geneid | 55005 |
---|---|
ensemblid | ENSG00000155906.20 |
hgncid | 21176 |
symbol | RMND1 |
name | required for meiotic nuclear division 1 homolog |
refseq_nuc | NM_017909.4 |
refseq_prot | NP_060379.2 |
ensembl_nuc | ENST00000444024.3 |
ensembl_prot | ENSP00000412708.2 |
mane_status | MANE Select |
chr | chr6 |
start | 151404762 |
end | 151452126 |
strand | - |
ver | v1.2 |
region | chr6:151404762-151452126 |
region5000 | chr6:151399762-151457126 |
regionname0 | RMND1_chr6_151404762_151452126 |
regionname5000 | RMND1_chr6_151399762_151457126 |
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 | 1/0 | 449 | 265 | 70 | 48 | 114 | 11 | 21 | 92 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0002 | 0/0 | 449 | 90 | 10 | 10 | 64 | 0 | 6 | 52 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003 | 0/1 | 449 | 28 | 4 | 8 | 4 | 3 | 8 | 2 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0004 | 0/0 | 449 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0005 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0006 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0007 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0008 | 0/0 | 449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
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 | 1/0 | 1350 | 234 | 41 | 47 | 114 | 11 | 20 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0002 | 0/0 | 1350 | 88 | 10 | 10 | 62 | 0 | 6 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0003 | 0/1 | 1350 | 27 | 3 | 8 | 4 | 3 | 8 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0004 | 0/0 | 1350 | 22 | 20 | 1 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0005 | 0/0 | 1350 | 6 | 6 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0006 | 0/0 | 1350 | 4 | 4 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0007 | 0/0 | 1350 | 3 | 3 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0008 | 0/0 | 1350 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0009 | 0/0 | 1350 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0010 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0011 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0012 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0013 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
c0014 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 603 | 161 | 54 | 13 | 81 | 2 | 11 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0002 | 1/0 | 599 | 152 | 31 | 32 | 67 | 7 | 14 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0003 | 0/0 | 603 | 42 | 1 | 12 | 26 | 1 | 2 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0004 | 0/1 | 599 | 20 | 0 | 6 | 2 | 3 | 8 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0005 | 0/0 | 603 | 5 | 0 | 2 | 2 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0006 | 0/0 | 599 | 3 | 0 | 1 | 1 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0007 | 0/0 | 603 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0008 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0009 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0010 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0011 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0012 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0013 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
t0014 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
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 | 1/0 | 1350 | 234 | 41 | 47 | 114 | 11 | 20 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0004 | 0/0 | 1350 | 22 | 20 | 1 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0005 | 0/0 | 1350 | 6 | 6 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0007 | 0/0 | 1350 | 3 | 3 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0002c0002 | 0/0 | 1350 | 88 | 10 | 10 | 62 | 0 | 6 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0002c0008 | 0/0 | 1350 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003c0003 | 0/1 | 1350 | 27 | 3 | 8 | 4 | 3 | 8 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003c0014 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0004c0006 | 0/0 | 1350 | 4 | 4 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0004c0010 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0005c0011 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0006c0013 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0007c0012 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0008c0009 | 0/0 | 1350 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1952 | 60 | 17 | 4 | 31 | 2 | 6 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0001t0002 | 1/0 | 1948 | 127 | 23 | 30 | 54 | 7 | 12 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0001t0003 | 0/0 | 1952 | 42 | 1 | 12 | 26 | 1 | 2 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0001t0006 | 0/0 | 1948 | 3 | 0 | 1 | 1 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0001t0012 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0001t0013 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0004t0001 | 0/0 | 1952 | 16 | 15 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0004t0002 | 0/0 | 1948 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0004t0005 | 0/0 | 1952 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0004t0007 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0004t0010 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0005t0001 | 0/0 | 1952 | 6 | 6 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0007t0001 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0001c0007t0002 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0002c0002t0001 | 0/0 | 1952 | 68 | 7 | 8 | 48 | 0 | 5 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0002c0002t0002 | 0/0 | 1948 | 19 | 3 | 2 | 13 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0002c0002t0009 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0002c0008t0001 | 0/0 | 1952 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003c0003t0001 | 0/0 | 1952 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003c0003t0004 | 0/1 | 1948 | 20 | 0 | 6 | 2 | 3 | 8 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003c0003t0005 | 0/0 | 1952 | 4 | 0 | 2 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003c0003t0011 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0003c0014t0001 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0004c0006t0001 | 0/0 | 1952 | 3 | 3 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0004c0006t0002 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0004c0010t0014 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0005c0011t0008 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0006c0013t0001 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0007c0012t0002 | 0/0 | 1948 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
a0008c0009t0002 | 0/0 | 1948 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | copy fasta | chr6 | 151399762 | 151457126 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0006g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0006g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0012g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0001t0013g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0007g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0007g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0004t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0005t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0005t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0005t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0007t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0007t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0001c0007t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0002t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0002c0008t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0003t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0003c0014t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0004c0006t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0004c0006t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0004c0006t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0004c0006t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0004c0010t0014g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0005c0011t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0006c0013t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0007c0012t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
a0008c0009t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0334 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00140 | hp1 | a0003 | c0003 | t0004 | g0029 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0296 | EUR | GBR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0327 | EUR | FIN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00408 | hp2 | a0001 | c0001 | t0013 | g0343 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00423 | hp1 | a0001 | c0001 | t0006 | g0351 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0360 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0366 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0362 | EAS | CHS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0332 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01069 | hp2 | a0003 | c0003 | t0005 | g0037 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01071 | hp1 | a0003 | c0003 | t0005 | g0036 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0081 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0333 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01168 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01169 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01175 | hp1 | a0001 | c0004 | t0001 | g0185 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0328 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01255 | hp2 | a0003 | c0003 | t0004 | g0025 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0331 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01261 | hp1 | a0003 | c0003 | t0004 | g0032 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0335 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0068 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0329 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01433 | hp1 | a0003 | c0003 | t0004 | g0041 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01496 | hp1 | a0003 | c0003 | t0004 | g0027 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0330 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01515 | hp2 | a0003 | c0003 | t0004 | g0031 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0286 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01517 | hp2 | a0003 | c0003 | t0004 | g0030 | EUR | IBS | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01884 | hp1 | a0001 | c0004 | t0010 | g0184 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01884 | hp2 | a0003 | c0014 | t0001 | g0323 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0319 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0345 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0134 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0363 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02040 | hp2 | a0003 | c0003 | t0005 | g0033 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0253 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02055 | hp2 | a0001 | c0007 | t0001 | g0244 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0368 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02135 | hp2 | a0002 | c0002 | t0009 | g0056 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0358 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02165 | hp1 | a0003 | c0003 | t0004 | g0039 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CDX | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0249 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0186 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02258 | hp1 | a0004 | c0010 | t0014 | g0371 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0364 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0135 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0190 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0247 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02647 | hp2 | a0001 | c0007 | t0002 | g0243 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02717 | hp2 | a0001 | c0005 | t0001 | g0262 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02735 | hp1 | a0003 | c0003 | t0004 | g0040 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0246 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02896 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0252 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02965 | hp1 | a0001 | c0004 | t0007 | g0370 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02970 | hp2 | a0001 | c0005 | t0001 | g0264 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0337 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03041 | hp1 | a0004 | c0006 | t0001 | g0259 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0105 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03098 | hp1 | a0001 | c0004 | t0002 | g0241 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03130 | hp1 | a0007 | c0012 | t0002 | g0254 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03139 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03195 | hp1 | a0001 | c0004 | t0007 | g0369 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03225 | hp2 | a0004 | c0006 | t0001 | g0258 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03486 | hp1 | a0003 | c0003 | t0001 | g0312 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03490 | hp2 | a0003 | c0003 | t0004 | g0035 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03491 | hp1 | a0003 | c0003 | t0004 | g0021 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03491 | hp2 | a0003 | c0003 | t0004 | g0038 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03516 | hp1 | a0005 | c0011 | t0008 | g0310 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03579 | hp1 | a0001 | c0007 | t0001 | g0242 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03579 | hp2 | a0001 | c0005 | t0001 | g0141 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03654 | hp1 | a0003 | c0003 | t0004 | g0026 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03704 | hp1 | a0003 | c0003 | t0004 | g0019 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03834 | hp1 | a0003 | c0003 | t0004 | g0023 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03834 | hp2 | a0008 | c0009 | t0002 | g0194 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03927 | hp1 | a0001 | c0004 | t0005 | g0020 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0122 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03942 | hp1 | a0003 | c0003 | t0004 | g0022 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0131 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0336 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | BEB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | STU | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0187 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18522 | hp2 | a0006 | c0013 | t0001 | g0245 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18906 | hp1 | a0004 | c0006 | t0001 | g0260 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18941 | hp2 | a0003 | c0003 | t0005 | g0024 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18977 | hp2 | a0003 | c0003 | t0004 | g0034 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19007 | hp2 | a0002 | c0008 | t0001 | g0115 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0320 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0251 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19063 | hp1 | a0002 | c0008 | t0001 | g0060 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19067 | hp1 | a0001 | c0001 | t0012 | g0342 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0365 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | ASW | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA20129 | hp2 | a0001 | c0004 | t0002 | g0189 | AFR | ASW | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0214 | EUR | TSI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0209 | EUR | TSI | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0344 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02109 | hp1 | a0001 | c0004 | t0001 | g0318 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0248 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02486 | hp2 | a0003 | c0003 | t0011 | g0265 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG02559 | hp2 | a0001 | c0004 | t0001 | g0250 | AFR | ACB | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG06807 | hp1 | a0001 | c0005 | t0001 | g0263 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA20300 | hp2 | a0004 | c0006 | t0002 | g0307 | AFR | USA | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
NA21309 | hp2 | a0003 | c0003 | t0001 | g0313 | AFR | LWK | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0004 | g0028 | REF | REF | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0276 | REF | REF | RMND1_chr6_151399762_151457126 | RMND1 | chr6 | 151399762 | 151457126 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:151405236
|
C | T | 1 | a0001 | 6 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
stop_retained_variant | LOW | c.1349G>A | p.Ter450Ter | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 1474/1948 | 1349/1350 | 450/449 | chr6 | 151405236 | ||
chr6:151422601
|
T | G | 1 | a0007 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.942A>C | p.Lys314Asn | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/12 | 1067/1948 | 942/1350 | 314/449 | chr6 | 151422601 | ||
chr6:151423604
|
T | A | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.858A>T | p.Glu286Asp | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/12 | 983/1948 | 858/1350 | 286/449 | chr6 | 151423604 | ||
chr6:151427517
|
G | C | 1 | a0005 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.795C>G | p.His265Gln | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/12 | 920/1948 | 795/1350 | 265/449 | chr6 | 151427517 | ||
chr6:151445417
|
G | A | 1 | a0002 | 90 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(87): Show |
missense_variant | MODERATE | c.395C>T | p.Thr132Met | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 520/1948 | 395/1350 | 132/449 | chr6 | 151445417 | ||
chr6:151445672
|
C | T | 2 | a0004a0005 | 6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
missense_variant | MODERATE | c.140G>A | p.Arg47His | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 265/1948 | 140/1350 | 47/449 | chr6 | 151445672 | ||
chr6:151445687
|
C | A | 1 | a0003 | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
missense_variant | MODERATE | c.125G>T | p.Ser42Ile | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 250/1948 | 125/1350 | 42/449 | chr6 | 151445687 | ||
chr6:151445736
|
C | T | 1 | a0008 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.76G>A | p.Gly26Ser | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 201/1948 | 76/1350 | 26/449 | chr6 | 151445736 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:151417312
|
C | T | 2 | a0003c0014a0004c0010 | 2 | HG01884.hp2 HG02258.hp1 |
synonymous_variant | LOW | c.1167G>A | p.Thr389Thr | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/12 | 1292/1948 | 1167/1350 | 389/449 | chr6 | 151417312 | ||
chr6:151423607
|
C | G | 1 | a0008c0009 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.855G>C | p.Gly285Gly | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/12 | 980/1948 | 855/1350 | 285/449 | chr6 | 151423607 | ||
chr6:151427529
|
G | A | 1 | a0001c0007 | 3 | HG02055.hp2 HG02647.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.783C>T | p.Ile261Ile | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/12 | 908/1948 | 783/1350 | 261/449 | chr6 | 151427529 | ||
chr6:151445353
|
G | A | 1 | a0002c0008 | 2 | NA19007.hp2 NA19063.hp1 |
synonymous_variant | LOW | c.459C>T | p.Thr153Thr | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 584/1948 | 459/1350 | 153/449 | chr6 | 151445353 | ||
chr6:151445365
|
T | C | 3 | a0001c0004a0001c0007a0006c0013 | 26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
synonymous_variant | LOW | c.447A>G | p.Lys149Lys | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/12 | 572/1948 | 447/1350 | 149/449 | chr6 | 151445365 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:151404857
|
A | G | 1 | a0005c0011t0008 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 378 | chr6 | 151404857 | |||||
chr6:151404858
|
C | CATTT | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(17): Show | 216 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*373_*376dupAAAT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 376 | chr6 | 151404858 | |||||
chr6:151404890
|
A | G | 1 | a0002c0002t0009 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*345T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 345 | chr6 | 151404890 | |||||
chr6:151405010
|
G | A | 1 | a0003c0003t0011 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 225 | chr6 | 151405010 | |||||
chr6:151405040
|
G | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(17): Show | 216 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*195C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 195 | chr6 | 151405040 | |||||
chr6:151405055
|
G | A | 1 | a0001c0001t0013 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 180 | chr6 | 151405055 | |||||
chr6:151405165
|
G | C | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(16): Show | 215 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*70C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 70 | chr6 | 151405165 | |||||
chr6:151405167
|
G | T | 1 | a0001c0001t0012 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 68 | chr6 | 151405167 | |||||
chr6:151405180
|
T | G | 2 | a0001c0004t0010a0003c0003t0011 | 2 | HG01884.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*55A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 12/12 | 55 | chr6 | 151405180 | |||||
chr6:151452029
|
G | A | 4 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(1): Show | 47 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-28C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | 6218 | chr6 | 151452029 | |||||
chr6:151452071
|
C | G | 3 | a0001c0004t0005a0003c0003t0004a0003c0003t0005 | 25 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | 6260 | chr6 | 151452071 | |||||
chr6:151452084
|
G | A | 1 | a0001c0004t0007 | 2 | HG02965.hp1 HG03195.hp1 |
5_prime_UTR_variant | MODIFIER | c.-83C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | 6273 | chr6 | 151452084 | |||||
chr6:151452121
|
T | A | 1 | a0004c0010t0014 | 1 | HG02258.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/12 | chr6 | 151452121 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:151405315
|
A | G | 1 | a0003c0014t0001g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1318-48T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405315 | ||||||
chr6:151405424
|
T | G | 1 | a0001c0001t0002g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1318-157A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405424 | ||||||
chr6:151405512
|
T | C | 1 | a0002c0002t0002g0043 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1317+208A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405512 | ||||||
chr6:151405621
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(200): Show | 214 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1317+99A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405621 | ||||||
chr6:151405624
|
G | C | 2 | a0001c0001t0002g0261a0001c0001t0002g0308 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1317+96C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405624 | ||||||
chr6:151405694
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 217 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1317+26G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 11/11 | chr6 | 151405694 | ||||||
chr6:151405951
|
C | T | 10 | a0001c0001t0003g0018a0001c0001t0003g0345a0001c0001t0003g0353others(7): Show | 11 | HG00408.hp2 HG00609.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1201-115G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151405951 | ||||||
chr6:151405995
|
T | C | 1 | a0001c0004t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1201-159A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151405995 | ||||||
chr6:151406073
|
A | G | 2 | a0001c0004t0007g0369a0001c0004t0007g0370 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1201-237T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406073 | ||||||
chr6:151406119
|
T | C | 2 | a0001c0004t0001g0190a0001c0004t0001g0320 | 2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1201-283A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406119 | ||||||
chr6:151406188
|
C | A | 1 | a0002c0002t0001g0135 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1201-352G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406188 | ||||||
chr6:151406351
|
CTTT | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 208 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1201-518_1201-516d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406351 | ||||||
chr6:151406356
|
T | TTTG | 6 | a0001c0005t0001g0013a0001c0005t0001g0141a0001c0005t0001g0262others(3): Show | 7 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-521_1201-520i others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406356 | ||||||
chr6:151406359
|
T | G | 9 | a0001c0005t0001g0013a0001c0005t0001g0141a0001c0005t0001g0262others(6): Show | 10 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1201-523A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406359 | ||||||
chr6:151406364
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0159 | 2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1201-528A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406364 | ||||||
chr6:151406382
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 217 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1201-546C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406382 | ||||||
chr6:151406410
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 258 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.1201-574G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406410 | ||||||
chr6:151406423
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1201-587G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406423 | ||||||
chr6:151406447
|
T | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0146others(142): Show | 148 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1201-611A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406447 | ||||||
chr6:151406458
|
A | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(201): Show | 215 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1201-622T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406458 | ||||||
chr6:151406522
|
C | T | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-686G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406522 | ||||||
chr6:151406523
|
G | A | 5 | a0001c0001t0002g0012a0001c0001t0002g0239a0001c0001t0002g0240others(2): Show | 6 | HG02572.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-687C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406523 | ||||||
chr6:151406561
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1201-725T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406561 | ||||||
chr6:151406937
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1201-1101G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406937 | ||||||
chr6:151406958
|
G | C | 2 | a0002c0002t0001g0055a0002c0002t0009g0056 | 2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1201-1122C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151406958 | ||||||
chr6:151407049
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(206): Show | 220 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.1201-1213T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407049 | ||||||
chr6:151407163
|
A | C | 6 | a0001c0005t0001g0013a0001c0005t0001g0141a0001c0005t0001g0262others(3): Show | 7 | HG02717.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-1327T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407163 | ||||||
chr6:151407164
|
CTG | C | 3 | a0001c0001t0002g0005a0001c0001t0002g0153a0001c0001t0002g0322 | 4 | HG02280.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-1330_1201-132 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407164 | ||||||
chr6:151407183
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0238 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1201-1347T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407183 | ||||||
chr6:151407268
|
A | G | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-1432T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407268 | ||||||
chr6:151407337
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(200): Show | 214 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1201-1501A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407337 | ||||||
chr6:151407531
|
C | T | 1 | a0004c0010t0014g0371 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1201-1695G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407531 | ||||||
chr6:151407579
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(247): Show | 266 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.1201-1743A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407579 | ||||||
chr6:151407615
|
A | G | 7 | a0001c0001t0006g0351a0001c0005t0001g0013a0001c0005t0001g0141others(4): Show | 8 | HG00423.hp1 HG02717.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-1779T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407615 | ||||||
chr6:151407689
|
C | T | 2 | a0001c0001t0001g0235a0002c0002t0001g0042 | 2 | NA18982.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1201-1853G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407689 | ||||||
chr6:151407732
|
C | A | 1 | a0001c0001t0006g0351 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1201-1896G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407732 | ||||||
chr6:151407764
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1201-1928G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407764 | ||||||
chr6:151407765
|
G | A | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-1929C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407765 | ||||||
chr6:151407835
|
C | T | 3 | a0002c0002t0001g0088a0002c0002t0001g0100a0002c0002t0002g0081 | 3 | HG00609.hp2 HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1201-1999G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407835 | ||||||
chr6:151407866
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1201-2030C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407866 | ||||||
chr6:151407868
|
G | A | 1 | a0002c0002t0001g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1201-2032C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407868 | ||||||
chr6:151407918
|
A | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 234 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1201-2082T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407918 | ||||||
chr6:151407920
|
A | C | 43 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0266others(40): Show | 46 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1201-2084T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407920 | ||||||
chr6:151407949
|
CTATT | C | 3 | a0001c0001t0002g0208a0001c0001t0002g0304a0001c0001t0002g0311 | 3 | NA18954.hp1 NA18965.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1201-2117_1201-211 others(8): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407949 | ||||||
chr6:151407978
|
C | T | 1 | a0001c0001t0002g0269 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1201-2142G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151407978 | ||||||
chr6:151408102
|
T | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(231): Show | 249 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1201-2266A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408102 | ||||||
chr6:151408104
|
G | A | 1 | a0005c0011t0008g0310 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1201-2268C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408104 | ||||||
chr6:151408161
|
T | C | 1 | a0002c0002t0001g0057 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1201-2325A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408161 | ||||||
chr6:151408220
|
G | A | 2 | a0003c0003t0011g0265a0004c0010t0014g0371 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1201-2384C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408220 | ||||||
chr6:151408221
|
G | A | 1 | a0004c0010t0014g0371 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1201-2385C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408221 | ||||||
chr6:151408265
|
C | A | 7 | a0001c0001t0001g0160a0001c0005t0001g0141a0001c0005t0001g0262others(4): Show | 7 | HG02717.hp2 HG03041.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-2429G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408265 | ||||||
chr6:151408270
|
G | A | 1 | a0001c0004t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1201-2434C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408270 | ||||||
chr6:151408321
|
G | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0213 | 3 | HG02809.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1201-2485C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408321 | ||||||
chr6:151408424
|
G | A | 1 | a0003c0003t0004g0003 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1201-2588C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408424 | ||||||
chr6:151408446
|
C | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0146others(151): Show | 158 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1201-2610G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408446 | ||||||
chr6:151408492
|
T | A | 3 | a0001c0001t0002g0274a0001c0001t0002g0277a0001c0001t0002g0315 | 3 | HG00735.hp2 HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1201-2656A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408492 | ||||||
chr6:151408682
|
A | G | 1 | a0003c0003t0011g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1201-2846T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408682 | ||||||
chr6:151408716
|
G | A | 1 | a0001c0001t0006g0344 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1201-2880C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408716 | ||||||
chr6:151408910
|
A | G | 6 | a0001c0001t0002g0229a0001c0001t0002g0274a0001c0001t0002g0277others(3): Show | 6 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1201-3074T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151408910 | ||||||
chr6:151409031
|
C | A | 2 | a0003c0003t0004g0019a0003c0003t0004g0040 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1201-3195G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409031 | ||||||
chr6:151409097
|
C | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(27): Show | 36 | HG00099.hp1 HG01074.hp1 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.1201-3261G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409097 | ||||||
chr6:151409231
|
G | A | 1 | a0002c0002t0001g0129 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1201-3395C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409231 | ||||||
chr6:151409307
|
T | G | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1201-3471A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409307 | ||||||
chr6:151409480
|
G | T | 1 | a0001c0001t0002g0281 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1201-3644C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409480 | ||||||
chr6:151409481
|
T | G | 1 | a0001c0001t0002g0281 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1201-3645A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409481 | ||||||
chr6:151409606
|
C | T | 1 | a0004c0010t0014g0371 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1201-3770G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409606 | ||||||
chr6:151409649
|
A | G | 126 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0151others(123): Show | 126 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1201-3813T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409649 | ||||||
chr6:151409667
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(162): Show | 174 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1201-3831G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409667 | ||||||
chr6:151409719
|
C | G | 1 | a0002c0002t0001g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1201-3883G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409719 | ||||||
chr6:151409768
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(24): Show | 33 | HG00099.hp1 HG00609.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1201-3932T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409768 | ||||||
chr6:151409796
|
A | G | 1 | a0002c0002t0001g0088 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1201-3960T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409796 | ||||||
chr6:151409812
|
C | T | 1 | a0002c0002t0001g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1201-3976G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151409812 | ||||||
chr6:151410041
|
C | T | 1 | a0002c0002t0001g0057 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1201-4205G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410041 | ||||||
chr6:151410057
|
A | AT | 162 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0152others(159): Show | 166 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1201-4222dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410057 | ||||||
chr6:151410057
|
A | ATT | 12 | a0001c0001t0002g0261a0001c0001t0002g0308a0001c0001t0003g0325others(9): Show | 12 | HG01433.hp2 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-4223_1201-422 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410057 | ||||||
chr6:151410057
|
AT | A | 6 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0280others(3): Show | 6 | HG03834.hp1 NA18955.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-4222delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410057 | ||||||
chr6:151410076
|
G | A | 1 | a0001c0001t0002g0225 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1201-4240C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410076 | ||||||
chr6:151410085
|
T | C | 6 | a0001c0001t0002g0207a0001c0001t0002g0269a0001c0001t0002g0271others(3): Show | 6 | NA18956.hp2 NA18963.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1201-4249A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410085 | ||||||
chr6:151410093
|
C | G | 46 | a0001c0001t0001g0309a0001c0001t0002g0182a0001c0001t0002g0201others(43): Show | 47 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1201-4257G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410093 | ||||||
chr6:151410094
|
A | G | 7 | a0001c0001t0002g0016a0001c0001t0002g0208a0001c0001t0002g0225others(4): Show | 8 | HG02074.hp1 NA18747.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1201-4258T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410094 | ||||||
chr6:151410106
|
C | G | 47 | a0001c0001t0001g0172a0001c0001t0001g0177a0001c0001t0002g0204others(44): Show | 48 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1201-4270G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410106 | ||||||
chr6:151410124
|
C | G | 1 | a0001c0001t0002g0199 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1201-4288G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410124 | ||||||
chr6:151410155
|
C | T | 2 | a0001c0001t0001g0145a0002c0002t0001g0100 | 2 | HG02886.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1201-4319G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410155 | ||||||
chr6:151410198
|
A | G | 8 | a0001c0001t0001g0306a0001c0001t0002g0239a0001c0001t0002g0240others(5): Show | 8 | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-4362T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410198 | ||||||
chr6:151410199
|
C | T | 2 | a0003c0003t0004g0028a0003c0003t0004g0032 | 2 | HG01261.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1201-4363G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410199 | ||||||
chr6:151410211
|
C | T | 1 | a0001c0004t0001g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1201-4375G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410211 | ||||||
chr6:151410212
|
G | A | 1 | a0002c0002t0001g0107 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1201-4376C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410212 | ||||||
chr6:151410246
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(145): Show | 155 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.1201-4410C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410246 | ||||||
chr6:151410251
|
C | T | 2 | a0002c0002t0001g0128a0002c0002t0002g0108 | 2 | HG02129.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1201-4415G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410251 | ||||||
chr6:151410257
|
A | G | 1 | a0002c0002t0001g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1201-4421T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410257 | ||||||
chr6:151410262
|
A | G | 15 | a0001c0007t0001g0242a0001c0007t0001g0244a0001c0007t0002g0243others(12): Show | 15 | HG02040.hp1 HG02055.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1201-4426T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410262 | ||||||
chr6:151410276
|
G | C | 6 | a0001c0001t0002g0016a0001c0001t0002g0279a0001c0001t0002g0290others(3): Show | 7 | HG02074.hp1 NA18946.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201-4440C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410276 | ||||||
chr6:151410284
|
T | C | 1 | a0003c0003t0004g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1201-4448A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410284 | ||||||
chr6:151410290
|
T | C | 26 | a0001c0001t0002g0005a0001c0001t0002g0153a0001c0001t0002g0175others(23): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1201-4454A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410290 | ||||||
chr6:151410297
|
C | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0239a0001c0001t0002g0240 | 4 | HG02572.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-4461G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410297 | ||||||
chr6:151410298
|
G | A | 2 | a0002c0002t0002g0108a0003c0003t0004g0028 | 2 | NA18941.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1201-4462C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410298 | ||||||
chr6:151410302
|
T | G | 2 | a0001c0001t0002g0271a0001c0004t0002g0189 | 2 | NA18994.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1201-4466A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410302 | ||||||
chr6:151410306
|
T | C | 1 | a0001c0001t0002g0271 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1201-4470A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410306 | ||||||
chr6:151410318
|
A | G | 1 | a0008c0009t0002g0194 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1201-4482T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410318 | ||||||
chr6:151410335
|
A | G | 13 | a0001c0001t0001g0166a0001c0001t0002g0006a0001c0001t0002g0154others(10): Show | 14 | HG01109.hp1 HG01884.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1201-4499T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410335 | ||||||
chr6:151410344
|
C | T | 72 | a0001c0001t0001g0151a0001c0001t0002g0215a0001c0001t0002g0301others(69): Show | 73 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1201-4508G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410344 | ||||||
chr6:151410346
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1201-4510G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410346 | ||||||
chr6:151410347
|
A | G | 1 | a0002c0002t0001g0130 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1201-4511T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410347 | ||||||
chr6:151410347
|
ACCCGGC | A | 4 | a0001c0001t0002g0196a0001c0001t0002g0221a0001c0001t0002g0226others(1): Show | 4 | NA18961.hp1 NA18975.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-4517_1201-451 others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410347 | ||||||
chr6:151410440
|
C | T | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1201-4604G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410440 | ||||||
chr6:151410580
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1201-4744A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410580 | ||||||
chr6:151410814
|
C | T | 2 | a0001c0001t0001g0094a0002c0002t0001g0088 | 2 | HG00609.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1201-4978G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410814 | ||||||
chr6:151410838
|
C | T | 40 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(37): Show | 42 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1201-5002G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410838 | ||||||
chr6:151410882
|
C | T | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(251): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1201-5046G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410882 | ||||||
chr6:151410982
|
A | G | 61 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(58): Show | 64 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.1201-5146T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151410982 | ||||||
chr6:151411100
|
C | A | 4 | a0001c0001t0001g0309a0004c0006t0001g0258a0004c0006t0001g0259others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-5264G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411100 | ||||||
chr6:151411250
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1201-5414A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411250 | ||||||
chr6:151411765
|
A | G | 44 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0006others(41): Show | 47 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1200+5514T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411765 | ||||||
chr6:151411820
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0257 | 2 | HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1200+5459C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411820 | ||||||
chr6:151411884
|
C | T | 1 | a0001c0001t0003g0325 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1200+5395G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411884 | ||||||
chr6:151411914
|
T | C | 1 | a0001c0004t0007g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1200+5365A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411914 | ||||||
chr6:151411951
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5328G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151411951 | ||||||
chr6:151412078
|
C | T | 41 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(38): Show | 43 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.1200+5201G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412078 | ||||||
chr6:151412091
|
C | A | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5188G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412091 | ||||||
chr6:151412141
|
A | G | 9 | a0001c0001t0002g0058a0001c0001t0002g0078a0001c0001t0002g0090others(6): Show | 9 | HG02155.hp2 NA18942.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+5138T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412141 | ||||||
chr6:151412209
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+5070G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412209 | ||||||
chr6:151412254
|
G | A | 1 | a0001c0001t0003g0363 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1200+5025C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412254 | ||||||
chr6:151412317
|
AT | A | 55 | a0001c0001t0002g0167a0001c0001t0002g0170a0001c0001t0002g0234others(52): Show | 56 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.1200+4961delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412317 | ||||||
chr6:151412317
|
ATT | A | 24 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(21): Show | 25 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1200+4960_1200+496 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412317 | ||||||
chr6:151412448
|
T | C | 116 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(113): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1200+4831A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412448 | ||||||
chr6:151412514
|
A | G | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1200+4765T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412514 | ||||||
chr6:151412598
|
A | G | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1200+4681T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412598 | ||||||
chr6:151412674
|
A | G | 7 | a0001c0001t0002g0183a0001c0001t0002g0197a0001c0001t0002g0199others(4): Show | 7 | HG00639.hp1 HG02602.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+4605T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412674 | ||||||
chr6:151412695
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1200+4584A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412695 | ||||||
chr6:151412784
|
C | T | 1 | a0004c0010t0014g0371 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1200+4495G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412784 | ||||||
chr6:151412830
|
G | T | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1200+4449C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412830 | ||||||
chr6:151412875
|
C | T | 2 | a0002c0002t0001g0095a0002c0002t0001g0140 | 2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1200+4404G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412875 | ||||||
chr6:151412916
|
C | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(136): Show | 148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1200+4363G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412916 | ||||||
chr6:151412916
|
C | G | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1200+4363G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412916 | ||||||
chr6:151412926
|
C | T | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1200+4353G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412926 | ||||||
chr6:151412999
|
T | TA | 99 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0152others(96): Show | 99 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1200+4279dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151412999 | ||||||
chr6:151413062
|
C | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(136): Show | 148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1200+4217G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413062 | ||||||
chr6:151413064
|
T | A | 116 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(113): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1200+4215A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413064 | ||||||
chr6:151413296
|
G | A | 2 | a0001c0004t0001g0250a0003c0003t0011g0265 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1200+3983C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413296 | ||||||
chr6:151413428
|
T | C | 116 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(113): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1200+3851A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413428 | ||||||
chr6:151413593
|
A | C | 1 | a0001c0004t0002g0189 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1200+3686T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413593 | ||||||
chr6:151413728
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1200+3551A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413728 | ||||||
chr6:151413760
|
C | T | 116 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(113): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1200+3519G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413760 | ||||||
chr6:151413863
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(44): Show | 56 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1200+3416A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413863 | ||||||
chr6:151413866
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1200+3413G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413866 | ||||||
chr6:151413877
|
G | C | 7 | a0001c0001t0001g0282a0001c0001t0002g0229a0001c0001t0002g0274others(4): Show | 7 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+3402C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151413877 | ||||||
chr6:151414244
|
T | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0292 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1200+3035A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414244 | ||||||
chr6:151414483
|
C | G | 1 | a0002c0002t0001g0097 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1200+2796G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414483 | ||||||
chr6:151414492
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1200+2787C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414492 | ||||||
chr6:151414643
|
T | C | 116 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(113): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1200+2636A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414643 | ||||||
chr6:151414747
|
A | G | 52 | a0001c0001t0003g0018a0001c0001t0003g0324a0001c0001t0003g0325others(49): Show | 53 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1200+2532T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414747 | ||||||
chr6:151414929
|
T | C | 7 | a0001c0004t0001g0246a0001c0004t0001g0247a0001c0004t0001g0248others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+2350A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414929 | ||||||
chr6:151414949
|
G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1200+2330C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151414949 | ||||||
chr6:151415049
|
GA | G | 74 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(71): Show | 76 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1200+2229delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415049 | ||||||
chr6:151415185
|
A | G | 2 | a0001c0005t0001g0013a0001c0005t0001g0264 | 3 | HG02965.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1200+2094T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415185 | ||||||
chr6:151415234
|
A | T | 1 | a0001c0001t0002g0214 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1200+2045T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415234 | ||||||
chr6:151415281
|
C | CT | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1200+1997dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415281 | ||||||
chr6:151415302
|
A | G | 1 | a0001c0001t0006g0334 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1200+1977T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415302 | ||||||
chr6:151415782
|
G | C | 2 | a0002c0002t0001g0136a0002c0002t0002g0132 | 2 | NA18950.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1200+1497C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415782 | ||||||
chr6:151415792
|
C | CA | 17 | a0001c0001t0001g0230a0001c0001t0002g0017a0001c0001t0002g0192others(14): Show | 18 | HG00423.hp2 HG00621.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1200+1486dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | ||||||
chr6:151415792
|
CA | C | 6 | a0001c0001t0001g0165a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 6 | HG02735.hp2 HG02809.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1200+1486delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | ||||||
chr6:151415792
|
CAA | C | 9 | a0001c0001t0001g0168a0001c0001t0003g0335a0001c0001t0003g0336others(6): Show | 9 | HG00609.hp1 HG01261.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1200+1485_1200+148 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | ||||||
chr6:151415792
|
CAAA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(145): Show | 159 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1200+1484_1200+148 others(7): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | ||||||
chr6:151415792
|
CAAAA | C | 95 | a0001c0001t0001g0177a0001c0001t0001g0309a0001c0001t0002g0005others(92): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1200+1483_1200+148 others(8): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415792 | ||||||
chr6:151415874
|
G | A | 1 | a0003c0003t0004g0022 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1200+1405C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415874 | ||||||
chr6:151415888
|
C | G | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1200+1391G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415888 | ||||||
chr6:151415963
|
A | G | 1 | a0002c0002t0001g0110 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1200+1316T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415963 | ||||||
chr6:151415988
|
G | GT | 44 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(41): Show | 46 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1200+1290dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151415988 | ||||||
chr6:151416042
|
G | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(27): Show | 36 | HG00099.hp1 HG01074.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1200+1237C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416042 | ||||||
chr6:151416171
|
G | C | 1 | a0002c0002t0001g0074 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1200+1108C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416171 | ||||||
chr6:151416270
|
G | A | 2 | a0001c0001t0001g0230a0002c0002t0001g0077 | 2 | NA18952.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1200+1009C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416270 | ||||||
chr6:151416420
|
C | CT | 12 | a0001c0001t0001g0144a0001c0001t0001g0165a0001c0001t0001g0256others(9): Show | 12 | HG01433.hp2 HG02132.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1200+858dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416420 | ||||||
chr6:151416420
|
CT | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0211others(110): Show | 120 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1200+858delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416420 | ||||||
chr6:151416420
|
CTT | C | 70 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(67): Show | 73 | HG00140.hp1 HG01069.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.1200+857_1200+858d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416420 | ||||||
chr6:151416446
|
C | T | 5 | a0001c0001t0001g0151a0001c0004t0001g0188a0001c0004t0001g0318others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+833G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416446 | ||||||
chr6:151416487
|
G | A | 1 | a0001c0001t0003g0366 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1200+792C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416487 | ||||||
chr6:151416754
|
A | G | 2 | a0001c0004t0001g0185a0001c0004t0001g0186 | 2 | HG01175.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1200+525T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416754 | ||||||
chr6:151416755
|
C | T | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1200+524G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416755 | ||||||
chr6:151416865
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+414G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416865 | ||||||
chr6:151416870
|
C | G | 8 | a0001c0004t0007g0369a0001c0004t0007g0370a0002c0002t0001g0082others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1200+409G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416870 | ||||||
chr6:151416911
|
G | A | 1 | a0005c0011t0008g0310 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1200+368C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416911 | ||||||
chr6:151416996
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1200+283T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151416996 | ||||||
chr6:151417235
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1200+44G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151417235 | ||||||
chr6:151417241
|
C | T | 21 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(18): Show | 21 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1200+38G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 10/11 | chr6 | 151417241 | ||||||
chr6:151417431
|
A | G | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1080-32T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417431 | ||||||
chr6:151417492
|
CT | C | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1080-94delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417492 | ||||||
chr6:151417719
|
A | G | 44 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(41): Show | 46 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1080-320T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417719 | ||||||
chr6:151417816
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1080-417A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417816 | ||||||
chr6:151417816
|
T | TA | 44 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(41): Show | 46 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1080-418_1080-417i others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417816 | ||||||
chr6:151417817
|
T | A | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1080-418A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417817 | ||||||
chr6:151417895
|
G | A | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1080-496C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151417895 | ||||||
chr6:151418021
|
G | A | 8 | a0001c0004t0007g0369a0001c0004t0007g0370a0002c0002t0001g0082others(5): Show | 8 | HG01884.hp2 HG02258.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1080-622C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418021 | ||||||
chr6:151418026
|
G | A | 26 | a0001c0001t0002g0005a0001c0001t0002g0153a0001c0001t0002g0175others(23): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1080-627C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418026 | ||||||
chr6:151418048
|
T | C | 5 | a0001c0004t0007g0369a0001c0004t0007g0370a0003c0003t0001g0313others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080-649A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418048 | ||||||
chr6:151418052
|
T | C | 72 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(69): Show | 75 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.1080-653A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418052 | ||||||
chr6:151418109
|
A | G | 72 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(69): Show | 75 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.1080-710T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418109 | ||||||
chr6:151418171
|
T | C | 2 | a0003c0014t0001g0323a0004c0010t0014g0371 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1080-772A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418171 | ||||||
chr6:151418178
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(88): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1080-779G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418178 | ||||||
chr6:151418272
|
G | A | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-873C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418272 | ||||||
chr6:151418369
|
G | A | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-970C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418369 | ||||||
chr6:151418417
|
T | TA | 38 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(35): Show | 39 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1080-1019dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418417 | ||||||
chr6:151418417
|
T | TAA | 33 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(30): Show | 35 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1080-1020_1080-101 others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418417 | ||||||
chr6:151418460
|
T | A | 72 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(69): Show | 75 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.1080-1061A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418460 | ||||||
chr6:151418466
|
A | T | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1080-1067T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418466 | ||||||
chr6:151418507
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1080-1108C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418507 | ||||||
chr6:151418675
|
G | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1080-1276C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418675 | ||||||
chr6:151418825
|
T | C | 72 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(69): Show | 75 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.1080-1426A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418825 | ||||||
chr6:151418833
|
C | T | 1 | a0001c0004t0001g0190 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1080-1434G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418833 | ||||||
chr6:151418858
|
C | A | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1080-1459G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418858 | ||||||
chr6:151418871
|
A | G | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1080-1472T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418871 | ||||||
chr6:151418928
|
G | A | 1 | a0001c0004t0007g0370 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1080-1529C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418928 | ||||||
chr6:151418946
|
T | C | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1080-1547A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418946 | ||||||
chr6:151418987
|
C | T | 1 | a0001c0001t0003g0365 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1080-1588G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151418987 | ||||||
chr6:151419301
|
G | A | 1 | a0002c0002t0002g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1080-1902C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419301 | ||||||
chr6:151419354
|
C | T | 1 | a0006c0013t0001g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1079+1891G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419354 | ||||||
chr6:151419368
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1079+1877G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419368 | ||||||
chr6:151419509
|
C | A | 1 | a0001c0001t0001g0143 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1079+1736G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419509 | ||||||
chr6:151419671
|
T | TA | 38 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(35): Show | 39 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1079+1573dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419671 | ||||||
chr6:151419671
|
TA | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(145): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1079+1573delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419671 | ||||||
chr6:151419717
|
T | A | 72 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(69): Show | 75 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.1079+1528A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419717 | ||||||
chr6:151419832
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(180): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1079+1413A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419832 | ||||||
chr6:151419978
|
G | GT | 72 | a0001c0001t0001g0151a0001c0001t0001g0309a0001c0001t0002g0005others(69): Show | 75 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(72): Show |
intron_variant | MODIFIER | c.1079+1266dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419978 | ||||||
chr6:151419991
|
A | G | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1079+1254T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151419991 | ||||||
chr6:151420042
|
C | T | 1 | a0001c0001t0003g0354 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1079+1203G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420042 | ||||||
chr6:151420121
|
G | A | 1 | a0004c0010t0014g0371 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1079+1124C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420121 | ||||||
chr6:151420152
|
A | G | 5 | a0001c0004t0007g0369a0001c0004t0007g0370a0003c0003t0001g0313others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1079+1093T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420152 | ||||||
chr6:151420292
|
G | A | 2 | a0001c0004t0007g0369a0001c0004t0007g0370 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1079+953C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420292 | ||||||
chr6:151420655
|
C | T | 3 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067 | 3 | HG02004.hp1 HG02148.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1079+590G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420655 | ||||||
chr6:151420840
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1079+405G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420840 | ||||||
chr6:151420880
|
T | A | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1079+365A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420880 | ||||||
chr6:151420990
|
T | C | 1 | a0001c0004t0001g0188 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1079+255A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151420990 | ||||||
chr6:151421032
|
CTT | C | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1079+211_1079+212d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151421032 | ||||||
chr6:151421096
|
A | G | 1 | a0001c0001t0003g0337 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1079+149T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151421096 | ||||||
chr6:151421151
|
G | A | 1 | a0002c0002t0002g0044 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1079+94C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 9/11 | chr6 | 151421151 | ||||||
chr6:151421406
|
T | C | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(366): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.1003-85A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421406 | ||||||
chr6:151421407
|
G | A | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1003-86C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421407 | ||||||
chr6:151421782
|
G | T | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1003-461C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421782 | ||||||
chr6:151421836
|
G | A | 2 | a0001c0001t0003g0340a0002c0002t0001g0129 | 2 | NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1003-515C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421836 | ||||||
chr6:151421888
|
G | T | 1 | a0002c0002t0002g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1003-567C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421888 | ||||||
chr6:151421949
|
A | C | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1002+592T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151421949 | ||||||
chr6:151422205
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1002+336C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422205 | ||||||
chr6:151422205
|
G | GC | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1002+335dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422205 | ||||||
chr6:151422234
|
TTTTCTTG others(3): Show |
T | 2 | a0001c0001t0002g0058a0001c0001t0002g0091 | 2 | NA18982.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1002+297_1002+306d others(12): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422234 | ||||||
chr6:151422273
|
CTATT | C | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1002+264_1002+267d others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422273 | ||||||
chr6:151422280
|
C | T | 1 | a0002c0002t0002g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1002+261G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422280 | ||||||
chr6:151422494
|
A | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1002+47T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 8/11 | chr6 | 151422494 | ||||||
chr6:151422661
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.938-56T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422661 | ||||||
chr6:151422803
|
T | C | 2 | a0002c0002t0001g0095a0002c0002t0001g0140 | 2 | NA18985.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.938-198A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422803 | ||||||
chr6:151422813
|
A | G | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.938-208T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422813 | ||||||
chr6:151422927
|
C | T | 44 | a0001c0001t0003g0018a0001c0001t0003g0324a0001c0001t0003g0325others(41): Show | 45 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.938-322G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422927 | ||||||
chr6:151422950
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.938-345G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151422950 | ||||||
chr6:151423014
|
C | T | 1 | a0001c0007t0001g0242 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.938-409G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423014 | ||||||
chr6:151423019
|
C | T | 21 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(18): Show | 21 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.938-414G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423019 | ||||||
chr6:151423148
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(255): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.937+377C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423148 | ||||||
chr6:151423173
|
C | G | 28 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(25): Show | 29 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.937+352G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423173 | ||||||
chr6:151423268
|
A | C | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.937+257T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423268 | ||||||
chr6:151423401
|
A | C | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.937+124T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423401 | ||||||
chr6:151423455
|
G | T | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.937+70C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 7/11 | chr6 | 151423455 | ||||||
chr6:151423676
|
C | A | 6 | a0002c0002t0001g0080a0002c0002t0001g0096a0002c0002t0001g0097others(3): Show | 6 | HG00408.hp1 NA18943.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.831-45G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423676 | ||||||
chr6:151423764
|
T | C | 1 | a0001c0004t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.831-133A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423764 | ||||||
chr6:151423802
|
T | TC | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.831-172dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423802 | ||||||
chr6:151423851
|
C | CT | 44 | a0001c0001t0002g0005a0001c0001t0002g0153a0001c0001t0002g0175others(41): Show | 46 | HG00140.hp1 HG00140.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.831-221dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423851 | ||||||
chr6:151423851
|
CT | C | 34 | a0001c0001t0001g0151a0001c0001t0002g0170a0001c0001t0002g0199others(31): Show | 35 | HG00323.hp1 HG01167.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.831-221delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423851 | ||||||
chr6:151423887
|
G | A | 5 | a0001c0004t0007g0369a0001c0004t0007g0370a0003c0003t0001g0313others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.831-256C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423887 | ||||||
chr6:151423909
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.831-278C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151423909 | ||||||
chr6:151424024
|
T | G | 1 | a0004c0006t0001g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.831-393A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424024 | ||||||
chr6:151424198
|
C | T | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-567G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424198 | ||||||
chr6:151424210
|
C | T | 1 | a0003c0003t0011g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.831-579G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424210 | ||||||
chr6:151424255
|
T | G | 1 | a0001c0004t0002g0189 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.831-624A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424255 | ||||||
chr6:151424322
|
G | T | 1 | a0001c0001t0002g0200 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.831-691C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424322 | ||||||
chr6:151424335
|
C | T | 2 | a0001c0004t0001g0185a0001c0004t0001g0186 | 2 | HG01175.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.831-704G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424335 | ||||||
chr6:151424387
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.831-756G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424387 | ||||||
chr6:151424407
|
A | G | 10 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(7): Show | 11 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.831-776T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424407 | ||||||
chr6:151424414
|
A | G | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-783T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424414 | ||||||
chr6:151424417
|
C | T | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-786G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424417 | ||||||
chr6:151424418
|
A | G | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.831-787T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424418 | ||||||
chr6:151424419
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.831-788G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424419 | ||||||
chr6:151424463
|
C | CA | 96 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0177others(93): Show | 96 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.831-833dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424463 | ||||||
chr6:151424463
|
CA | C | 8 | a0001c0001t0001g0147a0001c0001t0001g0171a0001c0001t0001g0172others(5): Show | 8 | HG00099.hp1 HG01074.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.831-833delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424463 | ||||||
chr6:151424550
|
T | G | 1 | a0001c0001t0002g0219 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.831-919A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424550 | ||||||
chr6:151424596
|
A | G | 3 | a0002c0002t0001g0062a0002c0002t0001g0137a0002c0002t0002g0131 | 3 | HG02683.hp1 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.831-965T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424596 | ||||||
chr6:151424759
|
CA | C | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.831-1129delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424759 | ||||||
chr6:151424852
|
C | T | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.831-1221G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424852 | ||||||
chr6:151424853
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831-1222C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424853 | ||||||
chr6:151424886
|
G | GGGCTGAG others(1): Show |
47 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(44): Show | 50 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.831-1256_831-1255i others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151424886 | ||||||
chr6:151425189
|
C | T | 4 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0294others(1): Show | 4 | NA18970.hp1 NA18983.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-1558G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425189 | ||||||
chr6:151425413
|
A | G | 1 | a0002c0008t0001g0115 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.831-1782T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425413 | ||||||
chr6:151425416
|
G | A | 3 | a0001c0001t0001g0306a0001c0001t0002g0012a0001c0001t0002g0240 | 4 | HG02572.hp1 HG02622.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.831-1785C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425416 | ||||||
chr6:151425425
|
CGT | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(86): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.831-1796_831-1795d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425425 | ||||||
chr6:151425451
|
T | C | 92 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0177others(89): Show | 92 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.831-1820A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425451 | ||||||
chr6:151425451
|
T | TAC | 18 | a0001c0001t0002g0207a0001c0001t0003g0018a0001c0001t0003g0324others(15): Show | 19 | HG00438.hp1 HG00609.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.831-1822_831-1821d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425451 | ||||||
chr6:151425589
|
A | G | 1 | a0001c0004t0002g0241 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.830+1893T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425589 | ||||||
chr6:151425597
|
G | A | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.830+1885C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425597 | ||||||
chr6:151425650
|
T | C | 2 | a0002c0008t0001g0060a0002c0008t0001g0115 | 2 | NA19007.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.830+1832A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425650 | ||||||
chr6:151425665
|
C | T | 2 | a0001c0004t0001g0250a0003c0003t0011g0265 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.830+1817G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425665 | ||||||
chr6:151425832
|
G | C | 1 | a0002c0002t0001g0110 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.830+1650C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425832 | ||||||
chr6:151425907
|
G | A | 5 | a0001c0004t0007g0369a0001c0004t0007g0370a0003c0003t0001g0313others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.830+1575C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425907 | ||||||
chr6:151425946
|
C | CT | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(122): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.830+1535dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425946 | ||||||
chr6:151425946
|
C | CTT | 78 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0174others(75): Show | 78 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.830+1534_830+1535d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425946 | ||||||
chr6:151425946
|
C | CTTT | 13 | a0001c0004t0001g0246a0001c0004t0001g0247a0001c0004t0001g0248others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.830+1533_830+1535d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425946 | ||||||
chr6:151425974
|
C | T | 1 | a0002c0002t0009g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.830+1508G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151425974 | ||||||
chr6:151426017
|
C | T | 92 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0177others(89): Show | 92 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.830+1465G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426017 | ||||||
chr6:151426054
|
T | TGCCTCC | 8 | a0001c0001t0002g0183a0001c0001t0002g0197a0001c0001t0002g0199others(5): Show | 8 | HG00639.hp1 HG00639.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.830+1422_830+1427d others(8): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426054 | ||||||
chr6:151426065
|
C | T | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+1417G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426065 | ||||||
chr6:151426097
|
C | T | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+1385G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426097 | ||||||
chr6:151426111
|
G | T | 33 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(30): Show | 35 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.830+1371C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426111 | ||||||
chr6:151426503
|
C | T | 1 | a0003c0014t0001g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.830+979G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426503 | ||||||
chr6:151426617
|
T | C | 1 | a0001c0001t0002g0220 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.830+865A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426617 | ||||||
chr6:151426749
|
T | A | 1 | a0003c0003t0004g0035 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.830+733A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426749 | ||||||
chr6:151426839
|
G | C | 1 | a0002c0002t0001g0085 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.830+643C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426839 | ||||||
chr6:151426849
|
A | G | 3 | a0002c0002t0001g0112a0002c0002t0002g0113a0004c0006t0002g0307 | 3 | HG02258.hp2 HG02451.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.830+633T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426849 | ||||||
chr6:151426854
|
C | T | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+628G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426854 | ||||||
chr6:151426855
|
C | T | 5 | a0001c0004t0007g0369a0001c0004t0007g0370a0003c0003t0001g0313others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.830+627G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426855 | ||||||
chr6:151426871
|
G | A | 33 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(30): Show | 35 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.830+611C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426871 | ||||||
chr6:151426944
|
A | AT | 23 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(20): Show | 23 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.830+537dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151426944 | ||||||
chr6:151427073
|
T | A | 1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.830+409A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427073 | ||||||
chr6:151427086
|
G | T | 370 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(367): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.830+396C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427086 | ||||||
chr6:151427087
|
T | G | 370 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(367): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.830+395A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427087 | ||||||
chr6:151427116
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.830+366G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427116 | ||||||
chr6:151427185
|
G | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG00099.hp1 HG01074.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.830+297C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427185 | ||||||
chr6:151427199
|
A | G | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.830+283T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427199 | ||||||
chr6:151427224
|
A | G | 1 | a0001c0001t0002g0311 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.830+258T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427224 | ||||||
chr6:151427237
|
G | A | 2 | a0003c0003t0004g0025a0003c0003t0004g0029 | 2 | HG00140.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.830+245C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427237 | ||||||
chr6:151427348
|
C | A | 1 | a0002c0002t0001g0098 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.830+134G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427348 | ||||||
chr6:151427375
|
C | CA | 58 | a0001c0001t0002g0283a0001c0001t0003g0360a0002c0002t0001g0042others(55): Show | 58 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.830+106dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427375 | ||||||
chr6:151427375
|
CA | C | 10 | a0001c0001t0001g0147a0001c0001t0002g0206a0001c0001t0002g0261others(7): Show | 11 | HG01074.hp1 HG01975.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.830+106delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427375 | ||||||
chr6:151427407
|
T | C | 1 | a0002c0002t0001g0122 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.830+75A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 6/11 | chr6 | 151427407 | ||||||
chr6:151427673
|
C | A | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.730-91G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427673 | ||||||
chr6:151427734
|
A | G | 3 | a0001c0001t0003g0328a0001c0001t0003g0330a0001c0001t0003g0331 | 3 | HG01175.hp2 HG01256.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.730-152T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427734 | ||||||
chr6:151427820
|
T | A | 2 | a0001c0001t0002g0227a0001c0001t0002g0288 | 2 | HG00735.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.730-238A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427820 | ||||||
chr6:151427860
|
T | C | 91 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0002g0321others(88): Show | 91 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.730-278A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427860 | ||||||
chr6:151427946
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0002g0012a0001c0001t0002g0239others(1): Show | 5 | HG02572.hp1 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.730-364G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427946 | ||||||
chr6:151427991
|
A | C | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-409T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151427991 | ||||||
chr6:151428087
|
G | T | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-505C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428087 | ||||||
chr6:151428398
|
G | T | 1 | a0002c0002t0001g0109 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.730-816C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428398 | ||||||
chr6:151428425
|
A | G | 1 | a0004c0006t0002g0307 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.730-843T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428425 | ||||||
chr6:151428584
|
T | G | 1 | a0004c0006t0002g0307 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.730-1002A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428584 | ||||||
chr6:151428634
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(86): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.730-1052G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428634 | ||||||
chr6:151428635
|
G | A | 1 | a0001c0001t0002g0224 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.730-1053C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428635 | ||||||
chr6:151428680
|
C | T | 5 | a0001c0004t0007g0369a0001c0004t0007g0370a0003c0003t0001g0313others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-1098G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428680 | ||||||
chr6:151428796
|
A | C | 1 | a0001c0001t0002g0237 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.730-1214T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428796 | ||||||
chr6:151428848
|
T | C | 12 | a0002c0002t0001g0077a0002c0002t0001g0095a0002c0002t0001g0110others(9): Show | 12 | HG01975.hp2 HG01993.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.730-1266A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428848 | ||||||
chr6:151428994
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.729+1144T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151428994 | ||||||
chr6:151429009
|
T | C | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+1129A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429009 | ||||||
chr6:151429064
|
T | C | 5 | a0001c0004t0007g0369a0001c0004t0007g0370a0003c0003t0001g0313others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+1074A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429064 | ||||||
chr6:151429073
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.729+1065G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429073 | ||||||
chr6:151429123
|
C | CT | 8 | a0001c0001t0001g0257a0001c0001t0002g0293a0002c0002t0001g0082others(5): Show | 8 | HG02683.hp2 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+1014dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429123 | ||||||
chr6:151429141
|
G | A | 1 | a0001c0001t0003g0365 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.729+997C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429141 | ||||||
chr6:151429162
|
C | T | 1 | a0002c0002t0001g0088 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.729+976G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429162 | ||||||
chr6:151429187
|
C | T | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+951G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429187 | ||||||
chr6:151429230
|
T | G | 11 | a0002c0002t0001g0061a0002c0002t0001g0062a0002c0002t0001g0063others(8): Show | 11 | HG00621.hp1 HG01346.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.729+908A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429230 | ||||||
chr6:151429363
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0002g0181a0001c0001t0002g0217others(3): Show | 8 | HG00741.hp1 HG01928.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.729+775A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429363 | ||||||
chr6:151429465
|
A | G | 1 | a0002c0002t0001g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.729+673T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429465 | ||||||
chr6:151429479
|
G | C | 2 | a0001c0004t0001g0250a0003c0003t0011g0265 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.729+659C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429479 | ||||||
chr6:151429491
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.729+647G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429491 | ||||||
chr6:151429535
|
G | GT | 40 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(37): Show | 42 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.729+602_729+603ins others(1): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429535 | ||||||
chr6:151429543
|
A | C | 1 | a0001c0001t0002g0197 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.729+595T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429543 | ||||||
chr6:151429563
|
G | T | 2 | a0001c0004t0001g0250a0003c0003t0011g0265 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.729+575C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429563 | ||||||
chr6:151429628
|
C | T | 40 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(37): Show | 42 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.729+510G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429628 | ||||||
chr6:151429803
|
T | C | 6 | a0001c0001t0002g0308a0001c0004t0007g0369a0001c0004t0007g0370others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+335A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429803 | ||||||
chr6:151429825
|
C | T | 4 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0198others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+313G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429825 | ||||||
chr6:151429902
|
G | A | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729+236C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 5/11 | chr6 | 151429902 | ||||||
chr6:151430277
|
C | T | 2 | a0001c0004t0001g0250a0003c0003t0011g0265 | 2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.690-100G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430277 | ||||||
chr6:151430505
|
G | C | 2 | a0003c0003t0004g0030a0003c0003t0004g0031 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.690-328C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430505 | ||||||
chr6:151430556
|
T | C | 1 | a0002c0002t0001g0098 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.690-379A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430556 | ||||||
chr6:151430750
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.690-573G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430750 | ||||||
chr6:151430773
|
C | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.690-596G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430773 | ||||||
chr6:151430881
|
T | TATTAATG others(307): Show |
1 | a0003c0003t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.690-705_690-704ins others(314): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430881 | ||||||
chr6:151430881
|
T | TATTAATG others(308): Show |
2 | a0003c0014t0001g0323a0004c0010t0014g0371 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.690-705_690-704ins others(315): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430881 | ||||||
chr6:151430914
|
C | CTTAAG | 4 | a0001c0001t0002g0308a0003c0003t0001g0313a0003c0014t0001g0323others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-738_690-737ins others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151430914 | ||||||
chr6:151431059
|
A | G | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.690-882T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431059 | ||||||
chr6:151431124
|
A | T | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.690-947T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431124 | ||||||
chr6:151431192
|
C | G | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.690-1015G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431192 | ||||||
chr6:151431487
|
C | T | 26 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(23): Show | 26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.690-1310G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431487 | ||||||
chr6:151431720
|
C | A | 37 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(34): Show | 39 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.689+1435G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431720 | ||||||
chr6:151431826
|
G | T | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.689+1329C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431826 | ||||||
chr6:151431876
|
A | G | 36 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(33): Show | 38 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.689+1279T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151431876 | ||||||
chr6:151432039
|
G | GA | 26 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(23): Show | 26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.689+1115dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432039 | ||||||
chr6:151432085
|
TCCA | T | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.689+1067_689+1069d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432085 | ||||||
chr6:151432260
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.689+895T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432260 | ||||||
chr6:151432286
|
C | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(252): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.689+869G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432286 | ||||||
chr6:151432305
|
C | T | 91 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0002g0321others(88): Show | 91 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.689+850G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432305 | ||||||
chr6:151432335
|
G | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(240): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.689+820C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432335 | ||||||
chr6:151432499
|
G | A | 7 | a0002c0002t0001g0064a0002c0002t0001g0066a0002c0002t0001g0067others(4): Show | 7 | HG02004.hp1 HG02148.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.689+656C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432499 | ||||||
chr6:151432531
|
C | CACTT | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(117): Show | 130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.689+623_689+624ins others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432531 | ||||||
chr6:151432559
|
G | C | 124 | a0001c0001t0001g0094a0001c0001t0001g0146a0001c0001t0001g0151others(121): Show | 124 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.689+596C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432559 | ||||||
chr6:151432567
|
T | C | 7 | a0001c0001t0002g0183a0001c0001t0002g0193a0001c0001t0002g0196others(4): Show | 7 | HG00639.hp1 HG01993.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.689+588A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432567 | ||||||
chr6:151432860
|
G | A | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.689+295C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432860 | ||||||
chr6:151432923
|
G | A | 30 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(27): Show | 30 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.689+232C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151432923 | ||||||
chr6:151433138
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(214): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.689+17A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 4/11 | chr6 | 151433138 | ||||||
chr6:151433292
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0002g0012a0001c0001t0002g0150others(3): Show | 7 | HG01891.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-62G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433292 | ||||||
chr6:151433437
|
A | C | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.614-207T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433437 | ||||||
chr6:151433609
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(213): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.614-379C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433609 | ||||||
chr6:151433825
|
G | GT | 12 | a0001c0001t0003g0327a0001c0001t0003g0328a0001c0001t0003g0329others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-596dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433825 | ||||||
chr6:151433827
|
T | G | 3 | a0002c0002t0001g0082a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG02896.hp1 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.614-597A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433827 | ||||||
chr6:151433869
|
CTG | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.614-641_614-640del others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433869 | ||||||
chr6:151433939
|
A | AC | 31 | a0001c0001t0001g0230a0001c0001t0001g0236a0001c0001t0001g0306others(28): Show | 31 | HG00621.hp2 HG00741.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.614-710dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433939 | ||||||
chr6:151433939
|
AC | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(72): Show | 86 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.614-710delG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433939 | ||||||
chr6:151433947
|
CCG | C | 27 | a0001c0001t0001g0151a0001c0001t0002g0271a0001c0001t0002g0314others(24): Show | 27 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.614-719_614-718del others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433947 | ||||||
chr6:151433948
|
CG | C | 78 | a0001c0001t0003g0018a0001c0001t0003g0326a0001c0001t0003g0328others(75): Show | 79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.614-719delC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433948 | ||||||
chr6:151433949
|
G | C | 61 | a0001c0001t0001g0146a0001c0001t0003g0361a0001c0004t0001g0187others(58): Show | 61 | HG00408.hp1 HG00621.hp1 HG01243.hp2 others(58): Show |
intron_variant | MODIFIER | c.614-719C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433949 | ||||||
chr6:151433953
|
C | A | 1 | a0001c0001t0006g0334 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.614-723G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151433953 | ||||||
chr6:151434000
|
C | T | 2 | a0001c0001t0002g0271a0001c0001t0002g0314 | 2 | NA18994.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.614-770G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434000 | ||||||
chr6:151434024
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.614-794A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434024 | ||||||
chr6:151434068
|
T | A | 7 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG02559.hp1 HG02615.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-838A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434068 | ||||||
chr6:151434135
|
G | A | 1 | a0001c0004t0001g0250 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.614-905C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434135 | ||||||
chr6:151434232
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.614-1002T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434232 | ||||||
chr6:151434276
|
TA | T | 4 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0071others(1): Show | 4 | NA18943.hp1 NA18944.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.614-1047delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434276 | ||||||
chr6:151434327
|
CAT | C | 91 | a0001c0001t0002g0321a0002c0002t0001g0042a0002c0002t0001g0048others(88): Show | 91 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.614-1099_614-1098d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434327 | ||||||
chr6:151434328
|
A | G | 2 | a0001c0004t0007g0369a0001c0004t0007g0370 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.614-1098T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434328 | ||||||
chr6:151434409
|
A | AT | 118 | a0001c0001t0001g0151a0001c0001t0002g0150a0001c0001t0002g0238others(115): Show | 118 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.614-1180dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434409 | ||||||
chr6:151434409
|
A | ATTTT | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1183_614-1180d others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434409 | ||||||
chr6:151434409
|
AT | A | 27 | a0001c0001t0001g0176a0001c0001t0002g0005a0001c0001t0002g0153others(24): Show | 29 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.614-1180delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434409 | ||||||
chr6:151434424
|
C | G | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1194G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434424 | ||||||
chr6:151434671
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(248): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.614-1441C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434671 | ||||||
chr6:151434814
|
T | C | 1 | a0002c0002t0001g0120 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.614-1584A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434814 | ||||||
chr6:151434845
|
T | C | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.613+1601A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434845 | ||||||
chr6:151434894
|
G | A | 1 | a0005c0011t0008g0310 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.613+1552C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434894 | ||||||
chr6:151434898
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.613+1548C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434898 | ||||||
chr6:151434918
|
G | C | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.613+1528C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434918 | ||||||
chr6:151434935
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(250): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.613+1511T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151434935 | ||||||
chr6:151435006
|
G | A | 1 | a0001c0005t0001g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.613+1440C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435006 | ||||||
chr6:151435030
|
G | A | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.613+1416C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435030 | ||||||
chr6:151435164
|
A | G | 129 | a0001c0001t0001g0151a0001c0001t0002g0261a0001c0001t0002g0308others(126): Show | 130 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.613+1282T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435164 | ||||||
chr6:151435192
|
T | C | 92 | a0001c0001t0002g0308a0001c0001t0002g0321a0002c0002t0001g0042others(89): Show | 92 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.613+1254A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435192 | ||||||
chr6:151435202
|
G | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0146others(46): Show | 51 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.613+1244C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435202 | ||||||
chr6:151435207
|
A | G | 98 | a0001c0001t0002g0261a0001c0001t0002g0308a0001c0001t0002g0321others(95): Show | 99 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.613+1239T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435207 | ||||||
chr6:151435254
|
T | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0204 | 2 | HG02155.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.613+1192A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435254 | ||||||
chr6:151435432
|
C | A | 1 | a0001c0001t0003g0325 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.613+1014G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435432 | ||||||
chr6:151435477
|
A | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(219): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.613+969T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435477 | ||||||
chr6:151435530
|
TTTAA | T | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.613+912_613+915del others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435530 | ||||||
chr6:151435589
|
T | A | 1 | a0001c0001t0002g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.613+857A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435589 | ||||||
chr6:151435744
|
T | C | 2 | a0001c0001t0002g0205a0001c0001t0002g0285 | 2 | HG00639.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.613+702A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435744 | ||||||
chr6:151435804
|
C | T | 31 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(28): Show | 31 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.613+642G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151435804 | ||||||
chr6:151436060
|
G | A | 1 | a0001c0001t0006g0351 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.613+386C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436060 | ||||||
chr6:151436105
|
C | CA | 10 | a0001c0001t0002g0308a0002c0002t0001g0086a0002c0002t0001g0101others(7): Show | 10 | HG02071.hp2 HG02451.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.613+340dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436105 | ||||||
chr6:151436110
|
A | AAAC | 6 | a0002c0002t0001g0048a0002c0002t0001g0055a0002c0002t0001g0084others(3): Show | 6 | HG02132.hp1 NA18978.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+335_613+336ins others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436110 | ||||||
chr6:151436111
|
A | AAC | 76 | a0001c0001t0002g0321a0002c0002t0001g0042a0002c0002t0001g0057others(73): Show | 76 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.613+334_613+335ins others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436111 | ||||||
chr6:151436112
|
C | A | 82 | a0001c0001t0002g0321a0002c0002t0001g0042a0002c0002t0001g0048others(79): Show | 82 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.613+334G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436112 | ||||||
chr6:151436112
|
C | CA | 30 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(27): Show | 32 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.613+333dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436112 | ||||||
chr6:151436112
|
CA | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(87): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.613+333delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436112 | ||||||
chr6:151436116
|
A | AC | 8 | a0002c0002t0001g0086a0002c0002t0001g0101a0002c0002t0001g0102others(5): Show | 8 | HG02071.hp2 HG02451.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.613+329_613+330ins others(1): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436116 | ||||||
chr6:151436116
|
A | C | 10 | a0001c0001t0001g0236a0001c0001t0002g0261a0001c0001t0003g0356others(7): Show | 11 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+330T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436116 | ||||||
chr6:151436117
|
A | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(119): Show | 132 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.613+329T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436117 | ||||||
chr6:151436192
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(250): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.613+254A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436192 | ||||||
chr6:151436197
|
T | C | 25 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(22): Show | 25 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.613+249A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 3/11 | chr6 | 151436197 | ||||||
chr6:151436610
|
C | T | 3 | a0003c0003t0001g0313a0003c0014t0001g0323a0004c0010t0014g0371 | 3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.505-56G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436610 | ||||||
chr6:151436772
|
C | T | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-218G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436772 | ||||||
chr6:151436825
|
G | A | 31 | a0001c0001t0001g0151a0001c0004t0001g0185a0001c0004t0001g0186others(28): Show | 31 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.505-271C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436825 | ||||||
chr6:151436894
|
A | AATG | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(250): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.505-343_505-341dup others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436894 | ||||||
chr6:151436907
|
C | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(89): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.505-353G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436907 | ||||||
chr6:151436961
|
C | T | 1 | a0002c0002t0002g0044 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.505-407G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151436961 | ||||||
chr6:151437266
|
A | G | 32 | a0001c0001t0001g0309a0001c0001t0002g0005a0001c0001t0002g0153others(29): Show | 34 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.505-712T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437266 | ||||||
chr6:151437297
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.505-743A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437297 | ||||||
chr6:151437426
|
A | G | 4 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0014t0001g0323others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-872T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437426 | ||||||
chr6:151437771
|
C | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0238 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.505-1217G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437771 | ||||||
chr6:151437900
|
G | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(246): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.505-1346C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151437900 | ||||||
chr6:151438057
|
T | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(194): Show | 208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.505-1503A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438057 | ||||||
chr6:151438107
|
A | G | 3 | a0001c0001t0001g0309a0001c0001t0002g0308a0003c0003t0011g0265 | 3 | HG02486.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.505-1553T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438107 | ||||||
chr6:151438359
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.505-1805A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438359 | ||||||
chr6:151438495
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.505-1941A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438495 | ||||||
chr6:151438504
|
C | T | 1 | a0002c0002t0001g0042 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.505-1950G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438504 | ||||||
chr6:151438723
|
C | T | 6 | a0004c0006t0001g0258a0004c0006t0001g0259a0004c0006t0001g0260others(3): Show | 6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2169G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438723 | ||||||
chr6:151438763
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.505-2209C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438763 | ||||||
chr6:151438764
|
C | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(88): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.505-2210G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438764 | ||||||
chr6:151438795
|
C | CT | 16 | a0001c0001t0001g0309a0001c0001t0002g0207a0001c0001t0002g0269others(13): Show | 16 | HG01175.hp1 HG02258.hp1 HG03041.hp1 others(13): Show |
intron_variant | MODIFIER | c.505-2242dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438795 | ||||||
chr6:151438809
|
T | C | 1 | a0001c0005t0001g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.505-2255A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438809 | ||||||
chr6:151438809
|
T | TTTC | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-2256_505-2255i others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438809 | ||||||
chr6:151438810
|
C | T | 2 | a0001c0001t0001g0309a0001c0001t0002g0308 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.505-2256G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438810 | ||||||
chr6:151438811
|
C | A | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-2257G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438811 | ||||||
chr6:151438812
|
A | C | 2 | a0001c0001t0001g0309a0001c0001t0002g0308 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.505-2258T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438812 | ||||||
chr6:151438819
|
A | C | 4 | a0002c0002t0001g0061a0002c0002t0001g0063a0002c0002t0002g0043others(1): Show | 4 | HG00621.hp1 HG02040.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-2265T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438819 | ||||||
chr6:151438820
|
C | A | 31 | a0001c0001t0003g0018a0001c0001t0003g0324a0001c0001t0003g0325others(28): Show | 32 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.505-2266G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438820 | ||||||
chr6:151438851
|
C | T | 33 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(30): Show | 35 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.505-2297G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438851 | ||||||
chr6:151438870
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(93): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.505-2316A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438870 | ||||||
chr6:151438984
|
C | A | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG02615.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-2430G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151438984 | ||||||
chr6:151439007
|
G | A | 1 | a0002c0002t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.505-2453C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439007 | ||||||
chr6:151439009
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.505-2455C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439009 | ||||||
chr6:151439072
|
C | T | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-2518G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439072 | ||||||
chr6:151439117
|
A | T | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-2563T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439117 | ||||||
chr6:151439183
|
T | C | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-2629A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439183 | ||||||
chr6:151439242
|
T | C | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-2688A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439242 | ||||||
chr6:151439247
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(134): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.505-2693G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439247 | ||||||
chr6:151439335
|
A | G | 3 | a0001c0001t0001g0235a0001c0001t0002g0149a0001c0001t0002g0218 | 3 | HG00423.hp2 NA18951.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.505-2781T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439335 | ||||||
chr6:151439362
|
T | C | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-2808A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439362 | ||||||
chr6:151439649
|
TG | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0174 | 3 | NA18957.hp1 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.505-3096delC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439649 | ||||||
chr6:151439651
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0174 | 3 | NA18957.hp1 NA19001.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.505-3097A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439651 | ||||||
chr6:151439803
|
G | A | 17 | a0002c0002t0001g0055a0002c0002t0001g0077a0002c0002t0001g0095others(14): Show | 17 | HG01975.hp2 HG01993.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.505-3249C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439803 | ||||||
chr6:151439887
|
C | G | 1 | a0001c0004t0001g0190 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.505-3333G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439887 | ||||||
chr6:151439996
|
G | T | 1 | a0001c0001t0002g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.505-3442C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151439996 | ||||||
chr6:151440209
|
G | A | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-3655C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440209 | ||||||
chr6:151440394
|
G | A | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-3840C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440394 | ||||||
chr6:151440411
|
T | C | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0002g0005others(2): Show | 6 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-3857A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440411 | ||||||
chr6:151440416
|
T | C | 1 | a0003c0003t0001g0313 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-3862A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440416 | ||||||
chr6:151440486
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(133): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.505-3932T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440486 | ||||||
chr6:151440548
|
T | C | 1 | a0002c0002t0002g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.505-3994A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440548 | ||||||
chr6:151440728
|
T | C | 1 | a0001c0001t0002g0268 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.505-4174A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440728 | ||||||
chr6:151440837
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.505-4283A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440837 | ||||||
chr6:151440953
|
T | C | 3 | a0002c0002t0001g0098a0002c0002t0001g0112a0002c0002t0002g0113 | 3 | HG02258.hp2 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.504+4355A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151440953 | ||||||
chr6:151441034
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+4274A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441034 | ||||||
chr6:151441155
|
G | C | 1 | a0001c0001t0003g0340 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.504+4153C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441155 | ||||||
chr6:151441157
|
T | C | 1 | a0002c0002t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+4151A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441157 | ||||||
chr6:151441170
|
A | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+4138T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441170 | ||||||
chr6:151441202
|
A | T | 26 | a0001c0004t0001g0185a0001c0004t0001g0186a0001c0004t0001g0187others(23): Show | 26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.504+4106T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441202 | ||||||
chr6:151441209
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(87): Show | 102 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(99): Show |
intron_variant | MODIFIER | c.504+4099T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441209 | ||||||
chr6:151441369
|
TG | T | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+3938delC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441369 | ||||||
chr6:151441419
|
C | T | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.504+3889G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441419 | ||||||
chr6:151441474
|
A | G | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.504+3834T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441474 | ||||||
chr6:151441475
|
G | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(41): Show | 53 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.504+3833C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441475 | ||||||
chr6:151441727
|
A | G | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.504+3581T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441727 | ||||||
chr6:151441740
|
A | C | 24 | a0001c0004t0001g0185a0001c0004t0001g0186a0001c0004t0001g0187others(21): Show | 24 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.504+3568T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441740 | ||||||
chr6:151441806
|
T | C | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.504+3502A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151441806 | ||||||
chr6:151442055
|
G | A | 3 | a0002c0002t0001g0083a0002c0002t0001g0114a0002c0002t0001g0128 | 3 | HG02080.hp2 HG02129.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.504+3253C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442055 | ||||||
chr6:151442091
|
C | T | 3 | a0001c0001t0001g0309a0001c0001t0002g0308a0001c0001t0002g0321 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+3217G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442091 | ||||||
chr6:151442148
|
A | G | 30 | a0001c0001t0001g0309a0001c0001t0002g0308a0001c0001t0002g0321others(27): Show | 31 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.504+3160T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442148 | ||||||
chr6:151442265
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+3043T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442265 | ||||||
chr6:151442285
|
C | CAAT | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(88): Show | 103 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.504+3020_504+3022d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442285 | ||||||
chr6:151442353
|
A | G | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2955T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442353 | ||||||
chr6:151442462
|
A | T | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.504+2846T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442462 | ||||||
chr6:151442528
|
T | C | 2 | a0001c0001t0002g0206a0001c0001t0002g0212 | 2 | NA18978.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.504+2780A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442528 | ||||||
chr6:151442586
|
G | A | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.504+2722C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442586 | ||||||
chr6:151442598
|
C | T | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2710G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442598 | ||||||
chr6:151442677
|
G | A | 6 | a0004c0006t0001g0258a0004c0006t0001g0259a0004c0006t0001g0260others(3): Show | 6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+2631C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442677 | ||||||
chr6:151442693
|
C | CT | 93 | a0001c0001t0002g0150a0001c0001t0002g0196a0001c0001t0002g0197others(90): Show | 93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.504+2614dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442693 | ||||||
chr6:151442693
|
CT | C | 51 | a0001c0001t0003g0018a0001c0001t0003g0325a0001c0001t0003g0327others(48): Show | 52 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.504+2614delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442693 | ||||||
chr6:151442711
|
TC | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(75): Show | 90 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(87): Show |
intron_variant | MODIFIER | c.504+2596delG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442711 | ||||||
chr6:151442712
|
C | T | 7 | a0001c0001t0001g0164a0001c0001t0001g0176a0001c0001t0001g0256others(4): Show | 7 | HG01884.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+2596G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442712 | ||||||
chr6:151442763
|
C | A | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2545G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442763 | ||||||
chr6:151442904
|
A | G | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+2404T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442904 | ||||||
chr6:151442945
|
T | C | 1 | a0001c0001t0002g0300 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.504+2363A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151442945 | ||||||
chr6:151443104
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(61): Show | 75 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.504+2204A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443104 | ||||||
chr6:151443115
|
A | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0195others(52): Show | 58 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.504+2193T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443115 | ||||||
chr6:151443129
|
G | A | 3 | a0001c0001t0001g0309a0001c0001t0002g0308a0001c0001t0002g0321 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+2179C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443129 | ||||||
chr6:151443404
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(61): Show | 75 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.504+1904G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443404 | ||||||
chr6:151443465
|
C | G | 1 | a0003c0003t0004g0025 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.504+1843G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443465 | ||||||
chr6:151443472
|
T | G | 1 | a0001c0004t0002g0189 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.504+1836A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443472 | ||||||
chr6:151443513
|
A | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(88): Show | 103 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.504+1795T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443513 | ||||||
chr6:151443530
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+1778G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443530 | ||||||
chr6:151443553
|
G | A | 3 | a0003c0003t0004g0019a0003c0003t0004g0040a0003c0014t0001g0323 | 3 | HG01884.hp2 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.504+1755C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443553 | ||||||
chr6:151443585
|
C | T | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.504+1723G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443585 | ||||||
chr6:151443588
|
C | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(88): Show | 103 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.504+1720G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443588 | ||||||
chr6:151443615
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.504+1693A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443615 | ||||||
chr6:151443634
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.504+1674G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443634 | ||||||
chr6:151443636
|
T | C | 6 | a0004c0006t0001g0258a0004c0006t0001g0259a0004c0006t0001g0260others(3): Show | 6 | HG02258.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+1672A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443636 | ||||||
chr6:151443659
|
C | T | 1 | a0002c0002t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+1649G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443659 | ||||||
chr6:151443721
|
T | C | 2 | a0002c0002t0002g0043a0002c0002t0002g0049 | 2 | HG02040.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.504+1587A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443721 | ||||||
chr6:151443741
|
C | T | 3 | a0001c0001t0001g0309a0001c0001t0002g0308a0001c0001t0002g0321 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+1567G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443741 | ||||||
chr6:151443820
|
C | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(61): Show | 75 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.504+1488G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151443820 | ||||||
chr6:151444161
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(88): Show | 103 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.504+1147A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444161 | ||||||
chr6:151444198
|
A | G | 1 | a0006c0013t0001g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.504+1110T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444198 | ||||||
chr6:151444221
|
G | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(88): Show | 103 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.504+1087C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444221 | ||||||
chr6:151444285
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.504+1023C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444285 | ||||||
chr6:151444333
|
A | G | 6 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0141others(3): Show | 7 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+975T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444333 | ||||||
chr6:151444376
|
G | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(41): Show | 53 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.504+932C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444376 | ||||||
chr6:151444599
|
C | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0002g0005others(2): Show | 6 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+709G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444599 | ||||||
chr6:151444650
|
T | TGCCTCTT others(19): Show |
27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.504+657_504+658ins others(26): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444650 | ||||||
chr6:151444656
|
C | T | 1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.504+652G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444656 | ||||||
chr6:151444820
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.504+488C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444820 | ||||||
chr6:151444951
|
C | T | 1 | a0002c0002t0001g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.504+357G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444951 | ||||||
chr6:151444954
|
G | T | 1 | a0002c0002t0001g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.504+354C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444954 | ||||||
chr6:151444955
|
A | T | 1 | a0002c0002t0001g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.504+353T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444955 | ||||||
chr6:151444978
|
TTTTTA | T | 6 | a0001c0001t0003g0324a0001c0001t0003g0341a0001c0001t0003g0346others(3): Show | 6 | HG00438.hp1 NA18993.hp2 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+325_504+329del others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151444978 | ||||||
chr6:151445027
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(178): Show | 193 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.504+281A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151445027 | ||||||
chr6:151445064
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+244T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151445064 | ||||||
chr6:151445262
|
G | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.504+46C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 2/11 | chr6 | 151445262 | ||||||
chr6:151446122
|
G | A | 1 | a0001c0004t0001g0190 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-14-297C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446122 | ||||||
chr6:151446209
|
G | C | 3 | a0001c0004t0001g0251a0001c0004t0001g0252a0001c0004t0001g0253 | 3 | HG02055.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-14-384C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446209 | ||||||
chr6:151446231
|
G | A | 1 | a0003c0014t0001g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-14-406C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446231 | ||||||
chr6:151446348
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(73): Show | 87 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.-14-523T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446348 | ||||||
chr6:151446422
|
G | GA | 11 | a0001c0001t0001g0213a0001c0001t0002g0181a0001c0001t0002g0212others(8): Show | 11 | HG01175.hp2 HG01261.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-598dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446422 | ||||||
chr6:151446422
|
GA | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(47): Show | 59 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.-14-598delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446422 | ||||||
chr6:151446535
|
C | T | 3 | a0003c0003t0004g0034a0003c0003t0005g0024a0003c0003t0005g0033 | 3 | HG02040.hp2 NA18941.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-14-710G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446535 | ||||||
chr6:151446772
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(250): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-14-947T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446772 | ||||||
chr6:151446900
|
CA | C | 152 | a0001c0001t0001g0309a0001c0001t0002g0183a0001c0001t0002g0261others(149): Show | 154 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-14-1076delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446900 | ||||||
chr6:151446923
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-14-1098C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151446923 | ||||||
chr6:151447000
|
A | T | 7 | a0002c0002t0001g0042a0002c0002t0001g0080a0002c0002t0001g0096others(4): Show | 7 | HG00408.hp1 NA18943.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1175T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447000 | ||||||
chr6:151447173
|
G | A | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-14-1348C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447173 | ||||||
chr6:151447216
|
C | T | 2 | a0001c0001t0003g0347a0001c0001t0003g0360 | 2 | HG00438.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-14-1391G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447216 | ||||||
chr6:151447240
|
T | C | 5 | a0004c0006t0001g0258a0004c0006t0001g0259a0004c0006t0001g0260others(2): Show | 5 | HG03041.hp1 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1415A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447240 | ||||||
chr6:151447327
|
ACAAATTT others(1): Show |
A | 93 | a0001c0001t0001g0309a0001c0001t0002g0308a0001c0001t0002g0321others(90): Show | 93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-1510_-14-1503d others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447327 | ||||||
chr6:151447336
|
T | G | 93 | a0001c0001t0001g0309a0001c0001t0002g0308a0001c0001t0002g0321others(90): Show | 93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-1511A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447336 | ||||||
chr6:151447360
|
A | G | 90 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0055others(87): Show | 90 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-1535T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447360 | ||||||
chr6:151447397
|
T | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(178): Show | 193 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-14-1572A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447397 | ||||||
chr6:151447483
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0215 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-14-1658C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447483 | ||||||
chr6:151447558
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-14-1733C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447558 | ||||||
chr6:151447565
|
C | T | 26 | a0001c0004t0001g0185a0001c0004t0001g0186a0001c0004t0001g0187others(23): Show | 26 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-14-1740G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447565 | ||||||
chr6:151447764
|
AGTTT | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(172): Show | 187 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-14-1943_-14-1940d others(6): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447764 | ||||||
chr6:151447800
|
T | A | 13 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(10): Show | 15 | HG01081.hp2 HG02615.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-1975A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447800 | ||||||
chr6:151447810
|
C | CT | 6 | a0001c0001t0002g0093a0001c0001t0002g0192a0001c0001t0002g0193others(3): Show | 6 | HG01993.hp1 HG02572.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-1986dupA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | ||||||
chr6:151447810
|
CT | C | 72 | a0001c0001t0001g0177a0001c0001t0001g0235a0001c0001t0002g0058others(69): Show | 73 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-14-1986delA | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | ||||||
chr6:151447810
|
CTT | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(80): Show | 94 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.-14-1987_-14-1986d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | ||||||
chr6:151447810
|
CTTT | C | 92 | a0001c0001t0002g0261a0001c0001t0002g0321a0001c0005t0001g0013others(89): Show | 93 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-1988_-14-1986d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447810 | ||||||
chr6:151447836
|
G | A | 1 | a0003c0014t0001g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-14-2011C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447836 | ||||||
chr6:151447916
|
C | T | 1 | a0003c0003t0004g0041 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-14-2091G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447916 | ||||||
chr6:151447997
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(73): Show | 87 | HG00099.hp1 HG00140.hp1 HG01069.hp2 others(84): Show |
intron_variant | MODIFIER | c.-14-2172C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151447997 | ||||||
chr6:151448028
|
C | A | 1 | a0001c0001t0002g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-14-2203G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448028 | ||||||
chr6:151448085
|
G | A | 1 | a0004c0006t0002g0307 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-2260C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448085 | ||||||
chr6:151448164
|
T | G | 1 | a0003c0003t0004g0039 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-14-2339A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448164 | ||||||
chr6:151448258
|
A | T | 3 | a0001c0001t0001g0309a0001c0001t0002g0308a0001c0001t0002g0321 | 3 | HG02886.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-14-2433T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448258 | ||||||
chr6:151448403
|
TC | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(221): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-14-2579delG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448403 | ||||||
chr6:151448652
|
A | C | 2 | a0001c0004t0001g0185a0001c0004t0001g0186 | 2 | HG01175.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-14-2827T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448652 | ||||||
chr6:151448718
|
C | T | 3 | a0002c0002t0001g0062a0002c0002t0001g0137a0002c0002t0002g0131 | 3 | HG02683.hp1 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-14-2893G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448718 | ||||||
chr6:151448878
|
A | G | 124 | a0001c0001t0002g0261a0001c0001t0002g0321a0001c0005t0001g0013others(121): Show | 126 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.-14-3053T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448878 | ||||||
chr6:151448941
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0002g0308 | 2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+3075C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448941 | ||||||
chr6:151448980
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-15+3036C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151448980 | ||||||
chr6:151449001
|
T | C | 23 | a0003c0003t0004g0003a0003c0003t0004g0019a0003c0003t0004g0021others(20): Show | 24 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-15+3015A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449001 | ||||||
chr6:151449060
|
C | CA | 75 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0222others(72): Show | 77 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-15+2955dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAA | 83 | a0001c0001t0001g0230a0001c0001t0001g0235a0001c0001t0001g0266others(80): Show | 83 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.-15+2954_-15+2955d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAAA | 36 | a0001c0001t0001g0309a0001c0001t0002g0308a0002c0002t0001g0074others(33): Show | 37 | HG01069.hp2 HG01071.hp1 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+2953_-15+2955d others(5): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0001g0151others(3): Show | 7 | HG01081.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+2948_-15+2955d others(10): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(7): Show | 13 | HG02280.hp2 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+2947_-15+2955d others(11): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG03098.hp2 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-15+2946_-15+2955d others(12): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-15+2945_-15+2955d others(13): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAAAAAAA others(6): Show |
1 | a0001c0004t0007g0369 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+2943_-15+2955d others(15): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
C | CAAAAAAA others(7): Show |
1 | a0001c0004t0007g0370 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-15+2942_-15+2955d others(16): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
CA | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0001g0144others(10): Show | 14 | HG01255.hp1 HG02155.hp1 HG03239.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+2955delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449060
|
CAA | C | 18 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(15): Show | 23 | HG00099.hp1 HG01074.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15+2954_-15+2955d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449060 | ||||||
chr6:151449097
|
G | A | 1 | a0001c0005t0001g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15+2919C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449097 | ||||||
chr6:151449164
|
C | T | 27 | a0003c0003t0001g0312a0003c0003t0001g0313a0003c0003t0004g0003others(24): Show | 28 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-15+2852G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449164 | ||||||
chr6:151449294
|
G | A | 1 | a0001c0001t0002g0321 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+2722C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449294 | ||||||
chr6:151449368
|
C | T | 211 | a0001c0001t0001g0094a0001c0001t0001g0309a0001c0001t0002g0058others(208): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-15+2648G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449368 | ||||||
chr6:151449369
|
G | GA | 49 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(46): Show | 59 | HG00099.hp1 HG00438.hp1 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.-15+2646dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449369 | ||||||
chr6:151449369
|
G | GAA | 6 | a0001c0001t0001g0148a0001c0001t0001g0180a0001c0001t0001g0256others(3): Show | 6 | HG02723.hp2 NA18979.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+2645_-15+2646d others(4): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449369 | ||||||
chr6:151449369
|
GA | G | 33 | a0001c0001t0002g0261a0001c0001t0003g0335a0001c0005t0001g0013others(30): Show | 35 | HG00140.hp1 HG00621.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15+2646delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449369 | ||||||
chr6:151449372
|
A | C | 5 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(2): Show | 6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+2644T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449372 | ||||||
chr6:151449637
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0238 | 2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-15+2379G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449637 | ||||||
chr6:151449656
|
T | TC | 9 | a0001c0001t0003g0335a0001c0001t0003g0336a0001c0001t0003g0366others(6): Show | 9 | HG00609.hp1 HG01261.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+2359dupG | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449656 | ||||||
chr6:151449660
|
CA | C | 3 | a0001c0001t0001g0309a0001c0001t0002g0308a0003c0003t0011g0265 | 3 | HG02486.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-15+2355delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449660 | ||||||
chr6:151449661
|
A | C | 184 | a0001c0001t0001g0094a0001c0001t0002g0058a0001c0001t0002g0075others(181): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-15+2355T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449661 | ||||||
chr6:151449662
|
C | CG | 20 | a0001c0001t0002g0078a0001c0001t0002g0261a0001c0001t0003g0328others(17): Show | 20 | HG00408.hp1 HG00621.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15+2353dupC | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449662 | ||||||
chr6:151449663
|
G | C | 4 | a0001c0001t0001g0309a0001c0001t0002g0308a0002c0002t0002g0052others(1): Show | 4 | HG02486.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+2353C>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449663 | ||||||
chr6:151449667
|
CCCCTCTC others(10): Show |
C | 1 | a0003c0003t0004g0039 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-15+2332_-15+2348d others(19): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449667 | ||||||
chr6:151449679
|
C | G | 11 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(8): Show | 12 | HG02109.hp2 HG02258.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+2337G>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449679 | ||||||
chr6:151449840
|
G | T | 1 | a0002c0002t0001g0077 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-15+2176C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449840 | ||||||
chr6:151449981
|
C | T | 11 | a0001c0001t0003g0327a0001c0001t0003g0328a0001c0001t0003g0329others(8): Show | 11 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+2035G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151449981 | ||||||
chr6:151450018
|
G | A | 82 | a0001c0001t0001g0094a0001c0001t0002g0058a0001c0001t0002g0078others(79): Show | 82 | HG00408.hp1 HG00609.hp2 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.-15+1998C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450018 | ||||||
chr6:151450043
|
G | A | 11 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(8): Show | 12 | HG02109.hp2 HG02258.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+1973C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450043 | ||||||
chr6:151450052
|
GCCTCTGC others(32): Show |
G | 1 | a0001c0001t0002g0267 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-15+1925_-15+1963d others(41): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450052 | ||||||
chr6:151450072
|
C | A | 1 | a0001c0001t0002g0321 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+1944G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450072 | ||||||
chr6:151450134
|
GCCCGGCC others(33): Show |
G | 101 | a0001c0001t0001g0094a0001c0001t0002g0058a0001c0001t0002g0075others(98): Show | 101 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-15+1842_-15+1881d others(42): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450134 | ||||||
chr6:151450141
|
C | T | 1 | a0004c0006t0002g0307 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-15+1875G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450141 | ||||||
chr6:151450168
|
A | G | 113 | a0001c0001t0001g0309a0001c0001t0002g0261a0001c0001t0002g0308others(110): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-15+1848T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450168 | ||||||
chr6:151450291
|
C | T | 12 | a0001c0004t0001g0185a0001c0004t0001g0186a0001c0004t0001g0187others(9): Show | 12 | HG01175.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+1725G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450291 | ||||||
chr6:151450322
|
C | CGGTCT | 29 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(26): Show | 31 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-15+1693_-15+1694i others(7): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450322 | ||||||
chr6:151450357
|
T | G | 7 | a0001c0001t0001g0306a0001c0001t0002g0012a0001c0001t0002g0150others(4): Show | 8 | HG01884.hp2 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+1659A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450357 | ||||||
chr6:151450359
|
GGGGTCAG others(37): Show |
G | 5 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(2): Show | 6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1613_-15+1656d others(46): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450359 | ||||||
chr6:151450361
|
GGTCAGCC others(118): Show |
G | 1 | a0001c0001t0003g0337 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-15+1530_-15+1654d others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450361 | ||||||
chr6:151450407
|
GGTCAGCC others(72): Show |
G | 44 | a0001c0001t0003g0018a0001c0001t0003g0324a0001c0001t0003g0325others(41): Show | 45 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-15+1530_-15+1608d others(81): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450407 | ||||||
chr6:151450408
|
GTCAGCCC others(71): Show |
G | 2 | a0001c0004t0007g0369a0001c0004t0007g0370 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15+1530_-15+1607d others(80): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450408 | ||||||
chr6:151450422
|
CGGCCAGC others(26): Show |
C | 8 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(5): Show | 9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+1561_-15+1593d others(35): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450422 | ||||||
chr6:151450431
|
A | G | 1 | a0003c0003t0001g0312 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+1585T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450431 | ||||||
chr6:151450436
|
G | A | 1 | a0001c0001t0003g0345 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1580C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450436 | ||||||
chr6:151450439
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(205): Show | 219 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-15+1577A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450439 | ||||||
chr6:151450442
|
G | A | 1 | a0003c0014t0001g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-15+1574C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450442 | ||||||
chr6:151450455
|
G | GGGGTCAG others(10): Show |
2 | a0002c0002t0001g0130a0002c0002t0002g0053 | 2 | HG03831.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-15+1560_-15+1561i others(19): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | ||||||
chr6:151450455
|
G | GGGTCAGC others(9): Show |
190 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(187): Show | 201 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-15+1560_-15+1561i others(18): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | ||||||
chr6:151450455
|
G | GGGTTAGC others(9): Show |
11 | a0001c0004t0001g0185a0001c0004t0001g0186a0001c0004t0001g0187others(8): Show | 11 | HG01175.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+1560_-15+1561i others(18): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | ||||||
chr6:151450455
|
G | GTCAGCCC others(52): Show |
1 | a0001c0001t0003g0345 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1560_-15+1561i others(61): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450455 | ||||||
chr6:151450456
|
GGCCAGCC others(23): Show |
G | 3 | a0001c0004t0010g0184a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG01884.hp1 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1530_-15+1559d others(32): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450456 | ||||||
chr6:151450458
|
C | T | 1 | a0002c0002t0002g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+1558G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450458 | ||||||
chr6:151450461
|
G | GCCCCCCG others(10): Show |
1 | a0002c0002t0002g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+1554_-15+1555i others(19): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450461 | ||||||
chr6:151450467
|
G | A | 1 | a0001c0001t0003g0345 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1549C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450467 | ||||||
chr6:151450477
|
A | G | 1 | a0001c0001t0003g0345 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15+1539T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450477 | ||||||
chr6:151450489
|
C | T | 1 | a0001c0004t0010g0184 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-15+1527G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450489 | ||||||
chr6:151450509
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-15+1507G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450509 | ||||||
chr6:151450518
|
C | T | 1 | a0001c0001t0003g0337 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-15+1498G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450518 | ||||||
chr6:151450525
|
G | A | 3 | a0001c0004t0010g0184a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG01884.hp1 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1491C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450525 | ||||||
chr6:151450529
|
TGGGGGGT others(42): Show |
T | 1 | a0001c0001t0002g0011 | 2 | NA18971.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-15+1438_-15+1486d others(51): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450529 | ||||||
chr6:151450534
|
G | T | 3 | a0001c0004t0010g0184a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG01884.hp1 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1482C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450534 | ||||||
chr6:151450546
|
G | A | 1 | a0002c0002t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-15+1470C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450546 | ||||||
chr6:151450564
|
TCCGGGAG others(25): Show |
T | 2 | a0001c0004t0007g0369a0001c0004t0007g0370 | 2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15+1420_-15+1451d others(34): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450564 | ||||||
chr6:151450629
|
C | T | 2 | a0003c0003t0004g0021a0003c0003t0004g0022 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1387G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450629 | ||||||
chr6:151450639
|
C | T | 32 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(29): Show | 34 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-15+1377G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450639 | ||||||
chr6:151450657
|
T | A | 2 | a0003c0003t0004g0021a0003c0003t0004g0022 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1359A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450657 | ||||||
chr6:151450658
|
G | T | 5 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0002g0005others(2): Show | 6 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1358C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450658 | ||||||
chr6:151450676
|
C | T | 2 | a0003c0003t0004g0021a0003c0003t0004g0022 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1340G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450676 | ||||||
chr6:151450702
|
A | G | 3 | a0001c0001t0013g0343a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1314T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450702 | ||||||
chr6:151450704
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(260): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-15+1312A>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450704 | ||||||
chr6:151450726
|
A | C | 3 | a0001c0001t0013g0343a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1290T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450726 | ||||||
chr6:151450728
|
G | A | 3 | a0001c0001t0013g0343a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1288C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450728 | ||||||
chr6:151450729
|
G | T | 3 | a0001c0001t0013g0343a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1287C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450729 | ||||||
chr6:151450750
|
G | A | 3 | a0001c0001t0013g0343a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1266C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450750 | ||||||
chr6:151450751
|
T | G | 3 | a0001c0001t0013g0343a0003c0003t0004g0021a0003c0003t0004g0022 | 3 | HG00408.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-15+1265A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450751 | ||||||
chr6:151450755
|
AGAAAGGG others(2): Show |
A | 29 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(26): Show | 35 | HG00099.hp1 HG01074.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15+1252_-15+1260d others(11): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450755 | ||||||
chr6:151450771
|
G | T | 116 | a0001c0001t0001g0094a0001c0001t0002g0058a0001c0001t0002g0075others(113): Show | 116 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.-15+1245C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450771 | ||||||
chr6:151450778
|
A | G | 116 | a0001c0001t0001g0094a0001c0001t0002g0058a0001c0001t0002g0075others(113): Show | 116 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-15+1238T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450778 | ||||||
chr6:151450804
|
T | G | 1 | a0001c0001t0002g0311 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-15+1212A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450804 | ||||||
chr6:151450809
|
G | T | 20 | a0003c0003t0004g0003a0003c0003t0004g0021a0003c0003t0004g0022others(17): Show | 21 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-15+1207C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450809 | ||||||
chr6:151450908
|
C | T | 5 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(2): Show | 6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1108G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450908 | ||||||
chr6:151450927
|
T | G | 5 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(2): Show | 5 | HG01975.hp2 HG01993.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+1089A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450927 | ||||||
chr6:151450984
|
A | G | 32 | a0001c0001t0002g0261a0001c0005t0001g0013a0001c0005t0001g0262others(29): Show | 34 | HG00140.hp1 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-15+1032T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151450984 | ||||||
chr6:151451004
|
C | T | 1 | a0003c0003t0004g0003 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-15+1012G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451004 | ||||||
chr6:151451043
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-15+973A>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451043 | ||||||
chr6:151451110
|
G | T | 1 | a0001c0001t0002g0182 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-15+906C>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451110 | ||||||
chr6:151451150
|
A | G | 3 | a0004c0006t0001g0258a0004c0006t0001g0259a0004c0006t0001g0260 | 3 | HG03041.hp1 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-15+866T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451150 | ||||||
chr6:151451198
|
T | TA | 95 | a0001c0001t0001g0094a0001c0001t0002g0075a0001c0001t0002g0076others(92): Show | 95 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-15+817dupT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | ||||||
chr6:151451198
|
T | TAA | 19 | a0001c0001t0003g0328a0001c0001t0003g0329a0001c0001t0003g0330others(16): Show | 19 | HG00099.hp2 HG00438.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15+816_-15+817dup others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | ||||||
chr6:151451198
|
T | TAAA | 29 | a0001c0001t0003g0018a0001c0001t0003g0345a0001c0001t0003g0346others(26): Show | 30 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+815_-15+817dup others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | ||||||
chr6:151451198
|
TA | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0195a0001c0001t0001g0210others(84): Show | 91 | HG00423.hp2 HG00621.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.-15+817delT | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | ||||||
chr6:151451198
|
TAA | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(41): Show | 53 | HG00099.hp1 HG01081.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.-15+816_-15+817del others(2): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | ||||||
chr6:151451198
|
TAAA | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG01074.hp1 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+815_-15+817del others(3): Show |
RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451198 | ||||||
chr6:151451199
|
A | T | 1 | a0003c0003t0004g0003 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-15+817T>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451199 | ||||||
chr6:151451212
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | NA18987.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-15+804T>G | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451212 | ||||||
chr6:151451220
|
C | A | 2 | a0001c0001t0002g0316a0001c0001t0002g0317 | 2 | NA18963.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-15+796G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451220 | ||||||
chr6:151451222
|
C | A | 2 | a0001c0001t0002g0316a0001c0001t0002g0317 | 2 | NA18963.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.-15+794G>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451222 | ||||||
chr6:151451260
|
T | A | 100 | a0001c0001t0001g0094a0001c0001t0002g0058a0001c0001t0002g0075others(97): Show | 100 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.-15+756A>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451260 | ||||||
chr6:151451373
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15+643T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451373 | ||||||
chr6:151451434
|
A | G | 100 | a0001c0001t0001g0094a0001c0001t0002g0058a0001c0001t0002g0075others(97): Show | 100 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.-15+582T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451434 | ||||||
chr6:151451450
|
A | G | 2 | a0002c0002t0001g0055a0002c0002t0009g0056 | 2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-15+566T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451450 | ||||||
chr6:151451468
|
C | T | 12 | a0002c0002t0001g0048a0002c0002t0002g0043a0002c0002t0002g0044others(9): Show | 12 | HG02040.hp1 NA18954.hp2 NA18979.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+548G>A | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451468 | ||||||
chr6:151451469
|
G | A | 3 | a0001c0004t0001g0318a0001c0004t0001g0319a0001c0004t0001g0320 | 3 | HG01891.hp2 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-15+547C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451469 | ||||||
chr6:151451488
|
G | A | 1 | a0001c0001t0002g0321 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-15+528C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451488 | ||||||
chr6:151451538
|
A | G | 1 | a0002c0002t0001g0042 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-15+478T>C | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451538 | ||||||
chr6:151451620
|
G | A | 1 | a0001c0001t0002g0322 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+396C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451620 | ||||||
chr6:151451977
|
G | A | 1 | a0003c0014t0001g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-15+39C>T | RMND1 | ENSG00000155906.20 | transcript | ENST00000444024.3 | protein_coding | 1/11 | chr6 | 151451977 |