0002t0001g0030a0002c0002t0001g0274a0002c0002t0001g0275others(6): Show | 9 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980+563_1980+634d others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866562 | |||||
chr7:866562
|
A | G | 260 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(257): Show | 278 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1980+495A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866562 | ||||||
chr7:866593
|
C | CCCGGGCC others(101): Show |
1 | a0001c0001t0001g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1980+562_1980+563i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866593 | |||||
chr7:866630
|
C | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0187 | 2 | HG03654.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1980+563C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866630 | ||||||
chr7:866631
|
C | CGGGCCTT others(101): Show |
12 | a0001c0006t0001g0039a0001c0006t0001g0040a0001c0006t0001g0049others(9): Show | 12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1980+634_1980+635i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866631 | |||||
chr7:866631
|
C | CGGGCCTT others(101): Show |
1 | a0001c0001t0001g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866631 | |||||
chr7:866631
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0187 | 2 | HG03654.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1980+564C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866631 | ||||||
chr7:866649
|
G | C | 1 | a0001c0001t0001g0025 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1980+582G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866649 | ||||||
chr7:866665
|
C | CGTGGGCC others(63): Show |
3 | a0002c0002t0001g0011a0002c0002t0001g0064a0002c0002t0001g0065 | 4 | NA18946.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+598_1980+599i others(72): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866665 | ||||||
chr7:866665
|
C | CGTGGGCC others(63): Show |
1 | a0001c0001t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1980+598_1980+599i others(72): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866665 | ||||||
chr7:866666
|
C | G | 13 | a0001c0001t0001g0151a0001c0001t0001g0173a0001c0001t0001g0179others(10): Show | 13 | HG00673.hp2 HG02040.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1980+599C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866666 | ||||||
chr7:866667
|
C | CGGGCCTT others(245): Show |
1 | a0003c0003t0001g0315 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1980+634_1980+635i others(254): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | CGGGCCTT others(137): Show |
3 | a0003c0003t0010g0361a0003c0003t0010g0362a0003c0021t0020g0337 | 3 | HG00323.hp2 HG00642.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1980+634_1980+635i others(146): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | CGGGCCTT others(101): Show |
2 | a0003c0003t0001g0357a0003c0003t0001g0358 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1980+634_1980+635i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | CGGGCCTT others(65): Show |
49 | a0001c0006t0018g0294a0002c0002t0001g0078a0002c0002t0001g0084others(46): Show | 50 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1980+634_1980+635i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | CGGGCCTT others(101): Show |
1 | a0020c0026t0001g0222 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1980+634_1980+635i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | CGGGCCTT others(29): Show |
19 | a0001c0004t0002g0026a0001c0004t0002g0242a0001c0004t0002g0243others(16): Show | 20 | HG01243.hp2 HG02132.hp2 HG02717.hp1 others(17): Show |
intron_variant | MODIFIER | c.1980+615_1980+650d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | CGGGCCTT others(65): Show |
7 | a0001c0001t0001g0035a0001c0001t0001g0118a0001c0001t0001g0138others(4): Show | 7 | HG01975.hp2 HG02273.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | CGT | 4 | a0001c0001t0001g0119a0002c0002t0001g0011a0002c0002t0001g0064others(1): Show | 5 | HG01261.hp1 NA18946.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1980+601_1980+602i others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | |||||
chr7:866667
|
C | T | 13 | a0001c0001t0001g0151a0001c0001t0001g0173a0001c0001t0001g0179others(10): Show | 13 | HG00673.hp2 HG02040.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1980+600C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866667 | ||||||
chr7:866668
|
G | GGGCCTTC others(65): Show |
1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1980+650_1980+651i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866668 | |||||
chr7:866678
|
CCCCACTG others(27): Show |
C | 1 | a0002c0002t0001g0073 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1980+615_1980+648d others(36): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866678 | |||||
chr7:866702
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0173a0001c0001t0001g0179others(1): Show | 4 | HG03471.hp2 HG03654.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+635G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866702 | ||||||
chr7:866702
|
G | C | 8 | a0001c0001t0001g0123a0001c0001t0001g0171a0001c0001t0001g0189others(5): Show | 8 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1980+635G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866702 | ||||||
chr7:866702
|
G | GTGGGCCT others(65): Show |
6 | a0001c0001t0001g0207a0001c0001t0001g0209a0002c0002t0009g0033others(3): Show | 7 | HG01256.hp2 HG01884.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866702 | |||||
chr7:866703
|
T | C | 8 | a0001c0001t0001g0123a0001c0001t0001g0171a0001c0001t0001g0189others(5): Show | 8 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1980+636T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866703 | ||||||
chr7:866712
|
G | GC | 83 | a0001c0001t0001g0035a0001c0001t0001g0119a0001c0001t0001g0150others(80): Show | 88 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1980+655dupC | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCC | 45 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0186others(42): Show | 51 | HG00544.hp1 HG01496.hp2 HG01891.hp1 others(48): Show |
intron_variant | MODIFIER | c.1980+654_1980+655d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(30): Show |
8 | a0001c0001t0001g0022a0001c0001t0001g0126a0001c0001t0001g0128others(5): Show | 9 | HG00673.hp2 HG01167.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(39): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(31): Show |
21 | a0001c0001t0001g0021a0001c0001t0001g0115a0001c0001t0001g0125others(18): Show | 22 | HG00408.hp1 HG00621.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(67): Show |
1 | a0001c0001t0001g0025 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(76): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(103): Show |
2 | a0001c0001t0001g0142a0001c0001t0001g0171 | 2 | HG01361.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(112): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(29): Show |
1 | a0001c0001t0001g0236 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(30): Show |
22 | a0001c0001t0001g0295a0001c0001t0021g0136a0001c0004t0002g0008others(19): Show | 24 | HG00544.hp2 HG00621.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(39): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(31): Show |
6 | a0001c0004t0022g0246a0002c0002t0001g0016a0002c0002t0001g0058others(3): Show | 7 | HG00639.hp1 HG01099.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(32): Show |
2 | a0002c0002t0001g0009a0002c0002t0001g0293 | 4 | HG02258.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(41): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(66): Show |
36 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0111others(33): Show | 39 | HG00099.hp1 HG00323.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(75): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(67): Show |
48 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(45): Show | 55 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(76): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(68): Show |
1 | a0001c0001t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(77): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(174): Show |
1 | a0001c0001t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(183): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(319): Show |
1 | a0001c0001t0001g0116 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1980+650_1980+651i others(328): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(66): Show |
3 | a0002c0002t0001g0002a0002c0002t0001g0285a0002c0002t0001g0289 | 7 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(75): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(67): Show |
5 | a0002c0002t0001g0005a0002c0002t0001g0286a0002c0002t0001g0287others(2): Show | 8 | HG01081.hp2 HG01175.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(76): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(102): Show |
6 | a0001c0001t0001g0123a0001c0001t0001g0185a0001c0001t0001g0189others(3): Show | 6 | HG03017.hp1 HG03490.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(111): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(103): Show |
3 | a0001c0001t0001g0193a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03927.hp2 HG03942.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(112): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(138): Show |
1 | a0001c0001t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(147): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(139): Show |
2 | a0001c0001t0001g0140a0004c0007t0004g0162 | 2 | HG04199.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(148): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(234): Show |
1 | a0003c0003t0001g0359 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(243): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(233): Show |
1 | a0003c0003t0001g0360 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(242): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCAC others(173): Show |
1 | a0001c0001t0001g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1980+650_1980+651i others(182): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866712
|
G | GCCCCCCC others(569): Show |
1 | a0001c0022t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1980+655_1980+656i others(578): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | |||||
chr7:866723
|
G | A | 1 | a0001c0004t0002g0251 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1980+656G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866723 | ||||||
chr7:866723
|
G | C | 1 | a0003c0003t0001g0341 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1980+656G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866723 | ||||||
chr7:866729
|
C | T | 1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1980+662C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866729 | ||||||
chr7:866730
|
G | A | 6 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(3): Show | 8 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1980+663G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866730 | ||||||
chr7:866771
|
G | A | 2 | a0009c0013t0001g0139a0009c0013t0001g0181 | 2 | NA18951.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1980+704G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866771 | ||||||
chr7:866991
|
A | G | 352 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(349): Show | 390 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(387): Show |
intron_variant | MODIFIER | c.1980+924A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866991 | ||||||
chr7:867013
|
G | T | 29 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(26): Show | 32 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1980+946G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867013 | ||||||
chr7:867036
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1980+969C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867036 | ||||||
chr7:867102
|
A | G | 269 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(266): Show | 287 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.1980+1035A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867102 | ||||||
chr7:867113
|
G | A | 1 | a0002c0002t0003g0070 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1980+1046G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867113 | ||||||
chr7:867143
|
G | A | 4 | a0006c0009t0001g0031a0006c0009t0001g0032a0006c0009t0001g0106others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+1076G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867143 | ||||||
chr7:867155
|
C | T | 1 | a0003c0003t0001g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1980+1088C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867155 | ||||||
chr7:867200
|
G | A | 31 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(28): Show | 34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.1980+1133G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867200 | ||||||
chr7:867346
|
C | T | 2 | a0001c0006t0018g0294a0022c0030t0001g0045 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1980+1279C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867346 | ||||||
chr7:867367
|
G | A | 1 | a0020c0026t0001g0222 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1980+1300G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867367 | ||||||
chr7:867390
|
T | C | 1 | a0001c0001t0024g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1980+1323T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867390 | ||||||
chr7:867510
|
G | T | 1 | a0001c0001t0001g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1980+1443G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867510 | ||||||
chr7:867733
|
C | A | 1 | a0002c0002t0001g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1981-1616C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867733 | ||||||
chr7:867755
|
A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.1981-1594A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867755 | ||||||
chr7:867762
|
G | A | 4 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(1): Show | 4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-1587G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867762 | ||||||
chr7:867778
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1981-1571C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867778 | ||||||
chr7:867812
|
G | A | 1 | a0001c0004t0002g0257 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1981-1537G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867812 | ||||||
chr7:867916
|
C | T | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1981-1433C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867916 | ||||||
chr7:867943
|
G | C | 1 | a0001c0004t0002g0261 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1981-1406G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867943 | ||||||
chr7:867951
|
G | A | 1 | a0002c0002t0009g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1981-1398G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867951 | ||||||
chr7:868035
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1981-1314C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868035 | ||||||
chr7:868035
|
C | T | 5 | a0006c0009t0001g0031a0006c0009t0001g0032a0006c0009t0001g0105others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981-1314C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868035 | ||||||
chr7:868109
|
C | T | 1 | a0003c0003t0001g0368 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1981-1240C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868109 | ||||||
chr7:868128
|
G | A | 1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1981-1221G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868128 | ||||||
chr7:868158
|
T | G | 1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1981-1191T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868158 | ||||||
chr7:868193
|
C | T | 2 | a0003c0003t0001g0324a0003c0003t0001g0327 | 2 | NA18978.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1981-1156C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868193 | ||||||
chr7:868195
|
T | C | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.1981-1154T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868195 | ||||||
chr7:868272
|
G | A | 61 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1981-1077G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868272 | ||||||
chr7:868373
|
C | T | 1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1981-976C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868373 | ||||||
chr7:868374
|
G | A | 61 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1981-975G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868374 | ||||||
chr7:868461
|
C | T | 1 | a0002c0002t0001g0016 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1981-888C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868461 | ||||||
chr7:868466
|
G | A | 4 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0300others(1): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981-883G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868466 | ||||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
1 | a0001c0001t0016g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1981-742_1981-741i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
3 | a0008c0011t0006g0304a0008c0011t0006g0306a0014c0018t0006g0305 | 3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1981-738_1981-737i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(257): Show |
1 | a0001c0001t0001g0186 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1981-720_1981-719i others(266): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
1 | a0001c0001t0001g0314 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
121 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0021others(118): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(335): Show |
1 | a0004c0007t0004g0212 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1981-667_1981-666i others(344): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
5 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981-699_1981-698i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(260): Show |
1 | a0001c0001t0001g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1981-736_1981-735i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1981-756_1981-755i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(221): Show |
1 | a0001c0004t0002g0255 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1981-819_1981-818i others(230): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(221): Show |
29 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(26): Show | 32 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1981-819_1981-818i others(230): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(223): Show |
1 | a0017c0015t0008g0259 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1981-850_1981-849i others(232): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
A | ATGTTGGT others(259): Show |
1 | a0001c0001t0001g0227 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1981-856_1981-855i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868480
|
ATGTTGGT others(31): Show |
A | 1 | a0002c0002t0001g0016 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1981-818_1981-781d others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | |||||
chr7:868492
|
T | TGGGGGGG others(260): Show |
1 | a0001c0001t0017g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1981-667_1981-666i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868492 | |||||
chr7:868530
|
T | TGGGGGGG others(260): Show |
1 | a0001c0001t0001g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1981-812_1981-811i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868530 | |||||
chr7:868531
|
G | C | 6 | a0002c0002t0001g0014a0002c0002t0001g0061a0002c0002t0001g0063others(3): Show | 7 | HG02015.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1981-818G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868531 | ||||||
chr7:868531
|
G | GGGGGGGC others(221): Show |
2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(230): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868531 | |||||
chr7:868531
|
G | T | 2 | a0001c0004t0002g0249a0002c0002t0001g0058 | 2 | HG03209.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1981-818G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868531 | ||||||
chr7:868538
|
C | CAGTGCTG others(259): Show |
2 | a0001c0001t0001g0191a0001c0001t0001g0199 | 2 | HG01978.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868538 | |||||
chr7:868568
|
T | TGGGGGGG others(220): Show |
1 | a0001c0004t0002g0249 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1981-781_1981-780i others(229): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868568 | ||||||
chr7:868569
|
T | TGGGGGGC others(525): Show |
4 | a0003c0003t0001g0029a0003c0003t0001g0351a0003c0003t0001g0352others(1): Show | 5 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981-705_1981-704i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | |||||
chr7:868569
|
T | TGGGGGGC others(525): Show |
1 | a0003c0003t0001g0349 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1981-705_1981-704i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | |||||
chr7:868569
|
T | TGGGGGGC others(107): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0166a0001c0001t0001g0178 | 4 | HG00423.hp1 NA18947.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-667_1981-666i others(116): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | |||||
chr7:868569
|
T | TGGGGGGC others(260): Show |
2 | a0001c0001t0001g0035a0001c0001t0001g0297 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | |||||
chr7:868569
|
T | TGGGGGGC others(526): Show |
1 | a0003c0003t0001g0329 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1981-736_1981-735i others(535): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | |||||
chr7:868569
|
T | TGGGGGGC others(526): Show |
1 | a0003c0003t0001g0318 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1981-736_1981-735i others(535): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | |||||
chr7:868570
|
G | T | 1 | a0001c0004t0002g0249 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1981-779G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868570 | ||||||
chr7:868602
|
C | CGGATGGG others(259): Show |
1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868602 | |||||
chr7:868607
|
G | T | 1 | a0001c0004t0002g0255 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1981-742G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868607 | ||||||
chr7:868626
|
T | C | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1981-723T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868626 | ||||||
chr7:868651
|
A | ACAGTGCT others(259): Show |
4 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(1): Show | 4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868651 | |||||
chr7:868651
|
A | G | 4 | a0001c0004t0002g0255a0008c0011t0006g0304a0008c0011t0006g0306others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-698A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868651 | ||||||
chr7:868660
|
G | GTTCCCTG others(260): Show |
1 | a0001c0001t0001g0295 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868660 | |||||
chr7:868679
|
G | A | 28 | a0001c0006t0018g0294a0002c0002t0001g0002a0002c0002t0001g0005others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1981-670G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868679 | ||||||
chr7:868682
|
T | TGGGGGGC others(259): Show |
1 | a0001c0001t0001g0213 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868682 | ||||||
chr7:868682
|
T | TGGGGGGG others(525): Show |
1 | a0003c0003t0001g0331 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868682 | ||||||
chr7:868683
|
T | G | 288 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(285): Show | 315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1981-666T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868683 | ||||||
chr7:868689
|
G | A | 8 | a0003c0003t0001g0029a0003c0003t0001g0318a0003c0003t0001g0329others(5): Show | 9 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1981-660G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868689 | ||||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0322 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1981-629_1981-628i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
4 | a0003c0003t0001g0325a0003c0003t0001g0333a0003c0003t0001g0338others(1): Show | 4 | HG01943.hp2 HG01981.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(563): Show |
1 | a0003c0003t0001g0342 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(572): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0353 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0330 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0357 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(639): Show |
1 | a0003c0003t0001g0316 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(648): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
2 | a0003c0003t0001g0335a0003c0003t0001g0368 | 2 | HG03669.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
34 | a0003c0003t0001g0311a0003c0003t0001g0312a0003c0003t0001g0313others(31): Show | 34 | HG00558.hp2 HG01074.hp1 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
2 | a0003c0003t0001g0319a0003c0003t0001g0320 | 2 | HG01123.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868689
|
G | GCAGTGCT others(525): Show |
1 | a0020c0026t0001g0222 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | |||||
chr7:868721
|
T | C | 1 | a0022c0030t0001g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1981-628T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868721 | ||||||
chr7:868721
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1981-628T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868721 | ||||||
chr7:868721
|
T | TGGGGGGC others(259): Show |
1 | a0005c0008t0001g0300 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1981-591_1981-590i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868721 | |||||
chr7:868721
|
T | TGGGGGGC others(259): Show |
3 | a0005c0008t0001g0027a0005c0008t0001g0028a0005c0008t0001g0301 | 5 | HG01243.hp1 HG01884.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981-553_1981-552i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868721 | |||||
chr7:868722
|
G | GGGGGGCA others(260): Show |
1 | a0001c0001t0001g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868722 | |||||
chr7:868727
|
G | GCAGTGCT others(487): Show |
1 | a0003c0003t0001g0343 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(496): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868727 | |||||
chr7:868727
|
G | GCAGTGCT others(31): Show |
1 | a0001c0001t0001g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1981-610_1981-609i others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868727 | |||||
chr7:868727
|
G | T | 28 | a0001c0006t0018g0294a0002c0002t0001g0002a0002c0002t0001g0005others(25): Show | 37 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1981-622G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868727 | ||||||
chr7:868760
|
G | GGGGGGCA others(259): Show |
2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | NA18954.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1981-553_1981-552i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868760 | |||||
chr7:868765
|
GCAGTGCT others(221): Show |
G | 7 | a0002c0002t0001g0271a0002c0002t0001g0272a0002c0002t0001g0273others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1981-562_1981-335d others(2): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868765 | |||||
chr7:868778
|
C | CCTGTGGT others(373): Show |
1 | a0003c0021t0020g0337 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(382): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868778 | |||||
chr7:868781
|
G | GTGGTGTT others(259): Show |
1 | a0011c0031t0014g0296 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868781 | |||||
chr7:868797
|
C | G | 281 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(278): Show | 308 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.1981-552C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868797 | ||||||
chr7:868797
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0229 | 2 | HG00673.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1981-552C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868797 | ||||||
chr7:868816
|
T | C | 4 | a0001c0001t0001g0153a0001c0006t0018g0294a0003c0003t0010g0361others(1): Show | 4 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-533T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868816 | ||||||
chr7:868835
|
G | T | 3 | a0001c0001t0001g0231a0003c0003t0010g0361a0003c0003t0010g0362 | 3 | HG00323.hp2 HG00642.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1981-514G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868835 | ||||||
chr7:868836
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1981-513G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868836 | ||||||
chr7:868872
|
T | TGGGGGGG others(70): Show |
1 | a0001c0001t0001g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1981-458_1981-457i others(79): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868872 | |||||
chr7:868874
|
G | C | 3 | a0001c0001t0001g0196a0002c0002t0009g0033a0002c0002t0009g0034 | 3 | HG01975.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1981-475G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868874 | ||||||
chr7:868879
|
G | GCAGTGCT others(31): Show |
1 | a0002c0002t0001g0066 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1981-372_1981-335d others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868879 | |||||
chr7:868879
|
G | GCAGTGCT others(563): Show |
2 | a0003c0003t0010g0361a0003c0003t0010g0362 | 2 | HG00323.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1981-458_1981-457i others(572): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868879 | |||||
chr7:868879
|
GCAGTGCT others(69): Show |
G | 3 | a0001c0001t0001g0231a0002c0002t0001g0287a0002c0002t0001g0289 | 3 | HG01978.hp1 HG03239.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1981-410_1981-335d others(78): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868879 | |||||
chr7:868892
|
C | T | 278 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(275): Show | 305 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1981-457C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868892 | ||||||
chr7:868900
|
G | A | 5 | a0006c0009t0001g0031a0006c0009t0001g0032a0006c0009t0001g0105others(2): Show | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981-449G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868900 | ||||||
chr7:868912
|
G | C | 18 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(15): Show | 27 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1981-437G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868912 | ||||||
chr7:868917
|
A | G | 1 | a0012c0016t0001g0372 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1981-432A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868917 | ||||||
chr7:868940
|
TGGTC | T | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1981-406_1981-403d others(6): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868940 | |||||
chr7:868987
|
G | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0153a0001c0001t0001g0166others(4): Show | 8 | HG00423.hp1 HG00673.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1981-362G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868987 | ||||||
chr7:868988
|
G | C | 21 | a0001c0006t0018g0294a0002c0002t0001g0002a0002c0002t0001g0005others(18): Show | 30 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1981-361G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868988 | ||||||
chr7:869130
|
G | A | 2 | a0001c0006t0001g0039a0001c0006t0001g0051 | 2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1981-219G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 869130 | ||||||
chr7:869202
|
C | T | 1 | a0001c0001t0016g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1981-147C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 869202 | ||||||
chr7:869262
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1981-87T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 869262 | ||||||
chr7:869529
|
G | A | 2 | a0002c0005t0001g0095a0002c0005t0001g0097 | 2 | HG00738.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2148+13G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869529 | ||||||
chr7:869615
|
G | A | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.2148+99G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869615 | ||||||
chr7:869713
|
T | C | 291 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(288): Show | 318 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.2148+197T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869713 | ||||||
chr7:869818
|
G | A | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+302G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869818 | ||||||
chr7:869859
|
C | A | 3 | a0003c0003t0007g0346a0003c0003t0007g0347a0003c0003t0007g0348 | 3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2148+343C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869859 | ||||||
chr7:869870
|
C | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+354C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869870 | ||||||
chr7:869933
|
C | T | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+417C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869933 | ||||||
chr7:869984
|
G | A | 1 | a0003c0012t0005g0309 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2148+468G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869984 | ||||||
chr7:870022
|
C | T | 3 | a0008c0011t0006g0304a0008c0011t0006g0306a0014c0018t0006g0305 | 3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2148+506C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870022 | ||||||
chr7:870040
|
C | CA | 21 | a0001c0001t0001g0109a0001c0001t0001g0168a0001c0001t0001g0235others(18): Show | 21 | HG01169.hp1 HG01175.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.2148+540dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870040 | |||||
chr7:870153
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2148+637T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870153 | ||||||
chr7:870196
|
C | A | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+680C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870196 | ||||||
chr7:870205
|
T | A | 1 | a0001c0004t0022g0246 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2148+689T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870205 | ||||||
chr7:870205
|
T | TA | 269 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(266): Show | 294 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.2148+707dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870205 | |||||
chr7:870205
|
T | TAA | 8 | a0001c0001t0001g0206a0001c0001t0016g0298a0002c0002t0001g0281others(5): Show | 10 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2148+706_2148+707d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870205 | |||||
chr7:870345
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2148+829T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870345 | ||||||
chr7:870498
|
A | C | 1 | a0001c0001t0001g0201 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2148+982A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870498 | ||||||
chr7:870565
|
A | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(259): Show | 280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+1049A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870565 | ||||||
chr7:870579
|
C | T | 2 | a0002c0002t0009g0033a0002c0002t0009g0034 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2148+1063C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870579 | ||||||
chr7:870685
|
GT | G | 68 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(65): Show | 69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.2148+1172delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870685 | |||||
chr7:870708
|
C | T | 61 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(58): Show | 62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.2148+1192C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870708 | ||||||
chr7:870737
|
CCCTGTGT others(10): Show |
C | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1225_2148+124 others(21): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870737 | |||||
chr7:870768
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2148+1252A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870768 | ||||||
chr7:870782
|
G | A | 27 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(24): Show | 36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2148+1266G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870782 | ||||||
chr7:870802
|
T | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1286T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870802 | ||||||
chr7:870808
|
C | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1292C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870808 | ||||||
chr7:870810
|
C | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1294C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870810 | ||||||
chr7:870810
|
C | T | 1 | a0002c0002t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2148+1294C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870810 | ||||||
chr7:870813
|
T | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1297T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870813 | ||||||
chr7:870823
|
C | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1307C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870823 | ||||||
chr7:870827
|
A | G | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1311A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870827 | ||||||
chr7:870831
|
T | G | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1315T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870831 | ||||||
chr7:870832
|
G | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1316G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870832 | ||||||
chr7:870834
|
T | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1318T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870834 | ||||||
chr7:870836
|
T | C | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1320T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870836 | ||||||
chr7:870841
|
C | G | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1325C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870841 | ||||||
chr7:870853
|
A | G | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2148+1337A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870853 | ||||||
chr7:870854
|
C | G | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1338C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870854 | ||||||
chr7:870855
|
T | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1339T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870855 | ||||||
chr7:870870
|
T | C | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1354T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870870 | ||||||
chr7:870873
|
T | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1357T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870873 | ||||||
chr7:870875
|
T | A | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1359T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870875 | ||||||
chr7:870887
|
C | CT | 10 | a0001c0004t0002g0249a0001c0004t0002g0256a0001c0004t0022g0246others(7): Show | 10 | HG02257.hp2 HG03209.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.2148+1391dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | |||||
chr7:870887
|
CT | C | 231 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(228): Show | 248 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.2148+1391delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | |||||
chr7:870887
|
CTT | C | 8 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(5): Show | 8 | HG01257.hp2 HG01975.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2148+1390_2148+139 others(6): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | |||||
chr7:870887
|
CTTTTTTT others(5): Show |
C | 10 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0281others(7): Show | 17 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2148+1380_2148+139 others(16): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | |||||
chr7:870897
|
T | C | 1 | a0003c0003t0001g0338 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1381T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870897 | ||||||
chr7:870973
|
CTCCGCCT others(490): Show |
C | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2149-1454_2149-958 others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870973 | |||||
chr7:871038
|
G | A | 7 | a0003c0003t0001g0029a0003c0003t0001g0349a0003c0003t0001g0351others(4): Show | 8 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.2149-1432G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871038 | ||||||
chr7:871038
|
G | T | 27 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(24): Show | 36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2149-1432G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871038 | ||||||
chr7:871154
|
G | C | 27 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(24): Show | 36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2149-1316G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871154 | ||||||
chr7:871247
|
A | G | 1 | a0002c0005t0001g0093 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2149-1223A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871247 | ||||||
chr7:871459
|
T | C | 36 | a0001c0006t0012g0037a0001c0006t0012g0038a0002c0002t0001g0002others(33): Show | 45 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.2149-1011T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871459 | ||||||
chr7:871473
|
C | T | 144 | a0001c0001t0001g0035a0001c0001t0001g0295a0001c0001t0001g0297others(141): Show | 160 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.2149-997C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871473 | ||||||
chr7:871476
|
C | T | 248 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(245): Show | 276 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.2149-994C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871476 | ||||||
chr7:871555
|
C | T | 27 | a0002c0002t0001g0002a0002c0002t0001g0005a0002c0002t0001g0009others(24): Show | 36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.2149-915C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871555 | ||||||
chr7:871598
|
C | T | 7 | a0001c0001t0001g0152a0001c0001t0001g0203a0001c0001t0001g0204others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2149-872C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871598 | ||||||
chr7:871626
|
G | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0295a0001c0001t0001g0297others(3): Show | 6 | HG02647.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2149-844G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871626 | ||||||
chr7:871683
|
CCACCCCG others(20): Show |
C | 1 | a0001c0001t0001g0152 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2149-786_2149-760d others(29): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871683 | ||||||
chr7:871722
|
A | G | 1 | a0001c0004t0002g0261 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2149-748A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871722 | ||||||
chr7:871731
|
A | G | 32 | a0001c0004t0002g0008a0001c0004t0002g0026a0001c0004t0002g0241others(29): Show | 35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.2149-739A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871731 | ||||||
chr7:871742
|
C | T | 1 | a0002c0002t0001g0030 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2149-728C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871742 | ||||||
chr7:871776
|
A | G | 1 | a0008c0011t0006g0306 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2149-694A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871776 | ||||||
chr7:871870
|
T | C | 291 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(288): Show | 318 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.2149-600T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871870 | ||||||
chr7:871877
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2149-593A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871877 | ||||||
chr7:872014
|
G | C | 2 | a0001c0006t0012g0037a0001c0006t0012g0038 | 2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2149-456G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872014 | ||||||
chr7:872016
|
C | T | 1 | a0002c0002t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2149-454C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872016 | ||||||
chr7:872020
|
A | G | 290 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(287): Show | 317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.2149-450A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872020 | ||||||
chr7:872204
|
T | C | 1 | a0001c0024t0001g0172 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2149-266T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872204 | ||||||
chr7:872264
|
A | G | 2 | a0001c0004t0002g0244a0001c0004t0002g0245 | 2 | HG02132.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2149-206A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872264 | ||||||
chr7:872319
|
G | A | 8 | a0001c0006t0001g0049a0001c0006t0001g0050a0001c0006t0001g0052others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2149-151G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872319 | ||||||
chr7:872815
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0183 | 2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2241+253G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 872815 | ||||||
chr7:872955
|
C | T | 2 | a0003c0003t0001g0357a0003c0003t0001g0358 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2242-260C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 872955 | ||||||
chr7:872960
|
G | A | 3 | a0002c0005t0001g0093a0002c0005t0001g0095a0002c0005t0001g0097 | 3 | HG00738.hp1 HG01884.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2242-255G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 872960 | ||||||
chr7:873012
|
G | A | 1 | a0002c0002t0009g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2242-203G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873012 | ||||||
chr7:873015
|
A | G | 7 | a0003c0003t0005g0307a0003c0003t0005g0308a0003c0012t0005g0309others(4): Show | 7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-200A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873015 | ||||||
chr7:873034
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2242-181C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873034 | ||||||
chr7:873083
|
T | A | 59 | a0003c0003t0001g0029a0003c0003t0001g0311a0003c0003t0001g0312others(56): Show | 60 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.2242-132T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873083 | ||||||
chr7:873091
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2242-124A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873091 | ||||||
chr7:873118
|
C | T | 289 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0020others(286): Show | 316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.2242-97C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873118 | ||||||
chr7:873137
|
G | A | 1 | a0001c0006t0018g0294 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2242-78G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873137 |