geneid | 222194 |
---|---|
ensemblid | ENSG00000187257.16 |
hgncid | 24765 |
symbol | RSBN1L |
name | round spermatid basic protein 1 like |
refseq_nuc | NM_198467.3 |
refseq_prot | NP_940869.2 |
ensembl_nuc | ENST00000334955.13 |
ensembl_prot | ENSP00000334040.7 |
mane_status | MANE Select |
chr | chr7 |
start | 77696459 |
end | 77783022 |
strand | + |
ver | v1.2 |
region | chr7:77696459-77783022 |
region5000 | chr7:77691459-77788022 |
regionname0 | RSBN1L_chr7_77696459_77783022 |
regionname5000 | RSBN1L_chr7_77691459_77788022 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 846 | 321 | 79 | 63 | 114 | 18 | 45 | 89 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0002 | 0/0 | 846 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0003 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0004 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0005 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0006 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0007 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0008 | 0/0 | 846 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2541 | 200 | 70 | 30 | 64 | 12 | 23 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0002 | 1/0 | 2541 | 115 | 8 | 29 | 50 | 6 | 21 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0003 | 0/0 | 2541 | 9 | 8 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0004 | 0/0 | 2541 | 4 | 0 | 4 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0005 | 0/0 | 2541 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0006 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0007 | 0/0 | 2541 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0008 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0009 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0010 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0011 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
c0012 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
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 | 1/0 | 3866 | 97 | 6 | 20 | 49 | 4 | 17 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0002 | 0/1 | 3867 | 50 | 4 | 10 | 28 | 1 | 6 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0003 | 0/0 | 3864 | 41 | 4 | 5 | 22 | 1 | 9 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0004 | 0/0 | 3866 | 37 | 14 | 4 | 10 | 8 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0005 | 0/0 | 3864 | 22 | 13 | 7 | 0 | 0 | 2 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0006 | 0/0 | 3867 | 9 | 1 | 3 | 2 | 1 | 2 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0007 | 0/0 | 3867 | 7 | 5 | 1 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0008 | 0/0 | 3864 | 7 | 7 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0009 | 0/0 | 3867 | 6 | 6 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0010 | 0/0 | 3868 | 5 | 0 | 1 | 2 | 0 | 2 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0011 | 0/0 | 3868 | 5 | 5 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0012 | 0/0 | 3865 | 4 | 4 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0013 | 0/0 | 3869 | 4 | 3 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0014 | 0/0 | 3866 | 3 | 1 | 1 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0015 | 0/0 | 3868 | 3 | 0 | 1 | 0 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0016 | 0/0 | 3868 | 3 | 1 | 2 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0017 | 0/0 | 3868 | 3 | 0 | 1 | 0 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0018 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0019 | 0/0 | 3865 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0020 | 0/0 | 3864 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0021 | 0/0 | 3866 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0022 | 0/0 | 3866 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0023 | 0/0 | 3864 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0024 | 0/0 | 3869 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0025 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0026 | 0/0 | 3866 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0027 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0028 | 0/0 | 3866 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0029 | 0/0 | 3866 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0030 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0031 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0032 | 0/0 | 3866 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0033 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0034 | 0/0 | 3866 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0035 | 0/0 | 3865 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0036 | 0/0 | 3866 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0037 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0038 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0039 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0040 | 0/0 | 3866 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0041 | 0/0 | 3866 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
t0042 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
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 | 2 | 0 | 0 | 0 | 2 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2541 | 200 | 70 | 30 | 64 | 12 | 23 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002 | 1/0 | 2541 | 115 | 8 | 29 | 50 | 6 | 21 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0004 | 0/0 | 2541 | 4 | 0 | 4 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0005 | 0/0 | 2541 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0009 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0002c0003 | 0/0 | 2541 | 9 | 8 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0003c0012 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0004c0011 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0005c0006 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0006c0010 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0007c0008 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0008c0007 | 0/0 | 2541 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 6407 | 50 | 4 | 10 | 28 | 1 | 6 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0003 | 0/0 | 6404 | 40 | 3 | 5 | 22 | 1 | 9 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0004 | 0/0 | 6406 | 30 | 7 | 4 | 10 | 8 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0005 | 0/0 | 6404 | 18 | 13 | 3 | 0 | 0 | 2 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0007 | 0/0 | 6407 | 5 | 4 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0008 | 0/0 | 6404 | 7 | 7 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0009 | 0/0 | 6407 | 6 | 6 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0010 | 0/0 | 6408 | 5 | 0 | 1 | 2 | 0 | 2 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0011 | 0/0 | 6408 | 5 | 5 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0012 | 0/0 | 6405 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0013 | 0/0 | 6409 | 4 | 3 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0014 | 0/0 | 6406 | 3 | 1 | 1 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0015 | 0/0 | 6408 | 3 | 0 | 1 | 0 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0016 | 0/0 | 6408 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0018 | 0/0 | 6407 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0019 | 0/0 | 6405 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0020 | 0/0 | 6404 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0022 | 0/0 | 6406 | 2 | 2 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0023 | 0/0 | 6404 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0024 | 0/0 | 6409 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0025 | 0/0 | 6407 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0026 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0027 | 0/0 | 6404 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0029 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0030 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0031 | 0/0 | 6404 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0032 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0033 | 0/0 | 6407 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0034 | 0/0 | 6406 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0001t0035 | 0/0 | 6405 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0001 | 1/0 | 6406 | 95 | 6 | 20 | 47 | 4 | 17 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0006 | 0/0 | 6407 | 8 | 1 | 3 | 2 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0016 | 0/0 | 6408 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0017 | 0/0 | 6408 | 3 | 0 | 1 | 0 | 1 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0021 | 0/0 | 6406 | 2 | 0 | 2 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0036 | 0/0 | 6406 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0037 | 0/0 | 6408 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0038 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0039 | 0/0 | 6408 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0041 | 0/0 | 6406 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0002t0042 | 0/0 | 6408 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0004t0005 | 0/0 | 6404 | 4 | 0 | 4 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0005t0040 | 0/0 | 6406 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0001c0009t0003 | 0/0 | 6404 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0002c0003t0004 | 0/0 | 6406 | 7 | 7 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0002c0003t0007 | 0/0 | 6407 | 2 | 1 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0003c0012t0012 | 0/0 | 6405 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0004c0011t0012 | 0/0 | 6405 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0005c0006t0001 | 0/0 | 6406 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0006c0010t0028 | 0/0 | 6406 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0007c0008t0001 | 0/0 | 6406 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
a0008c0007t0006 | 0/0 | 6407 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | copy fasta | chr7 | 77691459 | 77788022 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0010g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0010g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0011g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0011g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0013g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0013g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0013g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0013g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0014g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0014g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0015g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0015g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0015g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0016g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0016g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0018g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0018g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0019g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0019g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0020g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0020g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0022g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0023g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0024g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0025g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0026g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0027g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0029g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0030g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0031g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0032g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0033g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0034g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0001t0035g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0016g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0017g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0017g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0017g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0021g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0021g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0036g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0037g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0038g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0039g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0041g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0002t0042g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0004t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0004t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0004t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0004t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0005t0040g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0001c0009t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0002c0003t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0003c0012t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0004c0011t0012g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0005c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0006c0010t0028g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0007c0008t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
a0008c0007t0006g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00099 | hp2 | a0001 | c0002 | t0017 | g0238 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00140 | hp1 | a0001 | c0001 | t0015 | g0030 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00140 | hp2 | a0001 | c0002 | t0006 | g0266 | EUR | GBR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0108 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0137 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0222 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0107 | EUR | FIN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | CHS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0123 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00642 | hp1 | a0001 | c0001 | t0010 | g0055 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0313 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0316 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01070 | hp1 | a0001 | c0004 | t0005 | g0209 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01070 | hp2 | a0001 | c0002 | t0041 | g0244 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01071 | hp1 | a0001 | c0004 | t0005 | g0210 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01071 | hp2 | a0001 | c0002 | t0021 | g0256 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01074 | hp2 | a0001 | c0002 | t0021 | g0255 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0315 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01109 | hp1 | a0001 | c0001 | t0025 | g0113 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01109 | hp2 | a0001 | c0002 | t0017 | g0240 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01169 | hp1 | a0001 | c0002 | t0006 | g0263 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01175 | hp1 | a0001 | c0002 | t0039 | g0286 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01192 | hp1 | a0002 | c0003 | t0007 | g0104 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01192 | hp2 | a0001 | c0004 | t0005 | g0195 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01256 | hp1 | a0001 | c0001 | t0015 | g0028 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01256 | hp2 | a0001 | c0001 | t0016 | g0006 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01258 | hp1 | a0001 | c0001 | t0016 | g0015 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01261 | hp1 | a0001 | c0002 | t0042 | g0245 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0318 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0267 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0271 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0290 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0138 | EUR | IBS | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0079 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01891 | hp1 | a0001 | c0001 | t0031 | g0216 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01891 | hp2 | a0001 | c0001 | t0022 | g0047 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0311 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01975 | hp1 | a0001 | c0001 | t0014 | g0082 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0284 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01981 | hp2 | a0001 | c0002 | t0006 | g0282 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0293 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02027 | hp1 | a0001 | c0002 | t0037 | g0327 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02074 | hp2 | a0007 | c0008 | t0001 | g0317 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0334 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02145 | hp1 | a0002 | c0003 | t0004 | g0052 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0136 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02165 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | CDX | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | CDX | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02258 | hp2 | a0001 | c0001 | t0018 | g0129 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02280 | hp1 | a0006 | c0010 | t0028 | g0140 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02293 | hp2 | a0001 | c0004 | t0005 | g0211 | AMR | PEL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02451 | hp1 | a0001 | c0001 | t0014 | g0130 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02451 | hp2 | a0001 | c0001 | t0035 | g0037 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0096 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02572 | hp2 | a0001 | c0001 | t0020 | g0215 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02615 | hp1 | a0001 | c0009 | t0003 | g0176 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02622 | hp1 | a0002 | c0003 | t0004 | g0117 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02622 | hp2 | a0001 | c0002 | t0006 | g0243 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0125 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02647 | hp1 | a0001 | c0001 | t0029 | g0142 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02683 | hp2 | a0001 | c0002 | t0006 | g0246 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0124 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0276 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02735 | hp2 | a0001 | c0002 | t0036 | g0272 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0331 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02818 | hp1 | a0001 | c0001 | t0027 | g0077 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02886 | hp1 | a0002 | c0003 | t0004 | g0050 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0132 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02922 | hp1 | a0001 | c0001 | t0022 | g0046 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02965 | hp1 | a0002 | c0003 | t0004 | g0051 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02965 | hp2 | a0001 | c0001 | t0020 | g0212 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0191 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02976 | hp1 | a0001 | c0001 | t0032 | g0033 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03041 | hp1 | a0002 | c0003 | t0007 | g0048 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03041 | hp2 | a0001 | c0002 | t0016 | g0219 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03130 | hp2 | a0003 | c0012 | t0012 | g0208 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0135 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0062 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03239 | hp2 | a0001 | c0001 | t0015 | g0029 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0060 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0270 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03516 | hp1 | a0001 | c0001 | t0019 | g0032 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | ESN | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03579 | hp2 | a0001 | c0001 | t0024 | g0061 | AFR | MSL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03654 | hp2 | a0001 | c0001 | t0010 | g0053 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0330 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0308 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03704 | hp1 | a0001 | c0001 | t0023 | g0112 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03704 | hp2 | a0001 | c0002 | t0017 | g0239 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03710 | hp1 | a0001 | c0005 | t0040 | g0262 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0197 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0332 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03927 | hp2 | a0001 | c0001 | t0010 | g0116 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0227 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04115 | hp2 | a0008 | c0007 | t0006 | g0283 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0273 | SAS | BEB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0307 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04204 | hp1 | a0001 | c0002 | t0038 | g0297 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG04228 | hp2 | a0001 | c0001 | t0034 | g0171 | SAS | STU | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | CHB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0093 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18906 | hp2 | a0004 | c0011 | t0012 | g0192 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18949 | hp1 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18974 | hp2 | a0001 | c0002 | t0006 | g0225 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18980 | hp2 | a0001 | c0001 | t0010 | g0042 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0170 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19056 | hp1 | a0005 | c0006 | t0001 | g0278 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19062 | hp2 | a0001 | c0002 | t0006 | g0300 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19063 | hp2 | a0001 | c0001 | t0014 | g0095 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | YRI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ASW | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20129 | hp2 | a0001 | c0001 | t0026 | g0114 | AFR | ASW | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0188 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20805 | hp1 | a0001 | c0001 | t0030 | g0027 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0139 | EUR | TSI | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0258 | SAS | GIH | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | GIH | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01123 | hp1 | a0001 | c0001 | t0033 | g0149 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG01123 | hp2 | a0001 | c0002 | t0006 | g0285 | AMR | CLM | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02109 | hp1 | a0002 | c0003 | t0004 | g0039 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0134 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02486 | hp1 | a0002 | c0003 | t0004 | g0115 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02486 | hp2 | a0001 | c0001 | t0013 | g0122 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG02559 | hp2 | a0001 | c0001 | t0019 | g0031 | AFR | ACB | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG06807 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20300 | hp1 | a0002 | c0003 | t0004 | g0049 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | USA | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | LWK | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0071 | REF | REF | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0257 | REF | REF | RSBN1L_chr7_77691459_77788022 | RSBN1L | chr7 | 77691459 | 77788022 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77696480
|
C | T | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.11C>T | p.Pro4Leu | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 22/6406 | 11/2541 | 4/846 | chr7 | 77696480 | ||
chr7:77696602
|
G | A | 1 | a0002 | 9 | HG01192.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
missense_variant | MODERATE | c.133G>A | p.Val45Ile | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 144/6406 | 133/2541 | 45/846 | chr7 | 77696602 | ||
chr7:77696810
|
C | T | 1 | a0004 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.341C>T | p.Ser114Phe | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 352/6406 | 341/2541 | 114/846 | chr7 | 77696810 | ||
chr7:77749523
|
G | A | 1 | a0005 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.803G>A | p.Arg268His | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/8 | 814/6406 | 803/2541 | 268/846 | chr7 | 77749523 | ||
chr7:77749526
|
C | T | 1 | a0006 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.806C>T | p.Pro269Leu | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/8 | 817/6406 | 806/2541 | 269/846 | chr7 | 77749526 | ||
chr7:77749861
|
G | A | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1141G>A | p.Ala381Thr | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/8 | 1152/6406 | 1141/2541 | 381/846 | chr7 | 77749861 | ||
chr7:77778896
|
A | G | 1 | a0007 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2269A>G | p.Ile757Val | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2280/6406 | 2269/2541 | 757/846 | chr7 | 77778896 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77696601
|
G | A | 1 | a0001c0005 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.132G>A | p.Lys44Lys | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 143/6406 | 132/2541 | 44/846 | chr7 | 77696601 | ||
chr7:77696757
|
C | T | 1 | a0001c0004 | 4 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
synonymous_variant | LOW | c.288C>T | p.Ser96Ser | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/8 | 299/6406 | 288/2541 | 96/846 | chr7 | 77696757 | ||
chr7:77736453
|
A | G | 7 | a0001c0001a0001c0004a0001c0009others(4): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
synonymous_variant | LOW | c.630A>G | p.Glu210Glu | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/8 | 641/6406 | 630/2541 | 210/846 | chr7 | 77736453 | ||
chr7:77765605
|
C | T | 1 | a0001c0009 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.1455C>T | p.Asp485Asp | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/8 | 1466/6406 | 1455/2541 | 485/846 | chr7 | 77765605 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77779334
|
C | T | 1 | a0001c0001t0022 | 2 | HG01891.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*166C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 166 | chr7 | 77779334 | |||||
chr7:77779432
|
G | A | 1 | a0001c0001t0018 | 2 | HG02145.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*264G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 264 | chr7 | 77779432 | |||||
chr7:77779443
|
C | CAT | 2 | a0001c0002t0017a0001c0002t0042 | 4 | HG00099.hp2 HG01109.hp2 HG01261.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*291_*292dupTA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 293 | INFO_REALIGN_3_PRIME | chr7 | 77779443 | ||||
chr7:77779443
|
CAT | C | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*291_*292delTA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 291 | INFO_REALIGN_3_PRIME | chr7 | 77779443 | ||||
chr7:77779924
|
G | A | 1 | a0001c0001t0013 | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*756G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 756 | chr7 | 77779924 | |||||
chr7:77780037
|
G | A | 1 | a0001c0002t0036 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*869G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 869 | chr7 | 77780037 | |||||
chr7:77780065
|
T | C | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*897T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 897 | chr7 | 77780065 | |||||
chr7:77780122
|
G | A | 8 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(5): Show | 71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*954G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 954 | chr7 | 77780122 | |||||
chr7:77780224
|
T | C | 22 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(19): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1056T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1056 | chr7 | 77780224 | |||||
chr7:77780273
|
A | G | 4 | a0001c0001t0003a0001c0001t0033a0001c0001t0034others(1): Show | 43 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1105A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1105 | chr7 | 77780273 | |||||
chr7:77780531
|
T | C | 1 | a0001c0001t0019 | 2 | HG02559.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1363T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1363 | chr7 | 77780531 | |||||
chr7:77780805
|
A | G | 1 | a0001c0002t0041 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1637A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1637 | chr7 | 77780805 | |||||
chr7:77780817
|
C | T | 1 | a0001c0005t0040 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1649 | chr7 | 77780817 | |||||
chr7:77780942
|
T | A | 1 | a0001c0002t0038 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1774 | chr7 | 77780942 | |||||
chr7:77780984
|
A | G | 1 | a0001c0001t0029 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1816A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1816 | chr7 | 77780984 | |||||
chr7:77780997
|
G | C | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1829G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1829 | chr7 | 77780997 | |||||
chr7:77781138
|
A | G | 1 | a0001c0002t0042 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1970A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1970 | chr7 | 77781138 | |||||
chr7:77781146
|
A | T | 2 | a0001c0001t0011a0001c0001t0024 | 6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1978A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 1978 | chr7 | 77781146 | |||||
chr7:77781335
|
G | C | 1 | a0001c0001t0008 | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2167G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2167 | chr7 | 77781335 | |||||
chr7:77781530
|
G | A | 2 | a0001c0001t0015a0001c0001t0030 | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2362G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2362 | chr7 | 77781530 | |||||
chr7:77781946
|
C | G | 1 | a0001c0002t0042 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2778C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2778 | chr7 | 77781946 | |||||
chr7:77781950
|
C | T | 3 | a0001c0001t0009a0001c0001t0018a0006c0010t0028 | 9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2782 | chr7 | 77781950 | |||||
chr7:77781963
|
C | T | 1 | a0001c0001t0032 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2795C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2795 | chr7 | 77781963 | |||||
chr7:77781972
|
C | CA | 11 | a0001c0001t0009a0001c0001t0012a0001c0001t0015others(8): Show | 28 | HG00140.hp1 HG00140.hp2 HG01123.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2824dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | ||||
chr7:77781972
|
C | CAA | 13 | a0001c0001t0004a0001c0001t0014a0001c0001t0016others(10): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2823_*2824dupAA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | ||||
chr7:77781972
|
C | CAAA | 7 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(4): Show | 68 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2822_*2824dupAAA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | ||||
chr7:77781972
|
C | CAAAA | 2 | a0001c0001t0010a0001c0001t0024 | 6 | HG00642.hp1 HG03579.hp2 HG03654.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2821_*2824dupAAAA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2825 | INFO_REALIGN_3_PRIME | chr7 | 77781972 | ||||
chr7:77782116
|
A | G | 2 | a0001c0001t0025a0001c0001t0026 | 2 | HG01109.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2948A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 2948 | chr7 | 77782116 | |||||
chr7:77782231
|
C | T | 1 | a0001c0001t0032 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3063 | chr7 | 77782231 | |||||
chr7:77782247
|
C | T | 2 | a0001c0001t0015a0001c0001t0030 | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3079C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3079 | chr7 | 77782247 | |||||
chr7:77782372
|
A | AG | 2 | a0001c0001t0011a0001c0001t0024 | 6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3206dupG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3207 | INFO_REALIGN_3_PRIME | chr7 | 77782372 | ||||
chr7:77782409
|
C | A | 9 | a0001c0001t0003a0001c0001t0005a0001c0001t0012others(6): Show | 69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*3241C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3241 | chr7 | 77782409 | |||||
chr7:77782635
|
T | C | 1 | a0001c0001t0031 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3467T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3467 | chr7 | 77782635 | |||||
chr7:77782716
|
A | AGTG | 2 | a0001c0001t0015a0001c0001t0030 | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3554_*3556dupGGT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3557 | INFO_REALIGN_3_PRIME | chr7 | 77782716 | ||||
chr7:77782791
|
G | A | 1 | a0001c0001t0027 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3623G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 8/8 | 3623 | chr7 | 77782791 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77697093
|
T | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.586+38T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697093 | ||||||
chr7:77697431
|
G | T | 68 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0153others(65): Show | 68 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.586+376G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697431 | ||||||
chr7:77697865
|
C | A | 1 | a0001c0001t0004g0003 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.586+810C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697865 | ||||||
chr7:77697885
|
T | C | 1 | a0001c0002t0001g0218 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.586+830T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77697885 | ||||||
chr7:77698016
|
G | A | 17 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(14): Show | 17 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.586+961G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698016 | ||||||
chr7:77698032
|
CTT | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+981_586+982del others(2): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77698032 | |||||
chr7:77698077
|
C | T | 1 | a0001c0001t0033g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.586+1022C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698077 | ||||||
chr7:77698176
|
T | G | 1 | a0001c0001t0005g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.586+1121T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698176 | ||||||
chr7:77698756
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.586+1701A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698756 | ||||||
chr7:77698783
|
A | C | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.586+1728A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698783 | ||||||
chr7:77698786
|
T | C | 1 | a0001c0001t0030g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.586+1731T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77698786 | ||||||
chr7:77699012
|
A | C | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.586+1957A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699012 | ||||||
chr7:77699071
|
T | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+2016T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699071 | ||||||
chr7:77699266
|
A | C | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.586+2211A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699266 | ||||||
chr7:77699325
|
CGAAA | C | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+2273_586+2276d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77699325 | |||||
chr7:77699376
|
T | G | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+2321T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699376 | ||||||
chr7:77699796
|
A | AT | 21 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0002g0120others(18): Show | 21 | HG00140.hp1 HG01256.hp1 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.586+2757dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77699796 | |||||
chr7:77699901
|
A | G | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.586+2846A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699901 | ||||||
chr7:77699922
|
G | A | 81 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(78): Show | 81 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.586+2867G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77699922 | ||||||
chr7:77700075
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3020G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700075 | ||||||
chr7:77700426
|
C | T | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.586+3371C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700426 | ||||||
chr7:77700436
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+3381G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700436 | ||||||
chr7:77700526
|
G | A | 47 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(44): Show | 47 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.586+3471G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700526 | ||||||
chr7:77700653
|
A | G | 1 | a0001c0002t0001g0329 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.586+3598A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700653 | ||||||
chr7:77700852
|
G | T | 1 | a0001c0002t0001g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.586+3797G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700852 | ||||||
chr7:77700879
|
G | A | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.586+3824G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77700879 | ||||||
chr7:77701057
|
C | T | 1 | a0001c0001t0031g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.586+4002C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701057 | ||||||
chr7:77701091
|
ACAGTAAG others(1): Show |
A | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+4037_586+4044d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701091 | ||||||
chr7:77701112
|
AC | A | 141 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.586+4058delC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701112 | ||||||
chr7:77701151
|
C | CA | 27 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0153others(24): Show | 27 | HG00323.hp1 HG01192.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.586+4115dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701151 | |||||
chr7:77701155
|
A | C | 7 | a0001c0001t0002g0111a0001c0001t0004g0107a0001c0001t0004g0108others(4): Show | 7 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+4100A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701155 | ||||||
chr7:77701159
|
A | C | 2 | a0001c0001t0002g0111a0001c0001t0023g0112 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.586+4104A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701159 | ||||||
chr7:77701166
|
AAAAACAA others(1): Show |
A | 8 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+4114_586+4121d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701166 | |||||
chr7:77701168
|
A | C | 2 | a0001c0002t0001g0326a0001c0002t0037g0327 | 2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.586+4113A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701168 | ||||||
chr7:77701169
|
AACAACAA others(1): Show |
A | 111 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(108): Show | 112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.586+4116_586+4123d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701169 | |||||
chr7:77701170
|
AC | A | 7 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(4): Show | 7 | HG00140.hp1 HG01256.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+4116delC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701170 | ||||||
chr7:77701170
|
ACAACAAC | A | 14 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(11): Show | 14 | HG00438.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.586+4116_586+4122d others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701170 | ||||||
chr7:77701171
|
C | A | 67 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(64): Show | 67 | HG00639.hp2 HG00741.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.586+4116C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701171 | ||||||
chr7:77701180
|
C | A | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.586+4125C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701180 | ||||||
chr7:77701189
|
C | A | 1 | a0001c0002t0001g0222 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.586+4134C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701189 | ||||||
chr7:77701189
|
C | CA | 11 | a0001c0001t0003g0151a0001c0001t0003g0157a0001c0001t0005g0193others(8): Show | 11 | HG01433.hp1 HG02074.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+4143dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701189 | |||||
chr7:77701192
|
A | C | 2 | a0001c0002t0001g0324a0001c0002t0001g0325 | 2 | NA18972.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.586+4137A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701192 | ||||||
chr7:77701196
|
A | G | 1 | a0001c0001t0020g0215 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.586+4141A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701196 | ||||||
chr7:77701199
|
C | T | 1 | a0001c0002t0001g0325 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.586+4144C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701199 | ||||||
chr7:77701514
|
C | T | 1 | a0001c0002t0001g0323 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.586+4459C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701514 | ||||||
chr7:77701515
|
G | A | 1 | a0001c0001t0002g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.586+4460G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701515 | ||||||
chr7:77701653
|
CT | C | 212 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(209): Show | 213 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.586+4614delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77701653 | |||||
chr7:77701734
|
C | T | 2 | a0001c0001t0005g0197a0001c0001t0005g0214 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.586+4679C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701734 | ||||||
chr7:77701755
|
A | G | 2 | a0001c0001t0005g0196a0001c0001t0005g0213 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.586+4700A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701755 | ||||||
chr7:77701792
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+4737C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701792 | ||||||
chr7:77701862
|
G | A | 137 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(134): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.586+4807G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701862 | ||||||
chr7:77701924
|
G | A | 5 | a0001c0002t0001g0224a0001c0002t0001g0234a0001c0002t0001g0235others(2): Show | 5 | HG00423.hp1 NA19054.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+4869G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77701924 | ||||||
chr7:77702025
|
A | G | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+4970A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702025 | ||||||
chr7:77702050
|
C | A | 9 | a0001c0001t0002g0111a0001c0001t0004g0107a0001c0001t0004g0108others(6): Show | 9 | HG00280.hp1 HG00323.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.586+4995C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702050 | ||||||
chr7:77702168
|
G | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.586+5113G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702168 | ||||||
chr7:77702417
|
A | G | 2 | a0001c0001t0004g0143a0001c0001t0004g0144 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.586+5362A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702417 | ||||||
chr7:77702741
|
G | C | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.586+5686G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702741 | ||||||
chr7:77702743
|
G | C | 58 | a0001c0001t0002g0111a0001c0001t0004g0001a0001c0001t0004g0003others(55): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+5688G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77702743 | ||||||
chr7:77703013
|
C | T | 1 | a0001c0001t0003g0184 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.586+5958C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703013 | ||||||
chr7:77703079
|
G | A | 1 | a0001c0001t0010g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.586+6024G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703079 | ||||||
chr7:77703087
|
G | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+6032G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703087 | ||||||
chr7:77703146
|
G | T | 1 | a0001c0002t0001g0233 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.586+6091G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703146 | ||||||
chr7:77703290
|
G | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+6235G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703290 | ||||||
chr7:77703438
|
C | T | 1 | a0001c0001t0005g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.586+6383C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703438 | ||||||
chr7:77703477
|
G | GT | 54 | a0001c0001t0002g0111a0001c0001t0004g0110a0001c0001t0004g0131others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.586+6452dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
G | GTT | 45 | a0001c0001t0004g0001a0001c0001t0004g0137a0001c0001t0004g0138others(42): Show | 47 | HG00280.hp2 HG00738.hp2 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.586+6451_586+6452d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
G | GTTT | 22 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0143others(19): Show | 22 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.586+6450_586+6452d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
G | GTTTT | 11 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0010others(8): Show | 11 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+6449_586+6452d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
G | GTTTTT | 6 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0009g0141others(3): Show | 6 | HG01258.hp1 HG02071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+6448_586+6452d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
GT | G | 32 | a0001c0001t0003g0151a0001c0001t0003g0157a0001c0001t0003g0178others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.586+6452delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
GTT | G | 45 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(42): Show | 45 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.586+6451_586+6452d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
GTTT | G | 8 | a0001c0001t0002g0045a0001c0001t0002g0100a0001c0001t0002g0101others(5): Show | 8 | HG01952.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+6450_586+6452d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
GTTTT | G | 15 | a0001c0001t0002g0038a0001c0001t0002g0091a0001c0001t0002g0092others(12): Show | 15 | HG00639.hp1 HG01258.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.586+6449_586+6452d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
GTTTTT | G | 49 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0043others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.586+6448_586+6452d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0004g0004 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.586+6443_586+6452d others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703477
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0002t0001g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.586+6440_586+6452d others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77703477 | |||||
chr7:77703530
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.586+6475C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703530 | ||||||
chr7:77703779
|
C | T | 137 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(134): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.586+6724C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703779 | ||||||
chr7:77703850
|
C | T | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+6795C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703850 | ||||||
chr7:77703872
|
C | T | 2 | a0001c0001t0004g0143a0001c0001t0004g0144 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.586+6817C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703872 | ||||||
chr7:77703950
|
G | A | 68 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(65): Show | 68 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.586+6895G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703950 | ||||||
chr7:77703990
|
A | T | 1 | a0003c0012t0012g0208 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+6935A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77703990 | ||||||
chr7:77704191
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7136G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704191 | ||||||
chr7:77704273
|
A | G | 2 | a0001c0001t0004g0143a0001c0001t0004g0144 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.586+7218A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704273 | ||||||
chr7:77704461
|
T | C | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+7406T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704461 | ||||||
chr7:77704556
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.586+7501C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704556 | ||||||
chr7:77704657
|
C | T | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+7602C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704657 | ||||||
chr7:77704844
|
C | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7789C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704844 | ||||||
chr7:77704923
|
G | A | 1 | a0001c0005t0040g0262 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.586+7868G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704923 | ||||||
chr7:77704937
|
A | G | 1 | a0001c0001t0007g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.586+7882A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704937 | ||||||
chr7:77704950
|
C | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+7895C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704950 | ||||||
chr7:77704990
|
G | A | 1 | a0001c0001t0008g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+7935G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704990 | ||||||
chr7:77704991
|
T | G | 1 | a0001c0001t0008g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+7936T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77704991 | ||||||
chr7:77704991
|
T | TTG | 208 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(205): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.586+7950_586+7951d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77704991 | |||||
chr7:77704991
|
TTGTG | T | 6 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(3): Show | 6 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+7948_586+7951d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77704991 | |||||
chr7:77705043
|
C | T | 4 | a0001c0001t0004g0001a0001c0001t0004g0137a0001c0001t0004g0138others(1): Show | 5 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+7988C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705043 | ||||||
chr7:77705076
|
T | G | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+8021T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705076 | ||||||
chr7:77705124
|
C | T | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.586+8069C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705124 | ||||||
chr7:77705144
|
T | G | 1 | a0001c0002t0001g0284 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.586+8089T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705144 | ||||||
chr7:77705427
|
A | T | 1 | a0001c0001t0004g0005 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.586+8372A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705427 | ||||||
chr7:77705502
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.586+8447T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705502 | ||||||
chr7:77705510
|
G | GT | 17 | a0001c0002t0001g0222a0001c0002t0001g0232a0001c0002t0001g0259others(14): Show | 17 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.586+8474dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | |||||
chr7:77705510
|
G | GTTT | 55 | a0001c0001t0002g0040a0001c0001t0002g0056a0001c0001t0002g0057others(52): Show | 55 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.586+8472_586+8474d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | |||||
chr7:77705510
|
G | GTTTT | 108 | a0001c0001t0002g0038a0001c0001t0002g0041a0001c0001t0002g0043others(105): Show | 108 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.586+8471_586+8474d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | |||||
chr7:77705510
|
G | GTTTTT | 42 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(39): Show | 43 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.586+8470_586+8474d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | |||||
chr7:77705510
|
G | GTTTTTT | 7 | a0001c0001t0008g0022a0001c0001t0008g0023a0001c0001t0008g0024others(4): Show | 7 | HG02055.hp2 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+8469_586+8474d others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77705510 | |||||
chr7:77705510
|
G | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+8455G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705510 | ||||||
chr7:77705736
|
T | C | 1 | a0001c0001t0020g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.586+8681T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705736 | ||||||
chr7:77705961
|
T | C | 1 | a0001c0002t0001g0261 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.586+8906T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77705961 | ||||||
chr7:77706003
|
C | T | 1 | a0001c0001t0013g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+8948C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706003 | ||||||
chr7:77706080
|
G | GT | 8 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+9038dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77706080 | |||||
chr7:77706356
|
C | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.586+9301C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706356 | ||||||
chr7:77706432
|
A | G | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+9377A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706432 | ||||||
chr7:77706433
|
A | G | 58 | a0001c0001t0002g0111a0001c0001t0004g0001a0001c0001t0004g0003others(55): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+9378A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706433 | ||||||
chr7:77706625
|
G | T | 1 | a0001c0001t0008g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.586+9570G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706625 | ||||||
chr7:77706832
|
A | G | 11 | a0001c0001t0004g0001a0001c0001t0004g0137a0001c0001t0004g0138others(8): Show | 12 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.586+9777A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77706832 | ||||||
chr7:77707022
|
A | AT | 75 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(72): Show | 75 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.586+9986dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77707022 | |||||
chr7:77707086
|
C | T | 2 | a0001c0001t0007g0044a0001c0001t0027g0077 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.586+10031C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707086 | ||||||
chr7:77707216
|
G | C | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+10161G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707216 | ||||||
chr7:77707251
|
C | T | 1 | a0001c0001t0004g0004 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.586+10196C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707251 | ||||||
chr7:77707756
|
A | G | 1 | a0001c0001t0034g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.586+10701A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707756 | ||||||
chr7:77707879
|
G | C | 1 | a0003c0012t0012g0208 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+10824G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707879 | ||||||
chr7:77707931
|
T | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+10876T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77707931 | ||||||
chr7:77708072
|
T | G | 1 | a0001c0002t0001g0241 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.586+11017T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708072 | ||||||
chr7:77708119
|
C | T | 69 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(66): Show | 69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.586+11064C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708119 | ||||||
chr7:77708356
|
G | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+11301G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708356 | ||||||
chr7:77708364
|
T | G | 1 | a0003c0012t0012g0208 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+11309T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708364 | ||||||
chr7:77708385
|
A | AT | 208 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(205): Show | 209 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.586+11345dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77708385 | |||||
chr7:77708385
|
A | ATT | 8 | a0001c0001t0002g0043a0001c0001t0002g0075a0001c0001t0002g0076others(5): Show | 8 | HG01109.hp1 HG01261.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+11344_586+1134 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77708385 | |||||
chr7:77708467
|
C | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.586+11412C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708467 | ||||||
chr7:77708512
|
G | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+11457G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708512 | ||||||
chr7:77708530
|
C | T | 211 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(208): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.586+11475C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708530 | ||||||
chr7:77708538
|
C | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586+11483C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708538 | ||||||
chr7:77708670
|
C | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+11615C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708670 | ||||||
chr7:77708681
|
C | T | 2 | a0001c0001t0009g0128a0001c0001t0009g0134 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.586+11626C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708681 | ||||||
chr7:77708865
|
A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.586+11810A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708865 | ||||||
chr7:77708989
|
G | A | 2 | a0001c0001t0002g0086a0001c0001t0002g0099 | 2 | NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.586+11934G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77708989 | ||||||
chr7:77709039
|
G | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+11984G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709039 | ||||||
chr7:77709152
|
TTG | T | 8 | a0001c0002t0001g0254a0001c0002t0001g0277a0001c0002t0001g0279others(5): Show | 8 | HG01071.hp2 HG01074.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+12141_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | |||||
chr7:77709152
|
TTGTG | T | 19 | a0001c0002t0001g0226a0001c0002t0001g0230a0001c0002t0001g0231others(16): Show | 19 | HG01243.hp2 HG01255.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.586+12139_586+1214 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | |||||
chr7:77709152
|
TTGTGTG | T | 81 | a0001c0002t0001g0002a0001c0002t0001g0218a0001c0002t0001g0220others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.586+12137_586+1214 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | |||||
chr7:77709152
|
TTGTGTGT others(1): Show |
T | 5 | a0001c0002t0001g0311a0001c0002t0001g0330a0001c0002t0006g0263others(2): Show | 5 | HG01123.hp2 HG01169.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.586+12135_586+1214 others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | |||||
chr7:77709152
|
TTGTGTGT others(3): Show |
T | 3 | a0001c0002t0001g0242a0001c0002t0001g0334a0001c0002t0006g0243 | 3 | HG02132.hp1 HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586+12133_586+1214 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | |||||
chr7:77709152
|
TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0002g0076a0001c0001t0002g0086a0001c0001t0002g0099 | 3 | NA18998.hp1 NA19066.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.586+12131_586+1214 others(16): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709152 | |||||
chr7:77709170
|
G | A | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+12115G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709170 | ||||||
chr7:77709174
|
G | A | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+12119G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709174 | ||||||
chr7:77709180
|
G | A | 6 | a0001c0001t0012g0187a0001c0001t0012g0191a0001c0001t0019g0031others(3): Show | 6 | HG02559.hp2 HG02970.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+12125G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709180 | ||||||
chr7:77709182
|
G | A | 8 | a0001c0001t0002g0075a0001c0001t0002g0087a0001c0001t0002g0118others(5): Show | 8 | HG02738.hp2 HG02818.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+12127G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709182 | ||||||
chr7:77709184
|
G | A | 6 | a0001c0001t0008g0022a0001c0001t0010g0055a0001c0001t0011g0079others(3): Show | 6 | HG00642.hp1 HG01884.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+12129G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709184 | ||||||
chr7:77709186
|
G | A | 69 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(66): Show | 69 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.586+12131G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709186 | ||||||
chr7:77709188
|
G | A | 15 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0088others(12): Show | 15 | HG00280.hp2 HG00642.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.586+12133G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709188 | ||||||
chr7:77709188
|
G | GTA | 38 | a0001c0001t0003g0034a0001c0001t0003g0151a0001c0001t0003g0152others(35): Show | 38 | HG00639.hp2 HG00741.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.586+12134_586+1213 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709188 | |||||
chr7:77709188
|
GTGTGTGT others(3): Show |
G | 11 | a0001c0001t0002g0075a0001c0001t0002g0087a0001c0001t0002g0118others(8): Show | 11 | HG02559.hp2 HG02738.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.586+12137_586+1214 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709188 | |||||
chr7:77709190
|
G | A | 94 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(91): Show | 95 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.586+12135G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709190 | ||||||
chr7:77709190
|
G | GTATGTA | 12 | a0001c0001t0003g0035a0001c0001t0003g0036a0001c0001t0003g0153others(9): Show | 12 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.586+12136_586+1213 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709190 | |||||
chr7:77709190
|
GTGTGTGT others(1): Show |
G | 3 | a0001c0001t0008g0022a0001c0001t0010g0055a0001c0001t0011g0079 | 3 | HG00642.hp1 HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.586+12139_586+1214 others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709190 | |||||
chr7:77709192
|
G | A | 75 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0088others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.586+12137G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709192 | ||||||
chr7:77709192
|
GTGTGTA | G | 59 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(56): Show | 59 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.586+12141_586+1214 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709192 | |||||
chr7:77709194
|
G | A | 46 | a0001c0001t0002g0089a0001c0001t0004g0001a0001c0001t0004g0003others(43): Show | 47 | HG00280.hp1 HG00323.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.586+12139G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709194 | ||||||
chr7:77709194
|
G | GTA | 4 | a0001c0001t0009g0133a0001c0001t0022g0046a0001c0001t0022g0047others(1): Show | 4 | HG01891.hp2 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+12140_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709194 | |||||
chr7:77709194
|
GTGTA | G | 8 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0088others(5): Show | 8 | HG00280.hp2 HG01255.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+12147_586+1215 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709194 | |||||
chr7:77709196
|
G | A | 39 | a0001c0001t0002g0111a0001c0001t0003g0035a0001c0001t0003g0036others(36): Show | 39 | HG00140.hp1 HG00733.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.586+12141G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709196 | ||||||
chr7:77709196
|
GTA | G | 33 | a0001c0001t0002g0089a0001c0001t0004g0001a0001c0001t0004g0003others(30): Show | 34 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.586+12143_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709196 | |||||
chr7:77709198
|
A | ATG | 57 | a0001c0001t0003g0034a0001c0001t0003g0151a0001c0001t0003g0152others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.586+12145_586+1214 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77709198 | |||||
chr7:77709198
|
A | G | 39 | a0001c0001t0002g0111a0001c0001t0003g0035a0001c0001t0003g0036others(36): Show | 39 | HG00140.hp1 HG00733.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.586+12143A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709198 | ||||||
chr7:77709299
|
T | G | 4 | a0001c0001t0004g0011a0001c0001t0004g0016a0001c0001t0004g0017others(1): Show | 4 | HG02071.hp2 NA18612.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+12244T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709299 | ||||||
chr7:77709324
|
G | C | 1 | a0002c0003t0007g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.586+12269G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709324 | ||||||
chr7:77709447
|
G | C | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+12392G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709447 | ||||||
chr7:77709526
|
G | A | 2 | a0001c0001t0018g0129a0001c0001t0018g0136 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.586+12471G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709526 | ||||||
chr7:77709679
|
C | G | 2 | a0001c0002t0001g0242a0001c0002t0006g0243 | 2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586+12624C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709679 | ||||||
chr7:77709782
|
G | C | 4 | a0001c0001t0005g0150a0001c0001t0012g0187a0001c0001t0012g0191others(1): Show | 4 | HG01175.hp2 HG02970.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+12727G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709782 | ||||||
chr7:77709816
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.586+12761A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709816 | ||||||
chr7:77709893
|
C | A | 1 | a0001c0001t0034g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.586+12838C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709893 | ||||||
chr7:77709976
|
T | C | 2 | a0001c0001t0005g0194a0001c0001t0005g0204 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.586+12921T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77709976 | ||||||
chr7:77710456
|
C | G | 1 | a0003c0012t0012g0208 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.586+13401C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710456 | ||||||
chr7:77710528
|
A | G | 1 | a0001c0001t0005g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.586+13473A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710528 | ||||||
chr7:77710592
|
T | C | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+13537T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710592 | ||||||
chr7:77710650
|
T | G | 18 | a0001c0001t0002g0111a0001c0001t0004g0107a0001c0001t0004g0108others(15): Show | 18 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.586+13595T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710650 | ||||||
chr7:77710702
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.586+13647T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710702 | ||||||
chr7:77710758
|
G | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+13703G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77710758 | ||||||
chr7:77711081
|
A | G | 2 | a0001c0002t0001g0324a0001c0002t0001g0325 | 2 | NA18972.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.586+14026A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711081 | ||||||
chr7:77711257
|
A | G | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+14202A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711257 | ||||||
chr7:77711293
|
A | G | 1 | a0001c0002t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+14238A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711293 | ||||||
chr7:77711322
|
A | AT | 6 | a0001c0001t0004g0017a0001c0002t0001g0236a0001c0002t0001g0251others(3): Show | 6 | HG02071.hp2 HG02698.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+14288dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | |||||
chr7:77711322
|
AT | A | 46 | a0001c0001t0002g0070a0001c0001t0002g0071a0001c0001t0002g0072others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.586+14288delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | |||||
chr7:77711322
|
ATT | A | 128 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(125): Show | 128 | HG00423.hp2 HG00438.hp1 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.586+14287_586+1428 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | |||||
chr7:77711322
|
ATTT | A | 6 | a0001c0001t0002g0094a0001c0001t0002g0103a0001c0001t0003g0152others(3): Show | 6 | HG02004.hp2 HG02572.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+14286_586+1428 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77711322 | |||||
chr7:77711346
|
C | T | 6 | a0001c0001t0005g0198a0001c0001t0005g0205a0001c0001t0005g0206others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+14291C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711346 | ||||||
chr7:77711424
|
C | T | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+14369C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711424 | ||||||
chr7:77711504
|
T | A | 72 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 72 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.586+14449T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711504 | ||||||
chr7:77711544
|
T | C | 2 | a0001c0002t0001g0242a0001c0002t0006g0243 | 2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.586+14489T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711544 | ||||||
chr7:77711557
|
G | T | 2 | a0001c0001t0022g0046a0001c0001t0022g0047 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.586+14502G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711557 | ||||||
chr7:77711578
|
G | A | 1 | a0001c0001t0003g0172 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.586+14523G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711578 | ||||||
chr7:77711631
|
A | G | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+14576A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711631 | ||||||
chr7:77711915
|
A | C | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+14860A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77711915 | ||||||
chr7:77712058
|
GT | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.586+15011delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77712058 | |||||
chr7:77712215
|
G | GTA | 58 | a0001c0001t0002g0111a0001c0001t0004g0001a0001c0001t0004g0003others(55): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+15165_586+1516 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77712215 | |||||
chr7:77712278
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+15223A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712278 | ||||||
chr7:77712287
|
A | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.586+15232A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712287 | ||||||
chr7:77712422
|
A | T | 58 | a0001c0001t0002g0111a0001c0001t0004g0001a0001c0001t0004g0003others(55): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+15367A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712422 | ||||||
chr7:77712436
|
A | G | 1 | a0001c0002t0001g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.586+15381A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712436 | ||||||
chr7:77712530
|
C | T | 1 | a0001c0002t0001g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.586+15475C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712530 | ||||||
chr7:77712780
|
T | TA | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+15726dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77712780 | |||||
chr7:77712819
|
C | CTT | 323 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(320): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.586+15764_586+1576 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712819 | ||||||
chr7:77712882
|
G | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.586+15827G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712882 | ||||||
chr7:77712971
|
A | G | 1 | a0001c0001t0004g0008 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.586+15916A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77712971 | ||||||
chr7:77713254
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+16199A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713254 | ||||||
chr7:77713268
|
T | C | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.586+16213T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713268 | ||||||
chr7:77713302
|
T | C | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.586+16247T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713302 | ||||||
chr7:77713311
|
C | A | 1 | a0001c0002t0001g0313 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.586+16256C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713311 | ||||||
chr7:77713356
|
T | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+16301T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713356 | ||||||
chr7:77713385
|
C | T | 4 | a0001c0004t0005g0195a0001c0004t0005g0209a0001c0004t0005g0210others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+16330C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713385 | ||||||
chr7:77713391
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.586+16336C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713391 | ||||||
chr7:77713482
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+16427G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713482 | ||||||
chr7:77713484
|
G | A | 1 | a0001c0002t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.586+16429G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713484 | ||||||
chr7:77713524
|
T | G | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.586+16469T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713524 | ||||||
chr7:77713546
|
C | T | 17 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(14): Show | 17 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.586+16491C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713546 | ||||||
chr7:77713665
|
C | CT | 74 | a0001c0001t0002g0045a0001c0001t0003g0034a0001c0001t0003g0035others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.586+16624dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77713665 | |||||
chr7:77713679
|
T | A | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+16624T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713679 | ||||||
chr7:77713680
|
A | T | 68 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(65): Show | 68 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.586+16625A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713680 | ||||||
chr7:77713807
|
C | G | 1 | a0001c0001t0009g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586+16752C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713807 | ||||||
chr7:77713885
|
A | G | 1 | a0001c0001t0007g0013 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.586+16830A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713885 | ||||||
chr7:77713951
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.586+16896A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77713951 | ||||||
chr7:77714340
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586+17285G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714340 | ||||||
chr7:77714381
|
T | C | 16 | a0001c0001t0002g0111a0001c0001t0004g0107a0001c0001t0004g0108others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.586+17326T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714381 | ||||||
chr7:77714467
|
C | T | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+17412C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714467 | ||||||
chr7:77714581
|
A | G | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+17526A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714581 | ||||||
chr7:77714611
|
G | A | 333 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(330): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.586+17556G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714611 | ||||||
chr7:77714685
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.586+17630G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714685 | ||||||
chr7:77714744
|
C | T | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.586+17689C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714744 | ||||||
chr7:77714843
|
G | A | 1 | a0001c0001t0005g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586+17788G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714843 | ||||||
chr7:77714957
|
T | C | 4 | a0001c0002t0001g0002a0001c0002t0001g0287a0001c0002t0001g0314others(1): Show | 5 | NA18747.hp2 NA18946.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+17902T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714957 | ||||||
chr7:77714958
|
C | CA | 7 | a0001c0002t0001g0220a0001c0002t0001g0232a0001c0002t0001g0242others(4): Show | 7 | HG01981.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+17924dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77714958 | |||||
chr7:77714958
|
CA | C | 204 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(201): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.586+17924delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77714958 | |||||
chr7:77714958
|
CAA | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+17923_586+1792 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77714958 | |||||
chr7:77714975
|
A | G | 2 | a0001c0002t0001g0299a0001c0002t0001g0318 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.586+17920A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77714975 | ||||||
chr7:77715117
|
C | A | 1 | a0006c0010t0028g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+18062C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715117 | ||||||
chr7:77715139
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.586+18084G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715139 | ||||||
chr7:77715267
|
C | T | 2 | a0001c0001t0009g0132a0001c0001t0009g0141 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.586+18212C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715267 | ||||||
chr7:77715330
|
AGTGGGAT others(21): Show |
A | 1 | a0001c0002t0001g0324 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.586+18276_586+1830 others(32): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715330 | ||||||
chr7:77715425
|
C | T | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.586+18370C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715425 | ||||||
chr7:77715462
|
A | G | 3 | a0001c0002t0001g0284a0001c0002t0001g0298a0001c0002t0001g0328 | 3 | HG01496.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.586+18407A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715462 | ||||||
chr7:77715465
|
C | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0068a0001c0001t0002g0083 | 3 | NA19056.hp2 NA19079.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.586+18410C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715465 | ||||||
chr7:77715977
|
A | G | 72 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 72 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.586+18922A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77715977 | ||||||
chr7:77715991
|
ACTC | A | 6 | a0001c0001t0005g0197a0001c0001t0005g0214a0001c0004t0005g0195others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+18939_586+1894 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77715991 | |||||
chr7:77716018
|
A | G | 1 | a0001c0001t0005g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.586+18963A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716018 | ||||||
chr7:77716260
|
C | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586+19205C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716260 | ||||||
chr7:77716456
|
C | CT | 209 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(206): Show | 210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.586+19414dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716456 | |||||
chr7:77716469
|
T | C | 1 | a0001c0002t0041g0244 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.586+19414T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716469 | ||||||
chr7:77716610
|
A | G | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.586+19555A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716610 | ||||||
chr7:77716618
|
C | G | 1 | a0006c0010t0028g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.586+19563C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716618 | ||||||
chr7:77716624
|
C | CT | 59 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.586+19595dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716624 | |||||
chr7:77716624
|
C | CTT | 18 | a0001c0001t0002g0043a0001c0001t0002g0065a0001c0001t0002g0066others(15): Show | 18 | HG01943.hp1 HG01952.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.586+19594_586+1959 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716624 | |||||
chr7:77716624
|
CT | C | 64 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(61): Show | 64 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.586+19595delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77716624 | |||||
chr7:77716650
|
T | TTA | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0100others(3): Show | 6 | NA18978.hp1 NA18981.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+19595_586+1959 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716650 | ||||||
chr7:77716654
|
C | T | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.586+19599C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716654 | ||||||
chr7:77716717
|
C | T | 4 | a0001c0001t0005g0150a0001c0001t0012g0187a0001c0001t0012g0191others(1): Show | 4 | HG01175.hp2 HG02970.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+19662C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716717 | ||||||
chr7:77716763
|
C | G | 1 | a0001c0001t0011g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.587-19647C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716763 | ||||||
chr7:77716777
|
G | A | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.587-19633G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716777 | ||||||
chr7:77716780
|
C | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.587-19630C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716780 | ||||||
chr7:77716781
|
A | G | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.587-19629A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716781 | ||||||
chr7:77716783
|
C | T | 4 | a0001c0001t0005g0198a0001c0001t0005g0205a0001c0001t0005g0206others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-19627C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77716783 | ||||||
chr7:77717152
|
T | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-19258T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717152 | ||||||
chr7:77717177
|
A | G | 1 | a0001c0001t0034g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587-19233A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717177 | ||||||
chr7:77717431
|
T | C | 2 | a0001c0001t0004g0131a0001c0001t0014g0130 | 2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.587-18979T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717431 | ||||||
chr7:77717477
|
T | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-18933T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717477 | ||||||
chr7:77717552
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.587-18858G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717552 | ||||||
chr7:77717669
|
A | G | 12 | a0001c0002t0001g0223a0001c0002t0001g0226a0001c0002t0001g0227others(9): Show | 12 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-18741A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717669 | ||||||
chr7:77717828
|
G | A | 1 | a0001c0005t0040g0262 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.587-18582G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717828 | ||||||
chr7:77717864
|
T | A | 5 | a0001c0001t0002g0041a0001c0001t0002g0058a0001c0001t0002g0065others(2): Show | 5 | HG00438.hp1 HG02071.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-18546T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717864 | ||||||
chr7:77717992
|
C | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-18418C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77717992 | ||||||
chr7:77718256
|
C | A | 1 | a0001c0001t0002g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-18154C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718256 | ||||||
chr7:77718278
|
C | A | 2 | a0001c0001t0022g0046a0001c0001t0022g0047 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.587-18132C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718278 | ||||||
chr7:77718380
|
T | G | 58 | a0001c0001t0002g0111a0001c0001t0004g0001a0001c0001t0004g0003others(55): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.587-18030T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718380 | ||||||
chr7:77718846
|
T | C | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.587-17564T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718846 | ||||||
chr7:77718993
|
G | A | 1 | a0001c0002t0001g0234 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.587-17417G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718993 | ||||||
chr7:77718999
|
T | C | 2 | a0001c0001t0013g0123a0001c0001t0013g0125 | 2 | HG00639.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.587-17411T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77718999 | ||||||
chr7:77719129
|
A | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-17281A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719129 | ||||||
chr7:77719285
|
TTTAA | T | 3 | a0001c0002t0001g0233a0001c0002t0001g0276a0001c0002t0001g0303 | 3 | HG02735.hp1 NA18945.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.587-17122_587-1711 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77719285 | |||||
chr7:77719448
|
G | A | 1 | a0001c0002t0001g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.587-16962G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719448 | ||||||
chr7:77719582
|
A | G | 3 | a0001c0002t0001g0302a0001c0002t0001g0305a0001c0002t0001g0319 | 3 | NA18995.hp1 NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.587-16828A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719582 | ||||||
chr7:77719911
|
C | T | 1 | a0001c0002t0001g0280 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.587-16499C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719911 | ||||||
chr7:77719920
|
G | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-16490G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77719920 | ||||||
chr7:77720073
|
C | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-16337C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720073 | ||||||
chr7:77720392
|
G | A | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-16018G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720392 | ||||||
chr7:77720484
|
G | A | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-15926G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720484 | ||||||
chr7:77720499
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-15911C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720499 | ||||||
chr7:77720520
|
T | C | 1 | a0001c0001t0005g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.587-15890T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720520 | ||||||
chr7:77720619
|
C | G | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-15791C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720619 | ||||||
chr7:77720630
|
A | G | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-15780A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720630 | ||||||
chr7:77720763
|
C | CT | 13 | a0001c0001t0003g0153a0001c0001t0005g0197a0001c0001t0005g0213others(10): Show | 13 | HG02717.hp1 HG02818.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.587-15627dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77720763 | |||||
chr7:77720763
|
CT | C | 124 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.587-15627delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77720763 | |||||
chr7:77720763
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0158 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.587-15636_587-1562 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77720763 | |||||
chr7:77720772
|
T | C | 1 | a0001c0001t0002g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.587-15638T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720772 | ||||||
chr7:77720881
|
T | C | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-15529T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77720881 | ||||||
chr7:77721009
|
TG | T | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-15398delG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77721009 | |||||
chr7:77721021
|
G | A | 1 | a0001c0002t0001g0323 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.587-15389G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721021 | ||||||
chr7:77721032
|
G | A | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587-15378G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721032 | ||||||
chr7:77721045
|
T | G | 1 | a0001c0001t0034g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587-15365T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721045 | ||||||
chr7:77721086
|
G | A | 1 | a0001c0002t0001g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.587-15324G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721086 | ||||||
chr7:77721148
|
G | T | 72 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 72 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.587-15262G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721148 | ||||||
chr7:77721226
|
G | GT | 30 | a0001c0001t0002g0070a0001c0001t0002g0072a0001c0001t0002g0073others(27): Show | 30 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.587-15172dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77721226 | |||||
chr7:77721238
|
T | C | 1 | a0001c0002t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.587-15172T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721238 | ||||||
chr7:77721276
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-15134A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721276 | ||||||
chr7:77721283
|
A | G | 2 | a0001c0001t0003g0185a0001c0001t0034g0171 | 2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.587-15127A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721283 | ||||||
chr7:77721508
|
T | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-14902T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721508 | ||||||
chr7:77721516
|
C | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-14894C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721516 | ||||||
chr7:77721729
|
A | G | 1 | a0001c0002t0036g0272 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.587-14681A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721729 | ||||||
chr7:77721767
|
A | C | 58 | a0001c0001t0002g0111a0001c0001t0004g0001a0001c0001t0004g0003others(55): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.587-14643A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721767 | ||||||
chr7:77721767
|
A | G | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-14643A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721767 | ||||||
chr7:77721925
|
C | T | 1 | a0001c0002t0001g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-14485C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721925 | ||||||
chr7:77721971
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-14439A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77721971 | ||||||
chr7:77722023
|
C | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-14387C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722023 | ||||||
chr7:77722147
|
C | T | 3 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0014 | 3 | HG00735.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.587-14263C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722147 | ||||||
chr7:77722232
|
T | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-14178T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722232 | ||||||
chr7:77722326
|
G | T | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-14084G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722326 | ||||||
chr7:77722388
|
G | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-14022G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722388 | ||||||
chr7:77722410
|
T | C | 1 | a0001c0001t0009g0141 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.587-14000T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722410 | ||||||
chr7:77722440
|
A | T | 1 | a0001c0002t0001g0324 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.587-13970A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722440 | ||||||
chr7:77722474
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-13936C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722474 | ||||||
chr7:77722600
|
C | T | 1 | a0001c0002t0001g0276 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.587-13810C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722600 | ||||||
chr7:77722624
|
T | A | 1 | a0001c0002t0001g0324 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.587-13786T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722624 | ||||||
chr7:77722968
|
C | CT | 122 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(119): Show | 123 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.587-13425dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77722968 | |||||
chr7:77722968
|
CT | C | 88 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(85): Show | 88 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.587-13425delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77722968 | |||||
chr7:77722998
|
C | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-13412C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77722998 | ||||||
chr7:77723037
|
G | A | 1 | a0001c0002t0001g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-13373G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723037 | ||||||
chr7:77723071
|
G | T | 5 | a0001c0002t0001g0270a0001c0002t0001g0273a0001c0002t0001g0275others(2): Show | 5 | HG03491.hp1 HG04115.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-13339G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723071 | ||||||
chr7:77723112
|
A | G | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.587-13298A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723112 | ||||||
chr7:77723216
|
T | G | 6 | a0001c0001t0011g0060a0001c0001t0011g0062a0001c0001t0011g0079others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-13194T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723216 | ||||||
chr7:77723310
|
A | G | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587-13100A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723310 | ||||||
chr7:77723383
|
A | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-13027A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723383 | ||||||
chr7:77723384
|
G | A | 5 | a0001c0001t0003g0153a0001c0001t0003g0160a0001c0001t0003g0161others(2): Show | 5 | NA18943.hp1 NA18954.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-13026G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723384 | ||||||
chr7:77723407
|
A | G | 1 | a0001c0002t0006g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.587-13003A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723407 | ||||||
chr7:77723502
|
C | T | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-12908C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723502 | ||||||
chr7:77723846
|
A | G | 1 | a0001c0001t0003g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.587-12564A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723846 | ||||||
chr7:77723921
|
T | C | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-12489T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723921 | ||||||
chr7:77723944
|
A | T | 1 | a0001c0002t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.587-12466A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723944 | ||||||
chr7:77723944
|
AT | A | 214 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(211): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.587-12453delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77723944 | |||||
chr7:77723946
|
T | A | 53 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(50): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.587-12464T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723946 | ||||||
chr7:77723976
|
CTGTGTTG others(14): Show |
C | 1 | a0001c0002t0001g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-12433_587-1241 others(25): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77723976 | ||||||
chr7:77724113
|
C | T | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-12297C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724113 | ||||||
chr7:77724216
|
A | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-12194A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724216 | ||||||
chr7:77724287
|
CCTT | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-12120_587-1211 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77724287 | |||||
chr7:77724476
|
A | C | 1 | a0001c0002t0001g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.587-11934A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724476 | ||||||
chr7:77724592
|
A | C | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-11818A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724592 | ||||||
chr7:77724711
|
C | G | 1 | a0001c0002t0001g0324 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.587-11699C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724711 | ||||||
chr7:77724711
|
C | T | 211 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(208): Show | 212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.587-11699C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724711 | ||||||
chr7:77724865
|
G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-11545G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77724865 | ||||||
chr7:77725243
|
A | AATTTTTT others(22): Show |
2 | a0001c0001t0005g0206a0003c0012t0012g0208 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.587-11167_587-1116 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725243 | ||||||
chr7:77725243
|
A | AATTTTTT others(24): Show |
2 | a0001c0001t0005g0198a0001c0001t0005g0207 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.587-11167_587-1116 others(35): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725243 | ||||||
chr7:77725243
|
A | AATTTTTT others(26): Show |
1 | a0001c0001t0005g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.587-11167_587-1116 others(37): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725243 | ||||||
chr7:77725244
|
C | CT | 33 | a0001c0001t0002g0111a0001c0001t0004g0107a0001c0001t0004g0108others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.587-11145dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTT | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-11146_587-1114 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(3): Show |
14 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0156others(11): Show | 14 | HG02074.hp1 HG02647.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-11154_587-1114 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0003g0165a0001c0001t0003g0179a0001c0001t0020g0212others(2): Show | 5 | HG02129.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-11155_587-1114 others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(5): Show |
19 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(16): Show | 19 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.587-11156_587-1114 others(16): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(6): Show |
27 | a0001c0001t0002g0038a0001c0001t0002g0045a0001c0001t0002g0056others(24): Show | 27 | HG00639.hp1 HG01074.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.587-11157_587-1114 others(17): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(7): Show |
28 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0063others(25): Show | 28 | HG00438.hp1 HG01167.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.587-11158_587-1114 others(18): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(8): Show |
20 | a0001c0001t0002g0064a0001c0001t0002g0081a0001c0001t0002g0091others(17): Show | 21 | HG00280.hp2 HG00423.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.587-11159_587-1114 others(19): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(9): Show |
12 | a0001c0001t0002g0097a0001c0001t0003g0182a0001c0001t0004g0003others(9): Show | 12 | HG00735.hp2 HG01123.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.587-11160_587-1114 others(20): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(10): Show |
8 | a0001c0001t0002g0101a0001c0001t0004g0004a0001c0001t0004g0012others(5): Show | 8 | HG02071.hp2 HG02080.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-11161_587-1114 others(21): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0011 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.587-11162_587-1114 others(22): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(12): Show |
4 | a0001c0001t0002g0040a0001c0001t0002g0068a0001c0001t0002g0083others(1): Show | 4 | NA19043.hp2 NA19056.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-11163_587-1114 others(23): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0004g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.587-11164_587-1114 others(24): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0005g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(27): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0005g0193a0001c0001t0005g0201a0001c0001t0005g0203 | 3 | HG01433.hp1 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(28): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(18): Show |
3 | a0001c0001t0003g0160a0001c0001t0003g0168a0001c0001t0003g0181 | 3 | HG02559.hp1 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(29): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(19): Show |
5 | a0001c0001t0003g0157a0001c0001t0003g0161a0001c0001t0004g0144others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-11145_587-1114 others(30): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(20): Show |
4 | a0001c0001t0003g0172a0001c0001t0034g0171a0001c0004t0005g0195others(1): Show | 4 | HG01192.hp2 HG02293.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-11145_587-1114 others(31): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0003g0034a0001c0001t0003g0189a0001c0009t0003g0176 | 3 | HG02615.hp1 NA19066.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(32): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0005g0214 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.587-11145_587-1114 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(34): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(24): Show |
5 | a0001c0001t0003g0036a0001c0001t0003g0169a0001c0001t0003g0173others(2): Show | 5 | HG03492.hp1 HG03710.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-11145_587-1114 others(35): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0003g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(36): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0003g0185 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(37): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(28): Show |
2 | a0001c0001t0003g0186a0001c0001t0005g0202 | 2 | HG03540.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.587-11145_587-1114 others(39): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | CTTTTTTT others(32): Show |
1 | a0001c0001t0005g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.587-11145_587-1114 others(43): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725244
|
C | T | 6 | a0001c0001t0005g0198a0001c0001t0005g0205a0001c0001t0005g0206others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-11166C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725244 | ||||||
chr7:77725244
|
CT | C | 11 | a0001c0001t0003g0162a0001c0001t0005g0194a0001c0001t0005g0204others(8): Show | 11 | HG00639.hp2 HG01099.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.587-11145delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725244 | |||||
chr7:77725381
|
T | TG | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-11027dupG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725381 | |||||
chr7:77725397
|
G | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-11013G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725397 | ||||||
chr7:77725398
|
C | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-11012C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725398 | ||||||
chr7:77725409
|
G | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-11001G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725409 | ||||||
chr7:77725414
|
A | ATTTTGTA others(51): Show |
215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-10980_587-1097 others(62): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77725414 | |||||
chr7:77725543
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0003g0174 | 2 | NA18975.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.587-10867G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725543 | ||||||
chr7:77725583
|
T | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10827T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725583 | ||||||
chr7:77725833
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.587-10577G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725833 | ||||||
chr7:77725947
|
G | T | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-10463G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725947 | ||||||
chr7:77725948
|
C | T | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-10462C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77725948 | ||||||
chr7:77726002
|
A | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10408A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726002 | ||||||
chr7:77726040
|
A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-10370A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726040 | ||||||
chr7:77726087
|
T | C | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-10323T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726087 | ||||||
chr7:77726282
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10128G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726282 | ||||||
chr7:77726303
|
A | G | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.587-10107A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726303 | ||||||
chr7:77726361
|
T | C | 2 | a0001c0001t0005g0194a0001c0001t0005g0204 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.587-10049T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726361 | ||||||
chr7:77726388
|
T | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-10022T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726388 | ||||||
chr7:77726466
|
G | A | 1 | a0001c0002t0001g0258 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-9944G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726466 | ||||||
chr7:77726547
|
A | G | 4 | a0002c0003t0004g0039a0002c0003t0004g0049a0002c0003t0004g0051others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-9863A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726547 | ||||||
chr7:77726776
|
A | AT | 148 | a0001c0001t0002g0100a0001c0001t0002g0111a0001c0001t0003g0034others(145): Show | 149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.587-9613dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | |||||
chr7:77726776
|
A | ATT | 72 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 72 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.587-9614_587-9613d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | |||||
chr7:77726776
|
A | ATTT | 6 | a0001c0001t0002g0045a0001c0001t0002g0097a0001c0001t0002g0099others(3): Show | 6 | HG01884.hp2 HG02738.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-9615_587-9613d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | |||||
chr7:77726776
|
ATT | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-9614_587-9613d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77726776 | |||||
chr7:77726872
|
C | T | 2 | a0001c0001t0004g0143a0001c0001t0004g0144 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.587-9538C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77726872 | ||||||
chr7:77727000
|
C | T | 3 | a0001c0002t0001g0231a0001c0002t0001g0296a0001c0002t0001g0321 | 3 | NA18983.hp1 NA19009.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.587-9410C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727000 | ||||||
chr7:77727002
|
C | T | 16 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0109others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.587-9408C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727002 | ||||||
chr7:77727033
|
G | T | 3 | a0001c0001t0004g0145a0001c0001t0004g0146a0001c0001t0004g0147 | 3 | HG02615.hp2 HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.587-9377G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727033 | ||||||
chr7:77727089
|
C | CT | 60 | a0001c0001t0002g0111a0001c0001t0003g0157a0001c0001t0004g0001others(57): Show | 61 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.587-9306dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77727089 | |||||
chr7:77727245
|
G | A | 1 | a0001c0001t0034g0171 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.587-9165G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727245 | ||||||
chr7:77727276
|
G | A | 6 | a0001c0002t0001g0223a0001c0002t0001g0247a0001c0002t0001g0259others(3): Show | 6 | HG01358.hp1 HG01516.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-9134G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727276 | ||||||
chr7:77727379
|
G | A | 1 | a0001c0001t0003g0161 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.587-9031G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727379 | ||||||
chr7:77727442
|
T | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-8968T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727442 | ||||||
chr7:77727600
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.587-8810C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727600 | ||||||
chr7:77727625
|
A | AT | 11 | a0001c0001t0007g0054a0001c0001t0007g0078a0001c0001t0008g0020others(8): Show | 11 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.587-8769dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77727625 | |||||
chr7:77727626
|
T | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.587-8784T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727626 | ||||||
chr7:77727643
|
C | T | 1 | a0001c0002t0001g0234 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.587-8767C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727643 | ||||||
chr7:77727716
|
T | A | 1 | a0001c0001t0003g0183 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.587-8694T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727716 | ||||||
chr7:77727729
|
G | A | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.587-8681G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727729 | ||||||
chr7:77727752
|
C | T | 2 | a0001c0001t0018g0129a0001c0001t0018g0136 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.587-8658C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727752 | ||||||
chr7:77727957
|
C | T | 72 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 72 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.587-8453C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77727957 | ||||||
chr7:77728052
|
C | T | 1 | a0004c0011t0012g0192 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.587-8358C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728052 | ||||||
chr7:77728074
|
A | G | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-8336A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728074 | ||||||
chr7:77728246
|
T | A | 67 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(64): Show | 67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.587-8164T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728246 | ||||||
chr7:77728355
|
T | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-8055T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728355 | ||||||
chr7:77728431
|
A | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.587-7979A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728431 | ||||||
chr7:77728546
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.587-7864C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728546 | ||||||
chr7:77728715
|
A | T | 4 | a0001c0002t0001g0284a0001c0002t0001g0298a0001c0002t0001g0328others(1): Show | 4 | HG01496.hp1 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-7695A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728715 | ||||||
chr7:77728755
|
A | G | 72 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 72 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.587-7655A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728755 | ||||||
chr7:77728784
|
T | C | 1 | a0001c0001t0007g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.587-7626T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728784 | ||||||
chr7:77728830
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-7580C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728830 | ||||||
chr7:77728959
|
G | A | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.587-7451G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77728959 | ||||||
chr7:77729168
|
A | T | 1 | a0001c0001t0004g0001 | 2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.587-7242A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729168 | ||||||
chr7:77729489
|
G | C | 1 | a0001c0001t0013g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.587-6921G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729489 | ||||||
chr7:77729666
|
T | C | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.587-6744T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729666 | ||||||
chr7:77729766
|
C | T | 1 | a0001c0001t0029g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.587-6644C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77729766 | ||||||
chr7:77730080
|
T | A | 1 | a0002c0003t0004g0050 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.587-6330T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730080 | ||||||
chr7:77730089
|
G | C | 1 | a0003c0012t0012g0208 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.587-6321G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730089 | ||||||
chr7:77730228
|
C | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-6182C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730228 | ||||||
chr7:77730526
|
T | TAAAAATC others(349): Show |
1 | a0001c0002t0001g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-5870_587-5869i others(358): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77730526 | |||||
chr7:77730620
|
T | C | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.587-5790T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77730620 | ||||||
chr7:77731014
|
G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-5396G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731014 | ||||||
chr7:77731092
|
A | G | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.587-5318A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731092 | ||||||
chr7:77731116
|
T | G | 1 | a0001c0002t0001g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.587-5294T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731116 | ||||||
chr7:77731290
|
T | G | 1 | a0001c0001t0003g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.587-5120T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731290 | ||||||
chr7:77731306
|
T | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.587-5104T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731306 | ||||||
chr7:77731410
|
A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-5000A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731410 | ||||||
chr7:77731423
|
A | G | 1 | a0001c0002t0001g0258 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.587-4987A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731423 | ||||||
chr7:77731534
|
C | T | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-4876C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731534 | ||||||
chr7:77731568
|
T | C | 1 | a0001c0002t0006g0266 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.587-4842T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731568 | ||||||
chr7:77731584
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-4826A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731584 | ||||||
chr7:77731772
|
T | A | 1 | a0001c0001t0002g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.587-4638T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731772 | ||||||
chr7:77731826
|
C | A | 2 | a0001c0001t0005g0197a0001c0001t0005g0214 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.587-4584C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731826 | ||||||
chr7:77731983
|
G | A | 1 | a0001c0001t0003g0153 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.587-4427G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77731983 | ||||||
chr7:77732189
|
T | A | 1 | a0001c0001t0002g0068 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.587-4221T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732189 | ||||||
chr7:77732210
|
A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.587-4200A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732210 | ||||||
chr7:77732629
|
C | G | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-3781C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732629 | ||||||
chr7:77732675
|
T | C | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.587-3735T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732675 | ||||||
chr7:77732763
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-3647A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732763 | ||||||
chr7:77732955
|
T | C | 1 | a0001c0001t0019g0032 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.587-3455T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77732955 | ||||||
chr7:77733091
|
C | T | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-3319C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733091 | ||||||
chr7:77733172
|
G | C | 76 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(73): Show | 76 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.587-3238G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733172 | ||||||
chr7:77733187
|
A | G | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-3223A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733187 | ||||||
chr7:77733368
|
C | T | 1 | a0001c0001t0011g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.587-3042C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733368 | ||||||
chr7:77733376
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-3034A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733376 | ||||||
chr7:77733430
|
C | T | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-2980C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733430 | ||||||
chr7:77733812
|
G | A | 212 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(209): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.587-2598G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77733812 | ||||||
chr7:77734140
|
A | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-2270A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734140 | ||||||
chr7:77734570
|
C | T | 6 | a0001c0001t0003g0153a0001c0001t0003g0177a0001c0002t0017g0238others(3): Show | 6 | HG00099.hp2 HG01109.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-1840C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734570 | ||||||
chr7:77734654
|
A | C | 1 | a0001c0002t0001g0329 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.587-1756A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734654 | ||||||
chr7:77734916
|
T | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-1494T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77734916 | ||||||
chr7:77735054
|
G | GA | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-1345dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 77735054 | |||||
chr7:77735065
|
A | C | 3 | a0001c0002t0001g0241a0001c0002t0001g0253a0001c0002t0001g0274 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.587-1345A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735065 | ||||||
chr7:77735068
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-1342A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735068 | ||||||
chr7:77735211
|
T | C | 1 | a0001c0002t0001g0242 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.587-1199T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735211 | ||||||
chr7:77735219
|
A | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.587-1191A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735219 | ||||||
chr7:77735709
|
A | G | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.587-701A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735709 | ||||||
chr7:77735762
|
T | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-648T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735762 | ||||||
chr7:77735779
|
TG | T | 3 | a0001c0002t0001g0241a0001c0002t0001g0253a0001c0002t0001g0274 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.587-630delG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735779 | ||||||
chr7:77735917
|
T | A | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.587-493T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735917 | ||||||
chr7:77735974
|
T | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-436T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77735974 | ||||||
chr7:77736048
|
T | C | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.587-362T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736048 | ||||||
chr7:77736095
|
C | A | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.587-315C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736095 | ||||||
chr7:77736165
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.587-245C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736165 | ||||||
chr7:77736213
|
A | G | 1 | a0001c0002t0001g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.587-197A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 1/7 | chr7 | 77736213 | ||||||
chr7:77736585
|
G | A | 3 | a0001c0004t0005g0195a0001c0004t0005g0209a0001c0004t0005g0210 | 3 | HG01070.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.703+59G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736585 | ||||||
chr7:77736664
|
A | G | 1 | a0001c0002t0001g0281 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.703+138A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736664 | ||||||
chr7:77736740
|
G | C | 5 | a0001c0002t0001g0224a0001c0002t0001g0234a0001c0002t0001g0235others(2): Show | 5 | HG00423.hp1 NA19054.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+214G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736740 | ||||||
chr7:77736751
|
G | A | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.703+225G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736751 | ||||||
chr7:77736828
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+302A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736828 | ||||||
chr7:77736860
|
A | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.703+334A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736860 | ||||||
chr7:77736941
|
T | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+415T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736941 | ||||||
chr7:77736983
|
C | T | 1 | a0001c0002t0001g0228 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.703+457C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736983 | ||||||
chr7:77736994
|
T | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+468T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77736994 | ||||||
chr7:77737034
|
T | G | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.703+508T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737034 | ||||||
chr7:77737558
|
G | T | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1032G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737558 | ||||||
chr7:77737671
|
G | A | 1 | a0001c0002t0017g0240 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703+1145G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737671 | ||||||
chr7:77737782
|
G | T | 2 | a0001c0001t0007g0054a0001c0001t0007g0078 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.703+1256G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737782 | ||||||
chr7:77737830
|
C | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+1304C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737830 | ||||||
chr7:77737835
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+1309C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737835 | ||||||
chr7:77737851
|
C | T | 2 | a0001c0001t0005g0194a0001c0001t0005g0204 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.703+1325C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737851 | ||||||
chr7:77737947
|
G | A | 1 | a0001c0001t0008g0022 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.703+1421G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77737947 | ||||||
chr7:77738041
|
G | T | 1 | a0001c0001t0014g0095 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.703+1515G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738041 | ||||||
chr7:77738089
|
A | AT | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1572dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77738089 | |||||
chr7:77738098
|
T | C | 1 | a0001c0002t0001g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.703+1572T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738098 | ||||||
chr7:77738212
|
T | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+1686T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738212 | ||||||
chr7:77738316
|
A | T | 2 | a0001c0001t0005g0194a0001c0001t0005g0204 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.703+1790A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738316 | ||||||
chr7:77738351
|
A | G | 2 | a0001c0001t0022g0046a0001c0001t0022g0047 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.703+1825A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738351 | ||||||
chr7:77738728
|
A | C | 1 | a0001c0002t0001g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.703+2202A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738728 | ||||||
chr7:77738763
|
G | C | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.703+2237G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738763 | ||||||
chr7:77738811
|
T | A | 1 | a0001c0002t0001g0291 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.703+2285T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738811 | ||||||
chr7:77738853
|
C | T | 72 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(69): Show | 72 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.703+2327C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738853 | ||||||
chr7:77738867
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.703+2341A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77738867 | ||||||
chr7:77739066
|
A | G | 2 | a0001c0001t0019g0031a0001c0001t0019g0032 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+2540A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739066 | ||||||
chr7:77739100
|
A | G | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703+2574A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739100 | ||||||
chr7:77739533
|
T | G | 1 | a0001c0001t0011g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+3007T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739533 | ||||||
chr7:77739574
|
G | A | 2 | a0001c0001t0019g0031a0001c0001t0019g0032 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+3048G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739574 | ||||||
chr7:77739711
|
G | GA | 67 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0045others(64): Show | 67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.703+3207dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | |||||
chr7:77739711
|
G | GAA | 9 | a0001c0001t0002g0097a0001c0001t0033g0149a0001c0002t0001g0221others(6): Show | 9 | HG00642.hp2 HG01123.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3206_703+3207d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | |||||
chr7:77739711
|
GA | G | 91 | a0001c0001t0002g0087a0001c0001t0003g0034a0001c0001t0003g0035others(88): Show | 92 | HG00280.hp2 HG00639.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.703+3207delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | |||||
chr7:77739711
|
GAA | G | 8 | a0001c0001t0009g0128a0001c0001t0009g0134a0001c0001t0015g0028others(5): Show | 8 | HG00140.hp1 HG01256.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+3206_703+3207d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | |||||
chr7:77739711
|
GAAAAAA | G | 15 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0109others(12): Show | 15 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.703+3202_703+3207d others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739711 | |||||
chr7:77739739
|
C | CT | 58 | a0001c0001t0005g0170a0001c0001t0005g0200a0001c0001t0005g0202others(55): Show | 59 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.703+3242dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTT | 52 | a0001c0001t0005g0193a0001c0001t0005g0197a0001c0001t0005g0198others(49): Show | 52 | HG00438.hp2 HG00738.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.703+3241_703+3242d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTT | 16 | a0001c0001t0005g0150a0001c0001t0005g0194a0001c0001t0005g0205others(13): Show | 16 | HG00140.hp2 HG00423.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.703+3240_703+3242d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTT | 12 | a0001c0001t0003g0035a0001c0001t0003g0162a0001c0001t0003g0166others(9): Show | 12 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+3239_703+3242d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTT | 19 | a0001c0001t0003g0036a0001c0001t0003g0153a0001c0001t0003g0155others(16): Show | 19 | HG00733.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.703+3238_703+3242d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTTT | 16 | a0001c0001t0003g0034a0001c0001t0003g0157a0001c0001t0003g0161others(13): Show | 16 | HG00735.hp2 HG01884.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+3237_703+3242d others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTTTT | 8 | a0001c0001t0003g0186a0001c0001t0004g0011a0001c0001t0004g0019others(5): Show | 8 | HG02647.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+3236_703+3242d others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTTTT others(1): Show |
9 | a0001c0001t0003g0154a0001c0001t0003g0156a0001c0001t0003g0175others(6): Show | 9 | HG01256.hp2 HG01258.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3235_703+3242d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTTTT others(2): Show |
9 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0159others(6): Show | 9 | HG02055.hp1 HG02074.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3234_703+3242d others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0003g0164a0001c0001t0004g0001a0001c0001t0004g0137others(2): Show | 6 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+3233_703+3242d others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0138a0001c0001t0025g0113a0001c0001t0026g0114 | 3 | HG01109.hp1 HG01517.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.703+3232_703+3242d others(13): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0183a0001c0001t0018g0136 | 2 | HG02145.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.703+3231_703+3242d others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
CTTTTTTT | C | 12 | a0001c0001t0002g0038a0001c0001t0002g0043a0001c0001t0002g0069others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+3236_703+3242d others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
CTTTTTTT others(1): Show |
C | 67 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(64): Show | 67 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.703+3235_703+3242d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739739
|
CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0109others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+3232_703+3242d others(13): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77739739 | |||||
chr7:77739813
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.703+3287G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739813 | ||||||
chr7:77739849
|
A | G | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.703+3323A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739849 | ||||||
chr7:77739894
|
C | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3368C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739894 | ||||||
chr7:77739899
|
G | A | 1 | a0001c0001t0005g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703+3373G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77739899 | ||||||
chr7:77740003
|
C | T | 1 | a0001c0001t0007g0078 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.703+3477C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740003 | ||||||
chr7:77740004
|
G | A | 6 | a0001c0001t0005g0193a0001c0001t0005g0199a0001c0001t0005g0200others(3): Show | 6 | HG01433.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+3478G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740004 | ||||||
chr7:77740119
|
C | A | 67 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(64): Show | 67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.703+3593C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740119 | ||||||
chr7:77740237
|
A | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+3711A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740237 | ||||||
chr7:77740320
|
CAT | C | 4 | a0001c0001t0004g0001a0001c0001t0004g0137a0001c0001t0004g0138others(1): Show | 5 | HG00280.hp2 HG01515.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3795_703+3796d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740320 | ||||||
chr7:77740353
|
A | G | 4 | a0001c0001t0005g0198a0001c0001t0005g0205a0001c0001t0005g0206others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+3827A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740353 | ||||||
chr7:77740454
|
C | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+3928C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740454 | ||||||
chr7:77740662
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4136A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740662 | ||||||
chr7:77740666
|
G | A | 73 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(70): Show | 73 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.703+4140G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740666 | ||||||
chr7:77740777
|
G | A | 1 | a0001c0002t0001g0304 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.703+4251G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740777 | ||||||
chr7:77740981
|
TTTTC | T | 24 | a0001c0001t0003g0159a0001c0001t0005g0150a0001c0001t0005g0193others(21): Show | 24 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.703+4459_703+4462d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740981 | |||||
chr7:77740982
|
TTTC | T | 44 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(41): Show | 44 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.703+4459_703+4461d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740982 | |||||
chr7:77740985
|
C | CT | 7 | a0001c0001t0002g0040a0001c0001t0002g0043a0001c0001t0004g0003others(4): Show | 7 | HG01981.hp1 HG02055.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+4478dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740985 | |||||
chr7:77740985
|
CT | C | 14 | a0001c0001t0002g0088a0001c0001t0014g0130a0001c0001t0026g0114others(11): Show | 14 | HG00323.hp1 HG01192.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+4478delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77740985 | |||||
chr7:77740990
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0032g0033 | 2 | HG02015.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.703+4464T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77740990 | ||||||
chr7:77741041
|
C | T | 1 | a0001c0001t0019g0032 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.703+4515C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741041 | ||||||
chr7:77741080
|
G | A | 1 | a0001c0002t0001g0220 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.703+4554G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741080 | ||||||
chr7:77741094
|
C | A | 5 | a0001c0001t0005g0198a0001c0001t0005g0205a0001c0001t0005g0206others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+4568C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741094 | ||||||
chr7:77741111
|
C | T | 2 | a0001c0001t0019g0031a0001c0001t0019g0032 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+4585C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741111 | ||||||
chr7:77741135
|
C | T | 2 | a0001c0001t0005g0194a0001c0001t0005g0204 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.703+4609C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741135 | ||||||
chr7:77741161
|
G | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.703+4635G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741161 | ||||||
chr7:77741199
|
C | T | 4 | a0001c0002t0001g0270a0001c0002t0001g0275a0001c0002t0038g0297others(1): Show | 4 | HG03491.hp1 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4673C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741199 | ||||||
chr7:77741230
|
A | G | 1 | a0001c0001t0003g0161 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.703+4704A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741230 | ||||||
chr7:77741345
|
A | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.703+4819A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741345 | ||||||
chr7:77741477
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+4951G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741477 | ||||||
chr7:77741552
|
C | T | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.703+5026C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741552 | ||||||
chr7:77741691
|
C | CA | 44 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(41): Show | 45 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.703+5180dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77741691 | |||||
chr7:77741691
|
C | CAA | 6 | a0001c0001t0011g0060a0001c0001t0011g0062a0001c0001t0011g0079others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+5179_703+5180d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77741691 | |||||
chr7:77741691
|
CA | C | 10 | a0001c0001t0002g0084a0001c0001t0002g0118a0001c0001t0003g0158others(7): Show | 10 | HG01257.hp2 HG01433.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+5180delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77741691 | |||||
chr7:77741773
|
G | A | 7 | a0001c0002t0001g0293a0001c0002t0001g0295a0001c0002t0001g0299others(4): Show | 7 | HG01099.hp1 HG01433.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+5247G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741773 | ||||||
chr7:77741999
|
G | T | 1 | a0001c0001t0002g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.703+5473G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77741999 | ||||||
chr7:77742038
|
T | C | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.703+5512T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742038 | ||||||
chr7:77742164
|
TA | T | 18 | a0001c0001t0004g0004a0001c0001t0004g0007a0001c0001t0004g0009others(15): Show | 18 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.703+5655delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742164 | |||||
chr7:77742179
|
AAATACAC others(2): Show |
A | 7 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0094others(4): Show | 7 | NA18946.hp1 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+5655_703+5663d others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742179 | |||||
chr7:77742179
|
AAATACAC others(12): Show |
A | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+5655_703+5673d others(21): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742179 | |||||
chr7:77742180
|
A | AT | 27 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0005others(24): Show | 28 | HG01099.hp2 HG01175.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(3): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | ATAC | 13 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0137others(10): Show | 13 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | ATACAC | 35 | a0001c0001t0002g0038a0001c0001t0002g0071a0001c0001t0002g0073others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | ATACACAC | 65 | a0001c0001t0002g0045a0001c0001t0002g0056a0001c0001t0002g0057others(62): Show | 65 | HG00423.hp2 HG00733.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(9): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | ATACACAC others(2): Show |
33 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0043others(30): Show | 33 | HG00438.hp1 HG01255.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | ATACACAC others(4): Show |
5 | a0001c0001t0002g0069a0001c0001t0002g0118a0001c0001t0002g0126others(2): Show | 5 | HG02071.hp1 HG02738.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+5654_703+5655i others(13): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | ATACACAC others(6): Show |
2 | a0001c0001t0007g0044a0001c0001t0025g0113 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.703+5654_703+5655i others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | ATACACAC others(8): Show |
1 | a0002c0003t0004g0117 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.703+5654_703+5655i others(17): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742180
|
A | C | 5 | a0001c0001t0002g0059a0001c0001t0003g0154a0001c0001t0003g0167others(2): Show | 5 | HG02015.hp1 HG03490.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+5654A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742180 | ||||||
chr7:77742182
|
T | C | 187 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.703+5656T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742182 | ||||||
chr7:77742182
|
T | TAC | 24 | a0001c0002t0001g0223a0001c0002t0001g0226a0001c0002t0001g0227others(21): Show | 24 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.703+5691_703+5692d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742182 | |||||
chr7:77742182
|
T | TACAC | 11 | a0001c0002t0001g0224a0001c0002t0001g0234a0001c0002t0001g0235others(8): Show | 11 | HG00423.hp1 HG00438.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.703+5689_703+5692d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742182 | |||||
chr7:77742182
|
TACACACA others(7): Show |
T | 2 | a0001c0002t0001g0277a0001c0002t0001g0279 | 2 | NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.703+5679_703+5692d others(16): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77742182 | |||||
chr7:77742184
|
C | T | 1 | a0006c0010t0028g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.703+5658C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742184 | ||||||
chr7:77742190
|
C | T | 7 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0094others(4): Show | 7 | NA18946.hp1 NA18978.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+5664C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742190 | ||||||
chr7:77742200
|
C | T | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+5674C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742200 | ||||||
chr7:77742463
|
G | C | 10 | a0001c0001t0004g0143a0001c0001t0004g0144a0002c0003t0004g0039others(7): Show | 10 | HG01192.hp1 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+5937G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742463 | ||||||
chr7:77742512
|
A | G | 15 | a0001c0002t0001g0223a0001c0002t0001g0226a0001c0002t0001g0227others(12): Show | 15 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+5986A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742512 | ||||||
chr7:77742674
|
C | G | 2 | a0001c0002t0001g0250a0001c0002t0001g0261 | 2 | HG01167.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.703+6148C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742674 | ||||||
chr7:77742737
|
C | A | 2 | a0001c0002t0001g0236a0001c0002t0001g0291 | 2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.703+6211C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742737 | ||||||
chr7:77742789
|
G | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+6263G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742789 | ||||||
chr7:77742816
|
C | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+6290C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742816 | ||||||
chr7:77742829
|
C | A | 1 | a0001c0001t0004g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.703+6303C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742829 | ||||||
chr7:77742956
|
T | G | 1 | a0001c0002t0001g0218 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.703+6430T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77742956 | ||||||
chr7:77743059
|
A | AT | 214 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(211): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.704-6354dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743059 | |||||
chr7:77743285
|
T | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-6139T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743285 | ||||||
chr7:77743311
|
T | A | 2 | a0001c0001t0003g0159a0001c0001t0003g0179 | 2 | HG02129.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.704-6113T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743311 | ||||||
chr7:77743460
|
TTTTG | T | 8 | a0001c0001t0005g0170a0001c0001t0008g0020a0001c0001t0008g0021others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-5960_704-5957d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743460 | |||||
chr7:77743461
|
TTTG | T | 47 | a0001c0001t0002g0059a0001c0001t0003g0034a0001c0001t0003g0035others(44): Show | 47 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.704-5960_704-5958d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743461 | |||||
chr7:77743462
|
TTG | T | 152 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(149): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.704-5960_704-5959d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743462 | |||||
chr7:77743463
|
TG | T | 8 | a0001c0001t0002g0080a0001c0001t0002g0087a0001c0001t0005g0194others(5): Show | 8 | HG01099.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-5960delG | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743463 | ||||||
chr7:77743464
|
G | T | 1 | a0001c0002t0001g0274 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.704-5960G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743464 | ||||||
chr7:77743480
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.704-5944A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743480 | ||||||
chr7:77743490
|
CT | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-5932delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77743490 | |||||
chr7:77743589
|
C | T | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.704-5835C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743589 | ||||||
chr7:77743683
|
CAAAT | C | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-5740_704-5737d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743683 | ||||||
chr7:77743717
|
G | T | 2 | a0001c0001t0002g0063a0001c0001t0002g0081 | 2 | HG00423.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.704-5707G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743717 | ||||||
chr7:77743845
|
G | T | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-5579G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77743845 | ||||||
chr7:77744120
|
C | T | 3 | a0001c0002t0001g0307a0001c0002t0001g0308a0001c0002t0001g0331 | 3 | HG02738.hp1 HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-5304C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744120 | ||||||
chr7:77744201
|
A | T | 1 | a0001c0001t0020g0212 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.704-5223A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744201 | ||||||
chr7:77744344
|
G | A | 5 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0109others(2): Show | 5 | HG00280.hp1 HG00323.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-5080G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744344 | ||||||
chr7:77744420
|
G | A | 1 | a0001c0001t0011g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704-5004G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744420 | ||||||
chr7:77744526
|
G | T | 1 | a0001c0001t0003g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.704-4898G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744526 | ||||||
chr7:77744637
|
C | T | 1 | a0001c0002t0006g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.704-4787C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77744637 | ||||||
chr7:77745116
|
C | T | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.704-4308C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745116 | ||||||
chr7:77745119
|
G | T | 13 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0154others(10): Show | 13 | HG02074.hp1 HG02129.hp2 NA18953.hp2 others(10): Show |
intron_variant | MODIFIER | c.704-4305G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745119 | ||||||
chr7:77745180
|
G | A | 1 | a0001c0001t0013g0125 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.704-4244G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745180 | ||||||
chr7:77745192
|
C | T | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.704-4232C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745192 | ||||||
chr7:77745262
|
CA | C | 55 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(52): Show | 55 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.704-4146delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77745262 | |||||
chr7:77745291
|
GA | G | 14 | a0001c0002t0001g0264a0001c0002t0001g0265a0001c0002t0001g0293others(11): Show | 14 | HG01099.hp1 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.704-4131delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77745291 | |||||
chr7:77745310
|
A | G | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704-4114A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745310 | ||||||
chr7:77745396
|
A | G | 2 | a0001c0002t0001g0241a0001c0002t0001g0253 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.704-4028A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745396 | ||||||
chr7:77745447
|
T | C | 131 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(128): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.704-3977T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745447 | ||||||
chr7:77745487
|
A | G | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.704-3937A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745487 | ||||||
chr7:77745529
|
C | T | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.704-3895C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745529 | ||||||
chr7:77745697
|
C | T | 1 | a0001c0001t0014g0095 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.704-3727C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745697 | ||||||
chr7:77745866
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.704-3558G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745866 | ||||||
chr7:77745994
|
A | G | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.704-3430A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77745994 | ||||||
chr7:77746020
|
A | C | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704-3404A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746020 | ||||||
chr7:77746079
|
A | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-3345A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746079 | ||||||
chr7:77746151
|
C | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-3273C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746151 | ||||||
chr7:77746208
|
T | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-3216T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746208 | ||||||
chr7:77746261
|
G | C | 1 | a0001c0001t0003g0183 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.704-3163G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746261 | ||||||
chr7:77746320
|
C | T | 1 | a0001c0004t0005g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.704-3104C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746320 | ||||||
chr7:77746327
|
C | T | 1 | a0001c0001t0022g0046 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704-3097C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746327 | ||||||
chr7:77746388
|
A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.704-3036A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746388 | ||||||
chr7:77746463
|
C | T | 1 | a0001c0002t0001g0328 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.704-2961C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746463 | ||||||
chr7:77746493
|
C | T | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-2931C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746493 | ||||||
chr7:77746494
|
G | A | 1 | a0001c0001t0004g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.704-2930G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746494 | ||||||
chr7:77746517
|
C | G | 1 | a0001c0002t0001g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.704-2907C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746517 | ||||||
chr7:77746688
|
T | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.704-2736T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746688 | ||||||
chr7:77746827
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.704-2597C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746827 | ||||||
chr7:77746828
|
G | A | 2 | a0001c0002t0001g0299a0001c0002t0001g0318 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.704-2596G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746828 | ||||||
chr7:77746913
|
C | G | 54 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(51): Show | 55 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.704-2511C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746913 | ||||||
chr7:77746961
|
G | T | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-2463G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77746961 | ||||||
chr7:77747004
|
G | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-2420G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747004 | ||||||
chr7:77747005
|
G | T | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.704-2419G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747005 | ||||||
chr7:77747097
|
C | A | 8 | a0001c0001t0004g0005a0001c0001t0004g0011a0001c0001t0004g0012others(5): Show | 8 | HG02071.hp2 HG02080.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-2327C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747097 | ||||||
chr7:77747150
|
C | T | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.704-2274C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747150 | ||||||
chr7:77747324
|
A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.704-2100A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747324 | ||||||
chr7:77747358
|
G | A | 2 | a0001c0001t0004g0143a0001c0001t0004g0144 | 2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.704-2066G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747358 | ||||||
chr7:77747689
|
G | C | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.704-1735G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747689 | ||||||
chr7:77747749
|
G | A | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.704-1675G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747749 | ||||||
chr7:77747793
|
C | T | 4 | a0001c0001t0009g0128a0001c0001t0009g0132a0001c0001t0009g0134others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1631C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747793 | ||||||
chr7:77747797
|
T | C | 1 | a0001c0001t0032g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704-1627T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747797 | ||||||
chr7:77747914
|
G | A | 2 | a0001c0001t0005g0194a0001c0001t0005g0204 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.704-1510G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747914 | ||||||
chr7:77747914
|
G | C | 1 | a0001c0002t0001g0230 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.704-1510G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747914 | ||||||
chr7:77747916
|
G | C | 36 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(33): Show | 37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.704-1508G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747916 | ||||||
chr7:77747919
|
A | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-1505A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747919 | ||||||
chr7:77747987
|
A | G | 1 | a0001c0002t0001g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.704-1437A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77747987 | ||||||
chr7:77748074
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1350A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748074 | ||||||
chr7:77748115
|
G | T | 1 | a0001c0002t0001g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.704-1309G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748115 | ||||||
chr7:77748378
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-1046A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748378 | ||||||
chr7:77748492
|
A | C | 1 | a0001c0001t0003g0185 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.704-932A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748492 | ||||||
chr7:77748536
|
G | A | 71 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(68): Show | 71 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-888G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748536 | ||||||
chr7:77748631
|
C | T | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.704-793C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748631 | ||||||
chr7:77748806
|
T | C | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-618T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748806 | ||||||
chr7:77748838
|
G | A | 16 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0109others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.704-586G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77748838 | ||||||
chr7:77748896
|
CGTCT | C | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.704-511_704-508del others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 77748896 | |||||
chr7:77749124
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.704-300C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77749124 | ||||||
chr7:77749236
|
A | G | 1 | a0003c0012t0012g0208 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.704-188A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 2/7 | chr7 | 77749236 | ||||||
chr7:77750199
|
A | G | 1 | a0001c0002t0001g0251 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1344+135A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750199 | ||||||
chr7:77750211
|
G | A | 1 | a0002c0003t0004g0115 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1344+147G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750211 | ||||||
chr7:77750280
|
ATAAT | A | 73 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(70): Show | 73 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1344+220_1344+223d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750280 | |||||
chr7:77750296
|
G | GT | 23 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0064others(20): Show | 23 | HG00423.hp2 HG00733.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1344+257dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750296
|
G | GTT | 7 | a0001c0001t0002g0067a0001c0001t0010g0042a0001c0001t0011g0096others(4): Show | 7 | HG01256.hp1 HG02572.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344+256_1344+257d others(4): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750296
|
G | GTTT | 10 | a0001c0001t0002g0118a0001c0001t0004g0107a0001c0001t0004g0108others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+255_1344+257d others(5): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750296
|
G | GTTTT | 6 | a0001c0001t0022g0047a0002c0003t0004g0039a0002c0003t0004g0050others(3): Show | 6 | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+254_1344+257d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750296
|
GT | G | 133 | a0001c0001t0002g0074a0001c0001t0003g0035a0001c0001t0003g0036others(130): Show | 134 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1344+257delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750296
|
GTTTT | G | 33 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(30): Show | 34 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.1344+254_1344+257d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750296
|
GTTTTTTT others(1): Show |
G | 10 | a0001c0001t0005g0193a0001c0001t0005g0196a0001c0001t0005g0200others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+250_1344+257d others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750296
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0003g0185 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1344+248_1344+257d others(12): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77750296 | |||||
chr7:77750302
|
T | G | 1 | a0001c0002t0001g0252 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1344+238T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750302 | ||||||
chr7:77750413
|
G | T | 67 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(64): Show | 67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1344+349G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750413 | ||||||
chr7:77750420
|
A | G | 2 | a0002c0003t0007g0048a0002c0003t0007g0104 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1344+356A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750420 | ||||||
chr7:77750439
|
G | A | 74 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(71): Show | 74 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1344+375G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750439 | ||||||
chr7:77750563
|
G | A | 14 | a0001c0001t0005g0193a0001c0001t0005g0196a0001c0001t0005g0197others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1344+499G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750563 | ||||||
chr7:77750600
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+536G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77750600 | ||||||
chr7:77751092
|
G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+1028G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751092 | ||||||
chr7:77751151
|
TTTTTTTG | T | 129 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(126): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1344+1102_1344+110 others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77751151 | |||||
chr7:77751289
|
A | ATCACCAT others(4): Show |
1 | a0001c0001t0004g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1344+1225_1344+122 others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751289 | ||||||
chr7:77751290
|
C | CCACCATG others(4): Show |
53 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(50): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1344+1227_1344+123 others(15): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77751290 | |||||
chr7:77751290
|
C | G | 1 | a0001c0001t0004g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1344+1226C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751290 | ||||||
chr7:77751328
|
CAG | C | 3 | a0001c0002t0001g0002a0001c0002t0001g0287a0001c0002t0001g0314 | 4 | NA18946.hp2 NA18949.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+1265_1344+126 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751328 | ||||||
chr7:77751448
|
A | T | 73 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(70): Show | 73 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.1344+1384A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751448 | ||||||
chr7:77751604
|
C | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+1540C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751604 | ||||||
chr7:77751674
|
G | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0175 | 2 | NA18988.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1344+1610G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751674 | ||||||
chr7:77751716
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1344+1652A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751716 | ||||||
chr7:77751744
|
G | C | 14 | a0001c0001t0005g0193a0001c0001t0005g0196a0001c0001t0005g0197others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1344+1680G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751744 | ||||||
chr7:77751844
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1344+1780C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751844 | ||||||
chr7:77751858
|
G | T | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+1794G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751858 | ||||||
chr7:77751860
|
C | T | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1344+1796C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751860 | ||||||
chr7:77751862
|
C | T | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1344+1798C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751862 | ||||||
chr7:77751878
|
G | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+1814G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77751878 | ||||||
chr7:77752055
|
C | G | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1344+1991C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752055 | ||||||
chr7:77752275
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+2211A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752275 | ||||||
chr7:77752415
|
T | TATC | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1344+2353_1344+235 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77752415 | |||||
chr7:77752448
|
A | T | 4 | a0001c0001t0003g0034a0001c0001t0003g0157a0001c0001t0003g0168others(1): Show | 4 | HG02135.hp2 NA18747.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2384A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752448 | ||||||
chr7:77752478
|
G | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2414G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752478 | ||||||
chr7:77752725
|
C | A | 3 | a0001c0002t0001g0311a0001c0002t0001g0312a0001c0002t0001g0316 | 3 | HG00738.hp1 HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.1344+2661C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752725 | ||||||
chr7:77752946
|
C | T | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1344+2882C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752946 | ||||||
chr7:77752971
|
G | A | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1344+2907G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77752971 | ||||||
chr7:77753006
|
T | G | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+2942T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753006 | ||||||
chr7:77753017
|
T | C | 2 | a0001c0001t0019g0031a0001c0001t0019g0032 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+2953T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753017 | ||||||
chr7:77753033
|
T | C | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1344+2969T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753033 | ||||||
chr7:77753106
|
A | C | 1 | a0001c0001t0004g0016 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1344+3042A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753106 | ||||||
chr7:77753419
|
A | G | 42 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(39): Show | 42 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1344+3355A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753419 | ||||||
chr7:77753427
|
T | C | 13 | a0001c0002t0001g0264a0001c0002t0001g0293a0001c0002t0001g0294others(10): Show | 13 | HG01099.hp1 HG01433.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1344+3363T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753427 | ||||||
chr7:77753619
|
A | G | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+3555A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753619 | ||||||
chr7:77753938
|
A | G | 69 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(66): Show | 69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1344+3874A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753938 | ||||||
chr7:77753980
|
G | T | 1 | a0001c0001t0031g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1344+3916G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77753980 | ||||||
chr7:77754231
|
G | A | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+4167G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754231 | ||||||
chr7:77754523
|
C | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1344+4459C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754523 | ||||||
chr7:77754614
|
A | G | 1 | a0001c0002t0001g0251 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1344+4550A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754614 | ||||||
chr7:77754720
|
C | G | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1344+4656C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754720 | ||||||
chr7:77754833
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1344+4769C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77754833 | ||||||
chr7:77754986
|
C | CTA | 69 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(66): Show | 69 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1344+4932_1344+493 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77754986 | |||||
chr7:77755013
|
A | T | 1 | a0001c0002t0001g0268 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1344+4949A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755013 | ||||||
chr7:77755031
|
G | C | 70 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(67): Show | 70 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1344+4967G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755031 | ||||||
chr7:77755250
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+5186A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755250 | ||||||
chr7:77755391
|
G | A | 1 | a0001c0001t0008g0023 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1344+5327G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755391 | ||||||
chr7:77755391
|
G | T | 1 | a0001c0001t0009g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1344+5327G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755391 | ||||||
chr7:77755671
|
CAAAACA | C | 209 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(206): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1344+5618_1344+562 others(10): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77755671 | |||||
chr7:77755679
|
AAACAAAA others(3): Show |
A | 1 | a0001c0001t0002g0086 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1344+5618_1344+562 others(14): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77755679 | |||||
chr7:77755933
|
C | T | 4 | a0001c0002t0001g0269a0001c0002t0001g0289a0001c0002t0001g0309others(1): Show | 4 | HG00438.hp2 HG02015.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+5869C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77755933 | ||||||
chr7:77756008
|
A | C | 80 | a0001c0001t0002g0097a0001c0001t0004g0148a0001c0002t0001g0002others(77): Show | 81 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1344+5944A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756008 | ||||||
chr7:77756050
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+5986A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756050 | ||||||
chr7:77756154
|
C | G | 47 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(44): Show | 47 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1344+6090C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756154 | ||||||
chr7:77756185
|
G | A | 6 | a0001c0002t0001g0237a0001c0002t0001g0311a0001c0002t0001g0312others(3): Show | 6 | HG00738.hp1 HG01257.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+6121G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756185 | ||||||
chr7:77756279
|
G | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+6215G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756279 | ||||||
chr7:77756322
|
G | A | 1 | a0001c0001t0003g0152 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1344+6258G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756322 | ||||||
chr7:77756323
|
G | T | 1 | a0001c0001t0003g0152 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1344+6259G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756323 | ||||||
chr7:77756377
|
C | G | 2 | a0001c0001t0003g0178a0001c0001t0003g0188 | 2 | HG00741.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1344+6313C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756377 | ||||||
chr7:77756774
|
G | A | 2 | a0001c0002t0001g0236a0001c0002t0001g0291 | 2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1344+6710G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756774 | ||||||
chr7:77756864
|
T | TAATG | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+6801_1344+680 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77756864 | |||||
chr7:77756876
|
T | C | 1 | a0001c0001t0031g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1344+6812T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756876 | ||||||
chr7:77756894
|
A | G | 1 | a0001c0001t0007g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1344+6830A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77756894 | ||||||
chr7:77757102
|
A | G | 2 | a0001c0001t0002g0111a0001c0001t0023g0112 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1344+7038A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757102 | ||||||
chr7:77757107
|
C | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+7043C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757107 | ||||||
chr7:77757280
|
C | T | 42 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(39): Show | 42 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1344+7216C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757280 | ||||||
chr7:77757714
|
T | C | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1344+7650T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77757714 | ||||||
chr7:77757990
|
CAG | C | 36 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(33): Show | 37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-7502_1345-750 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77757990 | |||||
chr7:77758174
|
T | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(33): Show | 37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-7321T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758174 | ||||||
chr7:77758177
|
T | C | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1345-7318T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758177 | ||||||
chr7:77758201
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1345-7294C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758201 | ||||||
chr7:77758397
|
A | G | 7 | a0001c0001t0005g0194a0001c0001t0005g0204a0001c0001t0019g0031others(4): Show | 7 | HG01099.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-7098A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758397 | ||||||
chr7:77758402
|
A | G | 1 | a0001c0002t0001g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1345-7093A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758402 | ||||||
chr7:77758477
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1345-7018C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758477 | ||||||
chr7:77758494
|
A | G | 2 | a0001c0001t0018g0129a0001c0001t0018g0136 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1345-7001A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758494 | ||||||
chr7:77758645
|
A | G | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1345-6850A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758645 | ||||||
chr7:77758827
|
T | C | 1 | a0001c0001t0008g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1345-6668T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758827 | ||||||
chr7:77758851
|
G | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-6644G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758851 | ||||||
chr7:77758978
|
T | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(33): Show | 37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-6517T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77758978 | ||||||
chr7:77759088
|
G | A | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1345-6407G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759088 | ||||||
chr7:77759151
|
C | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(18): Show | 21 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1345-6344C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759151 | ||||||
chr7:77759228
|
C | A | 6 | a0001c0001t0011g0060a0001c0001t0011g0062a0001c0001t0011g0079others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-6267C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759228 | ||||||
chr7:77759364
|
A | G | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-6131A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759364 | ||||||
chr7:77759392
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1345-6103C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759392 | ||||||
chr7:77759423
|
G | A | 1 | a0001c0001t0009g0133 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1345-6072G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759423 | ||||||
chr7:77759551
|
A | G | 1 | a0001c0002t0001g0230 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1345-5944A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759551 | ||||||
chr7:77759647
|
A | G | 3 | a0001c0002t0001g0231a0001c0002t0001g0296a0001c0002t0001g0321 | 3 | NA18983.hp1 NA19009.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1345-5848A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759647 | ||||||
chr7:77759684
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1345-5811C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759684 | ||||||
chr7:77759835
|
G | A | 3 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0148 | 3 | HG02135.hp1 NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1345-5660G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77759835 | ||||||
chr7:77760002
|
G | A | 2 | a0001c0001t0009g0128a0001c0001t0009g0134 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1345-5493G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760002 | ||||||
chr7:77760149
|
T | A | 1 | a0001c0001t0003g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1345-5346T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760149 | ||||||
chr7:77760234
|
T | G | 3 | a0001c0001t0007g0054a0001c0001t0007g0078a0001c0001t0007g0090 | 3 | HG02970.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1345-5261T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760234 | ||||||
chr7:77760664
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-4831A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760664 | ||||||
chr7:77760722
|
T | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-4773T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760722 | ||||||
chr7:77760736
|
A | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-4759A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760736 | ||||||
chr7:77760786
|
C | T | 3 | a0001c0002t0001g0241a0001c0002t0001g0253a0001c0002t0001g0274 | 3 | HG01243.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1345-4709C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760786 | ||||||
chr7:77760852
|
T | C | 2 | a0001c0001t0005g0198a0001c0001t0005g0207 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1345-4643T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77760852 | ||||||
chr7:77761063
|
A | T | 74 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(71): Show | 74 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1345-4432A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761063 | ||||||
chr7:77761139
|
T | C | 2 | a0001c0001t0002g0070a0001c0001t0002g0072 | 2 | HG00741.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1345-4356T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761139 | ||||||
chr7:77761204
|
A | G | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1345-4291A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761204 | ||||||
chr7:77761712
|
A | G | 7 | a0001c0001t0005g0194a0001c0001t0005g0204a0001c0001t0019g0031others(4): Show | 7 | HG01099.hp2 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-3783A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761712 | ||||||
chr7:77761967
|
G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1345-3528G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77761967 | ||||||
chr7:77762152
|
A | G | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1345-3343A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762152 | ||||||
chr7:77762364
|
A | C | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1345-3131A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762364 | ||||||
chr7:77762414
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1345-3081A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762414 | ||||||
chr7:77762663
|
A | C | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.1345-2832A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762663 | ||||||
chr7:77762697
|
A | G | 2 | a0001c0001t0009g0132a0001c0001t0009g0141 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1345-2798A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762697 | ||||||
chr7:77762699
|
G | T | 38 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(35): Show | 39 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.1345-2796G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762699 | ||||||
chr7:77762799
|
C | G | 1 | a0001c0002t0006g0266 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1345-2696C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762799 | ||||||
chr7:77762945
|
C | G | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-2550C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762945 | ||||||
chr7:77762950
|
G | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1345-2545G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77762950 | ||||||
chr7:77763015
|
C | A | 1 | a0001c0002t0001g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1345-2480C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763015 | ||||||
chr7:77763148
|
A | C | 1 | a0001c0002t0001g0331 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1345-2347A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763148 | ||||||
chr7:77763149
|
C | CT | 83 | a0001c0001t0003g0168a0001c0001t0004g0001a0001c0001t0004g0003others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1345-2326dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77763149 | |||||
chr7:77763149
|
C | CTT | 53 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(50): Show | 53 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1345-2327_1345-232 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77763149 | |||||
chr7:77763149
|
CTTTTTTT | C | 73 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(70): Show | 73 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1345-2332_1345-232 others(11): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77763149 | |||||
chr7:77763220
|
C | T | 2 | a0001c0001t0002g0111a0001c0001t0023g0112 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1345-2275C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763220 | ||||||
chr7:77763295
|
G | C | 4 | a0001c0001t0013g0122a0001c0001t0013g0123a0001c0001t0013g0124others(1): Show | 4 | HG00639.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-2200G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763295 | ||||||
chr7:77763392
|
C | T | 1 | a0001c0001t0004g0148 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1345-2103C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763392 | ||||||
chr7:77763768
|
C | T | 4 | a0001c0001t0005g0194a0001c0001t0005g0204a0001c0001t0020g0212others(1): Show | 4 | HG01099.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-1727C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763768 | ||||||
chr7:77763798
|
T | C | 6 | a0001c0001t0011g0060a0001c0001t0011g0062a0001c0001t0011g0079others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-1697T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77763798 | ||||||
chr7:77764013
|
A | C | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-1482A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764013 | ||||||
chr7:77764052
|
T | C | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1345-1443T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764052 | ||||||
chr7:77764187
|
C | G | 2 | a0001c0001t0005g0205a0001c0001t0005g0206 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1345-1308C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764187 | ||||||
chr7:77764422
|
T | C | 67 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(64): Show | 67 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1345-1073T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764422 | ||||||
chr7:77764499
|
A | G | 1 | a0001c0001t0003g0177 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1345-996A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764499 | ||||||
chr7:77764631
|
CT | C | 7 | a0001c0001t0002g0041a0001c0001t0002g0058a0001c0001t0002g0065others(4): Show | 7 | HG00438.hp1 HG01256.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-851delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 77764631 | |||||
chr7:77764779
|
G | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-716G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77764779 | ||||||
chr7:77765267
|
A | G | 36 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(33): Show | 37 | HG00280.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1345-228A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765267 | ||||||
chr7:77765362
|
T | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-133T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765362 | ||||||
chr7:77765446
|
C | A | 1 | a0001c0002t0041g0244 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1345-49C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765446 | ||||||
chr7:77765458
|
A | T | 6 | a0001c0001t0005g0197a0001c0001t0005g0214a0001c0004t0005g0195others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-37A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 3/7 | chr7 | 77765458 | ||||||
chr7:77765671
|
T | A | 18 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0004g0109others(15): Show | 18 | HG00280.hp1 HG00323.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1482+39T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765671 | ||||||
chr7:77765672
|
A | T | 1 | a0001c0001t0026g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1482+40A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765672 | ||||||
chr7:77765698
|
G | A | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1482+66G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765698 | ||||||
chr7:77765705
|
A | T | 2 | a0001c0001t0022g0046a0001c0001t0022g0047 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1482+73A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765705 | ||||||
chr7:77765769
|
C | T | 1 | a0001c0002t0001g0288 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1482+137C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765769 | ||||||
chr7:77765848
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1482+216C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765848 | ||||||
chr7:77765855
|
T | C | 1 | a0001c0001t0003g0161 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1482+223T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77765855 | ||||||
chr7:77766263
|
A | G | 5 | a0001c0001t0002g0041a0001c0001t0002g0058a0001c0001t0002g0065others(2): Show | 5 | HG00438.hp1 HG02071.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1482+631A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766263 | ||||||
chr7:77766520
|
C | CT | 14 | a0001c0001t0005g0214a0001c0001t0013g0122a0001c0001t0013g0123others(11): Show | 14 | HG00639.hp1 HG01192.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1482+902dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77766520 | |||||
chr7:77766520
|
CT | C | 6 | a0001c0001t0002g0088a0001c0001t0020g0212a0001c0002t0001g0218others(3): Show | 6 | HG01070.hp1 HG01975.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+902delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77766520 | |||||
chr7:77766599
|
G | A | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1482+967G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766599 | ||||||
chr7:77766654
|
A | G | 2 | a0001c0001t0015g0030a0001c0001t0031g0216 | 2 | HG00140.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1482+1022A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766654 | ||||||
chr7:77766918
|
G | A | 213 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(210): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1482+1286G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77766918 | ||||||
chr7:77767008
|
TCCTTTCC others(22): Show |
T | 2 | a0001c0001t0005g0194a0001c0001t0005g0204 | 2 | HG01099.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1482+1381_1482+140 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767008 | |||||
chr7:77767013
|
T | TCCTTCCC others(22): Show |
7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+1436_1482+146 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767013 | |||||
chr7:77767013
|
TCCTTCCC others(22): Show |
T | 2 | a0001c0001t0022g0046a0001c0001t0022g0047 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1482+1436_1482+146 others(33): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767013 | |||||
chr7:77767120
|
G | A | 1 | a0001c0001t0030g0027 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1482+1488G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767120 | ||||||
chr7:77767290
|
AT | A | 320 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1483-1357delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767290 | |||||
chr7:77767290
|
ATT | A | 11 | a0001c0001t0003g0035a0001c0001t0009g0128a0001c0001t0009g0132others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1483-1358_1483-135 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767290 | |||||
chr7:77767405
|
G | A | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-1256G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767405 | ||||||
chr7:77767499
|
G | A | 1 | a0001c0002t0001g0281 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1483-1162G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767499 | ||||||
chr7:77767726
|
GCCTCC | G | 58 | a0001c0001t0004g0001a0001c0001t0004g0004a0001c0001t0004g0005others(55): Show | 59 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1483-917_1483-913d others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767726 | |||||
chr7:77767731
|
C | G | 1 | a0001c0001t0002g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1483-930C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767731 | ||||||
chr7:77767743
|
C | T | 1 | a0001c0001t0004g0019 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1483-918C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767743 | ||||||
chr7:77767744
|
T | C | 1 | a0001c0001t0004g0019 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1483-917T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767744 | ||||||
chr7:77767750
|
C | CT | 3 | a0001c0001t0010g0106a0001c0001t0019g0032a0001c0004t0005g0211 | 3 | HG02293.hp2 HG03516.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1483-906dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767750 | |||||
chr7:77767755
|
T | C | 1 | a0001c0001t0003g0151 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1483-906T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767755 | ||||||
chr7:77767776
|
T | TC | 8 | a0001c0001t0002g0127a0001c0001t0003g0035a0001c0001t0008g0025others(5): Show | 8 | HG02055.hp2 HG03209.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.1483-879dupC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767776 | |||||
chr7:77767825
|
C | T | 1 | a0001c0002t0001g0292 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1483-836C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767825 | ||||||
chr7:77767834
|
T | TC | 12 | a0001c0001t0002g0041a0001c0001t0002g0101a0001c0001t0002g0127others(9): Show | 12 | HG00438.hp1 HG01192.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1483-821dupC | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77767834 | |||||
chr7:77767843
|
C | T | 129 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(126): Show | 130 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1483-818C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767843 | ||||||
chr7:77767942
|
C | T | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1483-719C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767942 | ||||||
chr7:77767998
|
G | A | 1 | a0001c0001t0010g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1483-663G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77767998 | ||||||
chr7:77768062
|
C | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1483-599C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768062 | ||||||
chr7:77768097
|
C | T | 2 | a0001c0002t0001g0267a0001c0002t0001g0290 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1483-564C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768097 | ||||||
chr7:77768320
|
A | G | 25 | a0001c0002t0001g0220a0001c0002t0001g0221a0001c0002t0001g0223others(22): Show | 25 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1483-341A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768320 | ||||||
chr7:77768373
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1483-288A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768373 | ||||||
chr7:77768417
|
T | C | 1 | a0001c0001t0003g0185 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1483-244T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768417 | ||||||
chr7:77768525
|
A | C | 1 | a0001c0001t0009g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1483-136A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768525 | ||||||
chr7:77768531
|
T | C | 5 | a0001c0001t0002g0084a0001c0001t0002g0085a0001c0001t0002g0088others(2): Show | 5 | HG01255.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483-130T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | chr7 | 77768531 | ||||||
chr7:77768589
|
ATAT | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1483-63_1483-61del others(3): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 77768589 | |||||
chr7:77768841
|
G | A | 1 | a0001c0002t0001g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1625+38G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77768841 | ||||||
chr7:77768864
|
T | C | 1 | a0001c0002t0001g0322 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1625+61T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77768864 | ||||||
chr7:77768874
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1625+71A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77768874 | ||||||
chr7:77769122
|
G | C | 1 | a0001c0001t0005g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1625+319G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769122 | ||||||
chr7:77769147
|
T | C | 1 | a0001c0001t0005g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1625+344T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769147 | ||||||
chr7:77769432
|
G | T | 1 | a0002c0003t0007g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1625+629G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769432 | ||||||
chr7:77769464
|
G | A | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1625+661G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769464 | ||||||
chr7:77769631
|
A | C | 9 | a0001c0001t0009g0128a0001c0001t0009g0132a0001c0001t0009g0133others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1625+828A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769631 | ||||||
chr7:77769688
|
A | C | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1625+885A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769688 | ||||||
chr7:77769898
|
A | G | 1 | a0001c0001t0010g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1625+1095A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769898 | ||||||
chr7:77769940
|
C | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1625+1137C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77769940 | ||||||
chr7:77770077
|
G | A | 1 | a0001c0001t0035g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1625+1274G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770077 | ||||||
chr7:77770182
|
T | A | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1625+1379T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770182 | ||||||
chr7:77770348
|
C | T | 1 | a0003c0012t0012g0208 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1625+1545C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770348 | ||||||
chr7:77770483
|
G | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1625+1680G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770483 | ||||||
chr7:77770518
|
A | G | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1625+1715A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770518 | ||||||
chr7:77770525
|
A | T | 212 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(209): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1625+1722A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770525 | ||||||
chr7:77770559
|
C | T | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1625+1756C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770559 | ||||||
chr7:77770600
|
G | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1625+1797G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770600 | ||||||
chr7:77770719
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1625+1916A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77770719 | ||||||
chr7:77771034
|
C | T | 2 | a0001c0001t0019g0031a0001c0001t0019g0032 | 2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1626-2113C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771034 | ||||||
chr7:77771068
|
A | T | 1 | a0001c0001t0002g0076 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1626-2079A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771068 | ||||||
chr7:77771148
|
G | A | 2 | a0001c0002t0001g0242a0001c0002t0006g0243 | 2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1626-1999G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771148 | ||||||
chr7:77771176
|
G | A | 4 | a0001c0001t0005g0193a0001c0001t0005g0200a0001c0001t0005g0201others(1): Show | 4 | HG01433.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626-1971G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771176 | ||||||
chr7:77771207
|
C | A | 215 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1626-1940C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771207 | ||||||
chr7:77771228
|
C | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626-1919C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771228 | ||||||
chr7:77771270
|
G | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1626-1877G>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771270 | ||||||
chr7:77771272
|
T | G | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1626-1875T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771272 | ||||||
chr7:77771506
|
C | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0087 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1626-1641C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771506 | ||||||
chr7:77771511
|
C | CT | 92 | a0001c0001t0003g0034a0001c0001t0003g0036a0001c0001t0003g0151others(89): Show | 92 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1626-1620dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771511 | |||||
chr7:77771511
|
C | CTT | 75 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0043others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1626-1621_1626-162 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771511 | |||||
chr7:77771511
|
C | CTTT | 58 | a0001c0001t0002g0038a0001c0001t0004g0001a0001c0001t0004g0003others(55): Show | 59 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.1626-1622_1626-162 others(7): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771511 | |||||
chr7:77771565
|
A | G | 1 | a0001c0001t0002g0119 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1626-1582A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771565 | ||||||
chr7:77771789
|
C | T | 1 | a0001c0001t0025g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1626-1358C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771789 | ||||||
chr7:77771826
|
A | AT | 210 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(207): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1626-1312dupT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771826 | |||||
chr7:77771826
|
A | ATT | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1626-1313_1626-131 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77771826 | |||||
chr7:77771990
|
T | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1626-1157T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77771990 | ||||||
chr7:77772221
|
C | G | 9 | a0001c0001t0009g0128a0001c0001t0009g0132a0001c0001t0009g0133others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-926C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772221 | ||||||
chr7:77772331
|
T | C | 164 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(161): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1626-816T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772331 | ||||||
chr7:77772731
|
TTAGA | T | 9 | a0001c0001t0009g0128a0001c0001t0009g0132a0001c0001t0009g0133others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-412_1626-409d others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 77772731 | |||||
chr7:77772780
|
G | A | 2 | a0001c0002t0001g0250a0001c0002t0001g0261 | 2 | HG01167.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1626-367G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772780 | ||||||
chr7:77772874
|
A | T | 9 | a0001c0001t0009g0128a0001c0001t0009g0132a0001c0001t0009g0133others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626-273A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77772874 | ||||||
chr7:77773082
|
T | G | 3 | a0001c0002t0001g0229a0001c0002t0001g0292a0001c0002t0001g0306 | 3 | HG02293.hp1 NA18943.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1626-65T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 5/7 | chr7 | 77773082 | ||||||
chr7:77773355
|
G | A | 1 | a0001c0001t0013g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1793+41G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773355 | ||||||
chr7:77773378
|
A | C | 1 | a0001c0001t0004g0008 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1793+64A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773378 | ||||||
chr7:77773429
|
A | G | 131 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(128): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1793+115A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773429 | ||||||
chr7:77773460
|
A | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+146A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773460 | ||||||
chr7:77773624
|
G | A | 2 | a0001c0001t0025g0113a0001c0001t0026g0114 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1793+310G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773624 | ||||||
chr7:77773680
|
T | G | 1 | a0001c0001t0003g0189 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1793+366T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773680 | ||||||
chr7:77773685
|
C | T | 1 | a0001c0002t0001g0306 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1793+371C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773685 | ||||||
chr7:77773718
|
G | A | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0173 | 3 | NA18969.hp1 NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1793+404G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773718 | ||||||
chr7:77773841
|
C | T | 49 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(46): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1793+527C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773841 | ||||||
chr7:77773961
|
C | T | 6 | a0001c0001t0002g0070a0001c0001t0002g0072a0001c0001t0002g0073others(3): Show | 6 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1793+647C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77773961 | ||||||
chr7:77774433
|
CA | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1124delA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77774433 | |||||
chr7:77774746
|
A | C | 16 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(13): Show | 16 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1793+1432A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774746 | ||||||
chr7:77774803
|
A | G | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1489A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774803 | ||||||
chr7:77774862
|
A | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1548A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774862 | ||||||
chr7:77774885
|
A | G | 2 | a0002c0003t0004g0115a0002c0003t0004g0117 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1793+1571A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774885 | ||||||
chr7:77774943
|
C | G | 71 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(68): Show | 71 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1793+1629C>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77774943 | ||||||
chr7:77774959
|
TCAAG | T | 3 | a0001c0001t0004g0109a0001c0001t0004g0110a0001c0001t0004g0148 | 3 | HG02135.hp1 NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1793+1651_1793+165 others(8): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77774959 | |||||
chr7:77775048
|
T | G | 2 | a0001c0001t0020g0212a0001c0001t0020g0215 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1793+1734T>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775048 | ||||||
chr7:77775080
|
C | T | 1 | a0001c0002t0006g0282 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1793+1766C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775080 | ||||||
chr7:77775122
|
T | C | 7 | a0001c0001t0008g0020a0001c0001t0008g0021a0001c0001t0008g0022others(4): Show | 7 | HG02055.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1793+1808T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775122 | ||||||
chr7:77775237
|
A | T | 2 | a0001c0002t0006g0263a0001c0002t0039g0286 | 2 | HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1793+1923A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775237 | ||||||
chr7:77775539
|
T | C | 1 | a0001c0002t0006g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1793+2225T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775539 | ||||||
chr7:77775573
|
T | A | 1 | a0001c0001t0005g0213 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1793+2259T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775573 | ||||||
chr7:77775608
|
G | A | 1 | a0001c0002t0001g0316 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1793+2294G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775608 | ||||||
chr7:77775701
|
A | T | 4 | a0001c0001t0015g0028a0001c0001t0015g0029a0001c0001t0015g0030others(1): Show | 4 | HG00140.hp1 HG01256.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1793+2387A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775701 | ||||||
chr7:77775776
|
C | T | 49 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(46): Show | 50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1793+2462C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775776 | ||||||
chr7:77775826
|
C | T | 4 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033others(1): Show | 4 | HG02559.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793+2512C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775826 | ||||||
chr7:77775885
|
A | T | 1 | a0001c0002t0006g0225 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1794-2453A>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775885 | ||||||
chr7:77775949
|
G | A | 4 | a0001c0001t0005g0198a0001c0001t0005g0205a0001c0001t0005g0206others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794-2389G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77775949 | ||||||
chr7:77776056
|
C | CA | 212 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(209): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1794-2272dupA | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77776056 | |||||
chr7:77776145
|
G | A | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1794-2193G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776145 | ||||||
chr7:77776180
|
G | A | 1 | a0001c0001t0004g0003 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1794-2158G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776180 | ||||||
chr7:77776232
|
T | A | 3 | a0001c0001t0019g0031a0001c0001t0019g0032a0001c0001t0032g0033 | 3 | HG02559.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1794-2106T>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776232 | ||||||
chr7:77776250
|
T | TTC | 217 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(214): Show | 218 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1794-2087_1794-208 others(6): Show |
RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77776250 | |||||
chr7:77776304
|
A | G | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1794-2034A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776304 | ||||||
chr7:77776424
|
T | C | 216 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1794-1914T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776424 | ||||||
chr7:77776526
|
G | A | 1 | a0001c0002t0001g0236 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1794-1812G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776526 | ||||||
chr7:77776581
|
A | G | 74 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(71): Show | 74 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1794-1757A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776581 | ||||||
chr7:77776727
|
CT | C | 13 | a0001c0001t0002g0038a0001c0001t0002g0070a0001c0001t0002g0071others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1794-1609delT | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 77776727 | |||||
chr7:77776796
|
A | C | 62 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(59): Show | 63 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1794-1542A>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776796 | ||||||
chr7:77776827
|
T | C | 4 | a0001c0002t0001g0269a0001c0002t0001g0289a0001c0002t0001g0309others(1): Show | 4 | HG00438.hp2 HG02015.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794-1511T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776827 | ||||||
chr7:77776925
|
G | T | 77 | a0001c0002t0001g0002a0001c0002t0001g0218a0001c0002t0001g0224others(74): Show | 78 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1794-1413G>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77776925 | ||||||
chr7:77777087
|
C | T | 130 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(127): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1794-1251C>T | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777087 | ||||||
chr7:77777171
|
C | A | 68 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(65): Show | 68 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1794-1167C>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777171 | ||||||
chr7:77777224
|
G | A | 75 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(72): Show | 75 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.1794-1114G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777224 | ||||||
chr7:77777249
|
T | C | 1 | a0001c0002t0001g0308 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1794-1089T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777249 | ||||||
chr7:77777422
|
G | A | 188 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(185): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1794-916G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777422 | ||||||
chr7:77777430
|
G | A | 68 | a0001c0001t0002g0038a0001c0001t0002g0040a0001c0001t0002g0041others(65): Show | 68 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1794-908G>A | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777430 | ||||||
chr7:77777642
|
T | C | 1 | a0001c0002t0001g0232 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1794-696T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777642 | ||||||
chr7:77777677
|
T | C | 1 | a0001c0001t0011g0093 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1794-661T>C | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777677 | ||||||
chr7:77777732
|
A | G | 5 | a0001c0002t0001g0270a0001c0002t0001g0273a0001c0002t0001g0275others(2): Show | 5 | HG03491.hp1 HG04115.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1794-606A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77777732 | ||||||
chr7:77778063
|
A | G | 70 | a0001c0001t0003g0034a0001c0001t0003g0035a0001c0001t0003g0036others(67): Show | 70 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.1794-275A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77778063 | ||||||
chr7:77778089
|
A | G | 1 | a0001c0001t0011g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1794-249A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77778089 | ||||||
chr7:77778239
|
A | G | 62 | a0001c0001t0004g0001a0001c0001t0004g0003a0001c0001t0004g0004others(59): Show | 63 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1794-99A>G | RSBN1L | ENSG00000187257.16 | transcript | ENST00000334955.13 | protein_coding | 6/7 | chr7 | 77778239 |