geneid | 80210 |
---|---|
ensemblid | ENSG00000135931.19 |
hgncid | 20730 |
symbol | ARMC9 |
name | armadillo repeat containing 9 |
refseq_nuc | NM_001352754.2 |
refseq_prot | NP_001339683.2 |
ensembl_nuc | ENST00000611582.5 |
ensembl_prot | ENSP00000484804.1 |
mane_status | MANE Select |
chr | chr2 |
start | 231198631 |
end | 231376848 |
strand | + |
ver | v1.2 |
region | chr2:231198631-231376848 |
region5000 | chr2:231193631-231381848 |
regionname0 | ARMC9_chr2_231198631_231376848 |
regionname5000 | ARMC9_chr2_231193631_231381848 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 818 | 192 | 3 | 40 | 105 | 10 | 33 | 73 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0002 | 0/0 | 818 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0003 | 0/0 | 818 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0004 | 0/0 | 818 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0005 | 0/0 | 818 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0006 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0007 | 1/0 | 818 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
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 | 2457 | 110 | 2 | 19 | 67 | 3 | 18 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0002 | 0/0 | 2457 | 40 | 1 | 10 | 18 | 2 | 9 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0003 | 0/0 | 2457 | 25 | 0 | 4 | 14 | 4 | 3 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0004 | 0/0 | 2457 | 14 | 0 | 6 | 5 | 1 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0005 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0006 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0007 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0008 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0009 | 1/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0010 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0011 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0012 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0013 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0014 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
c0015 | 0/0 | 2457 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5416 | 32 | 0 | 7 | 16 | 2 | 7 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0002 | 0/0 | 5409 | 23 | 0 | 3 | 14 | 1 | 5 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0003 | 0/0 | 5411 | 10 | 1 | 3 | 5 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0004 | 0/0 | 5423 | 9 | 0 | 1 | 8 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0005 | 0/0 | 5425 | 8 | 0 | 0 | 8 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0006 | 0/0 | 5418 | 7 | 0 | 2 | 3 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0007 | 0/0 | 5412 | 6 | 0 | 3 | 1 | 1 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0008 | 0/0 | 5427 | 6 | 0 | 0 | 6 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0009 | 0/0 | 5431 | 6 | 0 | 0 | 6 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0010 | 0/0 | 5417 | 5 | 0 | 1 | 2 | 1 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0011 | 0/0 | 5421 | 5 | 0 | 1 | 2 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0012 | 0/0 | 5403 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0013 | 0/0 | 5410 | 4 | 0 | 1 | 0 | 1 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0014 | 0/0 | 5417 | 4 | 1 | 1 | 0 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0015 | 0/0 | 5414 | 3 | 0 | 1 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0016 | 0/0 | 5416 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0017 | 0/0 | 5420 | 3 | 0 | 1 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0018 | 0/0 | 5429 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0019 | 0/0 | 5423 | 3 | 0 | 0 | 1 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0020 | 0/0 | 5390 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0021 | 0/0 | 5407 | 2 | 0 | 0 | 0 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0022 | 0/0 | 5413 | 2 | 0 | 0 | 1 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0023 | 0/0 | 5415 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0024 | 0/0 | 5419 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0025 | 0/0 | 5421 | 2 | 0 | 1 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0026 | 1/0 | 5423 | 2 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0027 | 0/0 | 5425 | 2 | 0 | 0 | 0 | 1 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0028 | 0/0 | 5429 | 2 | 0 | 1 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0029 | 0/0 | 5421 | 2 | 0 | 0 | 0 | 1 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0030 | 0/0 | 5433 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0031 | 0/0 | 5426 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0032 | 0/0 | 5423 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0033 | 0/0 | 5425 | 2 | 1 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0034 | 0/0 | 5418 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0035 | 0/0 | 5420 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0036 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0037 | 0/0 | 5409 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0038 | 0/0 | 5408 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0039 | 0/0 | 5415 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0040 | 0/0 | 5414 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0041 | 0/0 | 5416 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0042 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0043 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0044 | 0/0 | 5423 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0045 | 0/0 | 5422 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0046 | 0/0 | 5424 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0047 | 0/0 | 5427 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0048 | 0/0 | 5427 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0049 | 0/0 | 5426 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0050 | 0/0 | 5433 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0051 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0052 | 0/0 | 5441 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0053 | 0/1 | 5395 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0054 | 0/0 | 5413 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0055 | 0/0 | 5415 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0056 | 0/0 | 5419 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0057 | 0/0 | 5423 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0058 | 0/0 | 5425 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0059 | 0/0 | 5395 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0060 | 0/0 | 5395 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
t0061 | 0/0 | 5425 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
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 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
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 | 2457 | 110 | 2 | 19 | 67 | 3 | 18 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002 | 0/0 | 2457 | 40 | 1 | 10 | 18 | 2 | 9 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003 | 0/0 | 2457 | 25 | 0 | 4 | 14 | 4 | 3 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004 | 0/0 | 2457 | 14 | 0 | 6 | 5 | 1 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0008 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0012 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0015 | 0/0 | 2457 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0002c0005 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0002c0006 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0003c0010 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0003c0011 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0004c0014 | 0/0 | 2457 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0005c0013 | 0/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0006c0007 | 0/0 | 2457 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0007c0009 | 1/0 | 2457 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7872 | 25 | 0 | 6 | 11 | 1 | 7 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0002 | 0/0 | 7865 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0003 | 0/0 | 7867 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0004 | 0/0 | 7879 | 8 | 0 | 0 | 8 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0005 | 0/0 | 7881 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0006 | 0/0 | 7874 | 6 | 0 | 2 | 2 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0007 | 0/0 | 7868 | 4 | 0 | 3 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0008 | 0/0 | 7883 | 5 | 0 | 0 | 5 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0009 | 0/0 | 7887 | 6 | 0 | 0 | 6 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0010 | 0/0 | 7873 | 4 | 0 | 1 | 2 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0011 | 0/0 | 7877 | 3 | 0 | 1 | 0 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0013 | 0/0 | 7866 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0014 | 0/0 | 7873 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0015 | 0/0 | 7870 | 3 | 0 | 1 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0016 | 0/0 | 7872 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0017 | 0/0 | 7876 | 3 | 0 | 1 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0018 | 0/0 | 7885 | 3 | 0 | 0 | 3 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0019 | 0/0 | 7879 | 3 | 0 | 0 | 1 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0020 | 0/0 | 7846 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0023 | 0/0 | 7871 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0029 | 0/0 | 7877 | 2 | 0 | 0 | 0 | 1 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0030 | 0/0 | 7889 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0031 | 0/0 | 7882 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0032 | 0/0 | 7879 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0033 | 0/0 | 7881 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0034 | 0/0 | 7874 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0038 | 0/0 | 7864 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0039 | 0/0 | 7871 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0040 | 0/0 | 7870 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0041 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0045 | 0/0 | 7878 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0046 | 0/0 | 7880 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0050 | 0/0 | 7889 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0052 | 0/0 | 7897 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0053 | 0/1 | 7851 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0054 | 0/0 | 7869 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0055 | 0/0 | 7871 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0056 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0057 | 0/0 | 7879 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0058 | 0/0 | 7881 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0001t0061 | 0/0 | 7881 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0002 | 0/0 | 7865 | 15 | 0 | 2 | 8 | 1 | 4 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0003 | 0/0 | 7867 | 7 | 1 | 3 | 2 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0006 | 0/0 | 7874 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0011 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0012 | 0/0 | 7859 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0014 | 0/0 | 7873 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0016 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0021 | 0/0 | 7863 | 2 | 0 | 0 | 0 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0022 | 0/0 | 7869 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0023 | 0/0 | 7871 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0025 | 0/0 | 7877 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0027 | 0/0 | 7881 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0028 | 0/0 | 7885 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0032 | 0/0 | 7879 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0033 | 0/0 | 7881 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0047 | 0/0 | 7883 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0051 | 0/0 | 7893 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0002t0060 | 0/0 | 7851 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0001 | 0/0 | 7872 | 5 | 0 | 1 | 3 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0003 | 0/0 | 7867 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0004 | 0/0 | 7879 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0005 | 0/0 | 7881 | 4 | 0 | 0 | 4 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0007 | 0/0 | 7868 | 2 | 0 | 0 | 1 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0010 | 0/0 | 7873 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0012 | 0/0 | 7859 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0013 | 0/0 | 7866 | 2 | 0 | 0 | 0 | 0 | 2 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0020 | 0/0 | 7846 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0022 | 0/0 | 7869 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0025 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0030 | 0/0 | 7889 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0035 | 0/0 | 7876 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0037 | 0/0 | 7865 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0044 | 0/0 | 7879 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0003t0049 | 0/0 | 7882 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0002 | 0/0 | 7865 | 3 | 0 | 1 | 1 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0003 | 0/0 | 7867 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0011 | 0/0 | 7877 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0012 | 0/0 | 7859 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0013 | 0/0 | 7866 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0014 | 0/0 | 7873 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0024 | 0/0 | 7875 | 2 | 0 | 2 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0028 | 0/0 | 7885 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0036 | 0/0 | 7861 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0042 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0004t0043 | 0/0 | 7875 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0008t0027 | 0/0 | 7881 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0012t0048 | 0/0 | 7883 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0001c0015t0059 | 0/0 | 7851 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0002c0005t0008 | 0/0 | 7883 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0002c0006t0002 | 0/0 | 7865 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0003c0010t0001 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0003c0011t0002 | 0/0 | 7865 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0004c0014t0001 | 0/0 | 7872 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0005c0013t0026 | 0/0 | 7879 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0006c0007t0014 | 0/0 | 7873 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
a0007c0009t0026 | 1/0 | 7879 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | copy fasta | chr2 | 231193631 | 231381848 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0007g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0009g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0010g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0011g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0013g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0014g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0015g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0015g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0016g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0016g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0017g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0017g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0017g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0018g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0018g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0019g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0019g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0019g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0020g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0023g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0029g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0029g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0030g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0031g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0031g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0032g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0033g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0034g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0038g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0039g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0040g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0041g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0045g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0046g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0050g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0052g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0053g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0054g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0055g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0056g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0057g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0058g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0001t0061g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0011g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0012g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0014g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0016g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0021g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0021g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0022g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0023g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0025g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0027g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0028g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0032g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0033g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0047g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0051g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0002t0060g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0010g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0012g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0013g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0013g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0020g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0022g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0025g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0030g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0035g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0037g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0044g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0003t0049g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0011g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0012g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0013g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0014g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0024g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0024g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0028g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0036g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0042g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0004t0043g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0008t0027g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0012t0048g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0001c0015t0059g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0002c0005t0008g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0002c0006t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0003c0010t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0003c0011t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0004c0014t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0005c0013t0026g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0006c0007t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
a0007c0009t0026g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0004 | t0013 | g0004 | EUR | FIN | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00280 | hp2 | a0001 | c0003 | t0010 | g0038 | EUR | FIN | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0098 | EUR | FIN | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00323 | hp2 | a0001 | c0003 | t0007 | g0028 | EUR | FIN | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00408 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00408 | hp2 | a0001 | c0001 | t0010 | g0187 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00438 | hp2 | a0001 | c0001 | t0041 | g0152 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00544 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00544 | hp2 | a0001 | c0001 | t0009 | g0103 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00558 | hp1 | a0004 | c0014 | t0001 | g0093 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00558 | hp2 | a0001 | c0001 | t0008 | g0122 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00621 | hp1 | a0001 | c0001 | t0052 | g0131 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00621 | hp2 | a0001 | c0001 | t0050 | g0040 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00639 | hp2 | a0001 | c0002 | t0023 | g0084 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00673 | hp2 | a0001 | c0002 | t0003 | g0185 | EAS | CHS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00735 | hp1 | a0001 | c0002 | t0047 | g0080 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0196 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00738 | hp2 | a0001 | c0001 | t0013 | g0051 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0085 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01069 | hp1 | a0001 | c0004 | t0042 | g0035 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01069 | hp2 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01070 | hp1 | a0001 | c0004 | t0024 | g0002 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01070 | hp2 | a0001 | c0001 | t0017 | g0127 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01071 | hp1 | a0001 | c0004 | t0024 | g0016 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01071 | hp2 | a0001 | c0001 | t0007 | g0047 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01074 | hp1 | a0001 | c0001 | t0011 | g0048 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01074 | hp2 | a0001 | c0002 | t0025 | g0095 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01081 | hp1 | a0001 | c0015 | t0059 | g0104 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01081 | hp2 | a0001 | c0003 | t0035 | g0027 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01168 | hp1 | a0001 | c0004 | t0002 | g0012 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01168 | hp2 | a0001 | c0001 | t0010 | g0063 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01175 | hp1 | a0001 | c0002 | t0014 | g0056 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01258 | hp1 | a0001 | c0001 | t0054 | g0197 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01346 | hp2 | a0001 | c0002 | t0060 | g0096 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01361 | hp1 | a0001 | c0003 | t0004 | g0032 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01433 | hp1 | a0001 | c0004 | t0028 | g0014 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | CLM | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01515 | hp1 | a0001 | c0003 | t0037 | g0003 | EUR | IBS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01515 | hp2 | a0001 | c0001 | t0029 | g0049 | EUR | IBS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0005 | EUR | IBS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01943 | hp1 | a0001 | c0002 | t0003 | g0160 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01943 | hp2 | a0001 | c0001 | t0045 | g0050 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01978 | hp1 | a0001 | c0001 | t0034 | g0061 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01978 | hp2 | a0001 | c0001 | t0015 | g0060 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01981 | hp1 | a0001 | c0003 | t0044 | g0020 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0057 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0180 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG01993 | hp2 | a0001 | c0004 | t0043 | g0034 | AMR | PEL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02015 | hp1 | a0001 | c0004 | t0036 | g0039 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0140 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02027 | hp1 | a0001 | c0001 | t0058 | g0199 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02027 | hp2 | a0003 | c0010 | t0001 | g0108 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02074 | hp2 | a0001 | c0001 | t0018 | g0192 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02080 | hp1 | a0001 | c0001 | t0040 | g0128 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02080 | hp2 | a0001 | c0002 | t0006 | g0191 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02135 | hp1 | a0001 | c0001 | t0017 | g0141 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02155 | hp1 | a0002 | c0005 | t0008 | g0010 | EAS | CDX | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02155 | hp2 | a0001 | c0001 | t0016 | g0134 | EAS | CDX | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02165 | hp1 | a0001 | c0002 | t0011 | g0170 | EAS | CDX | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02165 | hp2 | a0003 | c0011 | t0002 | g0089 | EAS | CDX | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02257 | hp1 | a0006 | c0007 | t0014 | g0018 | AFR | ACB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02257 | hp2 | a0001 | c0001 | t0033 | g0157 | AFR | ACB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02523 | hp1 | a0001 | c0002 | t0033 | g0172 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02523 | hp2 | a0001 | c0001 | t0019 | g0097 | EAS | KHV | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02602 | hp1 | a0001 | c0001 | t0019 | g0067 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0066 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0070 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02738 | hp1 | a0001 | c0003 | t0013 | g0001 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG02738 | hp2 | a0001 | c0001 | t0011 | g0165 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03017 | hp2 | a0001 | c0003 | t0013 | g0011 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03490 | hp1 | a0001 | c0002 | t0028 | g0163 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0159 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03491 | hp2 | a0001 | c0003 | t0049 | g0008 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0167 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03654 | hp1 | a0001 | c0001 | t0061 | g0130 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03654 | hp2 | a0001 | c0002 | t0021 | g0064 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0094 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03704 | hp1 | a0005 | c0013 | t0026 | g0077 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03704 | hp2 | a0001 | c0002 | t0021 | g0107 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03710 | hp1 | a0001 | c0001 | t0029 | g0194 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03834 | hp2 | a0001 | c0004 | t0002 | g0026 | SAS | BEB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03927 | hp1 | a0001 | c0004 | t0014 | g0019 | SAS | BEB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03927 | hp2 | a0001 | c0001 | t0014 | g0118 | SAS | BEB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03942 | hp1 | a0001 | c0002 | t0022 | g0145 | SAS | BEB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG03942 | hp2 | a0001 | c0001 | t0019 | g0052 | SAS | BEB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG04115 | hp1 | a0001 | c0001 | t0011 | g0120 | SAS | STU | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0115 | SAS | STU | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
HG04228 | hp2 | a0001 | c0008 | t0027 | g0017 | SAS | STU | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | CHB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0114 | EAS | CHB | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18943 | hp1 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18944 | hp1 | a0001 | c0003 | t0005 | g0029 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18944 | hp2 | a0001 | c0003 | t0020 | g0055 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18945 | hp1 | a0001 | c0001 | t0031 | g0166 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18945 | hp2 | a0001 | c0001 | t0031 | g0062 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18950 | hp1 | a0001 | c0002 | t0012 | g0139 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18950 | hp2 | a0001 | c0001 | t0023 | g0164 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0153 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18951 | hp2 | a0001 | c0003 | t0025 | g0009 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18957 | hp1 | a0001 | c0001 | t0015 | g0083 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18957 | hp2 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18963 | hp1 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18963 | hp2 | a0001 | c0002 | t0032 | g0177 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18964 | hp1 | a0001 | c0001 | t0016 | g0146 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18965 | hp1 | a0001 | c0001 | t0009 | g0041 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18965 | hp2 | a0002 | c0006 | t0002 | g0021 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18969 | hp1 | a0001 | c0002 | t0016 | g0123 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18969 | hp2 | a0001 | c0001 | t0056 | g0200 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18970 | hp1 | a0001 | c0001 | t0032 | g0111 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18979 | hp1 | a0001 | c0001 | t0009 | g0100 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18979 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18981 | hp1 | a0001 | c0001 | t0017 | g0121 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18981 | hp2 | a0001 | c0001 | t0008 | g0183 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18983 | hp2 | a0001 | c0001 | t0015 | g0150 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18984 | hp2 | a0001 | c0001 | t0018 | g0136 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18993 | hp1 | a0001 | c0001 | t0057 | g0125 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18995 | hp1 | a0001 | c0002 | t0012 | g0088 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18995 | hp2 | a0001 | c0001 | t0018 | g0137 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18997 | hp1 | a0001 | c0004 | t0011 | g0110 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18997 | hp2 | a0001 | c0003 | t0022 | g0024 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18998 | hp1 | a0001 | c0003 | t0005 | g0006 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA18998 | hp2 | a0001 | c0004 | t0003 | g0030 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19002 | hp1 | a0001 | c0003 | t0030 | g0036 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19005 | hp1 | a0001 | c0004 | t0012 | g0007 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19005 | hp2 | a0001 | c0003 | t0005 | g0031 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19011 | hp2 | a0001 | c0001 | t0010 | g0162 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19012 | hp2 | a0001 | c0001 | t0030 | g0132 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19056 | hp1 | a0001 | c0003 | t0012 | g0015 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19056 | hp2 | a0001 | c0002 | t0051 | g0147 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19070 | hp1 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19070 | hp2 | a0001 | c0001 | t0046 | g0173 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19074 | hp2 | a0001 | c0003 | t0007 | g0025 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19081 | hp1 | a0001 | c0001 | t0009 | g0144 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19081 | hp2 | a0001 | c0001 | t0055 | g0193 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19082 | hp1 | a0001 | c0004 | t0002 | g0109 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19082 | hp2 | a0001 | c0012 | t0048 | g0156 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19088 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19090 | hp1 | a0001 | c0003 | t0005 | g0042 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA19090 | hp2 | a0001 | c0001 | t0020 | g0092 | EAS | JPT | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA20752 | hp1 | a0001 | c0002 | t0027 | g0117 | EUR | TSI | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA20752 | hp2 | a0001 | c0001 | t0038 | g0154 | EUR | TSI | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA20905 | hp1 | a0001 | c0001 | t0010 | g0186 | SAS | GIH | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0071 | SAS | GIH | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA21309 | hp1 | a0001 | c0002 | t0003 | g0155 | AFR | LWK | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
NA21309 | hp2 | a0001 | c0001 | t0039 | g0119 | AFR | LWK | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0053 | g0116 | REF | REF | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
homoSapiens_grch38 | hp1 | a0007 | c0009 | t0026 | g0086 | REF | REF | ARMC9_chr2_231193631_231381848 | ARMC9 | chr2 | 231193631 | 231381848 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231222761
|
A | G | 6 | a0001a0002a0003others(3): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
missense_variant | MODERATE | c.538A>G | p.Ile180Val | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/25 | 647/7879 | 538/2457 | 180/818 | chr2 | 231222761 | ||
chr2:231222762
|
T | A | 6 | a0001a0002a0003others(3): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
missense_variant | MODERATE | c.539T>A | p.Ile180Lys | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/25 | 648/7879 | 539/2457 | 180/818 | chr2 | 231222762 | ||
chr2:231235266
|
G | A | 1 | a0002 | 2 | HG02155.hp1 NA18965.hp2 |
missense_variant | MODERATE | c.665G>A | p.Arg222His | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/25 | 774/7879 | 665/2457 | 222/818 | chr2 | 231235266 | ||
chr2:231271015
|
G | A | 1 | a0003 | 2 | HG02027.hp2 HG02165.hp2 |
missense_variant | MODERATE | c.1153G>A | p.Asp385Asn | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/25 | 1262/7879 | 1153/2457 | 385/818 | chr2 | 231271015 | ||
chr2:231271067
|
C | T | 1 | a0006 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1205C>T | p.Ala402Val | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/25 | 1314/7879 | 1205/2457 | 402/818 | chr2 | 231271067 | ||
chr2:231291443
|
G | A | 1 | a0005 | 1 | HG03704.hp1 | missense_variant&splice_region_variant | MODERATE | c.1717G>A | p.Glu573Lys | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/25 | 1826/7879 | 1717/2457 | 573/818 | chr2 | 231291443 | ||
chr2:231360835
|
G | A | 1 | a0004 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.2213G>A | p.Arg738His | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/25 | 2322/7879 | 2213/2457 | 738/818 | chr2 | 231360835 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231208199
|
T | C | 6 | a0001c0003a0001c0004a0001c0008others(3): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
synonymous_variant | LOW | c.124T>C | p.Leu42Leu | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/25 | 233/7879 | 124/2457 | 42/818 | chr2 | 231208199 | ||
chr2:231208216
|
C | T | 1 | a0001c0008 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.141C>T | p.Gly47Gly | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/25 | 250/7879 | 141/2457 | 47/818 | chr2 | 231208216 | ||
chr2:231271029
|
G | A | 1 | a0001c0012 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.1167G>A | p.Gln389Gln | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/25 | 1276/7879 | 1167/2457 | 389/818 | chr2 | 231271029 | ||
chr2:231331852
|
C | T | 7 | a0001c0002a0001c0004a0001c0008others(4): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
synonymous_variant | LOW | c.1833C>T | p.Leu611Leu | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/25 | 1942/7879 | 1833/2457 | 611/818 | chr2 | 231331852 | ||
chr2:231331885
|
G | A | 7 | a0001c0002a0001c0004a0001c0008others(4): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
synonymous_variant | LOW | c.1866G>A | p.Thr622Thr | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/25 | 1975/7879 | 1866/2457 | 622/818 | chr2 | 231331885 | ||
chr2:231360851
|
G | A | 1 | a0001c0015 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.2229G>A | p.Ala743Ala | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/25 | 2338/7879 | 2229/2457 | 743/818 | chr2 | 231360851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231371560
|
C | T | 1 | a0001c0001t0061 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 25 | chr2 | 231371560 | |||||
chr2:231371728
|
A | G | 2 | a0001c0002t0060a0001c0015t0059 | 2 | HG01081.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*193A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 193 | chr2 | 231371728 | |||||
chr2:231371810
|
C | T | 16 | a0001c0001t0010a0001c0001t0011a0001c0001t0019others(13): Show | 23 | HG00280.hp2 HG00408.hp2 HG01074.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*275C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 275 | chr2 | 231371810 | |||||
chr2:231371916
|
A | G | 36 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(33): Show | 69 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*381A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 381 | chr2 | 231371916 | |||||
chr2:231372356
|
G | A | 2 | a0001c0001t0034a0001c0003t0035 | 2 | HG01081.hp2 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*821G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 821 | chr2 | 231372356 | |||||
chr2:231372699
|
G | GGT | 9 | a0001c0001t0005a0001c0001t0033a0001c0001t0046others(6): Show | 15 | HG02015.hp2 HG02027.hp1 HG02257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1219_*1220dupGT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
G | GGTGT | 5 | a0001c0001t0008a0001c0002t0047a0001c0003t0049others(2): Show | 9 | HG00558.hp2 HG00735.hp1 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1217_*1220dupGTGT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
G | GGTGTGT | 3 | a0001c0001t0018a0001c0002t0028a0001c0004t0028 | 5 | HG01433.hp1 HG02074.hp2 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1215_*1220dupGTGT others(2): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
G | GGTGTGTG others(1): Show |
1 | a0001c0001t0009 | 6 | HG00544.hp1 HG00544.hp2 NA18943.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1213_*1220dupGTGT others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
G | GGTGTGTG others(3): Show |
3 | a0001c0001t0030a0001c0001t0050a0001c0003t0030 | 3 | HG00621.hp2 NA19002.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1211_*1220dupGTGT others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
G | GGTGTGTG others(7): Show |
1 | a0001c0002t0051 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1207_*1220dupGTGT others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
G | GGTGTGTG others(11): Show |
1 | a0001c0001t0052 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1203_*1220dupGTGT others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1221 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
G | GTGT | 1 | a0001c0001t0031 | 2 | NA18945.hp1 NA18945.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1164_*1165insTGT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1165 | chr2 | 231372699 | |||||
chr2:231372699
|
GGT | G | 8 | a0001c0001t0011a0001c0001t0017a0001c0001t0029others(5): Show | 13 | HG01070.hp2 HG01074.hp1 HG01074.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1219_*1220delGT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1219 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGT | G | 7 | a0001c0001t0006a0001c0001t0034a0001c0001t0056others(4): Show | 13 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1217_*1220delGTGT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1217 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGT | G | 13 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(10): Show | 45 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1215_*1220delGTGT others(2): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1215 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(1): Show |
G | 6 | a0001c0001t0015a0001c0001t0023a0001c0001t0039others(3): Show | 8 | HG00639.hp2 HG01978.hp2 HG02080.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1213_*1220delGTGT others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1213 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(3): Show |
G | 5 | a0001c0001t0007a0001c0001t0054a0001c0002t0022others(2): Show | 9 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1211_*1220delGTGT others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1211 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(5): Show |
G | 7 | a0001c0001t0003a0001c0001t0013a0001c0002t0003others(4): Show | 14 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1209_*1220delGTGT others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1209 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(7): Show |
G | 10 | a0001c0001t0002a0001c0001t0038a0001c0002t0002others(7): Show | 29 | HG00323.hp1 HG00423.hp1 HG00738.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1220delGTGT others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1207 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(9): Show |
G | 1 | a0001c0002t0021 | 2 | HG03654.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1205_*1220delGTGT others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1205 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0004t0036 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1203_*1220delGTGT others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1203 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(21): Show |
G | 1 | a0001c0001t0053 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1193_*1220delGTGT others(24): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1193 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372699
|
GGTGTGTG others(25): Show |
G | 2 | a0001c0001t0020a0001c0003t0020 | 2 | NA18944.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1189_*1220delGTGT others(28): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1189 | INFO_REALIGN_3_PRIME | chr2 | 231372699 | ||||
chr2:231372731
|
TGTGTGTG others(21): Show |
T | 2 | a0001c0002t0060a0001c0015t0059 | 2 | HG01081.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1201_*1228delGTGT others(24): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1201 | INFO_REALIGN_3_PRIME | chr2 | 231372731 | ||||
chr2:231373015
|
G | C | 1 | a0001c0003t0044 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1480G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1480 | chr2 | 231373015 | |||||
chr2:231373120
|
C | T | 1 | a0001c0001t0040 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1585C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1585 | chr2 | 231373120 | |||||
chr2:231373412
|
G | A | 1 | a0001c0015t0059 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1877G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 1877 | chr2 | 231373412 | |||||
chr2:231373807
|
G | A | 1 | a0001c0001t0050 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2272G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 2272 | chr2 | 231373807 | |||||
chr2:231373893
|
G | A | 2 | a0001c0001t0020a0001c0003t0020 | 2 | NA18944.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2358G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 2358 | chr2 | 231373893 | |||||
chr2:231373895
|
CA | C | 25 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(22): Show | 68 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2376delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 2376 | INFO_REALIGN_3_PRIME | chr2 | 231373895 | ||||
chr2:231373912
|
T | A | 4 | a0001c0001t0032a0001c0001t0058a0001c0002t0032others(1): Show | 4 | HG02027.hp1 NA18963.hp2 NA18970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2377T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 2377 | chr2 | 231373912 | |||||
chr2:231374482
|
G | A | 1 | a0001c0004t0042 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2947G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 2947 | chr2 | 231374482 | |||||
chr2:231374675
|
C | G | 1 | a0001c0001t0057 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3140C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 3140 | chr2 | 231374675 | |||||
chr2:231374688
|
T | G | 2 | a0001c0001t0016a0001c0002t0016 | 3 | HG02155.hp2 NA18964.hp1 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3153T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 3153 | chr2 | 231374688 | |||||
chr2:231374863
|
A | C | 1 | a0001c0001t0041 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3328A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 3328 | chr2 | 231374863 | |||||
chr2:231375278
|
A | C | 1 | a0001c0001t0053 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3743A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 3743 | chr2 | 231375278 | |||||
chr2:231375336
|
G | A | 1 | a0001c0012t0048 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3801G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 3801 | chr2 | 231375336 | |||||
chr2:231375371
|
TGGCCAA | T | 3 | a0001c0002t0012a0001c0003t0012a0001c0004t0012 | 4 | NA18950.hp1 NA18995.hp1 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3841_*3846delAAGG others(2): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 3841 | INFO_REALIGN_3_PRIME | chr2 | 231375371 | ||||
chr2:231376281
|
T | C | 2 | a0001c0002t0060a0001c0015t0059 | 2 | HG01081.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4746T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 4746 | chr2 | 231376281 | |||||
chr2:231376588
|
A | G | 1 | a0001c0003t0037 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5053A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 5053 | chr2 | 231376588 | |||||
chr2:231376600
|
C | G | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(14): Show | 43 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5065C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 5065 | chr2 | 231376600 | |||||
chr2:231376826
|
C | T | 4 | a0001c0001t0039a0001c0003t0044a0001c0004t0042others(1): Show | 4 | HG01069.hp1 HG01981.hp1 HG01993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5291C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 25/25 | 5291 | chr2 | 231376826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:231198788
|
C | G | 43 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-42+90C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231198788 | ||||||
chr2:231198814
|
A | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-42+116A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231198814 | ||||||
chr2:231198852
|
C | G | 37 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.-42+154C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231198852 | ||||||
chr2:231198864
|
G | A | 39 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.-42+166G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231198864 | ||||||
chr2:231198976
|
T | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-42+278T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231198976 | ||||||
chr2:231199000
|
A | G | 41 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-42+302A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199000 | ||||||
chr2:231199176
|
C | T | 1 | a0001c0001t0014g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-42+478C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199176 | ||||||
chr2:231199183
|
G | A | 1 | a0001c0001t0011g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-42+485G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199183 | ||||||
chr2:231199232
|
T | C | 40 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.-42+534T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199232 | ||||||
chr2:231199238
|
A | G | 1 | a0001c0001t0056g0200 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-42+540A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199238 | ||||||
chr2:231199283
|
A | T | 40 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.-42+585A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199283 | ||||||
chr2:231199468
|
G | A | 28 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-42+770G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199468 | ||||||
chr2:231199738
|
C | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-42+1040C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199738 | ||||||
chr2:231199743
|
T | C | 1 | a0001c0001t0050g0040 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-42+1045T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231199743 | ||||||
chr2:231200027
|
A | G | 80 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.-42+1329A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200027 | ||||||
chr2:231200145
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-42+1447G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200145 | ||||||
chr2:231200250
|
G | T | 37 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.-42+1552G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200250 | ||||||
chr2:231200253
|
C | A | 40 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.-42+1555C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200253 | ||||||
chr2:231200263
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-42+1565G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200263 | ||||||
chr2:231200593
|
G | A | 40 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.-42+1895G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200593 | ||||||
chr2:231200675
|
A | AAACAACA others(2): Show |
41 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-42+1985_-42+1986i others(11): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231200675 | |||||
chr2:231200746
|
A | G | 39 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.-42+2048A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200746 | ||||||
chr2:231200757
|
C | T | 1 | a0001c0002t0027g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-42+2059C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231200757 | ||||||
chr2:231200842
|
G | GA | 5 | a0001c0001t0009g0041a0001c0001t0017g0121a0001c0002t0002g0043others(2): Show | 5 | HG02074.hp1 HG02738.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+2158dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231200842 | |||||
chr2:231201151
|
G | C | 41 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-42+2453G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231201151 | ||||||
chr2:231201549
|
G | T | 1 | a0001c0003t0007g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-42+2851G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231201549 | ||||||
chr2:231201938
|
T | C | 131 | a0001c0001t0001g0046a0001c0001t0001g0126a0001c0001t0001g0129others(128): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-42+3240T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231201938 | ||||||
chr2:231201991
|
T | G | 41 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-42+3293T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231201991 | ||||||
chr2:231202003
|
CT | C | 90 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(87): Show | 90 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-42+3321delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231202003 | |||||
chr2:231202003
|
CTT | C | 33 | a0001c0001t0010g0162a0001c0001t0033g0157a0001c0002t0002g0159others(30): Show | 33 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-42+3320_-42+3321d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231202003 | |||||
chr2:231202008
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-42+3310T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231202008 | ||||||
chr2:231202161
|
G | A | 39 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.-42+3463G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231202161 | ||||||
chr2:231202319
|
C | CT | 15 | a0001c0001t0001g0046a0001c0001t0002g0198a0001c0001t0007g0045others(12): Show | 15 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.-42+3642dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231202319 | |||||
chr2:231202319
|
CT | C | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0008g0122others(6): Show | 9 | HG00323.hp2 HG00558.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42+3642delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231202319 | |||||
chr2:231202384
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-42+3686G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231202384 | ||||||
chr2:231202661
|
C | T | 1 | a0001c0002t0002g0043 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-41-3537C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231202661 | ||||||
chr2:231203685
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41-2513C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231203685 | ||||||
chr2:231203828
|
C | T | 40 | a0001c0002t0002g0115a0001c0003t0001g0005a0001c0003t0001g0013others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.-41-2370C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231203828 | ||||||
chr2:231203978
|
A | C | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-41-2220A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231203978 | ||||||
chr2:231204176
|
G | GA | 8 | a0001c0001t0004g0059a0001c0001t0006g0057a0001c0001t0014g0118others(5): Show | 8 | HG01175.hp1 HG01361.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41-2001dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231204176 | |||||
chr2:231204176
|
GA | G | 44 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.-41-2001delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231204176 | |||||
chr2:231204176
|
GAA | G | 74 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(71): Show | 74 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-41-2002_-41-2001d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr2 | 231204176 | |||||
chr2:231204238
|
G | C | 1 | a0001c0001t0031g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-41-1960G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231204238 | ||||||
chr2:231204370
|
T | G | 39 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.-41-1828T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231204370 | ||||||
chr2:231204408
|
G | A | 37 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.-41-1790G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231204408 | ||||||
chr2:231204440
|
T | C | 1 | a0001c0002t0014g0056 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-41-1758T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231204440 | ||||||
chr2:231204949
|
G | A | 1 | a0001c0001t0010g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-41-1249G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231204949 | ||||||
chr2:231205138
|
C | T | 1 | a0001c0001t0008g0114 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-41-1060C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231205138 | ||||||
chr2:231206179
|
T | C | 1 | a0001c0002t0021g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-41-19T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231206179 | ||||||
chr2:231206193
|
T | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.-41-5T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 1/24 | chr2 | 231206193 | ||||||
chr2:231206487
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.51+198C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231206487 | ||||||
chr2:231206522
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.51+233G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231206522 | ||||||
chr2:231206797
|
C | T | 1 | a0001c0001t0019g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.51+508C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231206797 | ||||||
chr2:231206919
|
G | A | 1 | a0001c0001t0006g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.51+630G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231206919 | ||||||
chr2:231206969
|
G | A | 80 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.51+680G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231206969 | ||||||
chr2:231207149
|
C | T | 2 | a0001c0002t0002g0043a0001c0002t0002g0112 | 2 | HG02074.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.51+860C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231207149 | ||||||
chr2:231207633
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.52-494G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231207633 | ||||||
chr2:231207664
|
C | T | 2 | a0001c0001t0031g0062a0001c0001t0032g0111 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.52-463C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231207664 | ||||||
chr2:231207690
|
G | T | 15 | a0001c0003t0001g0033a0001c0003t0001g0037a0001c0003t0004g0032others(12): Show | 15 | HG00280.hp2 HG01069.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.52-437G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231207690 | ||||||
chr2:231207762
|
C | T | 1 | a0003c0010t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.52-365C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | chr2 | 231207762 | ||||||
chr2:231208083
|
ATTTG | A | 45 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.52-36_52-33delGTTT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr2 | 231208083 | |||||
chr2:231208393
|
G | A | 42 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.177+141G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231208393 | ||||||
chr2:231208569
|
G | A | 43 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.177+317G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231208569 | ||||||
chr2:231209015
|
C | T | 80 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.177+763C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209015 | ||||||
chr2:231209058
|
C | T | 2 | a0001c0002t0014g0056a0001c0002t0021g0107 | 2 | HG01175.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.177+806C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209058 | ||||||
chr2:231209098
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.177+846C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209098 | ||||||
chr2:231209144
|
C | T | 5 | a0001c0003t0001g0022a0001c0003t0003g0023a0001c0003t0007g0025others(2): Show | 5 | HG03834.hp2 NA18963.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+892C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209144 | ||||||
chr2:231209148
|
C | T | 11 | a0001c0003t0001g0033a0001c0003t0001g0037a0001c0003t0004g0032others(8): Show | 11 | HG00280.hp2 HG01069.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.177+896C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209148 | ||||||
chr2:231209155
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0019g0067 | 3 | HG02602.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.177+903G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209155 | ||||||
chr2:231209233
|
T | C | 1 | a0001c0001t0002g0198 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.177+981T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209233 | ||||||
chr2:231209407
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.177+1155A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209407 | ||||||
chr2:231209422
|
T | C | 1 | a0001c0003t0001g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.177+1170T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209422 | ||||||
chr2:231209581
|
G | A | 22 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0072others(19): Show | 22 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.177+1329G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209581 | ||||||
chr2:231209766
|
C | G | 43 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.177+1514C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231209766 | ||||||
chr2:231210680
|
C | T | 1 | a0001c0001t0038g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.177+2428C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231210680 | ||||||
chr2:231210804
|
T | C | 1 | a0001c0003t0003g0023 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.177+2552T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231210804 | ||||||
chr2:231210815
|
C | T | 39 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.177+2563C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231210815 | ||||||
chr2:231211008
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.177+2756G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231211008 | ||||||
chr2:231211137
|
T | TAC | 34 | a0001c0001t0001g0168a0001c0001t0001g0171a0001c0001t0001g0178others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.177+2906_177+2907d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr2 | 231211137 | |||||
chr2:231211137
|
TAC | T | 37 | a0001c0001t0039g0119a0001c0003t0001g0013a0001c0003t0001g0022others(34): Show | 37 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.177+2906_177+2907d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr2 | 231211137 | |||||
chr2:231211158
|
A | C | 1 | a0001c0001t0008g0153 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.177+2906A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231211158 | ||||||
chr2:231211162
|
C | A | 2 | a0001c0003t0001g0005a0001c0004t0013g0004 | 2 | HG00280.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.177+2910C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231211162 | ||||||
chr2:231211238
|
G | T | 1 | a0001c0001t0011g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.177+2986G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231211238 | ||||||
chr2:231211819
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.178-3012T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231211819 | ||||||
chr2:231212011
|
A | C | 42 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.178-2820A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231212011 | ||||||
chr2:231212362
|
A | G | 44 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.178-2469A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231212362 | ||||||
chr2:231212378
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.178-2453G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231212378 | ||||||
chr2:231212606
|
T | A | 1 | a0001c0004t0036g0039 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.178-2225T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231212606 | ||||||
chr2:231212668
|
G | T | 32 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0072others(29): Show | 32 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.178-2163G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231212668 | ||||||
chr2:231212817
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047 | 3 | HG01069.hp2 HG01071.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.178-2014G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231212817 | ||||||
chr2:231212957
|
T | C | 44 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.178-1874T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231212957 | ||||||
chr2:231213164
|
C | CT | 82 | a0001c0001t0001g0099a0001c0001t0001g0126a0001c0001t0001g0129others(79): Show | 82 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.178-1652dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr2 | 231213164 | |||||
chr2:231213235
|
C | T | 42 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.178-1596C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231213235 | ||||||
chr2:231213481
|
G | GT | 5 | a0001c0001t0001g0081a0001c0001t0015g0060a0001c0001t0033g0157others(2): Show | 5 | HG01978.hp2 HG02257.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1337dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr2 | 231213481 | |||||
chr2:231213734
|
C | T | 1 | a0001c0002t0047g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.178-1097C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231213734 | ||||||
chr2:231213746
|
A | C | 6 | a0001c0001t0001g0151a0001c0001t0003g0149a0001c0001t0006g0148others(3): Show | 6 | HG00438.hp2 HG00609.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-1085A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231213746 | ||||||
chr2:231214335
|
A | G | 1 | a0001c0001t0054g0197 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.178-496A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231214335 | ||||||
chr2:231214403
|
T | C | 38 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.178-428T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231214403 | ||||||
chr2:231214487
|
C | T | 1 | a0001c0003t0044g0020 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.178-344C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231214487 | ||||||
chr2:231214527
|
T | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.178-304T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231214527 | ||||||
chr2:231214696
|
C | T | 6 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-135C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 3/24 | chr2 | 231214696 | ||||||
chr2:231215368
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0017g0127 | 2 | HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.348+367T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 4/24 | chr2 | 231215368 | ||||||
chr2:231215711
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.348+710A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 4/24 | chr2 | 231215711 | ||||||
chr2:231215814
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.348+813C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 4/24 | chr2 | 231215814 | ||||||
chr2:231215873
|
T | C | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-765T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 4/24 | chr2 | 231215873 | ||||||
chr2:231215919
|
G | A | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.349-719G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 4/24 | chr2 | 231215919 | ||||||
chr2:231216537
|
G | A | 1 | a0001c0001t0031g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.349-101G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 4/24 | chr2 | 231216537 | ||||||
chr2:231217202
|
A | G | 1 | a0001c0001t0058g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.504+409A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231217202 | ||||||
chr2:231217269
|
A | G | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.504+476A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231217269 | ||||||
chr2:231217394
|
G | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0019g0067 | 3 | HG02602.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.504+601G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231217394 | ||||||
chr2:231217440
|
C | T | 1 | a0001c0001t0004g0188 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.504+647C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231217440 | ||||||
chr2:231217445
|
G | A | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+652G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231217445 | ||||||
chr2:231217567
|
CA | C | 35 | a0001c0001t0039g0119a0001c0002t0002g0098a0001c0003t0001g0005others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.504+791delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231217567 | |||||
chr2:231217970
|
G | A | 1 | a0001c0001t0056g0200 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.504+1177G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231217970 | ||||||
chr2:231217982
|
C | T | 1 | a0001c0003t0005g0029 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.504+1189C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231217982 | ||||||
chr2:231217987
|
CTTGT | C | 39 | a0001c0001t0039g0119a0001c0003t0001g0005a0001c0003t0001g0013others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+1205_504+1208d others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231217987 | |||||
chr2:231218505
|
T | C | 1 | a0001c0003t0005g0006 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.504+1712T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231218505 | ||||||
chr2:231218544
|
G | A | 2 | a0001c0002t0002g0159a0001c0002t0002g0167 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.504+1751G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231218544 | ||||||
chr2:231218815
|
A | G | 40 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.504+2022A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231218815 | ||||||
chr2:231218941
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.504+2148G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231218941 | ||||||
chr2:231219143
|
CT | C | 39 | a0001c0001t0001g0168a0001c0003t0001g0005a0001c0003t0001g0013others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.504+2361delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231219143 | |||||
chr2:231219306
|
G | A | 6 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+2513G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231219306 | ||||||
chr2:231219492
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.504+2699G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231219492 | ||||||
chr2:231219698
|
T | G | 38 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.504+2905T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231219698 | ||||||
chr2:231219810
|
C | T | 1 | a0001c0001t0016g0146 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.505-2918C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231219810 | ||||||
chr2:231219928
|
T | C | 1 | a0001c0001t0054g0197 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.505-2800T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231219928 | ||||||
chr2:231220057
|
T | C | 1 | a0001c0003t0013g0001 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.505-2671T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220057 | ||||||
chr2:231220336
|
G | C | 40 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.505-2392G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220336 | ||||||
chr2:231220521
|
C | T | 80 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.505-2207C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220521 | ||||||
chr2:231220561
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.505-2167C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220561 | ||||||
chr2:231220585
|
A | G | 38 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.505-2143A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220585 | ||||||
chr2:231220596
|
C | CA | 19 | a0001c0001t0001g0081a0001c0001t0001g0113a0001c0001t0001g0129others(16): Show | 19 | HG00642.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.505-2108dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231220596 | |||||
chr2:231220596
|
CA | C | 11 | a0001c0001t0001g0054a0001c0001t0007g0045a0001c0001t0011g0120others(8): Show | 11 | HG00280.hp2 HG01069.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.505-2108delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231220596 | |||||
chr2:231220682
|
C | T | 2 | a0001c0003t0001g0037a0001c0003t0030g0036 | 2 | NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.505-2046C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220682 | ||||||
chr2:231220800
|
C | T | 1 | a0001c0004t0014g0019 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.505-1928C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220800 | ||||||
chr2:231220938
|
T | G | 1 | a0001c0003t0007g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.505-1790T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220938 | ||||||
chr2:231220953
|
A | G | 2 | a0001c0003t0001g0005a0001c0004t0013g0004 | 2 | HG00280.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.505-1775A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231220953 | ||||||
chr2:231221167
|
T | G | 3 | a0001c0001t0001g0171a0001c0001t0004g0169a0001c0002t0011g0170 | 3 | HG00438.hp1 HG02165.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.505-1561T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231221167 | ||||||
chr2:231221197
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505-1531G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231221197 | ||||||
chr2:231221307
|
G | T | 1 | a0001c0002t0060g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.505-1421G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231221307 | ||||||
chr2:231221342
|
C | T | 38 | a0001c0003t0001g0005a0001c0003t0001g0013a0001c0003t0001g0022others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.505-1386C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231221342 | ||||||
chr2:231221507
|
C | T | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.505-1221C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231221507 | ||||||
chr2:231221666
|
C | CA | 6 | a0001c0001t0033g0157a0001c0002t0002g0058a0001c0002t0002g0098others(3): Show | 6 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-1048dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231221666 | |||||
chr2:231221830
|
C | CAAA | 43 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.505-882_505-880dup others(3): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231221830 | |||||
chr2:231221830
|
C | CAAAA | 72 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.505-883_505-880dup others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr2 | 231221830 | |||||
chr2:231222597
|
C | T | 1 | a0001c0001t0011g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.505-131C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231222597 | ||||||
chr2:231222672
|
A | G | 3 | a0001c0003t0010g0038a0001c0004t0042g0035a0001c0004t0043g0034 | 3 | HG00280.hp2 HG01069.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.505-56A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 5/24 | chr2 | 231222672 | ||||||
chr2:231222884
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.597+64C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231222884 | ||||||
chr2:231223136
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.597+316T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223136 | ||||||
chr2:231223281
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.597+461A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223281 | ||||||
chr2:231223302
|
C | T | 1 | a0001c0001t0010g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.597+482C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223302 | ||||||
chr2:231223582
|
A | T | 43 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.597+762A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223582 | ||||||
chr2:231223676
|
A | C | 37 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.597+856A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223676 | ||||||
chr2:231223697
|
C | T | 198 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(195): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.597+877C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223697 | ||||||
chr2:231223775
|
G | A | 197 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(194): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.597+955G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223775 | ||||||
chr2:231223916
|
G | C | 37 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.597+1096G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223916 | ||||||
chr2:231223934
|
A | G | 2 | a0001c0001t0001g0168a0001c0002t0028g0163 | 2 | HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.597+1114A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231223934 | ||||||
chr2:231224078
|
A | G | 1 | a0001c0001t0004g0124 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.597+1258A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231224078 | ||||||
chr2:231224361
|
C | T | 1 | a0001c0001t0013g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.597+1541C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231224361 | ||||||
chr2:231224865
|
C | T | 1 | a0001c0001t0006g0094 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.598-1909C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231224865 | ||||||
chr2:231225034
|
A | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(1): Show | 4 | HG00741.hp2 HG01175.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.598-1740A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231225034 | ||||||
chr2:231225079
|
T | C | 1 | a0001c0003t0007g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.598-1695T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231225079 | ||||||
chr2:231225335
|
C | G | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598-1439C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231225335 | ||||||
chr2:231226192
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598-582C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231226192 | ||||||
chr2:231226698
|
A | G | 1 | a0001c0001t0006g0196 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.598-76A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231226698 | ||||||
chr2:231226699
|
T | C | 1 | a0001c0001t0040g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.598-75T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231226699 | ||||||
chr2:231226760
|
C | G | 1 | a0001c0002t0027g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.598-14C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231226760 | ||||||
chr2:231226766
|
C | T | 34 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.598-8C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 6/24 | chr2 | 231226766 | ||||||
chr2:231226925
|
G | C | 1 | a0001c0002t0033g0172 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.622+127G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231226925 | ||||||
chr2:231226969
|
G | A | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.622+171G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231226969 | ||||||
chr2:231227044
|
C | T | 38 | a0001c0001t0033g0157a0001c0001t0039g0119a0001c0003t0001g0005others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.622+246C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231227044 | ||||||
chr2:231227235
|
C | G | 120 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.622+437C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231227235 | ||||||
chr2:231227487
|
C | T | 1 | a0004c0014t0001g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.622+689C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231227487 | ||||||
chr2:231227588
|
C | T | 42 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.622+790C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231227588 | ||||||
chr2:231227716
|
A | G | 45 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.622+918A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231227716 | ||||||
chr2:231228242
|
A | G | 3 | a0001c0001t0001g0168a0001c0004t0024g0002a0001c0004t0024g0016 | 3 | HG01070.hp1 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.622+1444A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231228242 | ||||||
chr2:231228291
|
A | C | 2 | a0001c0001t0010g0186a0001c0001t0010g0187 | 2 | HG00408.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.622+1493A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231228291 | ||||||
chr2:231228584
|
C | A | 36 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0106others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.622+1786C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231228584 | ||||||
chr2:231228636
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081 | 3 | HG00741.hp2 HG01175.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.622+1838C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231228636 | ||||||
chr2:231228748
|
G | A | 1 | a0001c0002t0022g0145 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.622+1950G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231228748 | ||||||
chr2:231229073
|
A | G | 50 | a0001c0001t0001g0113a0001c0001t0001g0158a0001c0001t0001g0168others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.622+2275A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231229073 | ||||||
chr2:231229205
|
C | T | 1 | a0001c0001t0004g0188 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.622+2407C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231229205 | ||||||
chr2:231229239
|
C | T | 1 | a0001c0002t0014g0056 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.622+2441C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231229239 | ||||||
chr2:231229270
|
A | G | 1 | a0001c0003t0012g0015 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.622+2472A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231229270 | ||||||
chr2:231229968
|
T | G | 2 | a0001c0001t0018g0192a0001c0002t0002g0190 | 2 | HG02074.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.622+3170T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231229968 | ||||||
chr2:231230031
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.622+3233T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230031 | ||||||
chr2:231230227
|
G | A | 2 | a0001c0001t0018g0192a0001c0002t0002g0190 | 2 | HG02074.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.622+3429G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230227 | ||||||
chr2:231230349
|
G | A | 29 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.622+3551G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230349 | ||||||
chr2:231230598
|
G | A | 1 | a0001c0002t0002g0190 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.622+3800G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230598 | ||||||
chr2:231230598
|
G | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.622+3800G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230598 | ||||||
chr2:231230625
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.622+3827C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230625 | ||||||
chr2:231230761
|
A | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.622+3963A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230761 | ||||||
chr2:231230771
|
G | A | 42 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.622+3973G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230771 | ||||||
chr2:231230805
|
A | G | 1 | a0001c0001t0007g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.622+4007A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230805 | ||||||
chr2:231230874
|
A | G | 78 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.622+4076A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230874 | ||||||
chr2:231230904
|
A | T | 1 | a0001c0004t0002g0026 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.622+4106A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231230904 | ||||||
chr2:231231121
|
G | A | 1 | a0001c0001t0011g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.623-4103G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231121 | ||||||
chr2:231231148
|
G | A | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.623-4076G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231148 | ||||||
chr2:231231255
|
A | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623-3969A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231255 | ||||||
chr2:231231367
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0039g0119 | 2 | HG02056.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.623-3857A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231367 | ||||||
chr2:231231440
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623-3784G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231440 | ||||||
chr2:231231501
|
G | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.623-3723G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231501 | ||||||
chr2:231231694
|
A | AT | 41 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.623-3518dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr2 | 231231694 | |||||
chr2:231231694
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.623-3530A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231694 | ||||||
chr2:231231728
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.623-3496G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231728 | ||||||
chr2:231231753
|
A | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623-3471A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231753 | ||||||
chr2:231231969
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623-3255G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231231969 | ||||||
chr2:231232010
|
G | A | 119 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.623-3214G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232010 | ||||||
chr2:231232025
|
C | CT | 43 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0065others(40): Show | 43 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.623-3180dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr2 | 231232025 | |||||
chr2:231232025
|
CTT | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.623-3181_623-3180d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr2 | 231232025 | |||||
chr2:231232175
|
G | A | 1 | a0001c0002t0021g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.623-3049G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232175 | ||||||
chr2:231232363
|
C | G | 41 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(38): Show | 41 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.623-2861C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232363 | ||||||
chr2:231232455
|
C | CT | 9 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(6): Show | 9 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.623-2756dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr2 | 231232455 | |||||
chr2:231232455
|
CTT | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.623-2757_623-2756d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr2 | 231232455 | |||||
chr2:231232554
|
C | T | 2 | a0001c0001t0053g0116a0001c0002t0002g0069 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.623-2670C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232554 | ||||||
chr2:231232604
|
A | G | 1 | a0001c0003t0035g0027 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.623-2620A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232604 | ||||||
chr2:231232670
|
T | C | 119 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.623-2554T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232670 | ||||||
chr2:231232743
|
G | A | 41 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(38): Show | 41 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.623-2481G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232743 | ||||||
chr2:231232914
|
G | A | 1 | a0001c0001t0011g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.623-2310G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232914 | ||||||
chr2:231232965
|
C | G | 2 | a0001c0001t0006g0196a0001c0001t0054g0197 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.623-2259C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231232965 | ||||||
chr2:231233082
|
C | G | 1 | a0001c0001t0040g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.623-2142C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233082 | ||||||
chr2:231233093
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623-2131C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233093 | ||||||
chr2:231233121
|
G | A | 1 | a0001c0001t0002g0198 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.623-2103G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233121 | ||||||
chr2:231233169
|
A | C | 1 | a0001c0003t0022g0024 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.623-2055A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233169 | ||||||
chr2:231233643
|
G | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623-1581G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233643 | ||||||
chr2:231233660
|
C | T | 2 | a0001c0001t0053g0116a0001c0002t0002g0069 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.623-1564C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233660 | ||||||
chr2:231233691
|
G | A | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.623-1533G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233691 | ||||||
chr2:231233708
|
G | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.623-1516G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233708 | ||||||
chr2:231233712
|
G | T | 8 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(5): Show | 8 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.623-1512G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231233712 | ||||||
chr2:231234319
|
C | T | 42 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.623-905C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234319 | ||||||
chr2:231234534
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.623-690A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234534 | ||||||
chr2:231234647
|
A | G | 2 | a0001c0002t0002g0159a0001c0002t0002g0167 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.623-577A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234647 | ||||||
chr2:231234666
|
C | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.623-558C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234666 | ||||||
chr2:231234798
|
A | G | 35 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.623-426A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234798 | ||||||
chr2:231234843
|
T | G | 2 | a0001c0001t0018g0192a0001c0002t0002g0190 | 2 | HG02074.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.623-381T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234843 | ||||||
chr2:231234863
|
C | T | 1 | a0001c0002t0002g0161 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.623-361C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234863 | ||||||
chr2:231234932
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.623-292A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 7/24 | chr2 | 231234932 | ||||||
chr2:231235657
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.780+276T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231235657 | ||||||
chr2:231235750
|
C | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.780+369C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231235750 | ||||||
chr2:231235862
|
G | A | 1 | a0001c0001t0009g0041 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.780+481G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231235862 | ||||||
chr2:231235884
|
C | T | 1 | a0001c0003t0001g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.780+503C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231235884 | ||||||
chr2:231235948
|
A | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.780+567A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231235948 | ||||||
chr2:231236027
|
T | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.780+646T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231236027 | ||||||
chr2:231236030
|
T | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.780+649T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231236030 | ||||||
chr2:231236257
|
G | T | 29 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.780+876G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231236257 | ||||||
chr2:231236263
|
T | C | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.780+882T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231236263 | ||||||
chr2:231236449
|
G | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.780+1068G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231236449 | ||||||
chr2:231236648
|
A | G | 1 | a0001c0001t0009g0144 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.780+1267A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231236648 | ||||||
chr2:231236909
|
C | T | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.780+1528C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231236909 | ||||||
chr2:231237175
|
C | CGT | 77 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0065others(74): Show | 77 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.780+1825_780+1826d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237175
|
C | CGTGT | 7 | a0001c0001t0001g0078a0001c0001t0001g0129a0001c0001t0011g0165others(4): Show | 7 | HG01175.hp2 HG01978.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+1823_780+1826d others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237175
|
C | CGTGTGT | 3 | a0001c0003t0025g0009a0002c0005t0008g0010a0002c0006t0002g0021 | 3 | HG02155.hp1 NA18951.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.780+1821_780+1826d others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237175
|
C | CGTGTGTG others(1): Show |
16 | a0001c0001t0009g0144a0001c0003t0001g0033a0001c0003t0001g0037others(13): Show | 16 | HG00280.hp2 HG01069.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.780+1819_780+1826d others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237175
|
C | CGTGTGTG others(3): Show |
17 | a0001c0001t0005g0143a0001c0001t0008g0122a0001c0003t0001g0005others(14): Show | 17 | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.780+1817_780+1826d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237175
|
C | CGTGTGTG others(5): Show |
5 | a0001c0003t0001g0013a0001c0003t0003g0023a0001c0003t0007g0028others(2): Show | 5 | HG00323.hp2 HG01433.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+1815_780+1826d others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237175
|
CGT | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.780+1825_780+1826d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237175
|
CGTGT | C | 2 | a0001c0001t0011g0048a0003c0010t0001g0108 | 2 | HG01074.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.780+1823_780+1826d others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237175 | |||||
chr2:231237459
|
A | T | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.780+2078A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237459 | ||||||
chr2:231237669
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.781-2274C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237669 | ||||||
chr2:231237753
|
GTA | G | 2 | a0001c0001t0040g0128a0001c0001t0050g0040 | 2 | HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.781-2162_781-2161d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237753 | |||||
chr2:231237753
|
GTATATAT others(3): Show |
G | 1 | a0001c0004t0014g0019 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.781-2170_781-2161d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237753 | |||||
chr2:231237757
|
A | ATATG | 2 | a0001c0001t0008g0153a0001c0002t0022g0145 | 2 | HG03942.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.781-2183_781-2182i others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237757 | |||||
chr2:231237759
|
A | ATG | 5 | a0001c0001t0018g0137a0001c0001t0033g0157a0001c0001t0057g0125others(2): Show | 5 | HG02257.hp2 HG03654.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.781-2183_781-2182i others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237759 | |||||
chr2:231237761
|
A | G | 26 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.781-2182A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237761 | ||||||
chr2:231237763
|
A | G | 1 | a0001c0001t0005g0138 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.781-2180A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237763 | ||||||
chr2:231237771
|
ATATATAT others(4): Show |
A | 1 | a0002c0005t0008g0010 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.781-2170_781-2160d others(13): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237771 | |||||
chr2:231237773
|
ATATATAT others(3): Show |
A | 9 | a0001c0001t0001g0171a0001c0001t0010g0162a0001c0002t0002g0190others(6): Show | 9 | HG02165.hp1 HG03834.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.781-2168_781-2159d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237773 | |||||
chr2:231237773
|
ATATATAT others(4): Show |
A | 1 | a0002c0006t0002g0021 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.781-2168_781-2158d others(13): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237773 | |||||
chr2:231237775
|
ATATATAT others(3): Show |
A | 27 | a0001c0001t0001g0158a0001c0001t0002g0182a0001c0001t0004g0184others(24): Show | 27 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.781-2166_781-2157d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237775 | |||||
chr2:231237775
|
ATATATAT others(4): Show |
A | 17 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0002g0198others(14): Show | 17 | HG00408.hp2 HG00673.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.781-2166_781-2156d others(13): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237775 | |||||
chr2:231237775
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0009g0176 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.781-2166_781-2155d others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237775 | |||||
chr2:231237775
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781-2166_781-2153d others(16): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237775 | |||||
chr2:231237777
|
ATATATTT others(3): Show |
A | 5 | a0001c0001t0029g0194a0001c0001t0055g0193a0001c0002t0028g0163others(2): Show | 5 | HG01433.hp2 HG03490.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-2164_781-2155d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237777 | |||||
chr2:231237777
|
ATATATTT others(5): Show |
A | 1 | a0001c0002t0002g0175 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.781-2164_781-2153d others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237777 | |||||
chr2:231237779
|
A | AT | 3 | a0001c0001t0032g0111a0001c0002t0002g0043a0001c0002t0002g0098 | 3 | HG00323.hp1 HG02074.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.781-2163dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237779 | |||||
chr2:231237779
|
ATATTTTT others(3): Show |
A | 4 | a0001c0003t0001g0005a0001c0003t0004g0032a0001c0003t0005g0031others(1): Show | 4 | HG01361.hp1 HG01516.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2162_781-2153d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237779 | |||||
chr2:231237779
|
ATATTTTT others(4): Show |
A | 1 | a0001c0002t0002g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.781-2162_781-2152d others(13): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237779 | |||||
chr2:231237779
|
ATATTTTT others(5): Show |
A | 1 | a0001c0003t0001g0037 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.781-2162_781-2151d others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237779 | |||||
chr2:231237779
|
ATATTTTT others(13): Show |
A | 1 | a0001c0001t0004g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.781-2162_781-2143d others(22): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237779 | |||||
chr2:231237780
|
TA | T | 6 | a0001c0001t0004g0105a0001c0001t0005g0102a0001c0001t0008g0114others(3): Show | 6 | HG01074.hp1 HG01074.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-2162delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237780 | ||||||
chr2:231237781
|
A | T | 8 | a0001c0001t0008g0076a0001c0001t0009g0103a0001c0001t0032g0111others(5): Show | 8 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-2162A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237781 | ||||||
chr2:231237781
|
AT | A | 16 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(13): Show | 16 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.781-2128delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237781 | |||||
chr2:231237781
|
ATT | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0009g0041others(4): Show | 7 | HG00280.hp1 HG00609.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-2129_781-2128d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237781 | |||||
chr2:231237781
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0002t0002g0115a0001c0004t0036g0039 | 2 | HG02015.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.781-2137_781-2128d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237781 | |||||
chr2:231237781
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0002t0021g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.781-2139_781-2128d others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr2 | 231237781 | |||||
chr2:231237782
|
T | TA | 17 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0151others(14): Show | 17 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.781-2161_781-2160i others(3): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237782 | ||||||
chr2:231237782
|
T | TATA | 6 | a0001c0001t0001g0072a0001c0001t0007g0071a0001c0001t0011g0120others(3): Show | 6 | HG00738.hp1 HG03017.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-2161_781-2160i others(5): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237782 | ||||||
chr2:231237783
|
T | A | 33 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0068others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.781-2160T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237783 | ||||||
chr2:231237784
|
T | A | 28 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0078others(25): Show | 28 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.781-2159T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237784 | ||||||
chr2:231237785
|
T | A | 22 | a0001c0001t0001g0113a0001c0001t0004g0124a0001c0001t0004g0135others(19): Show | 22 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.781-2158T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237785 | ||||||
chr2:231237786
|
T | A | 17 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(14): Show | 17 | HG00438.hp2 HG00609.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.781-2157T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237786 | ||||||
chr2:231237787
|
T | A | 10 | a0001c0001t0004g0124a0001c0001t0005g0138a0001c0001t0005g0140others(7): Show | 10 | HG00280.hp1 HG00423.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.781-2156T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237787 | ||||||
chr2:231237788
|
T | A | 4 | a0001c0001t0006g0094a0001c0001t0029g0049a0001c0001t0041g0152others(1): Show | 4 | HG00438.hp2 HG01515.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-2155T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237788 | ||||||
chr2:231237789
|
T | A | 3 | a0001c0001t0004g0124a0001c0001t0034g0061a0001c0004t0013g0004 | 3 | HG00280.hp1 HG00423.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.781-2154T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237789 | ||||||
chr2:231237790
|
T | A | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.781-2153T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237790 | ||||||
chr2:231237791
|
T | A | 1 | a0001c0003t0030g0036 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.781-2152T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237791 | ||||||
chr2:231237793
|
T | A | 1 | a0001c0002t0002g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.781-2150T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231237793 | ||||||
chr2:231238041
|
G | A | 31 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(28): Show | 31 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.781-1902G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238041 | ||||||
chr2:231238358
|
T | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.781-1585T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238358 | ||||||
chr2:231238379
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781-1564C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238379 | ||||||
chr2:231238396
|
C | G | 1 | a0001c0002t0002g0043 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.781-1547C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238396 | ||||||
chr2:231238413
|
A | G | 39 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0065others(36): Show | 39 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.781-1530A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238413 | ||||||
chr2:231238695
|
A | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781-1248A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238695 | ||||||
chr2:231238742
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781-1201C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238742 | ||||||
chr2:231238868
|
G | T | 1 | a0001c0003t0013g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.781-1075G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238868 | ||||||
chr2:231238934
|
G | T | 1 | a0001c0003t0005g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.781-1009G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238934 | ||||||
chr2:231238981
|
G | C | 2 | a0001c0003t0001g0005a0001c0004t0013g0004 | 2 | HG00280.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.781-962G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231238981 | ||||||
chr2:231239016
|
A | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.781-927A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231239016 | ||||||
chr2:231239366
|
C | T | 42 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.781-577C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231239366 | ||||||
chr2:231239633
|
C | A | 1 | a0001c0003t0022g0024 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.781-310C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231239633 | ||||||
chr2:231239712
|
C | T | 1 | a0001c0003t0001g0033 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.781-231C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231239712 | ||||||
chr2:231239853
|
G | A | 11 | a0001c0003t0001g0033a0001c0003t0001g0037a0001c0003t0004g0032others(8): Show | 11 | HG00280.hp2 HG01069.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.781-90G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 8/24 | chr2 | 231239853 | ||||||
chr2:231240347
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.879+306C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231240347 | ||||||
chr2:231240579
|
A | G | 1 | a0001c0002t0012g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.879+538A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231240579 | ||||||
chr2:231241039
|
C | A | 34 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.879+998C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241039 | ||||||
chr2:231241198
|
C | CA | 17 | a0001c0001t0001g0158a0001c0001t0006g0196a0001c0001t0007g0195others(14): Show | 17 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.879+1175dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231241198 | |||||
chr2:231241198
|
CA | C | 27 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+1175delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231241198 | |||||
chr2:231241198
|
CAAA | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+1173_879+1175d others(5): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231241198 | |||||
chr2:231241298
|
C | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+1257C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241298 | ||||||
chr2:231241318
|
C | G | 4 | a0001c0001t0001g0171a0001c0001t0004g0169a0001c0001t0058g0199others(1): Show | 4 | HG00438.hp1 HG02027.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1277C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241318 | ||||||
chr2:231241421
|
C | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+1380C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241421 | ||||||
chr2:231241430
|
A | C | 1 | a0001c0003t0049g0008 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.879+1389A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241430 | ||||||
chr2:231241532
|
G | C | 44 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.879+1491G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241532 | ||||||
chr2:231241614
|
C | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+1573C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241614 | ||||||
chr2:231241709
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.879+1668G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241709 | ||||||
chr2:231241780
|
C | A | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+1739C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241780 | ||||||
chr2:231241898
|
C | A | 1 | a0001c0012t0048g0156 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.879+1857C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231241898 | ||||||
chr2:231242144
|
C | T | 76 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(73): Show | 76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.879+2103C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231242144 | ||||||
chr2:231242206
|
T | C | 86 | a0001c0001t0001g0046a0001c0001t0001g0126a0001c0001t0001g0129others(83): Show | 86 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.879+2165T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231242206 | ||||||
chr2:231242650
|
G | T | 31 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(28): Show | 31 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+2609G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231242650 | ||||||
chr2:231242675
|
C | T | 2 | a0002c0005t0008g0010a0002c0006t0002g0021 | 2 | HG02155.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.879+2634C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231242675 | ||||||
chr2:231243241
|
C | T | 1 | a0001c0002t0002g0044 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.879+3200C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231243241 | ||||||
chr2:231243246
|
C | CA | 35 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(32): Show | 35 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.879+3222dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231243246 | |||||
chr2:231243533
|
A | G | 42 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.879+3492A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231243533 | ||||||
chr2:231243980
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.879+3939A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231243980 | ||||||
chr2:231244022
|
A | G | 1 | a0001c0002t0051g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.879+3981A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231244022 | ||||||
chr2:231244056
|
C | G | 31 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(28): Show | 31 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+4015C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231244056 | ||||||
chr2:231244364
|
C | CT | 8 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0106others(5): Show | 8 | HG00639.hp1 HG00735.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.879+4343dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231244364 | |||||
chr2:231244497
|
C | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.879+4456C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231244497 | ||||||
chr2:231244522
|
T | A | 3 | a0001c0001t0004g0188a0001c0001t0023g0164a0001c0001t0056g0200 | 3 | NA18950.hp2 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.879+4481T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231244522 | ||||||
chr2:231244795
|
C | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.879+4754C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231244795 | ||||||
chr2:231245103
|
T | G | 75 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.879+5062T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245103 | ||||||
chr2:231245139
|
C | T | 1 | a0003c0010t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.879+5098C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245139 | ||||||
chr2:231245176
|
C | T | 31 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(28): Show | 31 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.879+5135C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245176 | ||||||
chr2:231245482
|
T | C | 1 | a0001c0001t0031g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.879+5441T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245482 | ||||||
chr2:231245756
|
G | C | 199 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(196): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.879+5715G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245756 | ||||||
chr2:231245770
|
T | C | 120 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.879+5729T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245770 | ||||||
chr2:231245786
|
A | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.879+5745A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245786 | ||||||
chr2:231245895
|
T | C | 1 | a0004c0014t0001g0093 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.879+5854T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231245895 | ||||||
chr2:231246273
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.879+6232A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231246273 | ||||||
chr2:231246290
|
A | C | 1 | a0001c0002t0022g0145 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.879+6249A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231246290 | ||||||
chr2:231246572
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0068 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.879+6531A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231246572 | ||||||
chr2:231246620
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.879+6579A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231246620 | ||||||
chr2:231246648
|
T | C | 1 | a0001c0002t0033g0172 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.879+6607T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231246648 | ||||||
chr2:231246658
|
A | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.879+6617A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231246658 | ||||||
chr2:231246664
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.879+6623A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231246664 | ||||||
chr2:231246959
|
A | AT | 43 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.879+6933dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231246959 | |||||
chr2:231247092
|
A | G | 4 | a0001c0002t0002g0058a0001c0002t0002g0098a0001c0002t0003g0085others(1): Show | 4 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+7051A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231247092 | ||||||
chr2:231247566
|
C | A | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.879+7525C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231247566 | ||||||
chr2:231247650
|
G | T | 1 | a0001c0004t0028g0014 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.879+7609G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231247650 | ||||||
chr2:231247737
|
C | G | 77 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.879+7696C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231247737 | ||||||
chr2:231247899
|
C | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.879+7858C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231247899 | ||||||
chr2:231248017
|
A | C | 45 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.879+7976A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248017 | ||||||
chr2:231248065
|
T | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.879+8024T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248065 | ||||||
chr2:231248100
|
A | G | 1 | a0003c0010t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.879+8059A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248100 | ||||||
chr2:231248447
|
C | A | 1 | a0001c0002t0011g0170 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.880-8139C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248447 | ||||||
chr2:231248531
|
C | T | 2 | a0001c0003t0005g0031a0001c0004t0003g0030 | 2 | NA18998.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.880-8055C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248531 | ||||||
chr2:231248550
|
G | C | 79 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(76): Show | 79 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.880-8036G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248550 | ||||||
chr2:231248739
|
G | A | 2 | a0001c0003t0044g0020a0001c0004t0028g0014 | 2 | HG01433.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.880-7847G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248739 | ||||||
chr2:231248797
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-7789G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248797 | ||||||
chr2:231248797
|
G | T | 8 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(5): Show | 8 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-7789G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248797 | ||||||
chr2:231248806
|
C | CA | 33 | a0001c0001t0001g0113a0001c0001t0001g0158a0001c0001t0001g0171others(30): Show | 33 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.880-7753dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231248806 | |||||
chr2:231248806
|
CA | C | 26 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0072others(23): Show | 26 | HG00544.hp2 HG00609.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.880-7753delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231248806 | |||||
chr2:231248807
|
A | AC | 3 | a0001c0003t0001g0033a0001c0003t0004g0032a0001c0003t0030g0036 | 3 | HG01361.hp1 HG01433.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.880-7779_880-7778i others(3): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248807 | ||||||
chr2:231248808
|
A | C | 8 | a0001c0003t0001g0037a0001c0003t0005g0029a0001c0003t0005g0031others(5): Show | 8 | HG00280.hp2 HG01069.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-7778A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248808 | ||||||
chr2:231248874
|
C | G | 1 | a0001c0001t0009g0142 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.880-7712C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231248874 | ||||||
chr2:231249175
|
T | A | 77 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.880-7411T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231249175 | ||||||
chr2:231249381
|
G | C | 2 | a0001c0003t0037g0003a0001c0004t0002g0012 | 2 | HG01168.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.880-7205G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231249381 | ||||||
chr2:231249660
|
C | G | 46 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0171others(43): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.880-6926C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231249660 | ||||||
chr2:231249801
|
A | ACCCACCC others(30): Show |
1 | a0001c0003t0007g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.880-6600_880-6564d others(39): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231249801 | |||||
chr2:231249801
|
ACCCACCC others(30): Show |
A | 2 | a0001c0001t0006g0057a0001c0001t0020g0092 | 2 | HG01981.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.880-6600_880-6564d others(39): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231249801 | |||||
chr2:231249801
|
ACCCACCC others(141): Show |
A | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.880-6711_880-6564d others(2): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231249801 | |||||
chr2:231249875
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-6711G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231249875 | ||||||
chr2:231249877
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-6709C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231249877 | ||||||
chr2:231249878
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-6708C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231249878 | ||||||
chr2:231250362
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.880-6224G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231250362 | ||||||
chr2:231250488
|
T | G | 1 | a0001c0002t0002g0043 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.880-6098T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231250488 | ||||||
chr2:231251174
|
C | T | 77 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.880-5412C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231251174 | ||||||
chr2:231251629
|
C | T | 2 | a0001c0002t0002g0043a0001c0002t0002g0112 | 2 | HG02074.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.880-4957C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231251629 | ||||||
chr2:231251778
|
C | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.880-4808C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231251778 | ||||||
chr2:231251847
|
T | C | 1 | a0001c0001t0054g0197 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.880-4739T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231251847 | ||||||
chr2:231251873
|
G | A | 38 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0072others(35): Show | 38 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.880-4713G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231251873 | ||||||
chr2:231251945
|
T | A | 7 | a0001c0003t0001g0037a0001c0003t0004g0032a0001c0003t0005g0029others(4): Show | 7 | HG01361.hp1 HG02015.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-4641T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231251945 | ||||||
chr2:231252332
|
C | T | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.880-4254C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231252332 | ||||||
chr2:231252348
|
C | G | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.880-4238C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231252348 | ||||||
chr2:231252488
|
G | A | 1 | a0001c0004t0013g0004 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.880-4098G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231252488 | ||||||
chr2:231252689
|
T | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.880-3897T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231252689 | ||||||
chr2:231252783
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.880-3803C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231252783 | ||||||
chr2:231252800
|
C | G | 44 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.880-3786C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231252800 | ||||||
chr2:231252985
|
C | G | 1 | a0001c0002t0060g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.880-3601C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231252985 | ||||||
chr2:231253106
|
T | TTTTTTG | 119 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.880-3454_880-3449d others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231253106 | |||||
chr2:231253367
|
G | A | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.880-3219G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231253367 | ||||||
chr2:231253415
|
G | C | 5 | a0001c0003t0001g0022a0001c0003t0003g0023a0001c0003t0007g0025others(2): Show | 5 | HG03834.hp2 NA18963.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-3171G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231253415 | ||||||
chr2:231254100
|
T | C | 78 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.880-2486T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231254100 | ||||||
chr2:231254318
|
A | T | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.880-2268A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231254318 | ||||||
chr2:231254660
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0019g0067 | 3 | HG02602.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.880-1896_880-1887d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231254660 | |||||
chr2:231254942
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | NA18948.hp1 NA18957.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-1644G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231254942 | ||||||
chr2:231254943
|
A | T | 6 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | NA18948.hp1 NA18957.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-1643A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231254943 | ||||||
chr2:231255180
|
A | AAC | 7 | a0001c0001t0004g0101a0001c0001t0006g0057a0001c0001t0010g0063others(4): Show | 7 | HG00621.hp2 HG00673.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-1366_880-1365d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231255180 | |||||
chr2:231255180
|
A | AACAC | 4 | a0001c0001t0001g0113a0001c0001t0034g0061a0001c0002t0002g0043others(1): Show | 4 | HG00642.hp2 HG00741.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-1368_880-1365d others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231255180 | |||||
chr2:231255180
|
AAC | A | 11 | a0001c0001t0001g0158a0001c0001t0002g0189a0001c0001t0002g0198others(8): Show | 11 | HG00642.hp1 HG01993.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.880-1366_880-1365d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231255180 | |||||
chr2:231255180
|
AACAC | A | 59 | a0001c0001t0001g0129a0001c0001t0001g0151a0001c0001t0001g0168others(56): Show | 59 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.880-1368_880-1365d others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231255180 | |||||
chr2:231255180
|
AACACAC | A | 5 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0002t0002g0161others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-1370_880-1365d others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231255180 | |||||
chr2:231255180
|
AACACACA others(1): Show |
A | 52 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0003g0149others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.880-1372_880-1365d others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231255180 | |||||
chr2:231255180
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.880-1374_880-1365d others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr2 | 231255180 | |||||
chr2:231255407
|
C | T | 1 | a0001c0008t0027g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.880-1179C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231255407 | ||||||
chr2:231255766
|
A | G | 120 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(117): Show | 120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.880-820A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231255766 | ||||||
chr2:231255891
|
T | A | 33 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.880-695T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231255891 | ||||||
chr2:231256070
|
C | T | 35 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.880-516C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231256070 | ||||||
chr2:231256312
|
C | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-274C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231256312 | ||||||
chr2:231256313
|
T | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-273T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231256313 | ||||||
chr2:231256335
|
C | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-251C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231256335 | ||||||
chr2:231256395
|
C | T | 1 | a0001c0002t0051g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.880-191C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231256395 | ||||||
chr2:231256430
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.880-156C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 9/24 | chr2 | 231256430 | ||||||
chr2:231256694
|
A | G | 2 | a0001c0003t0001g0005a0001c0004t0013g0004 | 2 | HG00280.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.914+74A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231256694 | ||||||
chr2:231256835
|
G | A | 2 | a0001c0001t0010g0162a0001c0001t0055g0193 | 2 | NA19011.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.914+215G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231256835 | ||||||
chr2:231256839
|
T | G | 1 | a0001c0001t0006g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.914+219T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231256839 | ||||||
chr2:231256929
|
G | C | 45 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.914+309G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231256929 | ||||||
chr2:231257285
|
A | G | 78 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.914+665A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231257285 | ||||||
chr2:231257460
|
G | A | 1 | a0001c0003t0035g0027 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.914+840G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231257460 | ||||||
chr2:231257635
|
T | C | 77 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.914+1015T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231257635 | ||||||
chr2:231257769
|
A | G | 119 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.914+1149A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231257769 | ||||||
chr2:231257863
|
T | C | 123 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.915-1128T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231257863 | ||||||
chr2:231257867
|
C | G | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.915-1124C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231257867 | ||||||
chr2:231257909
|
G | A | 2 | a0001c0003t0037g0003a0001c0004t0002g0012 | 2 | HG01168.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.915-1082G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231257909 | ||||||
chr2:231258141
|
A | G | 2 | a0001c0002t0002g0043a0001c0002t0002g0112 | 2 | HG02074.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.915-850A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258141 | ||||||
chr2:231258184
|
T | C | 2 | a0001c0001t0007g0045a0001c0001t0007g0047 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.915-807T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258184 | ||||||
chr2:231258342
|
C | T | 1 | a0003c0010t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.915-649C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258342 | ||||||
chr2:231258401
|
G | A | 1 | a0001c0003t0013g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.915-590G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258401 | ||||||
chr2:231258500
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.915-491C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258500 | ||||||
chr2:231258528
|
C | T | 2 | a0001c0001t0006g0196a0001c0001t0054g0197 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.915-463C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258528 | ||||||
chr2:231258601
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.915-390G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258601 | ||||||
chr2:231258639
|
C | T | 1 | a0001c0001t0031g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.915-352C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 10/24 | chr2 | 231258639 | ||||||
chr2:231259414
|
G | T | 43 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1026+312G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231259414 | ||||||
chr2:231259476
|
C | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1026+374C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231259476 | ||||||
chr2:231259529
|
A | G | 1 | a0001c0001t0009g0041 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1026+427A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231259529 | ||||||
chr2:231259758
|
C | T | 2 | a0001c0003t0049g0008a0006c0007t0014g0018 | 2 | HG02257.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1026+656C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231259758 | ||||||
chr2:231259869
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1026+767G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231259869 | ||||||
chr2:231260253
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0017g0127 | 2 | HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1026+1151T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231260253 | ||||||
chr2:231260688
|
G | A | 1 | a0001c0001t0055g0193 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1026+1586G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231260688 | ||||||
chr2:231260765
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1027-1541T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231260765 | ||||||
chr2:231260919
|
T | C | 77 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1027-1387T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231260919 | ||||||
chr2:231260990
|
C | T | 1 | a0001c0002t0002g0044 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1027-1316C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231260990 | ||||||
chr2:231261182
|
T | C | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1027-1124T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261182 | ||||||
chr2:231261404
|
A | G | 1 | a0001c0002t0003g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1027-902A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261404 | ||||||
chr2:231261542
|
C | T | 1 | a0001c0002t0023g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1027-764C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261542 | ||||||
chr2:231261577
|
A | G | 78 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1027-729A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261577 | ||||||
chr2:231261665
|
A | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1027-641A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261665 | ||||||
chr2:231261821
|
C | T | 77 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1027-485C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261821 | ||||||
chr2:231261884
|
G | A | 30 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1027-422G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261884 | ||||||
chr2:231261972
|
G | GC | 199 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(196): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1027-333dupC | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr2 | 231261972 | |||||
chr2:231261979
|
A | G | 2 | a0002c0005t0008g0010a0002c0006t0002g0021 | 2 | HG02155.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1027-327A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261979 | ||||||
chr2:231261985
|
C | A | 43 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1027-321C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 11/24 | chr2 | 231261985 | ||||||
chr2:231262993
|
A | T | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1119+595A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231262993 | ||||||
chr2:231262999
|
TA | T | 76 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(73): Show | 76 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1119+603delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231262999 | |||||
chr2:231263028
|
C | G | 2 | a0001c0002t0002g0043a0001c0002t0002g0112 | 2 | HG02074.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1119+630C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231263028 | ||||||
chr2:231263397
|
C | T | 2 | a0001c0002t0002g0043a0001c0002t0002g0112 | 2 | HG02074.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1119+999C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231263397 | ||||||
chr2:231263492
|
A | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1119+1094A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231263492 | ||||||
chr2:231263709
|
T | C | 1 | a0001c0003t0012g0015 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1119+1311T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231263709 | ||||||
chr2:231263991
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1119+1593A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231263991 | ||||||
chr2:231264240
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1119+1842G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231264240 | ||||||
chr2:231264752
|
C | A | 1 | a0001c0002t0003g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1119+2354C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231264752 | ||||||
chr2:231264799
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1119+2401G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231264799 | ||||||
chr2:231264861
|
C | A | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1119+2463C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231264861 | ||||||
chr2:231264872
|
C | T | 1 | a0001c0003t0005g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1119+2474C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231264872 | ||||||
chr2:231264969
|
G | A | 2 | a0001c0001t0001g0168a0001c0002t0028g0163 | 2 | HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1119+2571G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231264969 | ||||||
chr2:231265029
|
C | T | 1 | a0001c0001t0004g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1119+2631C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231265029 | ||||||
chr2:231265096
|
C | CA | 11 | a0001c0001t0033g0157a0001c0003t0001g0037a0001c0003t0004g0032others(8): Show | 11 | HG00280.hp2 HG01069.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1119+2710dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231265096 | |||||
chr2:231265369
|
G | A | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1119+2971G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231265369 | ||||||
chr2:231265460
|
C | T | 1 | a0001c0001t0019g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1119+3062C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231265460 | ||||||
chr2:231265462
|
G | A | 1 | a0001c0001t0009g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1119+3064G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231265462 | ||||||
chr2:231265703
|
T | TA | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1119+3317dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231265703 | |||||
chr2:231265782
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1119+3384C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231265782 | ||||||
chr2:231265996
|
T | TA | 7 | a0001c0003t0001g0033a0001c0003t0005g0006a0001c0003t0010g0038others(4): Show | 7 | HG00280.hp2 HG01069.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+3615dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231265996 | |||||
chr2:231265996
|
T | TAA | 6 | a0001c0003t0001g0037a0001c0003t0004g0032a0001c0003t0005g0029others(3): Show | 6 | HG01361.hp1 NA18944.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+3614_1119+361 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231265996 | |||||
chr2:231266236
|
C | T | 1 | a0001c0001t0016g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1119+3838C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231266236 | ||||||
chr2:231266252
|
A | G | 1 | a0001c0003t0005g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1119+3854A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231266252 | ||||||
chr2:231266267
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | NA18948.hp1 NA18957.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.1119+3869G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231266267 | ||||||
chr2:231266504
|
A | G | 43 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(40): Show | 43 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1119+4106A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231266504 | ||||||
chr2:231266869
|
A | G | 50 | a0001c0001t0001g0046a0001c0001t0001g0158a0001c0001t0001g0168others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1120-4113A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231266869 | ||||||
chr2:231266989
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1120-3993G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231266989 | ||||||
chr2:231267232
|
A | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1120-3750A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231267232 | ||||||
chr2:231267300
|
G | A | 1 | a0001c0002t0032g0177 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1120-3682G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231267300 | ||||||
chr2:231267661
|
G | A | 117 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(114): Show | 117 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1120-3321G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231267661 | ||||||
chr2:231267801
|
A | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1120-3181A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231267801 | ||||||
chr2:231267820
|
A | G | 2 | a0001c0003t0005g0006a0001c0003t0025g0009 | 2 | NA18951.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1120-3162A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231267820 | ||||||
chr2:231268271
|
C | G | 45 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0005g0143others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1120-2711C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231268271 | ||||||
chr2:231268294
|
T | C | 1 | a0001c0001t0017g0127 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1120-2688T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231268294 | ||||||
chr2:231268345
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1120-2637T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231268345 | ||||||
chr2:231268412
|
G | A | 2 | a0001c0001t0016g0134a0001c0001t0016g0146 | 2 | HG02155.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1120-2570G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231268412 | ||||||
chr2:231268606
|
A | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1120-2376A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231268606 | ||||||
chr2:231268699
|
A | G | 4 | a0001c0002t0002g0058a0001c0002t0002g0098a0001c0002t0003g0085others(1): Show | 4 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120-2283A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231268699 | ||||||
chr2:231268790
|
A | G | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1120-2192A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231268790 | ||||||
chr2:231269215
|
T | C | 3 | a0001c0002t0002g0058a0001c0002t0003g0085a0001c0002t0023g0084 | 3 | HG00639.hp2 HG00741.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1120-1767T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231269215 | ||||||
chr2:231269398
|
C | CT | 7 | a0001c0001t0018g0192a0001c0001t0033g0157a0001c0001t0050g0040others(4): Show | 7 | HG00621.hp2 HG01361.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120-1563dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231269398 | |||||
chr2:231269398
|
C | CTT | 31 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1120-1564_1120-156 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr2 | 231269398 | |||||
chr2:231269401
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1120-1581T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231269401 | ||||||
chr2:231270028
|
G | A | 1 | a0003c0010t0001g0108 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1120-954G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231270028 | ||||||
chr2:231270085
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1120-897C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231270085 | ||||||
chr2:231270225
|
C | T | 2 | a0001c0001t0011g0120a0001c0001t0019g0067 | 2 | HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1120-757C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231270225 | ||||||
chr2:231270301
|
G | C | 9 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(6): Show | 9 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-681G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231270301 | ||||||
chr2:231270720
|
C | T | 1 | a0001c0001t0015g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1120-262C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231270720 | ||||||
chr2:231270828
|
A | T | 115 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(112): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1120-154A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 12/24 | chr2 | 231270828 | ||||||
chr2:231271144
|
G | A | 1 | a0001c0002t0002g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1210+72G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231271144 | ||||||
chr2:231271584
|
G | A | 1 | a0001c0001t0010g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1210+512G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231271584 | ||||||
chr2:231271682
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1210+610G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231271682 | ||||||
chr2:231272151
|
AGTTTTGT others(4): Show |
A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1211-795_1211-785d others(13): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272151 | |||||
chr2:231272166
|
T | TTG | 28 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(25): Show | 28 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1211-773_1211-772d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272166 | |||||
chr2:231272187
|
G | GT | 36 | a0001c0001t0001g0081a0001c0001t0001g0126a0001c0001t0001g0151others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1211-745dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272187 | |||||
chr2:231272187
|
GT | G | 39 | a0001c0001t0001g0129a0001c0001t0001g0158a0001c0001t0001g0168others(36): Show | 39 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1211-745delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272187 | |||||
chr2:231272297
|
A | G | 2 | a0001c0003t0044g0020a0001c0004t0028g0014 | 2 | HG01433.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1211-658A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231272297 | ||||||
chr2:231272418
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1211-537C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231272418 | ||||||
chr2:231272433
|
A | C | 42 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1211-522A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231272433 | ||||||
chr2:231272449
|
C | T | 9 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(6): Show | 9 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1211-506C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231272449 | ||||||
chr2:231272500
|
G | GTGTT | 41 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0087others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1211-425_1211-422d others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272500 | |||||
chr2:231272500
|
G | GTGTTTGT others(1): Show |
25 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(22): Show | 25 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.1211-429_1211-422d others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272500 | |||||
chr2:231272500
|
G | GTGTTTGT others(5): Show |
1 | a0001c0001t0004g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1211-433_1211-422d others(14): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272500 | |||||
chr2:231272500
|
GTGTT | G | 10 | a0001c0001t0002g0189a0001c0001t0002g0198a0001c0001t0011g0048others(7): Show | 10 | HG00741.hp1 HG01074.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.1211-425_1211-422d others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr2 | 231272500 | |||||
chr2:231272571
|
T | C | 118 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1211-384T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231272571 | ||||||
chr2:231272707
|
G | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1211-248G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231272707 | ||||||
chr2:231272808
|
G | A | 4 | a0001c0003t0001g0022a0001c0003t0007g0025a0001c0003t0022g0024others(1): Show | 4 | HG03834.hp2 NA18997.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211-147G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 13/24 | chr2 | 231272808 | ||||||
chr2:231273245
|
T | A | 1 | a0001c0001t0053g0116 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1334+167T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273245 | ||||||
chr2:231273248
|
G | A | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1334+170G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273248 | ||||||
chr2:231273528
|
C | T | 36 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1334+450C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273528 | ||||||
chr2:231273532
|
A | G | 2 | a0001c0001t0001g0168a0001c0002t0028g0163 | 2 | HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1334+454A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273532 | ||||||
chr2:231273658
|
G | A | 42 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1334+580G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273658 | ||||||
chr2:231273678
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1334+600G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273678 | ||||||
chr2:231273829
|
T | C | 1 | a0001c0002t0002g0161 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1334+751T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273829 | ||||||
chr2:231273917
|
A | G | 1 | a0001c0004t0036g0039 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1334+839A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273917 | ||||||
chr2:231273924
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1334+846G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231273924 | ||||||
chr2:231274411
|
C | T | 1 | a0001c0001t0038g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1334+1333C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231274411 | ||||||
chr2:231274542
|
C | T | 26 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1334+1464C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231274542 | ||||||
chr2:231274707
|
C | A | 2 | a0001c0001t0008g0153a0001c0001t0017g0121 | 2 | NA18951.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1334+1629C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231274707 | ||||||
chr2:231274798
|
G | A | 25 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1334+1720G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231274798 | ||||||
chr2:231275004
|
TTAAG | T | 40 | a0001c0001t0001g0129a0001c0001t0005g0143a0001c0001t0008g0122others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1335-1628_1335-162 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr2 | 231275004 | |||||
chr2:231275255
|
G | A | 5 | a0001c0001t0019g0097a0001c0002t0012g0088a0001c0003t0005g0042others(2): Show | 5 | HG02027.hp2 HG02165.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335-1381G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231275255 | ||||||
chr2:231275258
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1335-1378C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231275258 | ||||||
chr2:231275371
|
T | C | 1 | a0001c0001t0056g0200 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1335-1265T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231275371 | ||||||
chr2:231275648
|
C | A | 26 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1335-988C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231275648 | ||||||
chr2:231275946
|
T | A | 26 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1335-690T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231275946 | ||||||
chr2:231276415
|
C | T | 5 | a0001c0001t0001g0158a0001c0001t0006g0196a0001c0001t0007g0195others(2): Show | 5 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335-221C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 14/24 | chr2 | 231276415 | ||||||
chr2:231277016
|
G | A | 42 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0178others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.1474+241G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | chr2 | 231277016 | ||||||
chr2:231277171
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1474+396A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | chr2 | 231277171 | ||||||
chr2:231277545
|
A | ATG | 69 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0126others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1474+771_1474+772d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr2 | 231277545 | |||||
chr2:231277562
|
C | CT | 6 | a0001c0001t0001g0074a0001c0001t0011g0120a0001c0001t0020g0092others(3): Show | 6 | HG00323.hp2 HG01258.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474+803dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr2 | 231277562 | |||||
chr2:231277562
|
CT | C | 64 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0001g0158others(61): Show | 64 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1474+803delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr2 | 231277562 | |||||
chr2:231277563
|
T | A | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1474+788T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | chr2 | 231277563 | ||||||
chr2:231277665
|
C | T | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1475-717C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | chr2 | 231277665 | ||||||
chr2:231277713
|
C | A | 5 | a0001c0001t0001g0158a0001c0001t0006g0196a0001c0001t0007g0195others(2): Show | 5 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1475-669C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | chr2 | 231277713 | ||||||
chr2:231277713
|
C | T | 7 | a0001c0003t0001g0037a0001c0003t0004g0032a0001c0003t0005g0029others(4): Show | 7 | HG01361.hp1 HG02015.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1475-669C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | chr2 | 231277713 | ||||||
chr2:231278331
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | NA18948.hp1 NA18957.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.1475-51G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 15/24 | chr2 | 231278331 | ||||||
chr2:231278727
|
A | ATC | 42 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0129others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1551+271_1551+272d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231278727 | |||||
chr2:231279511
|
C | CT | 48 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0179others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1551+1070dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231279511 | |||||
chr2:231279511
|
CT | C | 27 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1551+1070delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr2 | 231279511 | |||||
chr2:231279755
|
C | G | 48 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0178others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1551+1297C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231279755 | ||||||
chr2:231280090
|
T | C | 2 | a0001c0001t0008g0153a0001c0001t0017g0121 | 2 | NA18951.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1551+1632T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231280090 | ||||||
chr2:231280142
|
A | C | 48 | a0001c0001t0001g0158a0001c0001t0001g0168a0001c0001t0001g0178others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1551+1684A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231280142 | ||||||
chr2:231280877
|
C | T | 1 | a0001c0001t0004g0188 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1552-1182C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231280877 | ||||||
chr2:231281139
|
G | A | 39 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0065others(36): Show | 39 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1552-920G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281139 | ||||||
chr2:231281142
|
A | G | 1 | a0001c0003t0020g0055 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1552-917A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281142 | ||||||
chr2:231281180
|
A | G | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1552-879A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281180 | ||||||
chr2:231281445
|
T | G | 3 | a0001c0001t0018g0136a0001c0001t0018g0137a0001c0003t0049g0008 | 3 | HG03491.hp2 NA18984.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1552-614T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281445 | ||||||
chr2:231281476
|
C | T | 1 | a0001c0002t0006g0191 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1552-583C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281476 | ||||||
chr2:231281588
|
G | C | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1552-471G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281588 | ||||||
chr2:231281629
|
T | C | 4 | a0001c0001t0011g0120a0001c0001t0019g0067a0001c0001t0038g0154others(1): Show | 4 | HG02602.hp1 HG03942.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1552-430T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281629 | ||||||
chr2:231281961
|
T | C | 15 | a0001c0001t0001g0178a0001c0001t0002g0182a0001c0001t0009g0176others(12): Show | 15 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.1552-98T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281961 | ||||||
chr2:231281965
|
C | A | 1 | a0001c0002t0002g0174 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1552-94C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231281965 | ||||||
chr2:231282005
|
G | C | 1 | a0001c0001t0019g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1552-54G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231282005 | ||||||
chr2:231282038
|
G | T | 1 | a0001c0002t0021g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1552-21G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 16/24 | chr2 | 231282038 | ||||||
chr2:231282159
|
G | A | 34 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1626+26G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231282159 | ||||||
chr2:231283036
|
A | C | 1 | a0001c0002t0003g0181 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1626+903A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231283036 | ||||||
chr2:231283145
|
A | C | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1626+1012A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231283145 | ||||||
chr2:231283629
|
C | T | 1 | a0001c0001t0019g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1626+1496C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231283629 | ||||||
chr2:231283694
|
C | T | 36 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1626+1561C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231283694 | ||||||
chr2:231283922
|
T | TA | 2 | a0001c0001t0031g0062a0001c0001t0032g0111 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1626+1790dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231283922 | |||||
chr2:231284469
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0003g0149a0001c0001t0006g0148others(3): Show | 6 | HG00438.hp2 HG00609.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1626+2336C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231284469 | ||||||
chr2:231284480
|
C | T | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1626+2347C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231284480 | ||||||
chr2:231285645
|
C | CA | 85 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(82): Show | 85 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1626+3524dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231285645 | |||||
chr2:231286005
|
GACA | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1626+3877_1626+387 others(7): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231286005 | |||||
chr2:231286053
|
C | T | 36 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1626+3920C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286053 | ||||||
chr2:231286105
|
G | A | 1 | a0001c0001t0006g0196 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1626+3972G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286105 | ||||||
chr2:231286141
|
C | A | 195 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(192): Show | 195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1626+4008C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286141 | ||||||
chr2:231286185
|
G | A | 4 | a0001c0003t0001g0033a0001c0003t0010g0038a0001c0004t0042g0035others(1): Show | 4 | HG00280.hp2 HG01069.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626+4052G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286185 | ||||||
chr2:231286304
|
C | A | 1 | a0001c0001t0030g0132 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1626+4171C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286304 | ||||||
chr2:231286305
|
G | A | 1 | a0001c0001t0008g0122 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1626+4172G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286305 | ||||||
chr2:231286443
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1626+4310C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286443 | ||||||
chr2:231286496
|
A | G | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1626+4363A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286496 | ||||||
chr2:231286908
|
C | T | 45 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1627-4445C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231286908 | ||||||
chr2:231287338
|
G | A | 1 | a0001c0004t0028g0014 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1627-4015G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231287338 | ||||||
chr2:231287495
|
T | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1627-3858T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231287495 | ||||||
chr2:231287576
|
G | T | 1 | a0001c0001t0013g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1627-3777G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231287576 | ||||||
chr2:231287584
|
A | G | 41 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0068others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1627-3769A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231287584 | ||||||
chr2:231288130
|
A | G | 1 | a0001c0004t0002g0012 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1627-3223A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231288130 | ||||||
chr2:231288351
|
T | C | 47 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1627-3002T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231288351 | ||||||
chr2:231288482
|
C | T | 40 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1627-2871C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231288482 | ||||||
chr2:231288494
|
T | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1627-2859T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231288494 | ||||||
chr2:231289110
|
G | A | 37 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1627-2243G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289110 | ||||||
chr2:231289167
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1627-2186T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289167 | ||||||
chr2:231289418
|
G | C | 1 | a0001c0001t0017g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1627-1935G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289418 | ||||||
chr2:231289480
|
G | A | 2 | a0001c0004t0024g0002a0001c0004t0024g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1627-1873G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289480 | ||||||
chr2:231289518
|
G | A | 25 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1627-1835G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289518 | ||||||
chr2:231289699
|
G | A | 70 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(67): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1627-1654G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289699 | ||||||
chr2:231289748
|
A | T | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1627-1605A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289748 | ||||||
chr2:231289843
|
T | C | 1 | a0001c0002t0002g0058 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1627-1510T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231289843 | ||||||
chr2:231290633
|
G | A | 26 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1627-720G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231290633 | ||||||
chr2:231290732
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1627-621A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231290732 | ||||||
chr2:231290928
|
T | G | 37 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1627-425T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | chr2 | 231290928 | ||||||
chr2:231290950
|
GT | G | 119 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0065others(116): Show | 119 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1627-386delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231290950 | |||||
chr2:231290950
|
GTT | G | 70 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(67): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1627-387_1627-386d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr2 | 231290950 | |||||
chr2:231291566
|
C | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | NA18948.hp1 NA18984.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717+123C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231291566 | ||||||
chr2:231291582
|
C | T | 1 | a0001c0002t0012g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1717+139C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231291582 | ||||||
chr2:231291740
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1717+297A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231291740 | ||||||
chr2:231292124
|
C | T | 37 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1717+681C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231292124 | ||||||
chr2:231292167
|
C | CA | 8 | a0001c0001t0009g0176a0001c0001t0014g0118a0001c0001t0016g0134others(5): Show | 8 | HG00423.hp1 HG00544.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1717+743dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231292167 | |||||
chr2:231292167
|
CA | C | 5 | a0001c0001t0001g0072a0001c0001t0009g0144a0001c0002t0002g0112others(2): Show | 5 | HG02155.hp1 HG03017.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717+743delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231292167 | |||||
chr2:231292501
|
C | T | 36 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(33): Show | 36 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1717+1058C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231292501 | ||||||
chr2:231292602
|
G | A | 20 | a0001c0001t0001g0075a0001c0001t0001g0106a0001c0001t0001g0171others(17): Show | 20 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.1717+1159G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231292602 | ||||||
chr2:231292613
|
G | A | 2 | a0002c0005t0008g0010a0002c0006t0002g0021 | 2 | HG02155.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1717+1170G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231292613 | ||||||
chr2:231292630
|
C | G | 34 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1717+1187C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231292630 | ||||||
chr2:231292959
|
A | C | 3 | a0001c0003t0010g0038a0001c0004t0042g0035a0001c0004t0043g0034 | 3 | HG00280.hp2 HG01069.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1717+1516A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231292959 | ||||||
chr2:231292966
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0068 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1717+1523A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231292966 | ||||||
chr2:231293026
|
G | T | 1 | a0001c0003t0005g0042 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1717+1583G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231293026 | ||||||
chr2:231293035
|
G | A | 1 | a0001c0001t0007g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1717+1592G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231293035 | ||||||
chr2:231293207
|
A | G | 3 | a0001c0002t0002g0161a0001c0002t0003g0160a0001c0002t0003g0180 | 3 | HG01943.hp1 HG01993.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1717+1764A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231293207 | ||||||
chr2:231293307
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1717+1864C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231293307 | ||||||
chr2:231293533
|
A | G | 118 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1717+2090A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231293533 | ||||||
chr2:231293670
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1717+2227C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231293670 | ||||||
chr2:231294071
|
CTG | C | 25 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1718-2124_1718-212 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr2 | 231294071 | |||||
chr2:231294086
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1718-2112C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231294086 | ||||||
chr2:231294172
|
C | T | 70 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(67): Show | 70 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1718-2026C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231294172 | ||||||
chr2:231294397
|
C | T | 3 | a0001c0001t0010g0186a0001c0001t0010g0187a0001c0002t0006g0191 | 3 | HG00408.hp2 HG02080.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1718-1801C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231294397 | ||||||
chr2:231294434
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1718-1764G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231294434 | ||||||
chr2:231294499
|
T | C | 168 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(165): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.1718-1699T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231294499 | ||||||
chr2:231294530
|
A | G | 37 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1718-1668A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231294530 | ||||||
chr2:231295578
|
G | A | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1718-620G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231295578 | ||||||
chr2:231295768
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1718-430A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231295768 | ||||||
chr2:231295841
|
C | A | 69 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(66): Show | 69 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.1718-357C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231295841 | ||||||
chr2:231295987
|
G | A | 1 | a0001c0001t0009g0144 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1718-211G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 18/24 | chr2 | 231295987 | ||||||
chr2:231296824
|
G | A | 1 | a0001c0003t0007g0028 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1773+571G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231296824 | ||||||
chr2:231296828
|
T | A | 1 | a0001c0001t0015g0150 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1773+575T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231296828 | ||||||
chr2:231296968
|
G | A | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1773+715G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231296968 | ||||||
chr2:231297231
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+978C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231297231 | ||||||
chr2:231297880
|
C | T | 37 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.1773+1627C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231297880 | ||||||
chr2:231298472
|
T | C | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1773+2219T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231298472 | ||||||
chr2:231298866
|
G | A | 26 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1773+2613G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231298866 | ||||||
chr2:231298867
|
G | C | 40 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1773+2614G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231298867 | ||||||
chr2:231299182
|
T | A | 1 | a0001c0002t0002g0098 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1773+2929T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231299182 | ||||||
chr2:231299457
|
A | G | 40 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1773+3204A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231299457 | ||||||
chr2:231299526
|
T | C | 1 | a0001c0001t0014g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1773+3273T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231299526 | ||||||
chr2:231299589
|
G | A | 1 | a0001c0002t0021g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1773+3336G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231299589 | ||||||
chr2:231299711
|
G | A | 1 | a0001c0002t0014g0056 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1773+3458G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231299711 | ||||||
chr2:231299776
|
T | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1773+3523T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231299776 | ||||||
chr2:231299778
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1773+3525T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231299778 | ||||||
chr2:231300013
|
A | G | 40 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1773+3760A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231300013 | ||||||
chr2:231300350
|
C | T | 39 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(36): Show | 39 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1773+4097C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231300350 | ||||||
chr2:231300495
|
G | C | 1 | a0001c0001t0007g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1773+4242G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231300495 | ||||||
chr2:231300520
|
C | G | 36 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1773+4267C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231300520 | ||||||
chr2:231300909
|
G | A | 39 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(36): Show | 39 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1773+4656G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231300909 | ||||||
chr2:231300999
|
C | A | 1 | a0001c0003t0049g0008 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1773+4746C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231300999 | ||||||
chr2:231301030
|
G | A | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1773+4777G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231301030 | ||||||
chr2:231301585
|
T | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+5332T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231301585 | ||||||
chr2:231301596
|
C | T | 1 | a0001c0002t0022g0145 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1773+5343C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231301596 | ||||||
chr2:231301999
|
C | T | 1 | a0001c0001t0007g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1773+5746C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231301999 | ||||||
chr2:231302433
|
G | GTT | 23 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(20): Show | 23 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1773+6182_1773+618 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231302433 | |||||
chr2:231302433
|
G | GTTT | 9 | a0001c0001t0008g0122a0001c0001t0011g0165a0001c0001t0054g0197others(6): Show | 9 | HG00558.hp2 HG01070.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1773+6181_1773+618 others(7): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231302433 | |||||
chr2:231302437
|
G | GT | 42 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0106others(39): Show | 42 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1773+6209dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231302437 | |||||
chr2:231302437
|
G | GTT | 11 | a0001c0001t0001g0179a0001c0001t0002g0182a0001c0001t0002g0189others(8): Show | 11 | HG00423.hp1 HG00621.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1773+6208_1773+620 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231302437 | |||||
chr2:231302437
|
G | T | 35 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1773+6184G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231302437 | ||||||
chr2:231302437
|
GT | G | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1773+6209delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231302437 | |||||
chr2:231302442
|
T | G | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1773+6189T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231302442 | ||||||
chr2:231302459
|
T | C | 2 | a0001c0001t0011g0120a0001c0001t0019g0067 | 2 | HG02602.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1773+6206T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231302459 | ||||||
chr2:231302531
|
G | T | 1 | a0001c0003t0005g0006 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1773+6278G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231302531 | ||||||
chr2:231302547
|
A | G | 1 | a0001c0001t0019g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1773+6294A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231302547 | ||||||
chr2:231302941
|
T | C | 8 | a0001c0001t0001g0151a0001c0001t0003g0149a0001c0001t0006g0148others(5): Show | 8 | HG00438.hp2 HG00609.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.1773+6688T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231302941 | ||||||
chr2:231303025
|
A | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+6772A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231303025 | ||||||
chr2:231303094
|
A | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+6841A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231303094 | ||||||
chr2:231303444
|
G | A | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+7191G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231303444 | ||||||
chr2:231303666
|
G | A | 7 | a0001c0003t0001g0037a0001c0003t0004g0032a0001c0003t0005g0029others(4): Show | 7 | HG01361.hp1 HG02015.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1773+7413G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231303666 | ||||||
chr2:231303768
|
T | C | 3 | a0001c0003t0001g0037a0001c0003t0004g0032a0001c0003t0030g0036 | 3 | HG01361.hp1 NA18968.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1773+7515T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231303768 | ||||||
chr2:231303900
|
C | T | 1 | a0001c0004t0014g0019 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1773+7647C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231303900 | ||||||
chr2:231304014
|
T | C | 111 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(108): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1773+7761T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304014 | ||||||
chr2:231304036
|
C | T | 1 | a0001c0002t0014g0056 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1773+7783C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304036 | ||||||
chr2:231304100
|
C | G | 1 | a0001c0002t0003g0085 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1773+7847C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304100 | ||||||
chr2:231304185
|
G | A | 1 | a0001c0001t0032g0111 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1773+7932G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304185 | ||||||
chr2:231304186
|
C | T | 8 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(5): Show | 8 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1773+7933C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304186 | ||||||
chr2:231304303
|
A | G | 2 | a0001c0001t0001g0168a0001c0002t0028g0163 | 2 | HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1773+8050A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304303 | ||||||
chr2:231304417
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0074 | 2 | HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1773+8164C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304417 | ||||||
chr2:231304712
|
T | A | 1 | a0001c0003t0012g0015 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1773+8459T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304712 | ||||||
chr2:231304788
|
A | C | 1 | a0001c0004t0014g0019 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1773+8535A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231304788 | ||||||
chr2:231305241
|
T | C | 1 | a0001c0002t0060g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1773+8988T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231305241 | ||||||
chr2:231305648
|
C | T | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1773+9395C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231305648 | ||||||
chr2:231305709
|
C | T | 1 | a0001c0001t0023g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1773+9456C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231305709 | ||||||
chr2:231306324
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1773+10071A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231306324 | ||||||
chr2:231306405
|
T | C | 1 | a0001c0001t0006g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1773+10152T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231306405 | ||||||
chr2:231306482
|
G | A | 110 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1773+10229G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231306482 | ||||||
chr2:231306489
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1773+10236T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231306489 | ||||||
chr2:231306662
|
A | G | 1 | a0001c0003t0005g0029 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1773+10409A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231306662 | ||||||
chr2:231307255
|
A | G | 27 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.1773+11002A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231307255 | ||||||
chr2:231307444
|
C | T | 1 | a0001c0001t0006g0094 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1773+11191C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231307444 | ||||||
chr2:231308038
|
G | A | 3 | a0001c0003t0001g0013a0001c0003t0012g0015a0001c0004t0012g0007 | 3 | NA19005.hp1 NA19056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1773+11785G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308038 | ||||||
chr2:231308166
|
G | A | 1 | a0001c0001t0023g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1773+11913G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308166 | ||||||
chr2:231308180
|
C | T | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1773+11927C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308180 | ||||||
chr2:231308220
|
G | A | 1 | a0001c0001t0014g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1773+11967G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308220 | ||||||
chr2:231308398
|
C | A | 36 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1773+12145C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308398 | ||||||
chr2:231308556
|
G | A | 1 | a0001c0003t0005g0042 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1773+12303G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308556 | ||||||
chr2:231308572
|
C | T | 7 | a0001c0001t0001g0106a0001c0001t0004g0101a0001c0001t0004g0105others(4): Show | 7 | HG00544.hp2 HG00673.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1773+12319C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308572 | ||||||
chr2:231308869
|
C | T | 1 | a0001c0001t0006g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1773+12616C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231308869 | ||||||
chr2:231309009
|
C | T | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1773+12756C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231309009 | ||||||
chr2:231309519
|
C | T | 7 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0005g0143others(4): Show | 7 | HG00558.hp2 NA18986.hp1 NA18997.hp2 others(4): Show |
intron_variant | MODIFIER | c.1773+13266C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231309519 | ||||||
chr2:231309572
|
C | G | 1 | a0001c0001t0017g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1773+13319C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231309572 | ||||||
chr2:231309615
|
A | G | 1 | a0001c0001t0017g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1773+13362A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231309615 | ||||||
chr2:231309926
|
A | G | 8 | a0001c0001t0033g0157a0001c0003t0001g0037a0001c0003t0004g0032others(5): Show | 8 | HG01361.hp1 HG02015.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1773+13673A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231309926 | ||||||
chr2:231310059
|
C | T | 1 | a0001c0001t0011g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1773+13806C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231310059 | ||||||
chr2:231310137
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1773+13884G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231310137 | ||||||
chr2:231310451
|
G | GC | 73 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(70): Show | 73 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1773+14199dupC | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231310451 | |||||
chr2:231310983
|
T | C | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+14730T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231310983 | ||||||
chr2:231311507
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0034g0061a0001c0003t0035g0027 | 3 | HG00642.hp2 HG01081.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1773+15254C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231311507 | ||||||
chr2:231311770
|
C | CA | 5 | a0001c0001t0001g0078a0001c0001t0001g0090a0001c0001t0019g0097others(2): Show | 5 | HG01175.hp1 HG01175.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1773+15543dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231311770 | |||||
chr2:231311770
|
CA | C | 81 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0065others(78): Show | 81 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.1773+15543delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231311770 | |||||
chr2:231311770
|
CAA | C | 67 | a0001c0001t0001g0126a0001c0001t0001g0129a0001c0001t0001g0151others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1773+15542_1773+15 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231311770 | |||||
chr2:231311828
|
G | A | 38 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1773+15575G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231311828 | ||||||
chr2:231312040
|
A | G | 1 | a0001c0004t0014g0019 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1773+15787A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231312040 | ||||||
chr2:231312165
|
C | T | 2 | a0001c0001t0008g0153a0001c0001t0017g0121 | 2 | NA18951.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1773+15912C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231312165 | ||||||
chr2:231312388
|
A | C | 3 | a0001c0003t0037g0003a0001c0004t0002g0012a0001c0015t0059g0104 | 3 | HG01081.hp1 HG01168.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1773+16135A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231312388 | ||||||
chr2:231312548
|
C | G | 2 | a0001c0001t0009g0142a0001c0002t0012g0139 | 2 | NA18943.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1773+16295C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231312548 | ||||||
chr2:231312598
|
C | CT | 6 | a0001c0001t0001g0078a0001c0001t0002g0198a0001c0001t0009g0041others(3): Show | 6 | HG00621.hp2 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1773+16362dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231312598 | |||||
chr2:231312800
|
A | G | 1 | a0001c0002t0027g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1773+16547A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231312800 | ||||||
chr2:231312861
|
G | T | 199 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(196): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1773+16608G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231312861 | ||||||
chr2:231313573
|
C | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+17320C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231313573 | ||||||
chr2:231313584
|
T | C | 1 | a0001c0001t0040g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1773+17331T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231313584 | ||||||
chr2:231313819
|
A | G | 34 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1773+17566A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231313819 | ||||||
chr2:231313866
|
C | CACCTCAG others(43): Show |
1 | a0001c0002t0002g0058 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1773+17614_1773+17 others(56): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231313866 | |||||
chr2:231313942
|
G | T | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1773+17689G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231313942 | ||||||
chr2:231313968
|
C | T | 25 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1773+17715C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231313968 | ||||||
chr2:231313969
|
A | T | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1773+17716A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231313969 | ||||||
chr2:231314071
|
T | C | 40 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(37): Show | 40 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1774-17722T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314071 | ||||||
chr2:231314077
|
T | G | 39 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0001g0158others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1774-17716T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314077 | ||||||
chr2:231314149
|
A | G | 114 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1774-17644A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314149 | ||||||
chr2:231314390
|
G | A | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1774-17403G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314390 | ||||||
chr2:231314427
|
G | A | 1 | a0002c0006t0002g0021 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1774-17366G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314427 | ||||||
chr2:231314527
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1774-17266A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314527 | ||||||
chr2:231314675
|
G | A | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1774-17118G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314675 | ||||||
chr2:231314944
|
A | G | 114 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1774-16849A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231314944 | ||||||
chr2:231315204
|
A | G | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1774-16589A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231315204 | ||||||
chr2:231315238
|
C | CA | 34 | a0001c0001t0001g0072a0001c0001t0003g0149a0001c0001t0004g0124others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1774-16537dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231315238 | |||||
chr2:231315396
|
A | G | 72 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1774-16397A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231315396 | ||||||
chr2:231315439
|
T | A | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1774-16354T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231315439 | ||||||
chr2:231315681
|
C | T | 199 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(196): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1774-16112C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231315681 | ||||||
chr2:231315735
|
A | AT | 71 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(68): Show | 71 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.1774-16056dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231315735 | |||||
chr2:231316160
|
A | ATG | 3 | a0001c0001t0009g0100a0001c0001t0031g0166a0001c0001t0033g0157 | 3 | HG02257.hp2 NA18945.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1774-15601_1774-15 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231316160 | |||||
chr2:231316160
|
ATG | A | 44 | a0001c0001t0001g0046a0001c0001t0001g0168a0001c0001t0001g0178others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1774-15601_1774-15 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231316160 | |||||
chr2:231316160
|
ATGTG | A | 30 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(27): Show | 30 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.1774-15603_1774-15 others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231316160 | |||||
chr2:231316160
|
ATGTGTG | A | 36 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0005g0143others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1774-15605_1774-15 others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231316160 | |||||
chr2:231316664
|
C | CAA | 37 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0005g0143others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1774-15118_1774-15 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231316664 | |||||
chr2:231317171
|
T | C | 1 | a0001c0001t0039g0119 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1774-14622T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231317171 | ||||||
chr2:231317193
|
C | T | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1774-14600C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231317193 | ||||||
chr2:231317210
|
G | A | 1 | a0001c0001t0031g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1774-14583G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231317210 | ||||||
chr2:231317316
|
G | T | 1 | a0001c0003t0044g0020 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1774-14477G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231317316 | ||||||
chr2:231317527
|
GT | G | 8 | a0001c0001t0055g0193a0001c0003t0001g0037a0001c0003t0004g0032others(5): Show | 8 | HG01361.hp1 HG02015.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.1774-14253delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231317527 | |||||
chr2:231317657
|
A | T | 6 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1774-14136A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231317657 | ||||||
chr2:231318255
|
A | AG | 34 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1774-13535dupG | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231318255 | |||||
chr2:231318681
|
G | A | 2 | a0001c0002t0003g0181a0001c0002t0032g0177 | 2 | NA18957.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1774-13112G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231318681 | ||||||
chr2:231318877
|
G | T | 1 | a0005c0013t0026g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1774-12916G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231318877 | ||||||
chr2:231318878
|
C | T | 73 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0001g0168others(70): Show | 73 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1774-12915C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231318878 | ||||||
chr2:231319212
|
C | T | 110 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1774-12581C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231319212 | ||||||
chr2:231319258
|
G | A | 37 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0005g0143others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1774-12535G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231319258 | ||||||
chr2:231319701
|
C | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1774-12092C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231319701 | ||||||
chr2:231320119
|
AGC | A | 37 | a0001c0001t0001g0054a0001c0001t0001g0129a0001c0001t0005g0143others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1774-11673_1774-11 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320119 | ||||||
chr2:231320259
|
C | T | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1774-11534C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320259 | ||||||
chr2:231320399
|
A | G | 2 | a0001c0004t0024g0002a0001c0004t0024g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1774-11394A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320399 | ||||||
chr2:231320558
|
CA | C | 70 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0001g0168others(67): Show | 70 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1774-11219delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231320558 | |||||
chr2:231320718
|
G | A | 39 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(36): Show | 39 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1774-11075G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320718 | ||||||
chr2:231320746
|
A | T | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1774-11047A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320746 | ||||||
chr2:231320788
|
G | A | 1 | a0001c0004t0002g0109 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1774-11005G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320788 | ||||||
chr2:231320853
|
A | C | 9 | a0001c0001t0006g0196a0001c0001t0007g0195a0001c0001t0054g0197others(6): Show | 9 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1774-10940A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320853 | ||||||
chr2:231320910
|
T | C | 1 | a0001c0004t0036g0039 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1774-10883T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320910 | ||||||
chr2:231320961
|
T | G | 1 | a0001c0001t0033g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1774-10832T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320961 | ||||||
chr2:231320975
|
G | C | 33 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1774-10818G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231320975 | ||||||
chr2:231321254
|
G | A | 32 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0003g0149others(29): Show | 32 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1774-10539G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231321254 | ||||||
chr2:231321419
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1774-10374C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231321419 | ||||||
chr2:231321508
|
T | C | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1774-10285T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231321508 | ||||||
chr2:231321521
|
C | T | 1 | a0001c0001t0032g0111 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1774-10272C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231321521 | ||||||
chr2:231321555
|
C | T | 39 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(36): Show | 39 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1774-10238C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231321555 | ||||||
chr2:231321754
|
C | T | 7 | a0001c0003t0001g0037a0001c0003t0004g0032a0001c0003t0005g0029others(4): Show | 7 | HG01361.hp1 HG02015.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1774-10039C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231321754 | ||||||
chr2:231321947
|
T | A | 2 | a0001c0004t0024g0002a0001c0004t0024g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1774-9846T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231321947 | ||||||
chr2:231322443
|
C | T | 108 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0129others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1774-9350C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231322443 | ||||||
chr2:231322505
|
T | G | 1 | a0001c0001t0001g0178 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1774-9288T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231322505 | ||||||
chr2:231322694
|
G | A | 1 | a0001c0002t0003g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1774-9099G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231322694 | ||||||
chr2:231323041
|
G | A | 37 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.1774-8752G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231323041 | ||||||
chr2:231323081
|
C | T | 74 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0001g0168others(71): Show | 74 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1774-8712C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231323081 | ||||||
chr2:231323098
|
A | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0014g0118 | 3 | HG00741.hp2 HG03927.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1774-8695A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231323098 | ||||||
chr2:231323568
|
A | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0074 | 2 | HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1774-8225A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231323568 | ||||||
chr2:231323590
|
G | A | 1 | a0001c0002t0003g0181 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1774-8203G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231323590 | ||||||
chr2:231323863
|
T | C | 6 | a0001c0003t0001g0037a0001c0003t0004g0032a0001c0003t0005g0031others(3): Show | 6 | HG01361.hp1 HG02015.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1774-7930T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231323863 | ||||||
chr2:231324123
|
C | CT | 136 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1774-7648dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231324123 | |||||
chr2:231324123
|
C | CTT | 15 | a0001c0001t0001g0106a0001c0001t0002g0182a0001c0001t0004g0169others(12): Show | 15 | HG00438.hp1 HG00639.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1774-7649_1774-764 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231324123 | |||||
chr2:231324123
|
CT | C | 6 | a0001c0001t0007g0045a0001c0001t0007g0047a0001c0001t0013g0051others(3): Show | 6 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1774-7648delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231324123 | |||||
chr2:231324166
|
T | C | 2 | a0001c0002t0002g0115a0006c0007t0014g0018 | 2 | HG02257.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1774-7627T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324166 | ||||||
chr2:231324167
|
G | C | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1774-7626G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324167 | ||||||
chr2:231324184
|
G | A | 4 | a0001c0003t0004g0032a0001c0003t0005g0031a0001c0004t0003g0030others(1): Show | 4 | HG01361.hp1 HG02015.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1774-7609G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324184 | ||||||
chr2:231324187
|
G | A | 1 | a0001c0001t0029g0049 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1774-7606G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324187 | ||||||
chr2:231324190
|
C | T | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1774-7603C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324190 | ||||||
chr2:231324191
|
A | G | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1774-7602A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324191 | ||||||
chr2:231324237
|
T | C | 2 | a0001c0001t0016g0134a0001c0003t0044g0020 | 2 | HG01981.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1774-7556T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324237 | ||||||
chr2:231324273
|
A | G | 1 | a0001c0002t0003g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1774-7520A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324273 | ||||||
chr2:231324409
|
G | C | 143 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0072others(140): Show | 143 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1774-7384G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324409 | ||||||
chr2:231324454
|
T | TA | 49 | a0001c0001t0001g0168a0001c0001t0001g0178a0001c0001t0001g0179others(46): Show | 49 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1774-7324dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231324454 | |||||
chr2:231324544
|
G | C | 2 | a0001c0001t0001g0168a0001c0002t0028g0163 | 2 | HG03490.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1774-7249G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324544 | ||||||
chr2:231324668
|
G | C | 123 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0065others(120): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1774-7125G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324668 | ||||||
chr2:231324763
|
A | C | 3 | a0001c0001t0040g0128a0001c0002t0002g0043a0001c0002t0002g0073 | 3 | HG02074.hp1 HG02080.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1774-7030A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324763 | ||||||
chr2:231324930
|
T | TAAAACAA others(2161): Show |
1 | a0001c0002t0003g0180 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1774-6850_1774-684 others(2172): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231324930 | |||||
chr2:231324995
|
G | A | 75 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0065others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1774-6798G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231324995 | ||||||
chr2:231325013
|
C | T | 75 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0065others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1774-6780C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231325013 | ||||||
chr2:231325192
|
T | C | 147 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(144): Show | 147 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1774-6601T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231325192 | ||||||
chr2:231325462
|
G | A | 2 | a0001c0003t0001g0013a0001c0004t0012g0007 | 2 | NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1774-6331G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231325462 | ||||||
chr2:231325486
|
G | A | 4 | a0001c0001t0007g0195a0001c0001t0054g0197a0001c0003t0007g0028others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774-6307G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231325486 | ||||||
chr2:231325716
|
G | A | 2 | a0001c0001t0032g0111a0003c0010t0001g0108 | 2 | HG02027.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1774-6077G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231325716 | ||||||
chr2:231325755
|
G | A | 8 | a0001c0001t0005g0138a0001c0002t0003g0155a0001c0003t0001g0037others(5): Show | 8 | HG01361.hp1 HG02015.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774-6038G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231325755 | ||||||
chr2:231326018
|
C | T | 1 | a0001c0002t0014g0056 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1774-5775C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326018 | ||||||
chr2:231326057
|
A | G | 70 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0151others(67): Show | 70 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1774-5736A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326057 | ||||||
chr2:231326213
|
T | C | 149 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1774-5580T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326213 | ||||||
chr2:231326273
|
C | A | 39 | a0001c0001t0001g0054a0001c0001t0001g0126a0001c0001t0001g0151others(36): Show | 39 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1774-5520C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326273 | ||||||
chr2:231326311
|
A | G | 1 | a0001c0003t0010g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1774-5482A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326311 | ||||||
chr2:231326342
|
G | C | 1 | a0001c0003t0001g0033 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1774-5451G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326342 | ||||||
chr2:231326366
|
G | A | 1 | a0001c0003t0010g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1774-5427G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326366 | ||||||
chr2:231326425
|
C | G | 2 | a0001c0001t0033g0157a0006c0007t0014g0018 | 2 | HG02257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1774-5368C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326425 | ||||||
chr2:231326523
|
A | G | 92 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0065others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1774-5270A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326523 | ||||||
chr2:231326538
|
G | A | 27 | a0001c0001t0001g0126a0001c0001t0001g0151a0001c0001t0004g0101others(24): Show | 27 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1774-5255G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326538 | ||||||
chr2:231326828
|
A | C | 1 | a0001c0012t0048g0156 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1774-4965A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326828 | ||||||
chr2:231326969
|
G | A | 1 | a0001c0004t0028g0014 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1774-4824G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231326969 | ||||||
chr2:231327085
|
T | C | 1 | a0001c0001t0017g0127 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1774-4708T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231327085 | ||||||
chr2:231327123
|
A | G | 1 | a0001c0002t0006g0191 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1774-4670A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231327123 | ||||||
chr2:231327323
|
G | A | 3 | a0001c0001t0008g0153a0001c0001t0017g0121a0001c0003t0001g0037 | 3 | NA18951.hp1 NA18968.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1774-4470G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231327323 | ||||||
chr2:231327593
|
C | T | 72 | a0001c0001t0001g0072a0001c0001t0001g0087a0001c0001t0001g0090others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1774-4200C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231327593 | ||||||
chr2:231328010
|
C | G | 65 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(62): Show | 65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1774-3783C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328010 | ||||||
chr2:231328320
|
G | C | 65 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(62): Show | 65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1774-3473G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328320 | ||||||
chr2:231328505
|
G | A | 63 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1774-3288G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328505 | ||||||
chr2:231328570
|
A | G | 1 | a0001c0001t0052g0131 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1774-3223A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328570 | ||||||
chr2:231328602
|
T | A | 65 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(62): Show | 65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1774-3191T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328602 | ||||||
chr2:231328740
|
T | C | 4 | a0001c0001t0009g0041a0001c0001t0009g0176a0001c0001t0050g0040others(1): Show | 4 | HG00544.hp1 HG00621.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774-3053T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328740 | ||||||
chr2:231328757
|
CAT | C | 65 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(62): Show | 65 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1774-3031_1774-303 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328757 | |||||
chr2:231328791
|
C | T | 63 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1774-3002C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328791 | ||||||
chr2:231328809
|
C | G | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-2984C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328809 | ||||||
chr2:231328814
|
C | CTTTT | 11 | a0001c0002t0002g0133a0001c0002t0002g0161a0001c0002t0002g0174others(8): Show | 11 | HG00423.hp1 HG00673.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1774-2978_1774-297 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(7): Show |
2 | a0001c0002t0003g0181a0001c0002t0032g0177 | 2 | NA18957.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1774-2975_1774-297 others(18): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(14): Show |
4 | a0001c0002t0028g0163a0001c0004t0024g0002a0001c0004t0024g0016others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774-2975_1774-297 others(25): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(15): Show |
16 | a0001c0002t0002g0069a0001c0002t0002g0098a0001c0002t0002g0112others(13): Show | 16 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1774-2975_1774-297 others(26): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(16): Show |
11 | a0001c0001t0058g0199a0001c0002t0002g0044a0001c0002t0002g0058others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1774-2975_1774-297 others(27): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(17): Show |
7 | a0001c0002t0002g0115a0001c0002t0021g0107a0001c0004t0013g0004others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1774-2975_1774-297 others(28): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(18): Show |
3 | a0001c0002t0002g0043a0001c0002t0022g0145a0001c0004t0014g0019 | 3 | HG02074.hp1 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1774-2975_1774-297 others(29): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(19): Show |
2 | a0001c0002t0012g0139a0001c0002t0051g0147 | 2 | NA18950.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1774-2975_1774-297 others(30): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(20): Show |
1 | a0001c0002t0012g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1774-2975_1774-297 others(31): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328814
|
C | CTTTTTTT others(21): Show |
1 | a0001c0004t0012g0007 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1774-2975_1774-297 others(32): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231328814 | |||||
chr2:231328819
|
C | T | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-2974C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328819 | ||||||
chr2:231328876
|
A | G | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-2917A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328876 | ||||||
chr2:231328877
|
C | A | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-2916C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328877 | ||||||
chr2:231328938
|
C | A | 1 | a0001c0001t0016g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1774-2855C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231328938 | ||||||
chr2:231329057
|
A | G | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-2736A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329057 | ||||||
chr2:231329084
|
G | A | 1 | a0001c0001t0013g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1774-2709G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329084 | ||||||
chr2:231329100
|
C | A | 58 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0058others(55): Show | 58 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.1774-2693C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329100 | ||||||
chr2:231329101
|
G | A | 1 | a0001c0001t0031g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1774-2692G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329101 | ||||||
chr2:231329116
|
C | T | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1774-2677C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329116 | ||||||
chr2:231329367
|
G | A | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-2426G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329367 | ||||||
chr2:231329733
|
C | T | 1 | a0001c0001t0058g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1774-2060C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329733 | ||||||
chr2:231329754
|
C | T | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-2039C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329754 | ||||||
chr2:231329778
|
C | T | 2 | a0001c0002t0002g0159a0001c0002t0002g0167 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1774-2015C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329778 | ||||||
chr2:231329876
|
C | A | 1 | a0001c0001t0005g0138 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1774-1917C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329876 | ||||||
chr2:231329889
|
A | G | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1904A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329889 | ||||||
chr2:231329897
|
T | C | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1896T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231329897 | ||||||
chr2:231330229
|
C | CTT | 13 | a0001c0002t0002g0159a0001c0002t0002g0161a0001c0002t0002g0190others(10): Show | 13 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1774-1549_1774-154 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231330229 | |||||
chr2:231330229
|
C | CTTT | 46 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(43): Show | 46 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.1774-1550_1774-154 others(7): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231330229 | |||||
chr2:231330229
|
CT | C | 90 | a0001c0001t0001g0046a0001c0001t0001g0072a0001c0001t0001g0151others(87): Show | 90 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1774-1548delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231330229 | |||||
chr2:231330254
|
A | G | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1539A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330254 | ||||||
chr2:231330283
|
G | A | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1510G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330283 | ||||||
chr2:231330384
|
C | T | 1 | a0001c0002t0003g0180 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1774-1409C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330384 | ||||||
chr2:231330389
|
C | T | 1 | a0001c0003t0049g0008 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1774-1404C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330389 | ||||||
chr2:231330423
|
G | A | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1370G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330423 | ||||||
chr2:231330506
|
C | T | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1287C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330506 | ||||||
chr2:231330575
|
A | G | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1218A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330575 | ||||||
chr2:231330762
|
A | G | 60 | a0001c0001t0058g0199a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1774-1031A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330762 | ||||||
chr2:231330812
|
GTAAAGGA others(13): Show |
G | 8 | a0001c0001t0001g0151a0001c0001t0005g0138a0001c0001t0006g0148others(5): Show | 8 | HG00558.hp1 HG00609.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1774-961_1774-942d others(22): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr2 | 231330812 | |||||
chr2:231330970
|
G | A | 3 | a0001c0001t0016g0134a0001c0002t0025g0095a0001c0004t0014g0019 | 3 | HG01074.hp2 HG02155.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1774-823G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231330970 | ||||||
chr2:231331240
|
T | C | 59 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0058others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1774-553T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331240 | ||||||
chr2:231331337
|
C | T | 1 | a0001c0001t0019g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1774-456C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331337 | ||||||
chr2:231331343
|
T | C | 4 | a0001c0001t0032g0111a0001c0001t0058g0199a0001c0003t0003g0023others(1): Show | 4 | HG02027.hp1 NA18963.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774-450T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331343 | ||||||
chr2:231331426
|
A | G | 1 | a0001c0002t0003g0085 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1774-367A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331426 | ||||||
chr2:231331456
|
CT | C | 59 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0058others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1774-336delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331456 | ||||||
chr2:231331523
|
G | A | 59 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0058others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1774-270G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331523 | ||||||
chr2:231331552
|
G | A | 59 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0058others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1774-241G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331552 | ||||||
chr2:231331760
|
T | A | 59 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0058others(56): Show | 59 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1774-33T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 19/24 | chr2 | 231331760 | ||||||
chr2:231331962
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1878+65G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231331962 | ||||||
chr2:231332026
|
A | G | 1 | a0001c0002t0027g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1878+129A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231332026 | ||||||
chr2:231332321
|
G | GGA | 60 | a0001c0001t0015g0060a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1878+432_1878+433d others(4): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231332321 | |||||
chr2:231332422
|
T | C | 60 | a0001c0001t0015g0060a0001c0002t0002g0043a0001c0002t0002g0044others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.1878+525T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231332422 | ||||||
chr2:231332769
|
G | A | 2 | a0001c0001t0029g0049a0001c0003t0004g0032 | 2 | HG01361.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1878+872G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231332769 | ||||||
chr2:231333459
|
C | T | 3 | a0001c0001t0034g0061a0001c0003t0035g0027a0001c0003t0037g0003 | 3 | HG01081.hp2 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1878+1562C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231333459 | ||||||
chr2:231333574
|
A | G | 2 | a0001c0001t0010g0186a0001c0001t0010g0187 | 2 | HG00408.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1878+1677A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231333574 | ||||||
chr2:231333580
|
A | G | 2 | a0001c0001t0001g0053a0001c0001t0001g0068 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1878+1683A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231333580 | ||||||
chr2:231333845
|
C | T | 1 | a0001c0012t0048g0156 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1878+1948C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231333845 | ||||||
chr2:231334182
|
G | T | 1 | a0001c0012t0048g0156 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1878+2285G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231334182 | ||||||
chr2:231334766
|
C | T | 5 | a0001c0001t0001g0113a0001c0001t0001g0158a0001c0001t0006g0066others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.1878+2869C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231334766 | ||||||
chr2:231334790
|
T | C | 2 | a0001c0004t0042g0035a0001c0004t0043g0034 | 2 | HG01069.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1878+2893T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231334790 | ||||||
chr2:231335393
|
C | T | 2 | a0001c0002t0012g0088a0001c0002t0051g0147 | 2 | NA18995.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1878+3496C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231335393 | ||||||
chr2:231335595
|
A | G | 199 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(196): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1878+3698A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231335595 | ||||||
chr2:231335771
|
T | C | 1 | a0001c0003t0049g0008 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1878+3874T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231335771 | ||||||
chr2:231335924
|
T | A | 2 | a0001c0001t0001g0113a0001c0003t0001g0005 | 2 | HG00642.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1878+4027T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231335924 | ||||||
chr2:231336051
|
C | A | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1878+4154C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231336051 | ||||||
chr2:231336467
|
C | T | 1 | a0002c0006t0002g0021 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1878+4570C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231336467 | ||||||
chr2:231336792
|
A | G | 1 | a0001c0001t0006g0082 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1878+4895A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231336792 | ||||||
chr2:231337154
|
C | T | 1 | a0001c0001t0053g0116 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1878+5257C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337154 | ||||||
chr2:231337270
|
G | GTA | 12 | a0001c0001t0001g0129a0001c0001t0001g0168a0001c0001t0004g0105others(9): Show | 12 | HG01071.hp1 HG01981.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.1878+5393_1878+539 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231337270 | |||||
chr2:231337272
|
A | G | 1 | a0001c0001t0008g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1878+5375A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337272 | ||||||
chr2:231337288
|
A | AT | 7 | a0001c0001t0023g0164a0001c0001t0031g0062a0001c0002t0003g0070others(4): Show | 7 | HG00735.hp1 HG01175.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1878+5392dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231337288 | |||||
chr2:231337290
|
A | AT | 93 | a0001c0001t0001g0046a0001c0001t0001g0091a0001c0001t0001g0151others(90): Show | 93 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1878+5418dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231337290 | |||||
chr2:231337290
|
A | ATT | 8 | a0001c0001t0002g0182a0001c0001t0004g0169a0001c0001t0011g0165others(5): Show | 8 | HG00438.hp1 HG02056.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1878+5417_1878+541 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231337290 | |||||
chr2:231337290
|
A | T | 14 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0074others(11): Show | 14 | HG00735.hp1 HG00735.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1878+5393A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337290 | ||||||
chr2:231337291
|
T | TA | 46 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0075others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1878+5394_1878+539 others(5): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337291 | ||||||
chr2:231337291
|
T | TATA | 2 | a0001c0001t0001g0054a0001c0001t0004g0059 | 2 | NA18986.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1878+5394_1878+539 others(7): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337291 | ||||||
chr2:231337292
|
T | A | 5 | a0001c0001t0001g0158a0001c0001t0005g0138a0001c0001t0006g0057others(2): Show | 5 | HG00642.hp1 HG01433.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1878+5395T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337292 | ||||||
chr2:231337293
|
T | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0178 | 3 | HG03490.hp2 HG03492.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1878+5396T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337293 | ||||||
chr2:231337404
|
C | G | 1 | a0001c0003t0013g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1878+5507C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337404 | ||||||
chr2:231337442
|
G | C | 3 | a0001c0001t0032g0111a0001c0001t0058g0199a0001c0003t0003g0023 | 3 | HG02027.hp1 NA18963.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1878+5545G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337442 | ||||||
chr2:231337469
|
G | GT | 33 | a0001c0001t0001g0081a0001c0001t0001g0171a0001c0001t0004g0169others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.1878+5590dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231337469 | |||||
chr2:231337469
|
G | T | 5 | a0001c0001t0001g0113a0001c0001t0001g0158a0001c0001t0006g0066others(2): Show | 5 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(2): Show |
intron_variant | MODIFIER | c.1878+5572G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337469 | ||||||
chr2:231337476
|
T | G | 3 | a0001c0002t0011g0170a0001c0002t0033g0172a0003c0011t0002g0089 | 3 | HG02165.hp1 HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1878+5579T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231337476 | ||||||
chr2:231337526
|
G | GTGGCGGG others(1): Show |
6 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(3): Show | 6 | HG00323.hp2 HG00738.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1878+5631_1878+563 others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231337526 | |||||
chr2:231337980
|
CAG | C | 7 | a0001c0002t0014g0056a0001c0002t0027g0117a0001c0002t0047g0080others(4): Show | 7 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1878+6088_1878+608 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231337980 | |||||
chr2:231338056
|
T | A | 1 | a0001c0004t0011g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1878+6159T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231338056 | ||||||
chr2:231338221
|
CT | C | 5 | a0001c0001t0001g0072a0001c0001t0017g0127a0001c0001t0019g0097others(2): Show | 5 | HG00323.hp2 HG01070.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1878+6341delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231338221 | |||||
chr2:231338256
|
C | T | 4 | a0001c0001t0010g0162a0001c0001t0055g0193a0001c0001t0056g0200others(1): Show | 4 | NA18969.hp2 NA18993.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878+6359C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231338256 | ||||||
chr2:231338330
|
TGCCTCA | T | 5 | a0001c0002t0027g0117a0001c0002t0047g0080a0001c0004t0024g0002others(2): Show | 5 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1878+6445_1878+645 others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231338330 | |||||
chr2:231338535
|
C | CT | 8 | a0001c0001t0001g0079a0001c0001t0001g0106a0001c0001t0002g0182others(5): Show | 8 | HG00741.hp2 HG02027.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1879-6418dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231338535 | |||||
chr2:231338564
|
G | A | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1879-6411G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231338564 | ||||||
chr2:231338595
|
G | A | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1879-6380G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231338595 | ||||||
chr2:231338758
|
A | T | 1 | a0001c0001t0053g0116 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1879-6217A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231338758 | ||||||
chr2:231339200
|
CATCTGT | C | 2 | a0001c0001t0008g0153a0001c0003t0005g0031 | 2 | NA18951.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1879-5773_1879-576 others(10): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231339200 | |||||
chr2:231339200
|
CATCTGTA | C | 37 | a0001c0001t0004g0059a0001c0001t0004g0101a0001c0001t0004g0105others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1879-5771_1879-576 others(11): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231339200 | |||||
chr2:231339807
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1879-5168C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231339807 | ||||||
chr2:231340041
|
G | A | 2 | a0001c0001t0002g0189a0001c0001t0002g0198 | 2 | NA18943.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1879-4934G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231340041 | ||||||
chr2:231340803
|
G | A | 1 | a0001c0004t0011g0110 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1879-4172G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231340803 | ||||||
chr2:231341313
|
C | T | 140 | a0001c0001t0001g0151a0001c0001t0002g0182a0001c0001t0003g0149others(137): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1879-3662C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231341313 | ||||||
chr2:231341640
|
T | TGATA | 71 | a0001c0001t0001g0078a0001c0001t0001g0178a0001c0001t0001g0179others(68): Show | 71 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1879-3300_1879-329 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231341640 | |||||
chr2:231341640
|
T | TGATAGAT others(1): Show |
76 | a0001c0001t0001g0046a0001c0001t0001g0079a0001c0001t0001g0081others(73): Show | 76 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1879-3304_1879-329 others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231341640 | |||||
chr2:231341640
|
T | TGATAGAT others(5): Show |
7 | a0001c0001t0001g0087a0001c0001t0004g0169a0001c0001t0005g0138others(4): Show | 7 | HG00323.hp2 HG00438.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1879-3308_1879-329 others(16): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231341640 | |||||
chr2:231341640
|
T | TGATAGAT others(9): Show |
3 | a0001c0001t0001g0171a0001c0001t0018g0192a0001c0004t0002g0012 | 3 | HG01168.hp1 HG02074.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1879-3312_1879-329 others(20): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231341640 | |||||
chr2:231341640
|
TGATA | T | 4 | a0001c0001t0001g0090a0001c0001t0004g0184a0001c0001t0011g0165others(1): Show | 4 | HG02738.hp2 NA18945.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879-3300_1879-329 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231341640 | |||||
chr2:231341640
|
TGATAGAT others(5): Show |
T | 1 | a0001c0001t0001g0129 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1879-3308_1879-329 others(16): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr2 | 231341640 | |||||
chr2:231342209
|
C | T | 1 | a0001c0002t0002g0112 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1879-2766C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231342209 | ||||||
chr2:231342332
|
C | T | 1 | a0001c0002t0003g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1879-2643C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231342332 | ||||||
chr2:231342385
|
C | T | 4 | a0001c0001t0009g0041a0001c0001t0009g0176a0001c0001t0013g0051others(1): Show | 4 | HG00544.hp1 HG00621.hp2 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1879-2590C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231342385 | ||||||
chr2:231342661
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1879-2314G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231342661 | ||||||
chr2:231343344
|
C | T | 13 | a0001c0002t0014g0056a0001c0002t0025g0095a0001c0002t0027g0117others(10): Show | 13 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1879-1631C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231343344 | ||||||
chr2:231343615
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1879-1360T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231343615 | ||||||
chr2:231343936
|
A | G | 1 | a0001c0002t0027g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1879-1039A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231343936 | ||||||
chr2:231344058
|
C | T | 1 | a0001c0003t0037g0003 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1879-917C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231344058 | ||||||
chr2:231344229
|
C | G | 154 | a0001c0001t0001g0046a0001c0001t0001g0151a0001c0001t0001g0171others(151): Show | 154 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1879-746C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231344229 | ||||||
chr2:231344717
|
C | T | 11 | a0001c0001t0004g0105a0001c0001t0005g0102a0001c0001t0005g0143others(8): Show | 11 | HG00544.hp2 HG00558.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.1879-258C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231344717 | ||||||
chr2:231344768
|
A | C | 1 | a0001c0003t0049g0008 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1879-207A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 20/24 | chr2 | 231344768 | ||||||
chr2:231345112
|
C | T | 1 | a0001c0002t0002g0098 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1994+22C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231345112 | ||||||
chr2:231345858
|
T | C | 14 | a0001c0002t0014g0056a0001c0002t0025g0095a0001c0002t0027g0117others(11): Show | 14 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1994+768T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231345858 | ||||||
chr2:231345965
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1994+875C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231345965 | ||||||
chr2:231345998
|
G | T | 2 | a0001c0004t0024g0002a0001c0004t0024g0016 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1994+908G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231345998 | ||||||
chr2:231346545
|
C | T | 1 | a0001c0001t0009g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1994+1455C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231346545 | ||||||
chr2:231347118
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1994+2028C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231347118 | ||||||
chr2:231347354
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1994+2264T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231347354 | ||||||
chr2:231348078
|
G | A | 41 | a0001c0001t0004g0059a0001c0001t0004g0101a0001c0001t0004g0105others(38): Show | 41 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1994+2988G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231348078 | ||||||
chr2:231348904
|
A | G | 2 | a0001c0004t0042g0035a0001c0004t0043g0034 | 2 | HG01069.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1994+3814A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231348904 | ||||||
chr2:231349299
|
T | C | 1 | a0001c0001t0058g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1994+4209T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231349299 | ||||||
chr2:231350026
|
TA | T | 12 | a0001c0001t0001g0099a0001c0001t0015g0083a0001c0001t0019g0097others(9): Show | 12 | HG02165.hp1 HG02165.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1994+4952delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231350026 | |||||
chr2:231350590
|
C | G | 1 | a0001c0002t0060g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1995-5208C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231350590 | ||||||
chr2:231350808
|
T | C | 57 | a0001c0001t0003g0149a0001c0002t0002g0043a0001c0002t0002g0044others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1995-4990T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231350808 | ||||||
chr2:231350946
|
C | CT | 56 | a0001c0001t0001g0054a0001c0001t0001g0078a0001c0001t0001g0091others(53): Show | 56 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1995-4822dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231350946 | |||||
chr2:231350967
|
T | TTTTTTTT others(2222): Show |
1 | a0001c0001t0030g0132 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1995-4456_1995-222 others(2233): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231350967 | |||||
chr2:231351043
|
C | G | 1 | a0001c0004t0013g0004 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1995-4755C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231351043 | ||||||
chr2:231351262
|
C | T | 1 | a0001c0003t0005g0042 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1995-4536C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231351262 | ||||||
chr2:231351334
|
G | A | 6 | a0001c0001t0004g0184a0001c0001t0018g0136a0001c0001t0018g0137others(3): Show | 6 | NA18944.hp1 NA18984.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1995-4464G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231351334 | ||||||
chr2:231352614
|
G | A | 1 | a0001c0001t0016g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1995-3184G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231352614 | ||||||
chr2:231352661
|
G | GGATA | 3 | a0001c0001t0001g0099a0001c0001t0009g0176a0001c0001t0019g0067 | 3 | HG00544.hp1 HG02602.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1995-3093_1995-309 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231352661 | |||||
chr2:231352661
|
GGATA | G | 83 | a0001c0001t0001g0046a0001c0001t0001g0078a0001c0001t0001g0079others(80): Show | 83 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1995-3093_1995-309 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231352661 | |||||
chr2:231352661
|
GGATAGAT others(1): Show |
G | 62 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0072others(59): Show | 62 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1995-3097_1995-309 others(12): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231352661 | |||||
chr2:231352661
|
GGATAGAT others(5): Show |
G | 10 | a0001c0001t0002g0189a0001c0001t0002g0198a0001c0001t0004g0124others(7): Show | 10 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.1995-3101_1995-309 others(16): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231352661 | |||||
chr2:231352705
|
A | G | 1 | a0001c0001t0007g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1995-3093A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231352705 | ||||||
chr2:231353259
|
C | T | 1 | a0001c0003t0001g0022 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1995-2539C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231353259 | ||||||
chr2:231353649
|
G | A | 1 | a0001c0001t0009g0041 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1995-2149G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231353649 | ||||||
chr2:231353980
|
T | C | 3 | a0001c0001t0004g0124a0001c0001t0030g0132a0001c0002t0023g0084 | 3 | HG00423.hp2 HG00639.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1995-1818T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231353980 | ||||||
chr2:231353980
|
T | TAC | 6 | a0001c0001t0007g0071a0001c0001t0011g0048a0001c0001t0045g0050others(3): Show | 6 | HG01074.hp1 HG01081.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1995-1783_1995-178 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231353980 | |||||
chr2:231353980
|
TAC | T | 5 | a0001c0001t0006g0148a0001c0001t0007g0045a0001c0001t0007g0047others(2): Show | 5 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1995-1783_1995-178 others(6): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231353980 | |||||
chr2:231353980
|
TACACACA others(9): Show |
T | 1 | a0006c0007t0014g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1995-1797_1995-178 others(20): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231353980 | |||||
chr2:231354263
|
T | TA | 24 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0091others(21): Show | 24 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1995-1512dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231354263 | |||||
chr2:231354322
|
C | G | 2 | a0001c0001t0010g0063a0001c0001t0033g0157 | 2 | HG01168.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1995-1476C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231354322 | ||||||
chr2:231354376
|
AT | A | 171 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(168): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1995-1399delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr2 | 231354376 | |||||
chr2:231354538
|
C | T | 1 | a0001c0001t0004g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1995-1260C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231354538 | ||||||
chr2:231355315
|
G | A | 1 | a0001c0003t0049g0008 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1995-483G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 21/24 | chr2 | 231355315 | ||||||
chr2:231355964
|
T | C | 2 | a0001c0001t0002g0189a0001c0001t0002g0198 | 2 | NA18943.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2131+30T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231355964 | ||||||
chr2:231356511
|
G | C | 1 | a0001c0002t0060g0096 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2131+577G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231356511 | ||||||
chr2:231357086
|
T | C | 1 | a0001c0001t0057g0125 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2131+1152T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231357086 | ||||||
chr2:231357107
|
C | G | 1 | a0001c0001t0014g0118 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2131+1173C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231357107 | ||||||
chr2:231357182
|
C | G | 1 | a0001c0001t0019g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2131+1248C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231357182 | ||||||
chr2:231357779
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2131+1845T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231357779 | ||||||
chr2:231357788
|
C | T | 1 | a0001c0001t0005g0140 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2131+1854C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231357788 | ||||||
chr2:231357975
|
C | T | 1 | a0001c0001t0019g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2131+2041C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231357975 | ||||||
chr2:231358034
|
G | C | 3 | a0001c0002t0025g0095a0001c0004t0014g0019a0005c0013t0026g0077 | 3 | HG01074.hp2 HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2131+2100G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231358034 | ||||||
chr2:231358350
|
A | AATTG | 3 | a0001c0001t0004g0184a0001c0002t0014g0056a0001c0003t0001g0013 | 3 | HG01175.hp1 NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2132-2375_2132-237 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr2 | 231358350 | |||||
chr2:231358350
|
AATTG | A | 2 | a0001c0001t0001g0168a0001c0001t0006g0094 | 2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2132-2375_2132-237 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr2 | 231358350 | |||||
chr2:231358490
|
C | G | 1 | a0001c0001t0046g0173 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2132-2264C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231358490 | ||||||
chr2:231358547
|
C | T | 1 | a0001c0001t0057g0125 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2132-2207C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231358547 | ||||||
chr2:231358635
|
C | T | 1 | a0001c0001t0034g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2132-2119C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231358635 | ||||||
chr2:231359082
|
G | GT | 7 | a0001c0001t0001g0126a0001c0001t0001g0171a0001c0001t0008g0183others(4): Show | 7 | HG01346.hp1 HG02683.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.2132-1651dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr2 | 231359082 | |||||
chr2:231359681
|
C | T | 1 | a0001c0001t0038g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2132-1073C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231359681 | ||||||
chr2:231359691
|
C | A | 2 | a0001c0001t0010g0162a0001c0001t0055g0193 | 2 | NA19011.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2132-1063C>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231359691 | ||||||
chr2:231359908
|
A | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2132-846A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231359908 | ||||||
chr2:231359931
|
A | G | 1 | a0001c0001t0040g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2132-823A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231359931 | ||||||
chr2:231360048
|
G | A | 1 | a0001c0002t0027g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2132-706G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231360048 | ||||||
chr2:231360063
|
C | T | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2132-691C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231360063 | ||||||
chr2:231360375
|
G | C | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2132-379G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231360375 | ||||||
chr2:231360483
|
A | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2132-271A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231360483 | ||||||
chr2:231360546
|
A | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2132-208A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231360546 | ||||||
chr2:231360635
|
C | T | 1 | a0001c0001t0017g0121 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2132-119C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 22/24 | chr2 | 231360635 | ||||||
chr2:231361007
|
G | T | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+124G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231361007 | ||||||
chr2:231361132
|
A | T | 1 | a0001c0003t0030g0036 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2261+249A>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231361132 | ||||||
chr2:231361235
|
G | A | 11 | a0001c0001t0001g0046a0001c0001t0007g0045a0001c0001t0007g0047others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.2261+352G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231361235 | ||||||
chr2:231361610
|
G | A | 2 | a0001c0001t0010g0186a0001c0001t0010g0187 | 2 | HG00408.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2261+727G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231361610 | ||||||
chr2:231362213
|
T | C | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+1330T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231362213 | ||||||
chr2:231362354
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2261+1471G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231362354 | ||||||
chr2:231362517
|
G | A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+1634G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231362517 | ||||||
chr2:231362681
|
T | C | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+1798T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231362681 | ||||||
chr2:231363344
|
G | T | 1 | a0001c0001t0031g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2261+2461G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231363344 | ||||||
chr2:231363585
|
A | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+2702A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231363585 | ||||||
chr2:231363849
|
A | C | 1 | a0001c0001t0007g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2261+2966A>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231363849 | ||||||
chr2:231363883
|
C | CA | 73 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0129others(70): Show | 73 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2261+3027dupA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231363883 | |||||
chr2:231363883
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0029g0049 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2261+3015_2261+302 others(17): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231363883 | |||||
chr2:231364010
|
T | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+3127T>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364010 | ||||||
chr2:231364080
|
A | G | 1 | a0001c0001t0058g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2261+3197A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364080 | ||||||
chr2:231364134
|
C | T | 3 | a0001c0001t0009g0041a0001c0001t0009g0176a0001c0001t0050g0040 | 3 | HG00544.hp1 HG00621.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2261+3251C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364134 | ||||||
chr2:231364313
|
T | C | 1 | a0001c0002t0002g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2261+3430T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364313 | ||||||
chr2:231364319
|
T | C | 126 | a0001c0001t0002g0182a0001c0001t0002g0189a0001c0001t0002g0198others(123): Show | 126 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2261+3436T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364319 | ||||||
chr2:231364354
|
A | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+3471A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364354 | ||||||
chr2:231364747
|
G | C | 5 | a0001c0001t0001g0087a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 5 | NA18948.hp1 NA18984.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2261+3864G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364747 | ||||||
chr2:231364877
|
G | A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+3994G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364877 | ||||||
chr2:231364898
|
G | A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2261+4015G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231364898 | ||||||
chr2:231365029
|
T | C | 199 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0054others(196): Show | 199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2261+4146T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365029 | ||||||
chr2:231365074
|
AGCCTGGA others(9): Show |
A | 1 | a0001c0002t0021g0064 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2261+4193_2261+420 others(20): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231365074 | |||||
chr2:231365115
|
G | T | 1 | a0001c0001t0009g0041 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2261+4232G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365115 | ||||||
chr2:231365278
|
G | A | 8 | a0001c0001t0016g0134a0001c0001t0016g0146a0001c0001t0017g0127others(5): Show | 8 | HG01070.hp2 HG02080.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.2261+4395G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365278 | ||||||
chr2:231365340
|
G | A | 1 | a0001c0002t0014g0056 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2261+4457G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365340 | ||||||
chr2:231365340
|
G | C | 1 | a0001c0002t0002g0112 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2261+4457G>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365340 | ||||||
chr2:231365419
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2262-4534A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365419 | ||||||
chr2:231365437
|
C | T | 1 | a0001c0001t0017g0127 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2262-4516C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365437 | ||||||
chr2:231365438
|
C | T | 1 | a0001c0001t0016g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2262-4515C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365438 | ||||||
chr2:231365538
|
G | T | 1 | a0001c0001t0019g0052 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2262-4415G>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365538 | ||||||
chr2:231365655
|
AGGAACCA others(19): Show |
A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-4272_2262-424 others(30): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231365655 | |||||
chr2:231365685
|
ACCAGCCG others(19): Show |
A | 1 | a0001c0002t0003g0181 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2262-4250_2262-422 others(30): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231365685 | |||||
chr2:231365891
|
C | T | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-4062C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365891 | ||||||
chr2:231365963
|
C | T | 10 | a0001c0001t0003g0149a0001c0002t0002g0133a0001c0002t0002g0161others(7): Show | 10 | HG00423.hp1 HG00673.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.2262-3990C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231365963 | ||||||
chr2:231366162
|
G | A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-3791G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366162 | ||||||
chr2:231366213
|
ATCAG | A | 2 | a0001c0001t0011g0048a0001c0003t0010g0038 | 2 | HG00280.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2262-3737_2262-373 others(8): Show |
ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231366213 | |||||
chr2:231366218
|
T | A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-3735T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366218 | ||||||
chr2:231366267
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2262-3686C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366267 | ||||||
chr2:231366438
|
T | C | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-3515T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366438 | ||||||
chr2:231366858
|
T | A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-3095T>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366858 | ||||||
chr2:231366900
|
G | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0106others(9): Show | 12 | HG00609.hp2 HG01981.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.2262-3053G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366900 | ||||||
chr2:231366960
|
C | G | 1 | a0001c0002t0002g0044 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2262-2993C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366960 | ||||||
chr2:231366976
|
G | A | 122 | a0001c0001t0002g0182a0001c0001t0002g0189a0001c0001t0002g0198others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2262-2977G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231366976 | ||||||
chr2:231367096
|
C | T | 12 | a0001c0001t0001g0054a0001c0001t0001g0075a0001c0001t0001g0106others(9): Show | 12 | HG00609.hp2 HG01981.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.2262-2857C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367096 | ||||||
chr2:231367110
|
A | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-2843A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367110 | ||||||
chr2:231367141
|
T | C | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-2812T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367141 | ||||||
chr2:231367205
|
G | A | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-2748G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367205 | ||||||
chr2:231367703
|
C | T | 1 | a0001c0001t0009g0144 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2262-2250C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367703 | ||||||
chr2:231367705
|
G | A | 1 | a0001c0003t0005g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2262-2248G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367705 | ||||||
chr2:231367709
|
G | A | 1 | a0001c0001t0008g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2262-2244G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367709 | ||||||
chr2:231367844
|
G | A | 1 | a0001c0003t0020g0055 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2262-2109G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231367844 | ||||||
chr2:231367978
|
CA | C | 6 | a0001c0001t0009g0041a0001c0001t0029g0194a0001c0001t0039g0119others(3): Show | 6 | HG03710.hp1 NA18965.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.2262-1961delA | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231367978 | |||||
chr2:231368019
|
T | C | 3 | a0001c0001t0003g0149a0001c0002t0002g0174a0001c0002t0003g0185 | 3 | HG00423.hp1 HG00673.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2262-1934T>C | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231368019 | ||||||
chr2:231368075
|
AT | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0068 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2262-1877delT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231368075 | ||||||
chr2:231368369
|
C | T | 1 | a0001c0001t0029g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2262-1584C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231368369 | ||||||
chr2:231368842
|
C | T | 4 | a0001c0001t0006g0148a0001c0001t0015g0150a0001c0001t0023g0164others(1): Show | 4 | NA18950.hp2 NA18979.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2262-1111C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231368842 | ||||||
chr2:231368990
|
A | G | 45 | a0001c0001t0002g0182a0001c0001t0002g0189a0001c0001t0002g0198others(42): Show | 45 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2262-963A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231368990 | ||||||
chr2:231369598
|
C | CT | 16 | a0001c0001t0001g0079a0001c0001t0004g0101a0001c0001t0004g0135others(13): Show | 16 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.2262-340dupT | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr2 | 231369598 | |||||
chr2:231369707
|
C | T | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-246C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231369707 | ||||||
chr2:231369782
|
C | T | 20 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0058others(17): Show | 20 | HG00639.hp2 HG00741.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.2262-171C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231369782 | ||||||
chr2:231369887
|
C | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2262-66C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 23/24 | chr2 | 231369887 | ||||||
chr2:231370178
|
C | G | 1 | a0001c0015t0059g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2434+53C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 24/24 | chr2 | 231370178 | ||||||
chr2:231370245
|
G | A | 1 | a0001c0001t0018g0192 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2434+120G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 24/24 | chr2 | 231370245 | ||||||
chr2:231370576
|
C | G | 3 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0004t0036g0039 | 3 | HG02015.hp1 HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.2434+451C>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 24/24 | chr2 | 231370576 | ||||||
chr2:231370611
|
G | A | 1 | a0001c0002t0002g0190 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2434+486G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 24/24 | chr2 | 231370611 | ||||||
chr2:231370669
|
C | T | 1 | a0001c0003t0049g0008 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2434+544C>T | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 24/24 | chr2 | 231370669 | ||||||
chr2:231371239
|
A | G | 2 | a0001c0002t0060g0096a0001c0015t0059g0104 | 2 | HG01081.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2435-274A>G | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 24/24 | chr2 | 231371239 | ||||||
chr2:231371357
|
G | A | 2 | a0001c0002t0060g0096a0001c0015t0059g0104 | 2 | HG01081.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2435-156G>A | ARMC9 | ENSG00000135931.19 | transcript | ENST00000611582.5 | protein_coding | 24/24 | chr2 | 231371357 |