geneid | 64795 |
---|---|
ensemblid | ENSG00000153561.13 |
hgncid | 25850 |
symbol | RMND5A |
name | required for meiotic nuclear division 5 homolog A |
refseq_nuc | NM_022780.4 |
refseq_prot | NP_073617.1 |
ensembl_nuc | ENST00000283632.5 |
ensembl_prot | ENSP00000283632.4 |
mane_status | MANE Select |
chr | chr2 |
start | 86720291 |
end | 86778041 |
strand | + |
ver | v1.2 |
region | chr2:86720291-86778041 |
region5000 | chr2:86715291-86783041 |
regionname0 | RMND5A_chr2_86720291_86778041 |
regionname5000 | RMND5A_chr2_86715291_86783041 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 391 | 304 | 86 | 66 | 100 | 14 | 36 | 82 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1176 | 178 | 51 | 35 | 58 | 9 | 24 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
c0002 | 1/0 | 1176 | 75 | 23 | 20 | 18 | 5 | 8 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
c0003 | 0/0 | 1176 | 34 | 1 | 5 | 24 | 0 | 4 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
c0004 | 0/0 | 1176 | 12 | 10 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
c0005 | 0/0 | 1176 | 5 | 1 | 4 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 5005 | 149 | 21 | 34 | 66 | 7 | 20 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0002 | 1/0 | 5008 | 35 | 2 | 16 | 6 | 3 | 7 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0003 | 0/0 | 5002 | 23 | 11 | 2 | 9 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0004 | 0/0 | 5006 | 20 | 7 | 0 | 12 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0005 | 0/0 | 5005 | 9 | 1 | 2 | 1 | 0 | 5 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0006 | 0/0 | 5004 | 7 | 3 | 3 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0007 | 0/0 | 5009 | 6 | 6 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0008 | 0/0 | 5007 | 4 | 3 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0009 | 0/0 | 5005 | 4 | 4 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0010 | 0/0 | 5005 | 3 | 0 | 3 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0011 | 0/0 | 5004 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0012 | 0/0 | 5005 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0013 | 0/0 | 5008 | 2 | 0 | 1 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0014 | 0/0 | 5003 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0015 | 0/0 | 5006 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0016 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0017 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0018 | 0/0 | 5008 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0019 | 0/0 | 5005 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0020 | 0/0 | 5005 | 2 | 0 | 0 | 0 | 2 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0021 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0022 | 0/0 | 5008 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0023 | 0/0 | 5002 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0024 | 0/0 | 5003 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0025 | 0/0 | 5008 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0026 | 0/0 | 5004 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0027 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0028 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0029 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0030 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0031 | 0/0 | 5005 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0032 | 0/0 | 5008 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0033 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0034 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0035 | 0/0 | 5008 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0036 | 0/0 | 5005 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0037 | 0/0 | 5006 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0038 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0039 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0040 | 0/0 | 5006 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0041 | 0/0 | 5002 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0042 | 0/0 | 5002 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0043 | 0/0 | 5005 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
t0044 | 0/0 | 5005 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
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 | 7 | 2 | 1 | 4 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0004 | 0/0 | 5 | 0 | 0 | 1 | 1 | 3 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1176 | 178 | 51 | 35 | 58 | 9 | 24 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002 | 1/0 | 1176 | 75 | 23 | 20 | 18 | 5 | 8 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0003 | 0/0 | 1176 | 34 | 1 | 5 | 24 | 0 | 4 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004 | 0/0 | 1176 | 12 | 10 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0005 | 0/0 | 1176 | 5 | 1 | 4 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6180 | 116 | 20 | 29 | 43 | 7 | 16 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0004 | 0/0 | 6181 | 20 | 7 | 0 | 12 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0005 | 0/0 | 6180 | 9 | 1 | 2 | 1 | 0 | 5 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0006 | 0/0 | 6179 | 6 | 3 | 2 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0009 | 0/0 | 6180 | 4 | 4 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0012 | 0/0 | 6180 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0015 | 0/0 | 6181 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0016 | 0/0 | 6182 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0017 | 0/0 | 6182 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0019 | 0/0 | 6180 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0020 | 0/0 | 6180 | 2 | 0 | 0 | 0 | 2 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0021 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0026 | 0/0 | 6179 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0028 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0029 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0036 | 0/0 | 6180 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0037 | 0/0 | 6181 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0038 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0039 | 0/0 | 6182 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0040 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0043 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0001t0044 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0001 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0002 | 1/0 | 6183 | 35 | 2 | 16 | 6 | 3 | 7 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0003 | 0/0 | 6177 | 23 | 11 | 2 | 9 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0007 | 0/0 | 6184 | 6 | 6 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0013 | 0/0 | 6183 | 2 | 0 | 1 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0014 | 0/0 | 6178 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0032 | 0/0 | 6183 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0033 | 0/0 | 6182 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0034 | 0/0 | 6182 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0035 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0041 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0002t0042 | 0/0 | 6177 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0003t0001 | 0/0 | 6180 | 32 | 1 | 4 | 23 | 0 | 4 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0003t0006 | 0/0 | 6179 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0003t0031 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0008 | 0/0 | 6182 | 4 | 3 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0018 | 0/0 | 6183 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0022 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0023 | 0/0 | 6177 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0024 | 0/0 | 6178 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0025 | 0/0 | 6183 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0027 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0004t0030 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0005t0010 | 0/0 | 6180 | 3 | 0 | 3 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
a0001c0005t0011 | 0/0 | 6179 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | copy fasta | chr2 | 86715291 | 86783041 |
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 | 6 | 1 | 1 | 4 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0163 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0015g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0016g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0016g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0017g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0019g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0020g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0020g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0021g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0026g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0029g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0036g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0037g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0038g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0039g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0040g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0043g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0001t0044g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0007g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0013g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0014g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0014g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0032g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0033g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0034g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0035g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0041g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0002t0042g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0003t0031g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0018g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0022g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0023g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0024g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0025g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0027g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0004t0030g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0005t0010g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0005t0010g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0005t0011g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
a0001c0005t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00099 | hp2 | a0001 | c0002 | t0042 | g0066 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0227 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00280 | hp2 | a0001 | c0001 | t0020 | g0135 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00323 | hp1 | a0001 | c0001 | t0020 | g0004 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00323 | hp2 | a0001 | c0002 | t0032 | g0233 | EUR | FIN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | CHS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0238 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0129 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0077 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01099 | hp2 | a0001 | c0003 | t0001 | g0035 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01109 | hp2 | a0001 | c0001 | t0019 | g0018 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01167 | hp1 | a0001 | c0004 | t0008 | g0249 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01167 | hp2 | a0001 | c0005 | t0011 | g0008 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01168 | hp1 | a0001 | c0001 | t0043 | g0021 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01168 | hp2 | a0001 | c0002 | t0002 | g0220 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0222 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01169 | hp2 | a0001 | c0005 | t0010 | g0008 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0221 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01358 | hp2 | a0001 | c0004 | t0023 | g0055 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01433 | hp2 | a0001 | c0002 | t0013 | g0106 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0244 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01884 | hp2 | a0001 | c0004 | t0030 | g0054 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01891 | hp1 | a0001 | c0002 | t0007 | g0020 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01891 | hp2 | a0001 | c0001 | t0017 | g0101 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0242 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01943 | hp2 | a0001 | c0003 | t0006 | g0036 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0038 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01993 | hp1 | a0001 | c0001 | t0006 | g0131 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0225 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02055 | hp1 | a0001 | c0002 | t0003 | g0065 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0230 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02145 | hp2 | a0001 | c0005 | t0011 | g0053 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0232 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02148 | hp2 | a0001 | c0005 | t0010 | g0052 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0241 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02273 | hp1 | a0001 | c0005 | t0010 | g0008 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02280 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02280 | hp2 | a0001 | c0001 | t0026 | g0113 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02451 | hp1 | a0001 | c0001 | t0028 | g0204 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02451 | hp2 | a0001 | c0002 | t0007 | g0020 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0071 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02622 | hp1 | a0001 | c0001 | t0015 | g0180 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0072 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02630 | hp2 | a0001 | c0004 | t0018 | g0014 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0120 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02698 | hp1 | a0001 | c0001 | t0036 | g0143 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0146 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02717 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0243 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0193 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02735 | hp2 | a0001 | c0003 | t0001 | g0030 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0074 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02809 | hp2 | a0001 | c0004 | t0008 | g0248 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02818 | hp1 | a0001 | c0001 | t0038 | g0184 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02818 | hp2 | a0001 | c0001 | t0016 | g0100 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02895 | hp2 | a0001 | c0004 | t0008 | g0029 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02897 | hp2 | a0001 | c0004 | t0008 | g0029 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02922 | hp1 | a0001 | c0001 | t0040 | g0098 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0064 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02970 | hp1 | a0001 | c0004 | t0025 | g0060 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02976 | hp1 | a0001 | c0004 | t0027 | g0061 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02976 | hp2 | a0001 | c0001 | t0017 | g0099 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03041 | hp2 | a0001 | c0002 | t0033 | g0250 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0062 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03139 | hp2 | a0001 | c0001 | t0015 | g0115 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03195 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | ESN | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03486 | hp2 | a0001 | c0001 | t0016 | g0097 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0216 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03540 | hp1 | a0001 | c0004 | t0018 | g0014 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03540 | hp2 | a0001 | c0002 | t0007 | g0010 | AFR | GWD | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03579 | hp2 | a0001 | c0002 | t0003 | g0067 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0123 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0031 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0122 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0228 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0050 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0234 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | STU | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18522 | hp1 | a0001 | c0002 | t0035 | g0103 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18522 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18747 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | CHB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0203 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18906 | hp2 | a0001 | c0001 | t0019 | g0018 | AFR | YRI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18940 | hp2 | a0001 | c0001 | t0037 | g0087 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18943 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18944 | hp1 | a0001 | c0003 | t0031 | g0002 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18975 | hp2 | a0001 | c0002 | t0013 | g0107 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18986 | hp1 | a0001 | c0002 | t0014 | g0069 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18987 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19001 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0105 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19030 | hp2 | a0001 | c0002 | t0007 | g0237 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19043 | hp2 | a0001 | c0004 | t0022 | g0247 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19055 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19065 | hp2 | a0001 | c0001 | t0039 | g0147 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19075 | hp1 | a0001 | c0002 | t0014 | g0078 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19082 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA19091 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20129 | hp1 | a0001 | c0002 | t0041 | g0063 | AFR | ASW | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | ASW | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0217 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0236 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | GIH | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | GIH | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02109 | hp1 | a0001 | c0002 | t0034 | g0112 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02109 | hp2 | a0001 | c0001 | t0044 | g0001 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02559 | hp1 | a0001 | c0001 | t0029 | g0202 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0245 | AFR | MSL | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG06807 | hp1 | a0001 | c0001 | t0021 | g0006 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA20300 | hp2 | a0001 | c0004 | t0024 | g0056 | AFR | USA | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
NA21309 | hp2 | a0001 | c0001 | t0009 | g0169 | AFR | LWK | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0224 | REF | REF | RMND5A_chr2_86715291_86783041 | RMND5A | chr2 | 86715291 | 86783041 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:86720724
|
A | G | 2 | a0001c0004a0001c0005 | 17 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
synonymous_variant | LOW | c.57A>G | p.Ser19Ser | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 434/6183 | 57/1176 | 19/391 | chr2 | 86720724 | ||
chr2:86720781
|
C | T | 1 | a0001c0005 | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
synonymous_variant | LOW | c.114C>T | p.Gly38Gly | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 491/6183 | 114/1176 | 38/391 | chr2 | 86720781 | ||
chr2:86741015
|
C | T | 1 | a0001c0003 | 34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
synonymous_variant | LOW | c.231C>T | p.Ser77Ser | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/9 | 608/6183 | 231/1176 | 77/391 | chr2 | 86741015 | ||
chr2:86751970
|
G | A | 3 | a0001c0001a0001c0003a0001c0005 | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
synonymous_variant | LOW | c.360G>A | p.Glu120Glu | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/9 | 737/6183 | 360/1176 | 120/391 | chr2 | 86751970 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:86720309
|
G | A | 2 | a0001c0005t0010a0001c0005t0011 | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-359G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 359 | chr2 | 86720309 | |||||
chr2:86720382
|
C | T | 1 | a0001c0001t0044 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-286C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 286 | chr2 | 86720382 | |||||
chr2:86720421
|
A | G | 2 | a0001c0005t0010a0001c0005t0011 | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-247A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 247 | chr2 | 86720421 | |||||
chr2:86720462
|
G | A | 2 | a0001c0005t0010a0001c0005t0011 | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-206G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 206 | chr2 | 86720462 | |||||
chr2:86720462
|
G | T | 1 | a0001c0001t0020 | 2 | HG00280.hp2 HG00323.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-206G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | chr2 | 86720462 | ||||||
chr2:86720467
|
G | T | 1 | a0001c0001t0043 | 1 | HG01168.hp1 | 5_prime_UTR_variant | MODIFIER | c.-201G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 201 | chr2 | 86720467 | |||||
chr2:86720517
|
C | A | 1 | a0001c0001t0021 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 151 | chr2 | 86720517 | |||||
chr2:86720523
|
G | T | 1 | a0001c0001t0019 | 2 | HG01109.hp2 NA18906.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-145G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | chr2 | 86720523 | ||||||
chr2:86720560
|
C | T | 1 | a0001c0002t0042 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-108C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | chr2 | 86720560 | ||||||
chr2:86720577
|
G | T | 1 | a0001c0004t0018 | 2 | HG02630.hp2 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-91G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 91 | chr2 | 86720577 | |||||
chr2:86720603
|
T | C | 14 | a0001c0001t0012a0001c0001t0026a0001c0001t0028others(11): Show | 22 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-65T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 65 | chr2 | 86720603 | |||||
chr2:86720624
|
G | A | 1 | a0001c0003t0031 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 44 | chr2 | 86720624 | |||||
chr2:86720641
|
G | A | 2 | a0001c0004t0008a0001c0004t0022 | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 27 | chr2 | 86720641 | |||||
chr2:86720660
|
C | T | 40 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(37): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/9 | 8 | chr2 | 86720660 | |||||
chr2:86773715
|
C | T | 1 | a0001c0001t0009 | 4 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*304C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 304 | chr2 | 86773715 | |||||
chr2:86773799
|
T | C | 1 | a0001c0002t0032 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 388 | chr2 | 86773799 | |||||
chr2:86774404
|
A | G | 1 | a0001c0002t0041 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*993A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 993 | chr2 | 86774404 | |||||
chr2:86774418
|
C | T | 1 | a0001c0001t0017 | 2 | HG01891.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1007 | chr2 | 86774418 | |||||
chr2:86774940
|
C | G | 1 | a0001c0004t0030 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1529C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1529 | chr2 | 86774940 | |||||
chr2:86775106
|
C | T | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(26): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1695C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1695 | chr2 | 86775106 | |||||
chr2:86775221
|
A | G | 3 | a0001c0001t0016a0001c0001t0017a0001c0001t0040 | 5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1810A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1810 | chr2 | 86775221 | |||||
chr2:86775316
|
TTTTC | T | 4 | a0001c0001t0006a0001c0001t0026a0001c0003t0006others(1): Show | 10 | HG01070.hp2 HG01167.hp2 HG01943.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1917_*1920delCTTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | INFO_REALIGN_3_PRIME | chr2 | 86775316 | ||||
chr2:86775325
|
TTTC | T | 15 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(12): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1917_*1919delCTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | INFO_REALIGN_3_PRIME | chr2 | 86775325 | ||||
chr2:86775326
|
TTC | T | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0037others(2): Show | 25 | HG00423.hp1 HG02135.hp1 HG02602.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1917_*1918delCT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | INFO_REALIGN_3_PRIME | chr2 | 86775326 | ||||
chr2:86775327
|
TC | T | 3 | a0001c0001t0016a0001c0001t0017a0001c0001t0039 | 5 | HG01891.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1917delC | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | chr2 | 86775327 | |||||
chr2:86775328
|
C | CT | 3 | a0001c0002t0007a0001c0002t0014a0001c0004t0024 | 9 | HG01891.hp1 HG02451.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1938dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1939 | INFO_REALIGN_3_PRIME | chr2 | 86775328 | ||||
chr2:86775328
|
C | T | 2 | a0001c0004t0018a0001c0004t0025 | 3 | HG02630.hp2 HG02970.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1917C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1917 | chr2 | 86775328 | |||||
chr2:86775328
|
CT | C | 3 | a0001c0002t0033a0001c0002t0034a0001c0004t0008 | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1938delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1938 | INFO_REALIGN_3_PRIME | chr2 | 86775328 | ||||
chr2:86775328
|
CTTT | C | 2 | a0001c0001t0005a0001c0001t0043 | 10 | HG01106.hp2 HG01168.hp1 HG01934.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1936_*1938delTTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1936 | INFO_REALIGN_3_PRIME | chr2 | 86775328 | ||||
chr2:86775349
|
T | A | 2 | a0001c0004t0008a0001c0004t0022 | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1938T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 1938 | chr2 | 86775349 | |||||
chr2:86775502
|
C | T | 2 | a0001c0001t0015a0001c0001t0038 | 3 | HG02622.hp1 HG02818.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2091C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2091 | chr2 | 86775502 | |||||
chr2:86775583
|
G | A | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(22): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*2172G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2172 | chr2 | 86775583 | |||||
chr2:86775763
|
G | A | 1 | a0001c0002t0013 | 2 | HG01433.hp2 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2352G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2352 | chr2 | 86775763 | |||||
chr2:86775905
|
C | T | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(22): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*2494C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2494 | chr2 | 86775905 | |||||
chr2:86775995
|
C | T | 1 | a0001c0001t0028 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2584C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2584 | chr2 | 86775995 | |||||
chr2:86776074
|
C | G | 29 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(26): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*2663C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2663 | chr2 | 86776074 | |||||
chr2:86776228
|
C | A | 1 | a0001c0002t0035 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2817C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 2817 | chr2 | 86776228 | |||||
chr2:86776421
|
C | G | 3 | a0001c0004t0023a0001c0004t0024a0001c0004t0030 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3010C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3010 | chr2 | 86776421 | |||||
chr2:86776723
|
C | A | 11 | a0001c0002t0003a0001c0002t0014a0001c0002t0034others(8): Show | 37 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3312C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3312 | chr2 | 86776723 | |||||
chr2:86776819
|
C | T | 1 | a0001c0001t0037 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3408C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3408 | chr2 | 86776819 | |||||
chr2:86776849
|
TTATCTC | T | 7 | a0001c0002t0003a0001c0002t0014a0001c0002t0041others(4): Show | 30 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3440_*3445delATCT others(2): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3440 | INFO_REALIGN_3_PRIME | chr2 | 86776849 | ||||
chr2:86776855
|
C | G | 1 | a0001c0002t0033 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3444C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3444 | chr2 | 86776855 | |||||
chr2:86777361
|
G | A | 1 | a0001c0004t0022 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3950G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 3950 | chr2 | 86777361 | |||||
chr2:86777631
|
T | C | 1 | a0001c0004t0030 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4220T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 4220 | chr2 | 86777631 | |||||
chr2:86777802
|
A | G | 1 | a0001c0001t0036 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4391A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 4391 | chr2 | 86777802 | |||||
chr2:86778003
|
A | G | 1 | a0001c0001t0038 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4592A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 9/9 | 4592 | chr2 | 86778003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:86720827
|
G | C | 27 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(24): Show | 33 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.142+18G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720827 | ||||||
chr2:86720840
|
T | G | 4 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+31T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720840 | ||||||
chr2:86720972
|
T | A | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+163T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720972 | ||||||
chr2:86720972
|
T | C | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0002t0002g0057 | 3 | HG01192.hp2 HG03239.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.142+163T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86720972 | ||||||
chr2:86721041
|
A | G | 30 | a0001c0002t0002g0251a0001c0002t0033g0250a0001c0003t0001g0002others(27): Show | 37 | HG01099.hp2 HG01109.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.142+232A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721041 | ||||||
chr2:86721045
|
G | T | 4 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(1): Show | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+236G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721045 | ||||||
chr2:86721109
|
G | A | 4 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(1): Show | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+300G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721109 | ||||||
chr2:86721143
|
T | C | 4 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+334T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721143 | ||||||
chr2:86721163
|
C | T | 4 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+354C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721163 | ||||||
chr2:86721191
|
T | C | 39 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(36): Show | 45 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.142+382T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721191 | ||||||
chr2:86721281
|
C | A | 7 | a0001c0004t0018g0014a0001c0004t0025g0060a0001c0004t0027g0061others(4): Show | 9 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+472C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721281 | ||||||
chr2:86721355
|
G | T | 29 | a0001c0001t0001g0246a0001c0003t0001g0002a0001c0003t0001g0011others(26): Show | 35 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.142+546G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721355 | ||||||
chr2:86721408
|
C | T | 6 | a0001c0001t0001g0239a0001c0001t0005g0240a0001c0001t0005g0242others(3): Show | 6 | HG01884.hp1 HG01934.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+599C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721408 | ||||||
chr2:86721477
|
C | T | 4 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+668C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721477 | ||||||
chr2:86721521
|
T | G | 4 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+712T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721521 | ||||||
chr2:86721566
|
C | A | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+757C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721566 | ||||||
chr2:86721593
|
G | A | 3 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008 | 4 | HG01167.hp2 HG01169.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+784G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721593 | ||||||
chr2:86721594
|
T | C | 10 | a0001c0001t0004g0009a0001c0001t0004g0084a0001c0001t0004g0085others(7): Show | 13 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+785T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721594 | ||||||
chr2:86721609
|
G | A | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+800G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721609 | ||||||
chr2:86721609
|
G | GT | 37 | a0001c0002t0002g0236a0001c0002t0002g0238a0001c0002t0002g0251others(34): Show | 44 | HG00639.hp2 HG01099.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.142+811dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86721609 | |||||
chr2:86721672
|
C | G | 4 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+863C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721672 | ||||||
chr2:86721688
|
G | C | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+879G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721688 | ||||||
chr2:86721699
|
T | C | 4 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(1): Show | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+890T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721699 | ||||||
chr2:86721712
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.142+903G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721712 | ||||||
chr2:86721722
|
T | C | 2 | a0001c0001t0004g0084a0001c0001t0004g0085 | 2 | NA18999.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.142+913T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721722 | ||||||
chr2:86721726
|
A | G | 3 | a0001c0005t0010g0008a0001c0005t0010g0052a0001c0005t0011g0008 | 4 | HG01167.hp2 HG01169.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+917A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721726 | ||||||
chr2:86721751
|
G | A | 23 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(20): Show | 28 | HG00642.hp1 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.142+942G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721751 | ||||||
chr2:86721946
|
A | G | 1 | a0001c0004t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+1137A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86721946 | ||||||
chr2:86722021
|
A | G | 7 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(4): Show | 9 | HG01167.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1212A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722021 | ||||||
chr2:86722063
|
T | C | 1 | a0001c0002t0035g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142+1254T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722063 | ||||||
chr2:86722149
|
A | G | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+1340A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722149 | ||||||
chr2:86722514
|
C | T | 1 | a0001c0003t0001g0013 | 2 | NA18983.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.142+1705C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722514 | ||||||
chr2:86722594
|
A | C | 32 | a0001c0001t0001g0027a0001c0001t0001g0211a0001c0002t0001g0083others(29): Show | 37 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.142+1785A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722594 | ||||||
chr2:86722763
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+1954C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722763 | ||||||
chr2:86722809
|
A | T | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+2000A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86722809 | ||||||
chr2:86722959
|
CCA | C | 4 | a0001c0003t0001g0013a0001c0003t0001g0049a0001c0003t0001g0050others(1): Show | 5 | HG03942.hp1 NA18950.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+2155_142+2156d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86722959 | |||||
chr2:86723015
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.142+2206C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723015 | ||||||
chr2:86723148
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.142+2339A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723148 | ||||||
chr2:86723159
|
G | A | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+2350G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723159 | ||||||
chr2:86723218
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.142+2409A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723218 | ||||||
chr2:86723324
|
A | AT | 4 | a0001c0002t0002g0028a0001c0002t0002g0234a0001c0002t0002g0235others(1): Show | 5 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+2516dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86723324 | |||||
chr2:86723491
|
C | T | 1 | a0001c0002t0034g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+2682C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723491 | ||||||
chr2:86723560
|
G | C | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+2751G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723560 | ||||||
chr2:86723721
|
G | A | 1 | a0001c0002t0035g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142+2912G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723721 | ||||||
chr2:86723758
|
G | A | 2 | a0001c0003t0001g0033a0001c0003t0001g0049 | 2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.142+2949G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723758 | ||||||
chr2:86723776
|
C | T | 1 | a0001c0001t0006g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.142+2967C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723776 | ||||||
chr2:86723830
|
C | T | 5 | a0001c0001t0016g0097a0001c0001t0016g0100a0001c0001t0017g0099others(2): Show | 5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+3021C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723830 | ||||||
chr2:86723960
|
C | G | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142+3151C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86723960 | ||||||
chr2:86724064
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(11): Show | 18 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.142+3255G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724064 | ||||||
chr2:86724249
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.142+3440C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724249 | ||||||
chr2:86724352
|
G | T | 10 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(7): Show | 12 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.142+3543G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724352 | ||||||
chr2:86724369
|
G | T | 1 | a0001c0001t0001g0019 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.142+3560G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724369 | ||||||
chr2:86724552
|
C | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.142+3743C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724552 | ||||||
chr2:86724555
|
C | G | 1 | a0001c0002t0001g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.142+3746C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724555 | ||||||
chr2:86724680
|
G | T | 1 | a0001c0002t0002g0235 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.142+3871G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86724680 | ||||||
chr2:86725012
|
A | C | 28 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(25): Show | 34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.142+4203A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725012 | ||||||
chr2:86725499
|
T | G | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+4690T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725499 | ||||||
chr2:86725547
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 222 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.142+4738T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725547 | ||||||
chr2:86725636
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.142+4827G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725636 | ||||||
chr2:86725637
|
C | T | 1 | a0001c0003t0001g0048 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.142+4828C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725637 | ||||||
chr2:86725643
|
G | A | 2 | a0001c0001t0004g0114a0001c0002t0034g0112 | 2 | HG02109.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.142+4834G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725643 | ||||||
chr2:86725648
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.142+4839T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725648 | ||||||
chr2:86725651
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+4842A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725651 | ||||||
chr2:86725683
|
G | A | 1 | a0001c0004t0008g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.142+4874G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725683 | ||||||
chr2:86725708
|
A | G | 1 | a0001c0002t0003g0082 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.142+4899A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725708 | ||||||
chr2:86725733
|
T | C | 5 | a0001c0001t0016g0097a0001c0001t0016g0100a0001c0001t0017g0099others(2): Show | 5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+4924T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725733 | ||||||
chr2:86725761
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+4952A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725761 | ||||||
chr2:86725951
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+5142T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86725951 | ||||||
chr2:86725976
|
CTT | C | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+5169_142+5170d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86725976 | |||||
chr2:86726002
|
T | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+5193T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726002 | ||||||
chr2:86726066
|
A | G | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+5257A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726066 | ||||||
chr2:86726090
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+5281A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726090 | ||||||
chr2:86726106
|
T | C | 1 | a0001c0001t0015g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.142+5297T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726106 | ||||||
chr2:86726121
|
C | T | 5 | a0001c0002t0003g0017a0001c0002t0003g0079a0001c0002t0003g0080others(2): Show | 6 | HG00423.hp2 HG00544.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+5312C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726121 | ||||||
chr2:86726133
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.142+5324A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726133 | ||||||
chr2:86726203
|
C | T | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+5394C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726203 | ||||||
chr2:86726250
|
C | A | 8 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(5): Show | 10 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+5441C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726250 | ||||||
chr2:86726376
|
C | T | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+5567C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726376 | ||||||
chr2:86726377
|
C | T | 8 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(5): Show | 10 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+5568C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726377 | ||||||
chr2:86726536
|
A | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.142+5727A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726536 | ||||||
chr2:86726568
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+5759A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726568 | ||||||
chr2:86726638
|
GT | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0119others(1): Show | 4 | HG00140.hp2 HG01106.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+5831delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86726638 | |||||
chr2:86726710
|
T | G | 1 | a0001c0004t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.142+5901T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726710 | ||||||
chr2:86726725
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.142+5916G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726725 | ||||||
chr2:86726758
|
G | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+5949G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726758 | ||||||
chr2:86726877
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.142+6068T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726877 | ||||||
chr2:86726957
|
A | G | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+6148A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726957 | ||||||
chr2:86726965
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.142+6156C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726965 | ||||||
chr2:86726991
|
T | C | 25 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(22): Show | 28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.142+6182T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86726991 | ||||||
chr2:86727176
|
T | G | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.142+6367T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727176 | ||||||
chr2:86727225
|
G | A | 10 | a0001c0001t0005g0021a0001c0001t0005g0120a0001c0001t0005g0122others(7): Show | 11 | HG01167.hp1 HG01168.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.142+6416G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727225 | ||||||
chr2:86727267
|
A | G | 1 | a0001c0002t0034g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+6458A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727267 | ||||||
chr2:86727295
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.142+6486A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727295 | ||||||
chr2:86727486
|
C | T | 1 | a0001c0002t0002g0231 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.142+6677C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727486 | ||||||
chr2:86727635
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.142+6826A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727635 | ||||||
chr2:86727677
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.142+6868G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727677 | ||||||
chr2:86727789
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.142+6980T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727789 | ||||||
chr2:86727940
|
G | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.142+7131G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86727940 | ||||||
chr2:86728008
|
A | C | 1 | a0001c0001t0001g0210 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.142+7199A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728008 | ||||||
chr2:86728140
|
A | T | 11 | a0001c0001t0001g0121a0001c0001t0006g0102a0001c0001t0016g0097others(8): Show | 11 | HG00609.hp1 HG01358.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.142+7331A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728140 | ||||||
chr2:86728164
|
AAC | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+7357_142+7358d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728164 | |||||
chr2:86728169
|
T | C | 9 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0034others(6): Show | 13 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+7360T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728169 | ||||||
chr2:86728183
|
G | T | 8 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(5): Show | 10 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.142+7374G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728183 | ||||||
chr2:86728215
|
A | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+7406A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728215 | ||||||
chr2:86728313
|
CTT | C | 9 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0002t0034g0112others(6): Show | 10 | HG01167.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.142+7518_142+7519d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728313 | |||||
chr2:86728313
|
CTTT | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.142+7517_142+7519d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728313 | |||||
chr2:86728323
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0004g0089a0001c0001t0019g0018 | 4 | HG01109.hp2 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+7514T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728323 | ||||||
chr2:86728437
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+7628G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728437 | ||||||
chr2:86728450
|
G | C | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+7641G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728450 | ||||||
chr2:86728491
|
A | G | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142+7682A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728491 | ||||||
chr2:86728516
|
C | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.142+7707C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728516 | ||||||
chr2:86728745
|
T | C | 1 | a0001c0002t0002g0104 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.142+7936T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728745 | ||||||
chr2:86728872
|
G | GC | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.142+8068dupC | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728872 | |||||
chr2:86728897
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.142+8088C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728897 | ||||||
chr2:86728900
|
A | G | 2 | a0001c0001t0006g0102a0001c0002t0041g0063 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.142+8091A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728900 | ||||||
chr2:86728918
|
A | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8109A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728918 | ||||||
chr2:86728929
|
G | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8120G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728929 | ||||||
chr2:86728931
|
A | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8122A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86728931 | ||||||
chr2:86728934
|
T | TTG | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8126_142+8127i others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86728934 | |||||
chr2:86729000
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0006g0025others(4): Show | 7 | HG01358.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.142+8191C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729000 | ||||||
chr2:86729018
|
T | A | 1 | a0001c0001t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.142+8209T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729018 | ||||||
chr2:86729022
|
A | G | 5 | a0001c0001t0001g0201a0001c0002t0002g0238a0001c0004t0023g0055others(2): Show | 5 | HG00639.hp2 HG01358.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+8213A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729022 | ||||||
chr2:86729174
|
TAAGA | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.142+8370_142+8373d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86729174 | |||||
chr2:86729204
|
T | A | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+8395T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729204 | ||||||
chr2:86729225
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+8416T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729225 | ||||||
chr2:86729253
|
C | T | 4 | a0001c0001t0001g0201a0001c0004t0023g0055a0001c0004t0024g0056others(1): Show | 4 | HG01358.hp2 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+8444C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729253 | ||||||
chr2:86729266
|
A | G | 4 | a0001c0001t0001g0201a0001c0004t0023g0055a0001c0004t0024g0056others(1): Show | 4 | HG01358.hp2 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+8457A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729266 | ||||||
chr2:86729283
|
G | T | 13 | a0001c0001t0001g0201a0001c0001t0001g0246a0001c0002t0034g0112others(10): Show | 15 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.142+8474G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729283 | ||||||
chr2:86729443
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.142+8634A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729443 | ||||||
chr2:86729501
|
C | T | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.142+8692C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729501 | ||||||
chr2:86729536
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.142+8727C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729536 | ||||||
chr2:86729537
|
G | A | 1 | a0001c0001t0016g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.142+8728G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729537 | ||||||
chr2:86729547
|
C | T | 1 | a0001c0002t0034g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.142+8738C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729547 | ||||||
chr2:86729588
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.142+8779G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729588 | ||||||
chr2:86729642
|
G | A | 8 | a0001c0001t0016g0097a0001c0002t0003g0064a0001c0002t0003g0065others(5): Show | 11 | HG01358.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.142+8833G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729642 | ||||||
chr2:86729667
|
C | CT | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.142+8858_142+8859i others(3): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729667 | ||||||
chr2:86729669
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.142+8860G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729669 | ||||||
chr2:86729797
|
G | T | 1 | a0001c0005t0011g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.142+8988G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729797 | ||||||
chr2:86729958
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.142+9149C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86729958 | ||||||
chr2:86730276
|
G | A | 30 | a0001c0001t0001g0128a0001c0002t0002g0105a0001c0002t0002g0212others(27): Show | 35 | HG01099.hp2 HG01109.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.142+9467G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730276 | ||||||
chr2:86730367
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142+9558A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730367 | ||||||
chr2:86730435
|
G | C | 4 | a0001c0002t0002g0236a0001c0002t0002g0238a0001c0002t0002g0251others(1): Show | 4 | HG00639.hp2 HG01346.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+9626G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730435 | ||||||
chr2:86730933
|
G | A | 1 | a0001c0002t0002g0218 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.143-9994G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86730933 | ||||||
chr2:86731075
|
T | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(19): Show | 31 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.143-9852T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731075 | ||||||
chr2:86731084
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.143-9843A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731084 | ||||||
chr2:86731206
|
G | A | 1 | a0001c0004t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-9721G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731206 | ||||||
chr2:86731246
|
T | G | 25 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(22): Show | 30 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.143-9681T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731246 | ||||||
chr2:86731496
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.143-9431T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731496 | ||||||
chr2:86731521
|
T | C | 2 | a0001c0004t0023g0055a0001c0004t0030g0054 | 2 | HG01358.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.143-9406T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731521 | ||||||
chr2:86731592
|
T | G | 1 | a0001c0004t0030g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-9335T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731592 | ||||||
chr2:86731635
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.143-9292G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731635 | ||||||
chr2:86731895
|
A | G | 1 | a0001c0004t0024g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.143-9032A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86731895 | ||||||
chr2:86732119
|
G | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(9): Show | 16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.143-8808G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732119 | ||||||
chr2:86732289
|
C | T | 1 | a0001c0001t0009g0244 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.143-8638C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732289 | ||||||
chr2:86732302
|
C | CAG | 12 | a0001c0001t0001g0121a0001c0002t0034g0112a0001c0004t0008g0029others(9): Show | 14 | HG00609.hp1 HG01167.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-8624_143-8623d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86732302 | |||||
chr2:86732346
|
G | A | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-8581G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732346 | ||||||
chr2:86732408
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.143-8519T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732408 | ||||||
chr2:86732420
|
T | C | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-8507T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732420 | ||||||
chr2:86732524
|
A | G | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.143-8403A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732524 | ||||||
chr2:86732527
|
G | A | 2 | a0001c0001t0006g0102a0001c0005t0011g0053 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.143-8400G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732527 | ||||||
chr2:86732650
|
AT | A | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-8275delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86732650 | |||||
chr2:86732754
|
C | G | 10 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(7): Show | 12 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-8173C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732754 | ||||||
chr2:86732756
|
A | G | 25 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(22): Show | 28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.143-8171A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732756 | ||||||
chr2:86732792
|
C | T | 1 | a0001c0001t0006g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.143-8135C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732792 | ||||||
chr2:86732916
|
G | T | 1 | a0001c0004t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.143-8011G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86732916 | ||||||
chr2:86733090
|
A | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.143-7837A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733090 | ||||||
chr2:86733095
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.143-7832G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733095 | ||||||
chr2:86733129
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.143-7798G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733129 | ||||||
chr2:86733305
|
G | A | 1 | a0001c0002t0042g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.143-7622G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733305 | ||||||
chr2:86733428
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0036g0143 | 3 | HG00099.hp1 HG00280.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.143-7499T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733428 | ||||||
chr2:86733512
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(25): Show | 34 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.143-7415A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733512 | ||||||
chr2:86733514
|
C | T | 22 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(19): Show | 27 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.143-7413C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733514 | ||||||
chr2:86733707
|
A | G | 8 | a0001c0002t0003g0016a0001c0002t0003g0064a0001c0002t0003g0065others(5): Show | 9 | HG02055.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-7220A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733707 | ||||||
chr2:86733750
|
G | C | 2 | a0001c0001t0001g0025a0001c0001t0006g0025 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.143-7177G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733750 | ||||||
chr2:86733949
|
C | A | 1 | a0001c0002t0035g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.143-6978C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733949 | ||||||
chr2:86733967
|
A | G | 12 | a0001c0002t0003g0076a0001c0002t0034g0112a0001c0004t0008g0029others(9): Show | 14 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.143-6960A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86733967 | ||||||
chr2:86734004
|
T | A | 1 | a0001c0002t0003g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.143-6923T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734004 | ||||||
chr2:86734071
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.143-6856G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734071 | ||||||
chr2:86734336
|
C | G | 2 | a0001c0002t0003g0015a0001c0002t0003g0077 | 3 | HG01074.hp2 HG01261.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.143-6591C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734336 | ||||||
chr2:86734370
|
G | T | 16 | a0001c0001t0001g0019a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 19 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.143-6557G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734370 | ||||||
chr2:86734478
|
C | T | 6 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(3): Show | 8 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.143-6449C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734478 | ||||||
chr2:86734519
|
A | G | 2 | a0001c0002t0002g0110a0001c0002t0002g0111 | 2 | NA18960.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.143-6408A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734519 | ||||||
chr2:86734555
|
A | G | 5 | a0001c0001t0016g0097a0001c0001t0016g0100a0001c0001t0017g0099others(2): Show | 5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-6372A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734555 | ||||||
chr2:86734659
|
T | C | 1 | a0001c0001t0004g0144 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.143-6268T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734659 | ||||||
chr2:86734682
|
T | A | 2 | a0001c0002t0007g0237a0001c0002t0035g0103 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.143-6245T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734682 | ||||||
chr2:86734707
|
G | A | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.143-6220G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734707 | ||||||
chr2:86734772
|
A | G | 21 | a0001c0001t0001g0019a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 24 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.143-6155A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734772 | ||||||
chr2:86734779
|
C | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.143-6148C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86734779 | ||||||
chr2:86734961
|
TTGTCTAT others(13): Show |
T | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-5963_143-5944d others(22): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86734961 | |||||
chr2:86735013
|
T | C | 1 | a0001c0001t0006g0129 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.143-5914T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735013 | ||||||
chr2:86735029
|
A | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.143-5898A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735029 | ||||||
chr2:86735061
|
G | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(21): Show | 30 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-5866G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735061 | ||||||
chr2:86735318
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0006g0193 | 2 | HG02735.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.143-5609G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735318 | ||||||
chr2:86735326
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-5601C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735326 | ||||||
chr2:86735361
|
A | G | 1 | a0001c0002t0003g0081 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.143-5566A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735361 | ||||||
chr2:86735419
|
G | A | 1 | a0001c0002t0003g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.143-5508G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735419 | ||||||
chr2:86735522
|
T | C | 1 | a0001c0002t0003g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.143-5405T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735522 | ||||||
chr2:86735550
|
C | CT | 5 | a0001c0001t0001g0027a0001c0001t0001g0189a0001c0001t0004g0085others(2): Show | 7 | NA18975.hp1 NA18983.hp1 NA18999.hp1 others(4): Show |
intron_variant | MODIFIER | c.143-5367dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86735550 | |||||
chr2:86735675
|
A | C | 1 | a0001c0004t0024g0056 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.143-5252A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735675 | ||||||
chr2:86735832
|
G | C | 25 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(22): Show | 30 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.143-5095G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86735832 | ||||||
chr2:86736190
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.143-4737C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736190 | ||||||
chr2:86736253
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.143-4674A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736253 | ||||||
chr2:86736341
|
C | A | 1 | a0001c0002t0003g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.143-4586C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736341 | ||||||
chr2:86736468
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.143-4459A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736468 | ||||||
chr2:86736484
|
CATT | C | 53 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(50): Show | 63 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.143-4442_143-4440d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736484 | ||||||
chr2:86736631
|
T | C | 10 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(7): Show | 12 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-4296T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736631 | ||||||
chr2:86736640
|
C | T | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.143-4287C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736640 | ||||||
chr2:86736732
|
G | T | 1 | a0001c0002t0002g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.143-4195G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736732 | ||||||
chr2:86736739
|
G | GTA | 1 | a0001c0002t0007g0010 | 3 | HG02717.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.143-4178_143-4177d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86736739 | |||||
chr2:86736748
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.143-4179T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736748 | ||||||
chr2:86736962
|
C | A | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-3965C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736962 | ||||||
chr2:86736964
|
G | C | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-3963G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86736964 | ||||||
chr2:86737123
|
T | C | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3804T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737123 | ||||||
chr2:86737278
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-3649A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737278 | ||||||
chr2:86737290
|
A | G | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3637A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737290 | ||||||
chr2:86737315
|
C | T | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3612C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737315 | ||||||
chr2:86737342
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.143-3585C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737342 | ||||||
chr2:86737444
|
G | A | 1 | a0001c0002t0002g0217 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.143-3483G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737444 | ||||||
chr2:86737462
|
A | G | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-3465A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737462 | ||||||
chr2:86737574
|
C | CATATATA others(7): Show |
1 | a0001c0001t0004g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.143-3346_143-3333d others(16): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(11): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0094others(3): Show | 9 | HG00642.hp1 HG02055.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-3350_143-3333d others(20): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(13): Show |
2 | a0001c0001t0001g0090a0001c0001t0019g0018 | 3 | HG01109.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.143-3352_143-3333d others(22): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(15): Show |
2 | a0001c0001t0001g0093a0001c0001t0004g0089 | 2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(24): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(19): Show |
1 | a0001c0001t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(28): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(21): Show |
1 | a0001c0001t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(30): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(25): Show |
1 | a0001c0001t0006g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(34): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(27): Show |
1 | a0001c0005t0011g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(36): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(29): Show |
1 | a0001c0001t0016g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(38): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(31): Show |
1 | a0001c0001t0017g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(40): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(33): Show |
2 | a0001c0001t0016g0100a0001c0001t0017g0099 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(42): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
C | CATATATA others(37): Show |
1 | a0001c0001t0040g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.143-3333_143-3332i others(46): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
CAT | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(71): Show | 89 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.143-3334_143-3333d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737574
|
CATAT | C | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(71): Show | 89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.143-3336_143-3333d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737574 | |||||
chr2:86737592
|
T | TATATATA | 13 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0145others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-3333_143-3332i others(9): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(2): Show |
3 | a0001c0001t0004g0150a0001c0003t0001g0032a0001c0004t0025g0060 | 3 | HG02970.hp1 NA19068.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(11): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(4): Show |
1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(13): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(7): Show |
1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(16): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(8): Show |
2 | a0001c0002t0034g0112a0001c0004t0024g0056 | 2 | HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(17): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(10): Show |
1 | a0001c0004t0030g0054 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(19): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(14): Show |
1 | a0001c0004t0022g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(23): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(16): Show |
1 | a0001c0004t0008g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.143-3333_143-3332i others(25): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(18): Show |
1 | a0001c0004t0008g0249 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.143-3333_143-3332i others(27): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737592
|
T | TATATATA others(24): Show |
1 | a0001c0004t0008g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.143-3333_143-3332i others(33): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86737592 | |||||
chr2:86737686
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.143-3241T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737686 | ||||||
chr2:86737725
|
C | G | 1 | a0001c0001t0001g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.143-3202C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737725 | ||||||
chr2:86737745
|
C | T | 1 | a0001c0001t0004g0088 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.143-3182C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737745 | ||||||
chr2:86737820
|
T | G | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-3107T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737820 | ||||||
chr2:86737959
|
G | A | 32 | a0001c0001t0001g0246a0001c0001t0012g0203a0001c0001t0012g0205others(29): Show | 38 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(35): Show |
intron_variant | MODIFIER | c.143-2968G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86737959 | ||||||
chr2:86738029
|
A | C | 1 | a0001c0002t0001g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.143-2898A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738029 | ||||||
chr2:86738047
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.143-2880T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738047 | ||||||
chr2:86738058
|
A | C | 1 | a0001c0002t0041g0063 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.143-2869A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738058 | ||||||
chr2:86738282
|
G | A | 50 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(47): Show | 60 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-2645G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738282 | ||||||
chr2:86738292
|
C | T | 34 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(31): Show | 39 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.143-2635C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738292 | ||||||
chr2:86738309
|
C | T | 1 | a0001c0002t0003g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.143-2618C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738309 | ||||||
chr2:86738416
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0006g0026 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.143-2511G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738416 | ||||||
chr2:86738467
|
C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(24): Show | 36 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.143-2460C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738467 | ||||||
chr2:86738514
|
G | C | 1 | a0001c0001t0029g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.143-2413G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738514 | ||||||
chr2:86738542
|
CA | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.143-2373delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86738542 | |||||
chr2:86738588
|
C | CA | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-2338dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86738588 | |||||
chr2:86738703
|
T | C | 1 | a0001c0003t0001g0040 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.143-2224T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738703 | ||||||
chr2:86738823
|
A | G | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-2104A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738823 | ||||||
chr2:86738955
|
G | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.143-1972G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738955 | ||||||
chr2:86738968
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.143-1959T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86738968 | ||||||
chr2:86739008
|
A | C | 1 | a0001c0001t0029g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.143-1919A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739008 | ||||||
chr2:86739108
|
G | T | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.143-1819G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739108 | ||||||
chr2:86739351
|
G | A | 9 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(6): Show | 11 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.143-1576G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739351 | ||||||
chr2:86739404
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.143-1523G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739404 | ||||||
chr2:86739485
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.143-1442G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739485 | ||||||
chr2:86739518
|
G | A | 4 | a0001c0002t0002g0028a0001c0002t0002g0234a0001c0002t0002g0235others(1): Show | 5 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-1409G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739518 | ||||||
chr2:86739894
|
G | A | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.143-1033G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739894 | ||||||
chr2:86739905
|
C | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.143-1022C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739905 | ||||||
chr2:86739923
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.143-1004G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86739923 | ||||||
chr2:86740082
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.143-845G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740082 | ||||||
chr2:86740122
|
A | G | 6 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(3): Show | 7 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-805A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740122 | ||||||
chr2:86740276
|
C | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(98): Show | 116 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.143-651C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740276 | ||||||
chr2:86740278
|
G | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.143-649G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740278 | ||||||
chr2:86740307
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.143-620C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740307 | ||||||
chr2:86740336
|
G | A | 34 | a0001c0002t0001g0083a0001c0002t0002g0105a0001c0002t0002g0236others(31): Show | 40 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.143-591G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740336 | ||||||
chr2:86740344
|
G | T | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-583G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740344 | ||||||
chr2:86740445
|
G | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.143-482G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | chr2 | 86740445 | ||||||
chr2:86740731
|
C | CA | 4 | a0001c0001t0001g0175a0001c0002t0002g0212a0001c0004t0018g0014others(1): Show | 5 | HG01934.hp2 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-191dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 86740731 | |||||
chr2:86741235
|
C | G | 1 | a0001c0002t0003g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.285+166C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741235 | ||||||
chr2:86741305
|
C | T | 2 | a0001c0003t0001g0033a0001c0003t0001g0049 | 2 | NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.285+236C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741305 | ||||||
chr2:86741518
|
C | T | 1 | a0001c0002t0002g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+449C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741518 | ||||||
chr2:86741565
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.285+496A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741565 | ||||||
chr2:86741662
|
A | C | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.285+593A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741662 | ||||||
chr2:86741774
|
G | A | 1 | a0001c0002t0003g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.285+705G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741774 | ||||||
chr2:86741849
|
T | C | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+780T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741849 | ||||||
chr2:86741850
|
T | G | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+781T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86741850 | ||||||
chr2:86742069
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0172a0001c0001t0001g0173 | 4 | HG01071.hp1 HG01106.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+1000A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742069 | ||||||
chr2:86742174
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.285+1105A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742174 | ||||||
chr2:86742198
|
T | A | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+1129T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742198 | ||||||
chr2:86742647
|
A | G | 4 | a0001c0002t0034g0112a0001c0003t0001g0030a0001c0003t0001g0031others(1): Show | 4 | HG02109.hp1 HG02735.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1578A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742647 | ||||||
chr2:86742648
|
G | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.285+1579G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742648 | ||||||
chr2:86742656
|
T | C | 3 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032 | 3 | HG02735.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.285+1587T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742656 | ||||||
chr2:86742670
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285+1601A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742670 | ||||||
chr2:86742740
|
G | A | 5 | a0001c0002t0002g0219a0001c0002t0002g0220a0001c0002t0002g0221others(2): Show | 5 | HG01074.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1671G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742740 | ||||||
chr2:86742770
|
T | C | 1 | a0001c0001t0040g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+1701T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742770 | ||||||
chr2:86742998
|
C | G | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.285+1929C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86742998 | ||||||
chr2:86743251
|
G | C | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+2182G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743251 | ||||||
chr2:86743283
|
T | A | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+2214T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743283 | ||||||
chr2:86743364
|
C | CT | 28 | a0001c0002t0041g0063a0001c0003t0001g0002a0001c0003t0001g0011others(25): Show | 34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.285+2308dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743364 | |||||
chr2:86743364
|
CT | C | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+2308delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743364 | |||||
chr2:86743498
|
CT | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.285+2434delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743498 | |||||
chr2:86743531
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.285+2462C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743531 | ||||||
chr2:86743567
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.285+2498C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743567 | ||||||
chr2:86743707
|
T | G | 1 | a0001c0002t0003g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.285+2638T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743707 | ||||||
chr2:86743710
|
G | A | 5 | a0001c0002t0002g0104a0001c0002t0002g0108a0001c0002t0002g0109others(2): Show | 5 | HG01433.hp2 HG02135.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+2641G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743710 | ||||||
chr2:86743748
|
G | A | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.285+2679G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743748 | ||||||
chr2:86743760
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.285+2691C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743760 | ||||||
chr2:86743884
|
AG | A | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.285+2817delG | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743884 | |||||
chr2:86743964
|
C | T | 5 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0005t0010g0008others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+2895C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743964 | ||||||
chr2:86743977
|
C | CA | 10 | a0001c0001t0001g0141a0001c0001t0001g0206a0001c0001t0001g0210others(7): Show | 11 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+2924dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743977 | |||||
chr2:86743977
|
CA | C | 35 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0239others(32): Show | 41 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.285+2924delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86743977 | |||||
chr2:86743994
|
T | A | 2 | a0001c0004t0023g0055a0001c0004t0030g0054 | 2 | HG01358.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.285+2925T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86743994 | ||||||
chr2:86744209
|
A | G | 2 | a0001c0002t0003g0074a0001c0002t0003g0075 | 2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.285+3140A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744209 | ||||||
chr2:86744224
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(9): Show | 16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.285+3155C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744224 | ||||||
chr2:86744246
|
A | C | 1 | a0001c0001t0029g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285+3177A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744246 | ||||||
chr2:86744729
|
T | TG | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.285+3662dupG | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86744729 | |||||
chr2:86744854
|
A | G | 1 | a0001c0001t0029g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285+3785A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744854 | ||||||
chr2:86744859
|
A | T | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3790A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744859 | ||||||
chr2:86744991
|
A | T | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3922A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744991 | ||||||
chr2:86744993
|
ATTTG | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.285+3927_285+3930d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86744993 | |||||
chr2:86744994
|
T | A | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+3925T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86744994 | ||||||
chr2:86745005
|
A | G | 1 | a0001c0001t0037g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.285+3936A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745005 | ||||||
chr2:86745008
|
A | AT | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+3952dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86745008 | |||||
chr2:86745008
|
AT | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.285+3952delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86745008 | |||||
chr2:86745014
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.285+3945T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745014 | ||||||
chr2:86745038
|
T | G | 4 | a0001c0002t0002g0236a0001c0002t0002g0238a0001c0002t0002g0251others(1): Show | 4 | HG00639.hp2 HG01346.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+3969T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745038 | ||||||
chr2:86745099
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.285+4030G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745099 | ||||||
chr2:86745293
|
T | C | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+4224T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745293 | ||||||
chr2:86745307
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.285+4238A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745307 | ||||||
chr2:86745959
|
T | C | 4 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(1): Show | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+4890T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745959 | ||||||
chr2:86745973
|
T | C | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+4904T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86745973 | ||||||
chr2:86746004
|
C | T | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+4935C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746004 | ||||||
chr2:86746070
|
T | A | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.285+5001T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746070 | ||||||
chr2:86746138
|
A | G | 1 | a0001c0002t0002g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+5069A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746138 | ||||||
chr2:86746499
|
G | A | 3 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032 | 3 | HG02735.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.286-5397G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746499 | ||||||
chr2:86746499
|
G | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0164others(5): Show | 12 | HG02015.hp1 HG02074.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.286-5397G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746499 | ||||||
chr2:86746661
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286-5235C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746661 | ||||||
chr2:86746711
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.286-5185A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746711 | ||||||
chr2:86746785
|
G | A | 1 | a0001c0002t0007g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.286-5111G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746785 | ||||||
chr2:86746828
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.286-5068C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746828 | ||||||
chr2:86746926
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.286-4970A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86746926 | ||||||
chr2:86747172
|
A | G | 1 | a0001c0001t0001g0163 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.286-4724A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747172 | ||||||
chr2:86747195
|
A | G | 23 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(20): Show | 26 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-4701A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747195 | ||||||
chr2:86747218
|
G | A | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.286-4678G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747218 | ||||||
chr2:86747343
|
TGTTAA | T | 1 | a0001c0002t0007g0010 | 3 | HG02717.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.286-4548_286-4544d others(7): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86747343 | |||||
chr2:86747566
|
A | G | 5 | a0001c0001t0012g0205a0001c0002t0002g0028a0001c0002t0002g0234others(2): Show | 6 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-4330A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747566 | ||||||
chr2:86747682
|
T | C | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.286-4214T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747682 | ||||||
chr2:86747711
|
A | C | 25 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(22): Show | 28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.286-4185A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747711 | ||||||
chr2:86747748
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.286-4148G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747748 | ||||||
chr2:86747756
|
C | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.286-4140C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747756 | ||||||
chr2:86747828
|
G | A | 1 | a0001c0001t0004g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.286-4068G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747828 | ||||||
chr2:86747936
|
G | A | 1 | a0001c0002t0007g0020 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.286-3960G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86747936 | ||||||
chr2:86748042
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.286-3854A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748042 | ||||||
chr2:86748097
|
T | C | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.286-3799T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748097 | ||||||
chr2:86748585
|
T | G | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-3311T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748585 | ||||||
chr2:86748847
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.286-3049G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86748847 | ||||||
chr2:86749064
|
C | T | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2832C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749064 | ||||||
chr2:86749116
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.286-2780G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749116 | ||||||
chr2:86749170
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0006g0026 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.286-2726G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749170 | ||||||
chr2:86749170
|
G | C | 1 | a0001c0005t0010g0052 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.286-2726G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749170 | ||||||
chr2:86749176
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0128a0001c0001t0001g0163others(2): Show | 6 | HG01071.hp1 HG01106.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2720G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749176 | ||||||
chr2:86749183
|
T | C | 1 | a0001c0001t0016g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.286-2713T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749183 | ||||||
chr2:86749225
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.286-2671G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749225 | ||||||
chr2:86749344
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.286-2552A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749344 | ||||||
chr2:86749396
|
CT | C | 23 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(20): Show | 26 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-2489delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86749396 | |||||
chr2:86749505
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0162a0001c0001t0004g0023 | 3 | NA18978.hp2 NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.286-2391C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749505 | ||||||
chr2:86749538
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.286-2358C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749538 | ||||||
chr2:86749578
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.286-2318C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749578 | ||||||
chr2:86749869
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.286-2027T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86749869 | ||||||
chr2:86750104
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.286-1792T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750104 | ||||||
chr2:86750442
|
C | A | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-1454C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750442 | ||||||
chr2:86750502
|
CAT | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.286-1393_286-1392d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750502 | ||||||
chr2:86750718
|
G | A | 1 | a0001c0002t0034g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.286-1178G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750718 | ||||||
chr2:86750729
|
C | T | 2 | a0001c0001t0016g0097a0001c0002t0002g0227 | 2 | HG00140.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.286-1167C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750729 | ||||||
chr2:86750771
|
GT | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.286-1109delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 86750771 | |||||
chr2:86750812
|
T | C | 1 | a0001c0002t0034g0112 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.286-1084T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86750812 | ||||||
chr2:86751010
|
T | C | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-886T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751010 | ||||||
chr2:86751072
|
G | A | 1 | a0001c0001t0004g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.286-824G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751072 | ||||||
chr2:86751741
|
A | G | 1 | a0001c0002t0002g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.286-155A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751741 | ||||||
chr2:86751772
|
G | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.286-124G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751772 | ||||||
chr2:86751773
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.286-123A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751773 | ||||||
chr2:86751774
|
C | T | 3 | a0001c0001t0006g0102a0001c0003t0001g0245a0001c0005t0011g0053 | 3 | HG02145.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.286-122C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 2/8 | chr2 | 86751774 | ||||||
chr2:86752294
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.420+264G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752294 | ||||||
chr2:86752297
|
G | A | 5 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0005t0010g0008others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+267G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752297 | ||||||
chr2:86752370
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.420+340A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752370 | ||||||
chr2:86752560
|
C | A | 1 | a0001c0002t0007g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.420+530C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752560 | ||||||
chr2:86752599
|
A | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.420+569A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752599 | ||||||
chr2:86752778
|
C | T | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-680C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752778 | ||||||
chr2:86752882
|
C | T | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-576C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752882 | ||||||
chr2:86752987
|
T | C | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-471T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86752987 | ||||||
chr2:86753115
|
G | A | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-343G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86753115 | ||||||
chr2:86753137
|
A | G | 3 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0047 | 3 | NA18955.hp2 NA18967.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.421-321A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86753137 | ||||||
chr2:86753387
|
A | G | 1 | a0001c0001t0016g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-71A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 3/8 | chr2 | 86753387 | ||||||
chr2:86753663
|
G | A | 1 | a0001c0004t0008g0029 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.521+105G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753663 | ||||||
chr2:86753711
|
A | T | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.521+153A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753711 | ||||||
chr2:86753744
|
A | G | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+186A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753744 | ||||||
chr2:86753963
|
G | A | 1 | a0001c0002t0002g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.521+405G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86753963 | ||||||
chr2:86754000
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(9): Show | 16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.521+442T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754000 | ||||||
chr2:86754534
|
C | G | 5 | a0001c0001t0016g0097a0001c0001t0016g0100a0001c0001t0017g0099others(2): Show | 5 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.521+976C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754534 | ||||||
chr2:86754595
|
G | T | 1 | a0001c0001t0004g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.521+1037G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754595 | ||||||
chr2:86754620
|
G | A | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.521+1062G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754620 | ||||||
chr2:86754654
|
C | T | 1 | a0001c0002t0003g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.521+1096C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754654 | ||||||
chr2:86754668
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(11): Show | 18 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.521+1110G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754668 | ||||||
chr2:86754705
|
G | A | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.521+1147G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754705 | ||||||
chr2:86754732
|
A | T | 2 | a0001c0001t0001g0201a0001c0001t0005g0118 | 2 | HG01106.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.521+1174A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86754732 | ||||||
chr2:86755076
|
C | T | 29 | a0001c0001t0001g0246a0001c0003t0001g0002a0001c0003t0001g0011others(26): Show | 35 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.521+1518C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755076 | ||||||
chr2:86755097
|
A | G | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.521+1539A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755097 | ||||||
chr2:86755112
|
C | CT | 28 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(25): Show | 34 | HG00642.hp1 HG01109.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.521+1570dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86755112 | |||||
chr2:86755158
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0161a0001c0001t0001g0162others(1): Show | 4 | HG03942.hp2 NA18978.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.521+1600C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755158 | ||||||
chr2:86755170
|
G | A | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.521+1612G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755170 | ||||||
chr2:86755319
|
A | G | 1 | a0001c0002t0003g0080 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.521+1761A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755319 | ||||||
chr2:86755381
|
C | G | 25 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(22): Show | 28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.521+1823C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755381 | ||||||
chr2:86755400
|
G | T | 1 | a0001c0001t0001g0019 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.521+1842G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755400 | ||||||
chr2:86755417
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.521+1859C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755417 | ||||||
chr2:86755521
|
T | C | 1 | a0001c0002t0035g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.521+1963T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755521 | ||||||
chr2:86755528
|
G | A | 23 | a0001c0002t0001g0083a0001c0002t0003g0015a0001c0002t0003g0016others(20): Show | 26 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.521+1970G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755528 | ||||||
chr2:86755659
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.521+2101A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755659 | ||||||
chr2:86755753
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.521+2195T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755753 | ||||||
chr2:86755832
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0004g0153 | 2 | NA18949.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.521+2274G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755832 | ||||||
chr2:86755955
|
T | C | 1 | a0001c0002t0003g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.521+2397T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86755955 | ||||||
chr2:86756263
|
T | C | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.521+2705T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756263 | ||||||
chr2:86756265
|
C | T | 1 | a0001c0002t0035g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.521+2707C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756265 | ||||||
chr2:86756538
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0197 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.521+2980A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756538 | ||||||
chr2:86756563
|
C | T | 1 | a0001c0003t0001g0040 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.521+3005C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756563 | ||||||
chr2:86756808
|
A | G | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.521+3250A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756808 | ||||||
chr2:86756856
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.521+3298A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86756856 | ||||||
chr2:86757030
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(9): Show | 16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.521+3472A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757030 | ||||||
chr2:86757042
|
G | A | 1 | a0001c0004t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.521+3484G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757042 | ||||||
chr2:86757059
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.521+3501G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757059 | ||||||
chr2:86757106
|
G | A | 1 | a0001c0001t0017g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.521+3548G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757106 | ||||||
chr2:86757174
|
C | CAAA | 7 | a0001c0002t0001g0083a0001c0002t0003g0064a0001c0002t0003g0071others(4): Show | 7 | HG00544.hp1 HG00738.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+3647_521+3649d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
C | CAAAA | 9 | a0001c0002t0003g0016a0001c0002t0003g0017a0001c0002t0003g0070others(6): Show | 11 | HG00099.hp2 HG00423.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.521+3646_521+3649d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
C | CAAAAAA | 5 | a0001c0002t0003g0067a0001c0002t0003g0068a0001c0002t0003g0072others(2): Show | 6 | HG00609.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.521+3644_521+3649d others(8): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
CA | C | 29 | a0001c0002t0002g0028a0001c0002t0002g0057a0001c0002t0002g0104others(26): Show | 32 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.521+3649delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
CAA | C | 7 | a0001c0002t0002g0105a0001c0002t0002g0111a0001c0002t0002g0229others(4): Show | 8 | HG00639.hp2 HG01074.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.521+3648_521+3649d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+3639_521+3649d others(13): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
CAAAAAAA others(7): Show |
C | 20 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0154others(17): Show | 21 | HG00733.hp2 HG01891.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.521+3636_521+3649d others(16): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
CAAAAAAA others(8): Show |
C | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.521+3635_521+3649d others(17): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0001g0026a0001c0001t0001g0151a0001c0001t0001g0162others(4): Show | 7 | HG01243.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.521+3634_521+3649d others(18): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757174
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0002t0003g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.521+3633_521+3649d others(19): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86757174 | |||||
chr2:86757269
|
C | T | 3 | a0001c0004t0018g0014a0001c0004t0025g0060a0001c0004t0027g0061 | 4 | HG02630.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.521+3711C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757269 | ||||||
chr2:86757274
|
C | T | 1 | a0001c0004t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.521+3716C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757274 | ||||||
chr2:86757403
|
T | C | 1 | a0001c0002t0013g0106 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.521+3845T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757403 | ||||||
chr2:86757419
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.521+3861C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757419 | ||||||
chr2:86757424
|
C | T | 3 | a0001c0004t0018g0014a0001c0004t0025g0060a0001c0004t0027g0061 | 4 | HG02630.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.521+3866C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757424 | ||||||
chr2:86757425
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.521+3867G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757425 | ||||||
chr2:86757964
|
A | G | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+4406A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86757964 | ||||||
chr2:86758161
|
CACA | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.521+4608_521+4610d others(5): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86758161 | |||||
chr2:86758360
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.521+4802A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758360 | ||||||
chr2:86758364
|
A | AT | 12 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0145others(9): Show | 13 | HG01978.hp1 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.521+4818dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86758364 | |||||
chr2:86758420
|
TA | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.521+4863delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758420 | ||||||
chr2:86758598
|
G | A | 11 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(8): Show | 13 | HG01167.hp1 HG01358.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.521+5040G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758598 | ||||||
chr2:86758612
|
G | A | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.521+5054G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758612 | ||||||
chr2:86758971
|
T | A | 1 | a0001c0002t0007g0010 | 3 | HG02717.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.521+5413T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86758971 | ||||||
chr2:86759079
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.521+5521A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759079 | ||||||
chr2:86759109
|
A | T | 1 | a0001c0001t0001g0132 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.521+5551A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759109 | ||||||
chr2:86759210
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(17): Show | 29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.521+5652G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759210 | ||||||
chr2:86759351
|
C | G | 1 | a0001c0003t0001g0040 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.522-5676C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759351 | ||||||
chr2:86759565
|
TA | T | 5 | a0001c0002t0003g0071a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02602.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-5455delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86759565 | |||||
chr2:86759566
|
A | T | 16 | a0001c0001t0001g0201a0001c0001t0001g0246a0001c0001t0009g0169others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.522-5461A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759566 | ||||||
chr2:86759612
|
G | GC | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0023others(82): Show | 100 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.522-5408dupC | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86759612 | |||||
chr2:86759620
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.522-5407G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759620 | ||||||
chr2:86759686
|
G | C | 4 | a0001c0002t0003g0070a0001c0004t0008g0029a0001c0004t0008g0248others(1): Show | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.522-5341G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759686 | ||||||
chr2:86759721
|
A | G | 1 | a0001c0005t0011g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.522-5306A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759721 | ||||||
chr2:86759724
|
C | T | 1 | a0001c0001t0005g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.522-5303C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759724 | ||||||
chr2:86759761
|
C | T | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.522-5266C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759761 | ||||||
chr2:86759879
|
C | T | 2 | a0001c0004t0027g0061a0001c0005t0011g0053 | 2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.522-5148C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86759879 | ||||||
chr2:86760002
|
T | G | 1 | a0001c0002t0002g0212 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.522-5025T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760002 | ||||||
chr2:86760194
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0005g0146 | 3 | HG00099.hp1 HG00280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.522-4833G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760194 | ||||||
chr2:86760295
|
C | T | 2 | a0001c0002t0003g0068a0001c0002t0014g0069 | 2 | HG00609.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.522-4732C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760295 | ||||||
chr2:86760355
|
T | C | 1 | a0001c0002t0003g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.522-4672T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760355 | ||||||
chr2:86760648
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.522-4379T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760648 | ||||||
chr2:86760762
|
GA | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.522-4260delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760762 | |||||
chr2:86760860
|
G | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.522-4167G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760860 | ||||||
chr2:86760864
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.522-4163G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86760864 | ||||||
chr2:86760965
|
A | AGT | 47 | a0001c0001t0001g0025a0001c0001t0001g0090a0001c0001t0001g0093others(44): Show | 50 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.522-4024_522-4023d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | |||||
chr2:86760965
|
A | AGTGT | 32 | a0001c0001t0001g0004a0001c0001t0001g0095a0001c0001t0001g0117others(29): Show | 36 | HG00323.hp1 HG00735.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.522-4026_522-4023d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | |||||
chr2:86760965
|
A | AGTGTGT | 24 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0130others(21): Show | 35 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.522-4028_522-4023d others(8): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | |||||
chr2:86760965
|
A | AGTGTGTG others(1): Show |
5 | a0001c0001t0006g0131a0001c0002t0041g0063a0001c0003t0001g0039others(2): Show | 5 | HG01993.hp1 HG02976.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.522-4030_522-4023d others(10): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | |||||
chr2:86760965
|
AGT | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(88): Show | 104 | HG00280.hp1 HG00544.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.522-4024_522-4023d others(4): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | |||||
chr2:86760965
|
AGTGT | A | 11 | a0001c0001t0001g0121a0001c0001t0001g0154a0001c0001t0004g0009others(8): Show | 13 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.522-4026_522-4023d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86760965 | |||||
chr2:86761208
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.522-3819G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761208 | ||||||
chr2:86761232
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.522-3795A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761232 | ||||||
chr2:86761655
|
A | G | 1 | a0001c0002t0002g0109 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.522-3372A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761655 | ||||||
chr2:86761672
|
T | A | 1 | a0001c0001t0004g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.522-3355T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761672 | ||||||
chr2:86761739
|
C | T | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.522-3288C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761739 | ||||||
chr2:86761849
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.522-3178G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761849 | ||||||
chr2:86761945
|
G | A | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-3082G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86761945 | ||||||
chr2:86762149
|
A | G | 4 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(1): Show | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.522-2878A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762149 | ||||||
chr2:86762343
|
A | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.522-2684A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762343 | ||||||
chr2:86762644
|
C | CA | 32 | a0001c0002t0002g0217a0001c0002t0003g0015a0001c0002t0003g0016others(29): Show | 36 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.522-2371dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762644 | |||||
chr2:86762644
|
CAAAA | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 218 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.522-2374_522-2371d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762644 | |||||
chr2:86762655
|
A | T | 1 | a0001c0005t0011g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.522-2372A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762655 | ||||||
chr2:86762658
|
A | T | 1 | a0001c0005t0011g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.522-2369A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762658 | ||||||
chr2:86762664
|
T | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(9): Show | 16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.522-2363T>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762664 | ||||||
chr2:86762671
|
T | TATATATA others(22): Show |
12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(9): Show | 16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.522-2337_522-2336i others(31): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762671 | |||||
chr2:86762671
|
TATATATA others(31): Show |
T | 1 | a0001c0003t0001g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.522-2338_522-2301d others(40): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762671 | |||||
chr2:86762682
|
TATATATA others(2): Show |
T | 37 | a0001c0002t0002g0028a0001c0002t0002g0057a0001c0002t0002g0104others(34): Show | 40 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.522-2291_522-2283d others(11): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | |||||
chr2:86762682
|
TATATATA others(11): Show |
T | 35 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(32): Show | 37 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.522-2300_522-2283d others(20): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | |||||
chr2:86762682
|
TATATATA others(20): Show |
T | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.522-2309_522-2283d others(29): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | |||||
chr2:86762682
|
TATATATA others(29): Show |
T | 10 | a0001c0001t0001g0157a0001c0001t0001g0199a0001c0001t0016g0097others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.522-2318_522-2283d others(38): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | |||||
chr2:86762682
|
TATATATA others(38): Show |
T | 10 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0164others(7): Show | 14 | HG00544.hp2 HG02015.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.522-2327_522-2283d others(47): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762682 | |||||
chr2:86762684
|
TATATATC others(18): Show |
T | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-2336_522-2312d others(27): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762684 | |||||
chr2:86762693
|
TATATATC others(9): Show |
T | 12 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(9): Show | 16 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.522-2327_522-2312d others(18): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762693 | |||||
chr2:86762709
|
C | CATATATA others(6): Show |
1 | a0001c0001t0006g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.522-2310_522-2309i others(15): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86762709 | |||||
chr2:86762808
|
A | C | 1 | a0001c0002t0042g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.522-2219A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762808 | ||||||
chr2:86762811
|
C | T | 2 | a0001c0002t0013g0106a0001c0002t0013g0107 | 2 | HG01433.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.522-2216C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762811 | ||||||
chr2:86762839
|
G | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.522-2188G>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86762839 | ||||||
chr2:86763124
|
T | C | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.522-1903T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763124 | ||||||
chr2:86763192
|
GTAGT | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.522-1832_522-1829d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 86763192 | |||||
chr2:86763295
|
C | G | 1 | a0001c0003t0001g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.522-1732C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763295 | ||||||
chr2:86763499
|
G | A | 1 | a0001c0004t0018g0014 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.522-1528G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763499 | ||||||
chr2:86763553
|
G | A | 2 | a0001c0002t0003g0062a0001c0002t0041g0063 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.522-1474G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763553 | ||||||
chr2:86763583
|
C | T | 7 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(4): Show | 9 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.522-1444C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763583 | ||||||
chr2:86763771
|
G | A | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.522-1256G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763771 | ||||||
chr2:86763904
|
A | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.522-1123A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86763904 | ||||||
chr2:86764178
|
G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0130a0001c0001t0001g0132others(2): Show | 9 | HG00642.hp2 HG00741.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.522-849G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764178 | ||||||
chr2:86764515
|
T | G | 1 | a0001c0002t0002g0230 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.522-512T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764515 | ||||||
chr2:86764680
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.522-347G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764680 | ||||||
chr2:86764723
|
C | T | 1 | a0001c0001t0037g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.522-304C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764723 | ||||||
chr2:86764751
|
C | A | 1 | a0001c0002t0014g0078 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.522-276C>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764751 | ||||||
chr2:86764770
|
A | C | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.522-257A>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 4/8 | chr2 | 86764770 | ||||||
chr2:86765214
|
T | TAA | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.688+22_688+23insAA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 86765214 | |||||
chr2:86765419
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0198 | 3 | HG01517.hp1 HG06807.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.688+226A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | chr2 | 86765419 | ||||||
chr2:86765489
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0157a0001c0001t0001g0199 | 3 | HG00609.hp1 NA18967.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.688+296C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | chr2 | 86765489 | ||||||
chr2:86765618
|
C | G | 2 | a0001c0004t0018g0014a0001c0004t0025g0060 | 3 | HG02630.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.689-241C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 5/8 | chr2 | 86765618 | ||||||
chr2:86766183
|
G | A | 1 | a0001c0001t0028g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.854+159G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766183 | ||||||
chr2:86766194
|
G | T | 4 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0225others(1): Show | 4 | HG01928.hp2 HG01943.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.854+170G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766194 | ||||||
chr2:86766403
|
C | T | 28 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(25): Show | 34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.854+379C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766403 | ||||||
chr2:86766405
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.854+381T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766405 | ||||||
chr2:86766516
|
T | C | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+492T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766516 | ||||||
chr2:86766525
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.854+501G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766525 | ||||||
chr2:86766537
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.854+513A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766537 | ||||||
chr2:86766597
|
G | A | 34 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(31): Show | 40 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(37): Show |
intron_variant | MODIFIER | c.854+573G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766597 | ||||||
chr2:86766633
|
C | T | 1 | a0001c0001t0036g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.854+609C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766633 | ||||||
chr2:86766647
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.854+623A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766647 | ||||||
chr2:86766651
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.854+627G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766651 | ||||||
chr2:86766661
|
C | CA | 42 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0001g0211others(39): Show | 47 | HG01074.hp1 HG01099.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.854+658dupA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | |||||
chr2:86766661
|
C | CAA | 5 | a0001c0001t0001g0188a0001c0003t0001g0013a0001c0004t0023g0055others(2): Show | 6 | HG01358.hp2 HG01884.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.854+657_854+658dup others(2): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | |||||
chr2:86766661
|
CA | C | 10 | a0001c0001t0001g0208a0001c0001t0005g0242a0001c0001t0016g0100others(7): Show | 10 | HG01070.hp1 HG01891.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.854+658delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | |||||
chr2:86766661
|
CAAAAAAA | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(26): Show | 38 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.854+652_854+658del others(7): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | |||||
chr2:86766661
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0002t0003g0070a0001c0002t0007g0237 | 2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.854+647_854+658del others(12): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86766661 | |||||
chr2:86766678
|
A | G | 1 | a0001c0002t0003g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.854+654A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766678 | ||||||
chr2:86766807
|
A | G | 1 | a0001c0002t0002g0028 | 2 | HG00733.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.854+783A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86766807 | ||||||
chr2:86767023
|
G | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(27): Show | 39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.854+999G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767023 | ||||||
chr2:86767158
|
G | A | 24 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(21): Show | 27 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.854+1134G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767158 | ||||||
chr2:86767167
|
G | A | 27 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(24): Show | 33 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.854+1143G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767167 | ||||||
chr2:86767314
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.854+1290T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767314 | ||||||
chr2:86767424
|
T | C | 1 | a0001c0002t0007g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.854+1400T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767424 | ||||||
chr2:86767425
|
C | CT | 6 | a0001c0002t0002g0028a0001c0002t0002g0110a0001c0002t0002g0234others(3): Show | 7 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+1422dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86767425 | |||||
chr2:86767425
|
CT | C | 8 | a0001c0002t0002g0111a0001c0002t0002g0215a0001c0002t0002g0221others(5): Show | 9 | HG01257.hp2 HG01943.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.854+1422delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86767425 | |||||
chr2:86767425
|
CTTTTTTT others(3): Show |
C | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.854+1413_854+1422d others(12): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86767425 | |||||
chr2:86767596
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.854+1572C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86767596 | ||||||
chr2:86768383
|
A | G | 1 | a0001c0001t0001g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.855-1640A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768383 | ||||||
chr2:86768428
|
C | T | 1 | a0001c0003t0001g0051 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.855-1595C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768428 | ||||||
chr2:86768801
|
G | T | 1 | a0001c0002t0003g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.855-1222G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768801 | ||||||
chr2:86768902
|
A | G | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.855-1121A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768902 | ||||||
chr2:86768989
|
A | G | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.855-1034A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86768989 | ||||||
chr2:86769012
|
C | T | 28 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(25): Show | 34 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.855-1011C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769012 | ||||||
chr2:86769047
|
C | T | 3 | a0001c0004t0023g0055a0001c0004t0024g0056a0001c0004t0030g0054 | 3 | HG01358.hp2 HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.855-976C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769047 | ||||||
chr2:86769305
|
A | T | 5 | a0001c0001t0012g0203a0001c0001t0012g0205a0001c0001t0026g0113others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.855-718A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769305 | ||||||
chr2:86769678
|
G | GT | 15 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(12): Show | 19 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.855-333dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86769678 | |||||
chr2:86769678
|
GT | G | 6 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(3): Show | 8 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.855-333delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 86769678 | |||||
chr2:86769725
|
A | G | 25 | a0001c0001t0016g0100a0001c0002t0003g0015a0001c0002t0003g0016others(22): Show | 28 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.855-298A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86769725 | ||||||
chr2:86770017
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG00738.hp2 HG00741.hp2 |
splice_region_variant&intron_variant | LOW | c.855-6T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 6/8 | chr2 | 86770017 | ||||||
chr2:86770193
|
T | G | 3 | a0001c0003t0001g0030a0001c0003t0001g0031a0001c0003t0001g0032 | 3 | HG02735.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.957+68T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770193 | ||||||
chr2:86770270
|
T | C | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.957+145T>C | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770270 | ||||||
chr2:86770425
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.957+300G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770425 | ||||||
chr2:86770510
|
C | T | 1 | a0001c0001t0004g0085 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.957+385C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770510 | ||||||
chr2:86770532
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.957+407G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770532 | ||||||
chr2:86770614
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.957+489C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770614 | ||||||
chr2:86770648
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.957+523C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770648 | ||||||
chr2:86770860
|
G | A | 1 | a0001c0004t0023g0055 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.958-698G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86770860 | ||||||
chr2:86771010
|
C | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0019a0001c0001t0001g0090others(11): Show | 18 | HG00642.hp1 HG01109.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.958-548C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771010 | ||||||
chr2:86771090
|
G | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.958-468G>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771090 | ||||||
chr2:86771157
|
G | A | 1 | a0001c0003t0001g0044 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.958-401G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771157 | ||||||
chr2:86771261
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0006g0026 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.958-297C>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771261 | ||||||
chr2:86771444
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG00738.hp2 HG00741.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.958-114C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771444 | ||||||
chr2:86771445
|
A | T | 1 | a0001c0001t0001g0185 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.958-113A>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771445 | ||||||
chr2:86771489
|
A | G | 1 | a0001c0005t0011g0053 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.958-69A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | chr2 | 86771489 | ||||||
chr2:86771536
|
C | CT | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.958-6dupT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 86771536 | |||||
chr2:86771536
|
CT | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
splice_region_variant&intron_variant | LOW | c.958-6delT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 86771536 | |||||
chr2:86771536
|
CTT | C | 9 | a0001c0001t0001g0145a0001c0001t0001g0168a0001c0001t0004g0084others(6): Show | 9 | HG01891.hp2 HG02818.hp2 HG02922.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.958-7_958-6delTT | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 86771536 | |||||
chr2:86771749
|
A | G | 4 | a0001c0004t0008g0029a0001c0004t0008g0248a0001c0004t0008g0249others(1): Show | 5 | HG01167.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112+37A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86771749 | ||||||
chr2:86771759
|
G | A | 1 | a0001c0004t0025g0060 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1112+47G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86771759 | ||||||
chr2:86771818
|
CTAAA | C | 27 | a0001c0003t0001g0002a0001c0003t0001g0011a0001c0003t0001g0012others(24): Show | 33 | HG01099.hp2 HG01109.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.1112+112_1112+115d others(6): Show |
RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 86771818 | |||||
chr2:86772021
|
G | A | 1 | a0001c0002t0002g0236 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1112+309G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772021 | ||||||
chr2:86772048
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1112+336C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772048 | ||||||
chr2:86772168
|
G | A | 1 | a0001c0004t0022g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1112+456G>A | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772168 | ||||||
chr2:86772224
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1112+512C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772224 | ||||||
chr2:86772311
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1112+599C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772311 | ||||||
chr2:86772323
|
C | T | 1 | a0001c0002t0035g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1112+611C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772323 | ||||||
chr2:86772379
|
C | T | 5 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(2): Show | 6 | HG01167.hp1 HG02109.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+667C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772379 | ||||||
chr2:86772695
|
A | G | 2 | a0001c0002t0002g0110a0001c0002t0002g0111 | 2 | NA18960.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1113-653A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772695 | ||||||
chr2:86772739
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(99): Show | 117 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1113-609C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772739 | ||||||
chr2:86772752
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.1113-596A>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772752 | ||||||
chr2:86772877
|
CA | C | 7 | a0001c0002t0034g0112a0001c0004t0008g0029a0001c0004t0008g0248others(4): Show | 9 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1113-467delA | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 86772877 | |||||
chr2:86772999
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1113-349C>T | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86772999 | ||||||
chr2:86773264
|
T | G | 24 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0017others(21): Show | 27 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1113-84T>G | RMND5A | ENSG00000153561.13 | transcript | ENST00000283632.5 | protein_coding | 8/8 | chr2 | 86773264 |