geneid | 4507 |
---|---|
ensemblid | ENSG00000099810.21 |
hgncid | 7413 |
symbol | MTAP |
name | methylthioadenosine phosphorylase |
refseq_nuc | NM_002451.4 |
refseq_prot | NP_002442.2 |
ensembl_nuc | ENST00000644715.2 |
ensembl_prot | ENSP00000494373.1 |
mane_status | MANE Select |
chr | chr9 |
start | 21802636 |
end | 21867081 |
strand | + |
ver | v1.2 |
region | chr9:21802636-21867081 |
region5000 | chr9:21797636-21872081 |
regionname0 | MTAP_chr9_21802636_21867081 |
regionname5000 | MTAP_chr9_21797636_21872081 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 283 | 243 | 47 | 37 | 123 | 10 | 25 | 96 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002 | 0/1 | 283 | 135 | 44 | 25 | 46 | 6 | 13 | 39 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0003 | 0/0 | 283 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0004 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0005 | 0/0 | 283 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 852 | 222 | 45 | 35 | 107 | 10 | 24 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0002 | 0/1 | 852 | 129 | 44 | 22 | 46 | 4 | 12 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0003 | 0/0 | 852 | 16 | 0 | 1 | 14 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0004 | 0/0 | 852 | 6 | 0 | 3 | 0 | 2 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0005 | 0/0 | 852 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0006 | 0/0 | 852 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0007 | 0/0 | 852 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0008 | 0/0 | 852 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0009 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
c0010 | 0/0 | 852 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 5181 | 123 | 16 | 24 | 57 | 11 | 14 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0002 | 0/0 | 5181 | 64 | 6 | 19 | 32 | 0 | 7 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0003 | 0/0 | 5180 | 58 | 13 | 5 | 29 | 1 | 10 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0004 | 0/0 | 5181 | 24 | 23 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0005 | 0/0 | 5180 | 15 | 0 | 0 | 15 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0006 | 0/0 | 5180 | 5 | 0 | 0 | 5 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0007 | 0/0 | 5180 | 5 | 3 | 0 | 0 | 2 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0008 | 0/0 | 5179 | 5 | 5 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0009 | 0/0 | 5180 | 4 | 3 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0010 | 0/0 | 5181 | 4 | 0 | 0 | 4 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0011 | 0/0 | 5181 | 4 | 0 | 1 | 0 | 1 | 2 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0012 | 0/0 | 5180 | 4 | 4 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0013 | 0/0 | 5181 | 4 | 0 | 0 | 4 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0014 | 0/0 | 5180 | 4 | 0 | 2 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0015 | 0/0 | 5180 | 4 | 0 | 4 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0016 | 0/0 | 5181 | 3 | 2 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0017 | 0/0 | 5181 | 3 | 0 | 0 | 3 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0018 | 0/0 | 5181 | 3 | 0 | 1 | 0 | 1 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0019 | 0/0 | 5180 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0020 | 0/0 | 5181 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0021 | 0/0 | 5167 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0022 | 0/0 | 5182 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0023 | 0/0 | 5180 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0024 | 0/0 | 5180 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0025 | 0/0 | 5181 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0026 | 0/0 | 5182 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0027 | 0/1 | 5181 | 2 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0028 | 0/0 | 5181 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0029 | 0/0 | 5181 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0030 | 0/0 | 5180 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0031 | 0/0 | 5181 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0032 | 0/0 | 5180 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0033 | 0/0 | 5180 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0034 | 0/0 | 5181 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0035 | 0/0 | 5181 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0036 | 0/0 | 5181 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0037 | 0/0 | 5181 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0038 | 0/0 | 5180 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0039 | 0/0 | 5181 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0040 | 0/0 | 5180 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0041 | 0/0 | 5181 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0042 | 0/0 | 5180 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0043 | 0/0 | 5180 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0044 | 0/0 | 5181 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0045 | 0/0 | 5181 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0046 | 0/0 | 5180 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0047 | 0/0 | 5180 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0048 | 0/0 | 5181 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0049 | 0/0 | 5179 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0050 | 0/0 | 5180 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0051 | 0/0 | 5179 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
t0052 | 0/0 | 5180 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
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 | 3 | 0 | 1 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0005 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 852 | 222 | 45 | 35 | 107 | 10 | 24 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0003 | 0/0 | 852 | 16 | 0 | 1 | 14 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0006 | 0/0 | 852 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0007 | 0/0 | 852 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0010 | 0/0 | 852 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002 | 0/1 | 852 | 129 | 44 | 22 | 46 | 4 | 12 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0004 | 0/0 | 852 | 6 | 0 | 3 | 0 | 2 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0003c0005 | 0/0 | 852 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0004c0008 | 0/0 | 852 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0005c0009 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6032 | 84 | 14 | 18 | 32 | 7 | 12 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0002 | 0/0 | 6032 | 13 | 1 | 4 | 7 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0003 | 0/0 | 6031 | 45 | 9 | 4 | 25 | 1 | 6 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0004 | 0/0 | 6032 | 3 | 3 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0005 | 0/0 | 6031 | 14 | 0 | 0 | 14 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0006 | 0/0 | 6031 | 5 | 0 | 0 | 5 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0008 | 0/0 | 6030 | 4 | 4 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0009 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0010 | 0/0 | 6032 | 4 | 0 | 0 | 4 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0011 | 0/0 | 6032 | 2 | 0 | 1 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0012 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0014 | 0/0 | 6031 | 4 | 0 | 2 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0015 | 0/0 | 6031 | 4 | 0 | 4 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0017 | 0/0 | 6032 | 3 | 0 | 0 | 3 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0018 | 0/0 | 6032 | 3 | 0 | 1 | 0 | 1 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0019 | 0/0 | 6031 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0020 | 0/0 | 6032 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0021 | 0/0 | 6018 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0023 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0024 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0025 | 0/0 | 6032 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0028 | 0/0 | 6032 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0029 | 0/0 | 6032 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0030 | 0/0 | 6031 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0031 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0032 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0035 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0036 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0041 | 0/0 | 6032 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0042 | 0/0 | 6031 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0043 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0044 | 0/0 | 6032 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0046 | 0/0 | 6031 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0047 | 0/0 | 6031 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0050 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0001t0051 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0003t0001 | 0/0 | 6032 | 15 | 0 | 1 | 13 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0003t0003 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0006t0001 | 0/0 | 6032 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0007t0003 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0001c0010t0009 | 0/0 | 6031 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0001 | 0/0 | 6032 | 16 | 2 | 2 | 10 | 2 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0002 | 0/0 | 6032 | 48 | 5 | 15 | 24 | 0 | 4 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0003 | 0/0 | 6031 | 10 | 2 | 1 | 3 | 0 | 4 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0004 | 0/0 | 6032 | 21 | 20 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0005 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0007 | 0/0 | 6031 | 5 | 3 | 0 | 0 | 2 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0008 | 0/0 | 6030 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0011 | 0/0 | 6032 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0012 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0013 | 0/0 | 6032 | 4 | 0 | 0 | 4 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0016 | 0/0 | 6032 | 3 | 2 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0022 | 0/0 | 6033 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0026 | 0/0 | 6033 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0027 | 0/1 | 6032 | 2 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0033 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0034 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0037 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0038 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0039 | 0/0 | 6032 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0040 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0045 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0048 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0049 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0002t0052 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0002c0004t0001 | 0/0 | 6032 | 6 | 0 | 3 | 0 | 2 | 1 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0003c0005t0002 | 0/0 | 6032 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0004c0008t0002 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
a0005c0009t0009 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | copy fasta | chr9 | 21797636 | 21872081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0009g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0010g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0010g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0010g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0011g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0011g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0015g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0015g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0015g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0015g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0017g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0017g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0017g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0018g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0018g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0018g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0019g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0020g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0020g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0021g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0021g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0023g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0023g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0024g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0024g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0025g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0025g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0028g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0028g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0029g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0029g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0030g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0031g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0032g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0035g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0036g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0041g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0042g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0043g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0044g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0046g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0047g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0050g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0051g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0006t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0007t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0007t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0010t0009g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0011g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0011g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0012g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0013g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0013g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0016g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0016g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0016g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0022g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0022g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0026g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0026g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0027g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0027g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0033g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0034g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0037g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0038g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0039g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0040g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0045g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0048g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0049g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0052g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0003c0005t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0004c0008t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0005c0009t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0018 | g0180 | EUR | GBR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0267 | EUR | GBR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00280 | hp2 | a0002 | c0004 | t0001 | g0186 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0157 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00323 | hp2 | a0001 | c0001 | t0011 | g0052 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00408 | hp1 | a0001 | c0001 | t0031 | g0141 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0281 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00544 | hp1 | a0002 | c0002 | t0003 | g0250 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0228 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00639 | hp2 | a0001 | c0001 | t0011 | g0171 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0202 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00738 | hp1 | a0002 | c0004 | t0001 | g0210 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01074 | hp1 | a0002 | c0002 | t0016 | g0320 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0225 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01081 | hp1 | a0002 | c0004 | t0001 | g0177 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01081 | hp2 | a0001 | c0001 | t0014 | g0161 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01106 | hp1 | a0001 | c0001 | t0018 | g0173 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0261 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0176 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01167 | hp1 | a0002 | c0002 | t0022 | g0156 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01169 | hp2 | a0002 | c0002 | t0022 | g0167 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01192 | hp2 | a0002 | c0002 | t0004 | g0035 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0153 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01361 | hp1 | a0001 | c0001 | t0015 | g0273 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0147 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01516 | hp2 | a0002 | c0002 | t0007 | g0110 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01517 | hp1 | a0002 | c0002 | t0007 | g0014 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01884 | hp1 | a0002 | c0002 | t0008 | g0340 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01884 | hp2 | a0002 | c0002 | t0040 | g0044 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0130 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01934 | hp2 | a0001 | c0001 | t0015 | g0258 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0193 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01975 | hp2 | a0001 | c0001 | t0015 | g0279 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01978 | hp2 | a0002 | c0004 | t0001 | g0207 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01981 | hp1 | a0001 | c0001 | t0046 | g0099 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02004 | hp2 | a0001 | c0001 | t0014 | g0106 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02027 | hp1 | a0001 | c0001 | t0028 | g0158 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02055 | hp2 | a0001 | c0001 | t0023 | g0132 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0295 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0298 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02258 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02273 | hp2 | a0001 | c0001 | t0015 | g0270 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02280 | hp1 | a0002 | c0002 | t0004 | g0128 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02523 | hp2 | a0001 | c0003 | t0003 | g0183 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02572 | hp2 | a0002 | c0002 | t0004 | g0089 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02602 | hp2 | a0001 | c0001 | t0041 | g0084 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0075 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02630 | hp1 | a0001 | c0001 | t0024 | g0092 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02630 | hp2 | a0002 | c0002 | t0016 | g0321 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0112 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02647 | hp2 | a0001 | c0001 | t0021 | g0336 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0137 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02717 | hp1 | a0002 | c0002 | t0004 | g0162 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02717 | hp2 | a0002 | c0002 | t0016 | g0319 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0310 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0002 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0304 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0262 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0083 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0045 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02896 | hp1 | a0002 | c0002 | t0004 | g0127 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02896 | hp2 | a0002 | c0002 | t0052 | g0036 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02897 | hp1 | a0002 | c0002 | t0004 | g0062 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02897 | hp2 | a0002 | c0002 | t0004 | g0061 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02922 | hp2 | a0001 | c0001 | t0020 | g0308 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02970 | hp1 | a0001 | c0001 | t0021 | g0069 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02970 | hp2 | a0001 | c0007 | t0003 | g0318 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0149 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03017 | hp2 | a0001 | c0001 | t0047 | g0268 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0024 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03041 | hp2 | a0002 | c0002 | t0034 | g0165 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0293 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03130 | hp2 | a0002 | c0002 | t0004 | g0111 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03139 | hp1 | a0002 | c0002 | t0007 | g0073 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03139 | hp2 | a0002 | c0002 | t0004 | g0181 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0155 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03225 | hp2 | a0002 | c0002 | t0007 | g0072 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03239 | hp1 | a0002 | c0004 | t0001 | g0178 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03239 | hp2 | a0001 | c0001 | t0042 | g0205 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03453 | hp1 | a0002 | c0002 | t0004 | g0164 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0299 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0101 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03490 | hp1 | a0002 | c0002 | t0011 | g0048 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03490 | hp2 | a0003 | c0005 | t0002 | g0009 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03492 | hp2 | a0003 | c0005 | t0002 | g0009 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03516 | hp1 | a0002 | c0002 | t0004 | g0022 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0065 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03540 | hp2 | a0002 | c0002 | t0004 | g0151 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03579 | hp1 | a0002 | c0002 | t0037 | g0114 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03579 | hp2 | a0002 | c0002 | t0045 | g0074 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03669 | hp1 | a0002 | c0002 | t0003 | g0260 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03688 | hp1 | a0002 | c0002 | t0039 | g0185 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0334 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03704 | hp2 | a0001 | c0001 | t0018 | g0172 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03710 | hp2 | a0001 | c0001 | t0044 | g0344 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0222 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03834 | hp1 | a0002 | c0002 | t0003 | g0242 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0086 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0214 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04199 | hp2 | a0002 | c0002 | t0011 | g0223 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0199 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04204 | hp2 | a0002 | c0002 | t0027 | g0360 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0327 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0229 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18522 | hp1 | a0001 | c0001 | t0035 | g0236 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0098 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18747 | hp2 | a0001 | c0001 | t0028 | g0195 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18906 | hp2 | a0002 | c0002 | t0004 | g0129 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18939 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18942 | hp2 | a0002 | c0002 | t0013 | g0211 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18947 | hp1 | a0001 | c0001 | t0019 | g0081 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18948 | hp1 | a0001 | c0001 | t0010 | g0351 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18949 | hp2 | a0001 | c0001 | t0043 | g0257 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18951 | hp1 | a0001 | c0001 | t0029 | g0352 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18951 | hp2 | a0002 | c0002 | t0026 | g0007 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18953 | hp1 | a0001 | c0001 | t0030 | g0010 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18957 | hp2 | a0002 | c0002 | t0013 | g0240 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18963 | hp1 | a0002 | c0002 | t0005 | g0209 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18968 | hp2 | a0001 | c0001 | t0030 | g0010 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18969 | hp1 | a0001 | c0001 | t0017 | g0169 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18974 | hp1 | a0002 | c0002 | t0049 | g0091 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18982 | hp1 | a0001 | c0001 | t0050 | g0012 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0244 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18990 | hp2 | a0001 | c0001 | t0010 | g0356 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18994 | hp2 | a0001 | c0001 | t0006 | g0296 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18997 | hp1 | a0001 | c0001 | t0051 | g0218 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18999 | hp2 | a0001 | c0006 | t0001 | g0078 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0297 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19006 | hp1 | a0001 | c0001 | t0017 | g0118 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19007 | hp1 | a0002 | c0002 | t0048 | g0030 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19007 | hp2 | a0001 | c0001 | t0029 | g0369 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19009 | hp1 | a0001 | c0001 | t0017 | g0136 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19010 | hp2 | a0001 | c0001 | t0010 | g0350 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0245 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19043 | hp1 | a0002 | c0002 | t0033 | g0208 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19056 | hp2 | a0002 | c0002 | t0013 | g0249 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19057 | hp2 | a0001 | c0001 | t0014 | g0366 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19058 | hp1 | a0001 | c0001 | t0025 | g0363 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19060 | hp1 | a0001 | c0001 | t0019 | g0033 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19060 | hp2 | a0004 | c0008 | t0002 | g0232 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19070 | hp1 | a0001 | c0001 | t0014 | g0008 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19070 | hp2 | a0002 | c0002 | t0013 | g0283 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19074 | hp2 | a0001 | c0001 | t0036 | g0354 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19082 | hp1 | a0001 | c0001 | t0025 | g0358 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19085 | hp1 | a0002 | c0002 | t0026 | g0246 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19088 | hp1 | a0001 | c0006 | t0001 | g0067 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0338 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0335 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19240 | hp1 | a0002 | c0002 | t0003 | g0341 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19240 | hp2 | a0001 | c0001 | t0032 | g0251 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ASW | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20129 | hp2 | a0001 | c0007 | t0003 | g0317 | AFR | ASW | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20752 | hp2 | a0002 | c0004 | t0001 | g0116 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0224 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01123 | hp1 | a0001 | c0010 | t0009 | g0197 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0002 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02109 | hp2 | a0002 | c0002 | t0012 | g0189 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02486 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02559 | hp1 | a0001 | c0001 | t0020 | g0286 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02559 | hp2 | a0002 | c0002 | t0038 | g0090 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03471 | hp1 | a0002 | c0002 | t0007 | g0148 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0233 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG06807 | hp2 | a0005 | c0009 | t0009 | g0013 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20300 | hp1 | a0001 | c0001 | t0009 | g0113 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0284 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA21309 | hp2 | a0002 | c0002 | t0012 | g0085 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0027 | g0005 | REF | REF | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0220 | REF | REF | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21816759
|
G | A | 2 | a0002a0004 | 136 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(133): Show |
missense_variant | MODERATE | c.166G>A | p.Val56Ile | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/8 | 279/6032 | 166/852 | 56/283 | chr9 | 21816759 | ||
chr9:21818168
|
G | A | 1 | a0003 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.313G>A | p.Gly105Ser | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/8 | 426/6032 | 313/852 | 105/283 | chr9 | 21818168 | ||
chr9:21854817
|
G | A | 1 | a0005 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.637G>A | p.Ala213Thr | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 750/6032 | 637/852 | 213/283 | chr9 | 21854817 | ||
chr9:21854826
|
G | A | 1 | a0004 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.646G>A | p.Ala216Thr | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 759/6032 | 646/852 | 216/283 | chr9 | 21854826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21818167
|
C | T | 1 | a0001c0007 | 2 | HG02970.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.312C>T | p.Pro104Pro | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/8 | 425/6032 | 312/852 | 104/283 | chr9 | 21818167 | ||
chr9:21818170
|
C | T | 1 | a0001c0006 | 2 | NA18999.hp2 NA19088.hp1 |
synonymous_variant | LOW | c.315C>T | p.Gly105Gly | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/8 | 428/6032 | 315/852 | 105/283 | chr9 | 21818170 | ||
chr9:21854741
|
C | T | 2 | a0001c0003a0002c0004 | 22 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(19): Show |
synonymous_variant | LOW | c.561C>T | p.Arg187Arg | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 674/6032 | 561/852 | 187/283 | chr9 | 21854741 | ||
chr9:21854774
|
A | G | 2 | a0001c0010a0005c0009 | 2 | HG01123.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.594A>G | p.Thr198Thr | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 707/6032 | 594/852 | 198/283 | chr9 | 21854774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21802646
|
C | G | 1 | a0002c0002t0052 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-103C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/8 | 103 | chr9 | 21802646 | |||||
chr9:21802702
|
C | A | 1 | a0001c0001t0031 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/8 | 47 | chr9 | 21802702 | |||||
chr9:21862119
|
C | T | 1 | a0001c0001t0030 | 2 | NA18953.hp1 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 105 | chr9 | 21862119 | |||||
chr9:21862272
|
A | C | 32 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(29): Show | 192 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*258A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 258 | chr9 | 21862272 | |||||
chr9:21862273
|
C | A | 13 | a0001c0001t0005a0001c0001t0009a0001c0001t0019others(10): Show | 31 | HG00597.hp1 HG00609.hp2 HG01074.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*259C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 259 | chr9 | 21862273 | |||||
chr9:21862317
|
G | T | 1 | a0001c0001t0029 | 2 | NA18951.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*303G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 303 | chr9 | 21862317 | |||||
chr9:21862320
|
G | C | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 306 | chr9 | 21862320 | |||||
chr9:21862322
|
G | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*308G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 308 | chr9 | 21862322 | |||||
chr9:21862323
|
G | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 309 | chr9 | 21862323 | |||||
chr9:21862324
|
G | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*310G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 310 | chr9 | 21862324 | |||||
chr9:21862326
|
A | C | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 312 | chr9 | 21862326 | |||||
chr9:21862329
|
C | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 315 | chr9 | 21862329 | |||||
chr9:21862332
|
T | C | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 318 | chr9 | 21862332 | |||||
chr9:21862334
|
C | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*320C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 320 | chr9 | 21862334 | |||||
chr9:21862336
|
T | C | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 322 | chr9 | 21862336 | |||||
chr9:21862337
|
T | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*323T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 323 | chr9 | 21862337 | |||||
chr9:21862338
|
C | G | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 324 | chr9 | 21862338 | |||||
chr9:21862342
|
T | C | 2 | a0001c0001t0010a0001c0001t0036 | 5 | NA18612.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*328T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 328 | chr9 | 21862342 | |||||
chr9:21862344
|
C | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 330 | chr9 | 21862344 | |||||
chr9:21862346
|
G | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 332 | chr9 | 21862346 | |||||
chr9:21862347
|
C | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*333C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 333 | chr9 | 21862347 | |||||
chr9:21862348
|
C | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*334C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 334 | chr9 | 21862348 | |||||
chr9:21862355
|
T | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 341 | chr9 | 21862355 | |||||
chr9:21862356
|
G | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 342 | chr9 | 21862356 | |||||
chr9:21862358
|
G | C | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 344 | chr9 | 21862358 | |||||
chr9:21862360
|
G | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 346 | chr9 | 21862360 | |||||
chr9:21862361
|
G | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 347 | chr9 | 21862361 | |||||
chr9:21862364
|
G | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 350 | chr9 | 21862364 | |||||
chr9:21862367
|
A | G | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 353 | chr9 | 21862367 | |||||
chr9:21862381
|
T | C | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 367 | chr9 | 21862381 | |||||
chr9:21862382
|
T | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 368 | chr9 | 21862382 | |||||
chr9:21862384
|
T | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 370 | chr9 | 21862384 | |||||
chr9:21862385
|
T | G | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 371 | chr9 | 21862385 | |||||
chr9:21862386
|
T | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 372 | chr9 | 21862386 | |||||
chr9:21862387
|
A | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 373 | chr9 | 21862387 | |||||
chr9:21862388
|
T | G | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*374T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 374 | chr9 | 21862388 | |||||
chr9:21862392
|
T | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 378 | chr9 | 21862392 | |||||
chr9:21862394
|
C | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 380 | chr9 | 21862394 | |||||
chr9:21862397
|
C | A | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 383 | chr9 | 21862397 | |||||
chr9:21862398
|
T | C | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 384 | chr9 | 21862398 | |||||
chr9:21862399
|
G | T | 1 | a0001c0001t0042 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 385 | chr9 | 21862399 | |||||
chr9:21862407
|
G | C | 3 | a0001c0001t0005a0001c0001t0019a0002c0002t0005 | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*393G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 393 | chr9 | 21862407 | |||||
chr9:21862550
|
G | A | 2 | a0001c0001t0011a0002c0002t0011 | 4 | HG00323.hp2 HG00639.hp2 HG03490.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 536 | chr9 | 21862550 | |||||
chr9:21862671
|
T | C | 2 | a0001c0001t0012a0002c0002t0012 | 4 | HG02109.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*657T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 657 | chr9 | 21862671 | |||||
chr9:21862782
|
C | CA | 2 | a0001c0001t0004a0002c0002t0004 | 24 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*775dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 776 | INFO_REALIGN_3_PRIME | chr9 | 21862782 | ||||
chr9:21862811
|
C | T | 2 | a0001c0001t0004a0002c0002t0004 | 24 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*797C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 797 | chr9 | 21862811 | |||||
chr9:21862818
|
T | C | 1 | a0002c0002t0016 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*804T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 804 | chr9 | 21862818 | |||||
chr9:21862824
|
TTGGGGGA others(7): Show |
T | 1 | a0001c0001t0021 | 2 | HG02647.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*815_*828delGGAGGG others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 815 | INFO_REALIGN_3_PRIME | chr9 | 21862824 | ||||
chr9:21862898
|
T | A | 52 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(49): Show | 232 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*884T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 884 | chr9 | 21862898 | |||||
chr9:21862916
|
T | A | 1 | a0001c0001t0032 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*902T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 902 | chr9 | 21862916 | |||||
chr9:21863052
|
A | G | 1 | a0002c0002t0016 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1038A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1038 | chr9 | 21863052 | |||||
chr9:21863117
|
AG | A | 2 | a0001c0001t0008a0002c0002t0008 | 5 | HG01884.hp1 HG02257.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1105delG | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1105 | INFO_REALIGN_3_PRIME | chr9 | 21863117 | ||||
chr9:21863195
|
A | G | 1 | a0001c0001t0024 | 2 | HG02630.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1181A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1181 | chr9 | 21863195 | |||||
chr9:21863537
|
G | C | 1 | a0001c0001t0043 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1523G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1523 | chr9 | 21863537 | |||||
chr9:21863622
|
CA | C | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | 199 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1622delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1622 | INFO_REALIGN_3_PRIME | chr9 | 21863622 | ||||
chr9:21863622
|
CAA | C | 11 | a0001c0001t0005a0001c0001t0009a0001c0001t0019others(8): Show | 26 | HG00597.hp1 HG00609.hp2 HG01123.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1621_*1622delAA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1621 | INFO_REALIGN_3_PRIME | chr9 | 21863622 | ||||
chr9:21863657
|
G | T | 3 | a0001c0001t0005a0001c0001t0019a0002c0002t0005 | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1643G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1643 | chr9 | 21863657 | |||||
chr9:21863743
|
G | A | 1 | a0002c0002t0013 | 4 | NA18942.hp2 NA18957.hp2 NA19056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1729G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1729 | chr9 | 21863743 | |||||
chr9:21863950
|
C | T | 2 | a0001c0001t0015a0001c0001t0030 | 6 | HG01361.hp1 HG01934.hp2 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1936C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1936 | chr9 | 21863950 | |||||
chr9:21864071
|
A | G | 1 | a0002c0002t0048 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2057 | chr9 | 21864071 | |||||
chr9:21864099
|
G | A | 33 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(30): Show | 121 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2085G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2085 | chr9 | 21864099 | |||||
chr9:21864202
|
C | T | 1 | a0001c0001t0025 | 2 | NA19058.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2188 | chr9 | 21864202 | |||||
chr9:21864269
|
A | G | 5 | a0001c0001t0020a0001c0001t0035a0002c0002t0016others(2): Show | 8 | HG01074.hp1 HG02559.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2255A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2255 | chr9 | 21864269 | |||||
chr9:21864350
|
A | AT | 23 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(20): Show | 105 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2348dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2349 | INFO_REALIGN_3_PRIME | chr9 | 21864350 | ||||
chr9:21864379
|
C | T | 50 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(47): Show | 230 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2365C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2365 | chr9 | 21864379 | |||||
chr9:21864536
|
A | G | 28 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(25): Show | 113 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2522A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2522 | chr9 | 21864536 | |||||
chr9:21864553
|
A | G | 4 | a0001c0001t0012a0001c0001t0023a0002c0002t0012others(1): Show | 7 | HG02055.hp2 HG02109.hp2 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2539A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2539 | chr9 | 21864553 | |||||
chr9:21864695
|
A | G | 1 | a0001c0001t0032 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2681A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2681 | chr9 | 21864695 | |||||
chr9:21864887
|
C | T | 2 | a0001c0001t0020a0001c0001t0035 | 3 | HG02559.hp1 HG02922.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2873C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2873 | chr9 | 21864887 | |||||
chr9:21865107
|
T | C | 31 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(28): Show | 120 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*3093T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3093 | chr9 | 21865107 | |||||
chr9:21865154
|
A | C | 1 | a0001c0001t0051 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3140A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3140 | chr9 | 21865154 | |||||
chr9:21865158
|
G | A | 1 | a0001c0001t0020 | 2 | HG02559.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3144G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3144 | chr9 | 21865158 | |||||
chr9:21865321
|
G | T | 1 | a0001c0001t0047 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3307G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3307 | chr9 | 21865321 | |||||
chr9:21865375
|
C | T | 1 | a0001c0001t0019 | 2 | NA18947.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3361C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3361 | chr9 | 21865375 | |||||
chr9:21865385
|
T | C | 1 | a0001c0001t0046 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3371T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3371 | chr9 | 21865385 | |||||
chr9:21865843
|
T | C | 53 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(50): Show | 233 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*3829T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3829 | chr9 | 21865843 | |||||
chr9:21865865
|
C | G | 2 | a0001c0001t0023a0002c0002t0037 | 3 | HG02055.hp2 HG03516.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3851C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3851 | chr9 | 21865865 | |||||
chr9:21865930
|
C | T | 1 | a0001c0001t0018 | 3 | HG00140.hp1 HG01106.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3916C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3916 | chr9 | 21865930 | |||||
chr9:21865960
|
A | C | 28 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(25): Show | 103 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3946A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3946 | chr9 | 21865960 | |||||
chr9:21866013
|
C | G | 1 | a0002c0002t0037 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3999C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3999 | chr9 | 21866013 | |||||
chr9:21866121
|
A | C | 1 | a0001c0001t0036 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4107A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4107 | chr9 | 21866121 | |||||
chr9:21866314
|
C | G | 33 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(30): Show | 193 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*4300C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4300 | chr9 | 21866314 | |||||
chr9:21866501
|
C | T | 50 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(47): Show | 229 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*4487C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4487 | chr9 | 21866501 | |||||
chr9:21866912
|
G | C | 1 | a0002c0002t0027 | 2 | HG04204.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4898G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4898 | chr9 | 21866912 | |||||
chr9:21866974
|
A | G | 1 | a0001c0001t0017 | 3 | NA18969.hp1 NA19006.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4960A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4960 | chr9 | 21866974 | |||||
chr9:21867053
|
T | C | 1 | a0002c0002t0007 | 5 | HG01516.hp2 HG01517.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5039T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 5039 | chr9 | 21867053 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21802923
|
C | G | 29 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0001g0346others(26): Show | 29 | HG01168.hp1 HG01169.hp1 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.33+142C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802923 | ||||||
chr9:21802951
|
G | A | 1 | a0005c0009t0009g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33+170G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802951 | ||||||
chr9:21802983
|
C | CACACACA others(12): Show |
1 | a0002c0002t0007g0014 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.33+202_33+203insAC others(17): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802983 | ||||||
chr9:21802985
|
A | AAC | 6 | a0001c0001t0012g0201a0001c0010t0009g0197a0002c0002t0002g0198others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.33+255_33+256dupAC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACAC | 7 | a0001c0001t0001g0196a0001c0001t0002g0194a0001c0001t0028g0195others(4): Show | 7 | HG01516.hp1 HG01975.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.33+253_33+256dupAC others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACAC | 8 | a0001c0001t0001g0188a0001c0003t0001g0182a0001c0003t0003g0183others(5): Show | 8 | HG00280.hp2 HG00621.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.33+251_33+256dupAC others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(1): Show |
10 | a0001c0001t0001g0179a0001c0001t0001g0365a0001c0001t0001g0367others(7): Show | 10 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+249_33+256dupAC others(6): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(3): Show |
13 | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0002g0175others(10): Show | 13 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.33+247_33+256dupAC others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(5): Show |
14 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0364others(11): Show | 14 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.33+245_33+256dupAC others(10): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(7): Show |
21 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0142others(18): Show | 21 | HG00408.hp1 HG01099.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.33+243_33+256dupAC others(12): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(9): Show |
23 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0123others(20): Show | 24 | HG00673.hp1 HG00735.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.33+241_33+256dupAC others(14): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(11): Show |
14 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0107others(11): Show | 14 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.33+239_33+256dupAC others(16): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(13): Show |
19 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(16): Show | 20 | HG01256.hp2 HG01981.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.33+237_33+256dupAC others(18): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(15): Show |
10 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0004g0077others(7): Show | 10 | HG02027.hp2 HG02257.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+235_33+256dupAC others(20): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(17): Show |
18 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0349others(15): Show | 19 | HG01168.hp1 HG01433.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.33+233_33+256dupAC others(22): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(19): Show |
19 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0057others(16): Show | 19 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.33+231_33+256dupAC others(24): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(21): Show |
10 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 10 | HG00423.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+229_33+256dupAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(23): Show |
10 | a0001c0001t0001g0034a0001c0001t0001g0345a0001c0001t0005g0031others(7): Show | 10 | HG01192.hp2 HG02896.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+227_33+256dupAC others(28): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(25): Show |
6 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0005g0026others(3): Show | 6 | HG00597.hp1 HG01496.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.33+225_33+256dupAC others(30): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(27): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0021a0002c0002t0004g0022 | 3 | HG01517.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.33+223_33+256dupAC others(32): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(29): Show |
1 | a0001c0001t0005g0019 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.33+221_33+256dupAC others(34): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(31): Show |
3 | a0001c0001t0001g0343a0001c0003t0001g0017a0001c0003t0001g0018 | 3 | NA18942.hp1 NA18948.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.33+219_33+256dupAC others(36): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(33): Show |
1 | a0001c0001t0005g0016 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.33+217_33+256dupAC others(38): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(39): Show |
1 | a0001c0001t0001g0015 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.33+211_33+256dupAC others(44): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | AACACACA others(102): Show |
1 | a0001c0001t0001g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.33+256_33+257insAC others(107): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0342 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.33+204_33+205insCA others(9): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | ||||||
chr9:21802985
|
A | ACACACAC others(12): Show |
1 | a0002c0002t0003g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.33+204_33+205insCA others(17): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | ||||||
chr9:21802985
|
A | ACACACAC others(16): Show |
2 | a0001c0001t0001g0339a0002c0002t0008g0340 | 2 | HG01884.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.33+204_33+205insCA others(21): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | ||||||
chr9:21802985
|
A | ACACACAC others(22): Show |
1 | a0001c0003t0001g0338 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.33+204_33+205insCA others(27): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | ||||||
chr9:21802985
|
A | ACACACAC others(26): Show |
1 | a0001c0001t0005g0337 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.33+204_33+205insCA others(31): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | ||||||
chr9:21802985
|
A | ACACACAC others(28): Show |
1 | a0001c0001t0021g0336 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33+204_33+205insCA others(33): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | ||||||
chr9:21802985
|
AAC | A | 18 | a0001c0001t0003g0234a0001c0001t0003g0235a0001c0001t0035g0236others(15): Show | 18 | HG00639.hp1 HG01071.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.33+255_33+256delAC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACAC | A | 25 | a0001c0001t0001g0253a0001c0001t0002g0256a0001c0001t0003g0239others(22): Show | 26 | HG00544.hp1 HG00673.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.33+253_33+256delAC others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACAC | A | 24 | a0001c0001t0001g0266a0001c0001t0002g0264a0001c0001t0002g0282others(21): Show | 26 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.33+251_33+256delAC others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(1): Show |
A | 19 | a0001c0001t0001g0294a0001c0001t0002g0008a0001c0001t0002g0289others(16): Show | 19 | HG00438.hp1 HG02074.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.33+249_33+256delAC others(6): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(3): Show |
A | 13 | a0001c0001t0001g0300a0001c0001t0001g0309a0001c0001t0003g0301others(10): Show | 14 | HG02055.hp1 HG02129.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.33+247_33+256delAC others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(5): Show |
A | 7 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 8 | HG01891.hp2 HG02738.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.33+245_33+256delAC others(10): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
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AACACACA others(7): Show |
A | 1 | a0002c0002t0002g0316 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.33+243_33+256delAC others(12): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(9): Show |
A | 11 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(8): Show | 12 | HG01074.hp1 HG01109.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.33+241_33+256delAC others(14): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(11): Show |
A | 1 | a0001c0001t0003g0327 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.33+239_33+256delAC others(16): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(13): Show |
A | 5 | a0002c0002t0001g0328a0002c0002t0001g0329a0002c0002t0001g0330others(2): Show | 5 | NA18940.hp1 NA18941.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+237_33+256delAC others(18): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(15): Show |
A | 1 | a0001c0001t0001g0333 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.33+235_33+256delAC others(20): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802985
|
AACACACA others(21): Show |
A | 1 | a0002c0002t0003g0334 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.33+229_33+256delAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | |||||
chr9:21802988
|
A | ACACACAC others(66): Show |
1 | a0001c0001t0042g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.33+211_33+283dupAC others(71): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802988 | |||||
chr9:21803012
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A | G | 1 | a0002c0002t0002g0335 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.33+231A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803012 | ||||||
chr9:21803036
|
A | ACACACAC others(21): Show |
1 | a0005c0009t0009g0013 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33+256_33+257insAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803036 | |||||
chr9:21803036
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A | ACACACAC others(19): Show |
1 | a0001c0001t0009g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.33+256_33+257insAC others(24): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803036 | |||||
chr9:21803036
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0009g0113 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33+256_33+257insAC others(18): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803036 | |||||
chr9:21803040
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C | CACACACA others(21): Show |
1 | a0001c0001t0002g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.33+259_33+260insAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803040 | ||||||
chr9:21803100
|
T | TC | 15 | a0001c0003t0001g0017a0001c0003t0001g0023a0001c0003t0001g0028others(12): Show | 15 | HG01496.hp2 HG02523.hp2 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.33+320dupC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803100 | |||||
chr9:21803166
|
A | G | 29 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(26): Show | 31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.33+385A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803166 | ||||||
chr9:21803184
|
G | C | 224 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(221): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.33+403G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803184 | ||||||
chr9:21803217
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T | C | 4 | a0002c0002t0002g0190a0002c0002t0002g0206a0002c0002t0002g0221others(1): Show | 4 | NA18612.hp2 NA18949.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+436T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803217 | ||||||
chr9:21803512
|
C | T | 8 | a0001c0001t0002g0008a0001c0001t0002g0282a0001c0001t0006g0281others(5): Show | 8 | HG00408.hp2 HG02083.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.33+731C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803512 | ||||||
chr9:21803560
|
G | A | 1 | a0002c0004t0001g0207 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.33+779G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803560 | ||||||
chr9:21803628
|
C | T | 1 | a0001c0001t0009g0113 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33+847C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803628 | ||||||
chr9:21803730
|
T | TCTTAA | 224 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(221): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.33+952_33+953insAA others(3): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803730 | |||||
chr9:21803760
|
A | G | 1 | a0002c0002t0002g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.33+979A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803760 | ||||||
chr9:21803859
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A | T | 73 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(70): Show | 76 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.33+1078A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803859 | ||||||
chr9:21803878
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.33+1097T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803878 | ||||||
chr9:21803881
|
C | A | 224 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(221): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.33+1100C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803881 | ||||||
chr9:21803898
|
A | G | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33+1117A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803898 | ||||||
chr9:21803949
|
T | C | 2 | a0002c0002t0002g0007a0002c0002t0026g0007 | 2 | NA18951.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.33+1168T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803949 | ||||||
chr9:21804522
|
C | T | 1 | a0001c0001t0020g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.33+1741C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804522 | ||||||
chr9:21804578
|
T | C | 1 | a0002c0002t0002g0238 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.33+1797T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804578 | ||||||
chr9:21804618
|
A | G | 224 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(221): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.33+1837A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804618 | ||||||
chr9:21804694
|
A | G | 224 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(221): Show | 232 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.33+1913A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804694 | ||||||
chr9:21804704
|
CAA | C | 73 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(70): Show | 76 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.33+1925_33+1926del others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21804704 | |||||
chr9:21804751
|
A | G | 1 | a0001c0003t0001g0088 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.33+1970A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804751 | ||||||
chr9:21804821
|
C | T | 1 | a0001c0001t0023g0065 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.33+2040C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804821 | ||||||
chr9:21804877
|
T | C | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0001t0032g0251others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+2096T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804877 | ||||||
chr9:21804887
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.33+2106G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804887 | ||||||
chr9:21805064
|
G | A | 3 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0001g0365 | 3 | NA18980.hp1 NA19011.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.33+2283G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805064 | ||||||
chr9:21805209
|
C | CAG | 223 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(220): Show | 231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.33+2428_33+2429ins others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805209 | ||||||
chr9:21805304
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.33+2523C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805304 | ||||||
chr9:21805924
|
A | T | 1 | a0002c0002t0002g0215 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.33+3143A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805924 | ||||||
chr9:21805925
|
T | G | 1 | a0002c0002t0002g0215 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.33+3144T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805925 | ||||||
chr9:21805934
|
G | C | 1 | a0001c0001t0020g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33+3153G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805934 | ||||||
chr9:21805990
|
A | G | 2 | a0002c0002t0012g0085a0002c0002t0012g0189 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+3209A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805990 | ||||||
chr9:21806254
|
T | C | 1 | a0001c0003t0001g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.33+3473T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806254 | ||||||
chr9:21806296
|
T | C | 3 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197 | 3 | HG01123.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.33+3515T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806296 | ||||||
chr9:21806330
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.33+3549G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806330 | ||||||
chr9:21806331
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.33+3550A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806331 | ||||||
chr9:21806422
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0041g0084 | 2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.33+3641A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806422 | ||||||
chr9:21806456
|
C | G | 1 | a0001c0001t0020g0308 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.33+3675C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806456 | ||||||
chr9:21806565
|
G | A | 101 | a0001c0001t0003g0239a0002c0002t0001g0115a0002c0002t0001g0154others(98): Show | 103 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.33+3784G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806565 | ||||||
chr9:21806918
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.33+4137C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806918 | ||||||
chr9:21806970
|
C | A | 100 | a0001c0001t0003g0239a0002c0002t0001g0115a0002c0002t0001g0154others(97): Show | 102 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.33+4189C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806970 | ||||||
chr9:21807073
|
C | T | 1 | a0002c0002t0002g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.33+4292C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807073 | ||||||
chr9:21807213
|
A | G | 3 | a0002c0002t0001g0330a0002c0002t0001g0331a0002c0002t0001g0332 | 3 | NA18941.hp1 NA18989.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.33+4432A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807213 | ||||||
chr9:21807321
|
A | G | 1 | a0002c0002t0001g0329 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.33+4540A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807321 | ||||||
chr9:21807328
|
G | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0203others(9): Show | 12 | HG00323.hp2 HG01099.hp1 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.33+4547G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807328 | ||||||
chr9:21807358
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0339 | 2 | NA18947.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.33+4577G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807358 | ||||||
chr9:21807518
|
A | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.33+4737A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807518 | ||||||
chr9:21807574
|
C | T | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33+4793C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807574 | ||||||
chr9:21807659
|
T | C | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33+4878T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807659 | ||||||
chr9:21807736
|
G | T | 1 | a0004c0008t0002g0232 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33+4955G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807736 | ||||||
chr9:21807835
|
C | T | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33+5054C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807835 | ||||||
chr9:21807995
|
A | G | 115 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(112): Show | 121 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.33+5214A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807995 | ||||||
chr9:21808011
|
C | G | 8 | a0001c0001t0002g0008a0001c0001t0002g0282a0001c0001t0006g0281others(5): Show | 8 | HG00408.hp2 HG02083.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.33+5230C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808011 | ||||||
chr9:21808024
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.33+5243A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808024 | ||||||
chr9:21808061
|
A | C | 1 | a0002c0002t0003g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.33+5280A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808061 | ||||||
chr9:21808209
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33+5428T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808209 | ||||||
chr9:21808265
|
A | G | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+5484A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808265 | ||||||
chr9:21808306
|
C | T | 3 | a0002c0002t0012g0085a0002c0002t0012g0189a0002c0002t0040g0044 | 3 | HG01884.hp2 HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+5525C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808306 | ||||||
chr9:21808353
|
G | A | 1 | a0002c0002t0011g0048 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.33+5572G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808353 | ||||||
chr9:21808410
|
C | G | 116 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(113): Show | 122 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.33+5629C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808410 | ||||||
chr9:21808421
|
C | CA | 14 | a0001c0003t0001g0017a0001c0003t0001g0023a0001c0003t0001g0028others(11): Show | 14 | HG01496.hp2 HG02523.hp2 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.33+5652dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21808421 | |||||
chr9:21808421
|
CA | C | 103 | a0001c0001t0003g0239a0001c0001t0004g0077a0001c0001t0012g0024others(100): Show | 104 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.33+5652delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21808421 | |||||
chr9:21808421
|
CAAA | C | 113 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(110): Show | 119 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.33+5650_33+5652del others(3): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21808421 | |||||
chr9:21808467
|
T | C | 1 | a0001c0001t0001g0362 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.33+5686T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808467 | ||||||
chr9:21808546
|
A | G | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33+5765A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808546 | ||||||
chr9:21808571
|
G | A | 3 | a0001c0001t0003g0011a0001c0007t0003g0317a0001c0007t0003g0318 | 4 | HG01433.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+5790G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808571 | ||||||
chr9:21808605
|
A | C | 1 | a0001c0001t0002g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.33+5824A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808605 | ||||||
chr9:21808606
|
AC | A | 208 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(205): Show | 215 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.33+5826delC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808606 | ||||||
chr9:21808607
|
C | A | 13 | a0001c0001t0001g0253a0001c0001t0003g0252a0001c0001t0003g0263others(10): Show | 13 | HG00621.hp2 HG01192.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.33+5826C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808607 | ||||||
chr9:21808753
|
T | G | 105 | a0001c0001t0003g0239a0002c0002t0001g0115a0002c0002t0001g0154others(102): Show | 106 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.33+5972T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808753 | ||||||
chr9:21808777
|
C | T | 1 | a0001c0001t0041g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.33+5996C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808777 | ||||||
chr9:21808779
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0044g0344 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.33+5998C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808779 | ||||||
chr9:21808914
|
C | T | 103 | a0001c0001t0003g0239a0002c0002t0001g0115a0002c0002t0001g0154others(100): Show | 104 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.33+6133C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808914 | ||||||
chr9:21809078
|
T | A | 100 | a0001c0001t0003g0239a0002c0002t0001g0115a0002c0002t0001g0154others(97): Show | 101 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.33+6297T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809078 | ||||||
chr9:21809334
|
C | T | 114 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(111): Show | 120 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.34-6099C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809334 | ||||||
chr9:21809361
|
C | T | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.34-6072C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809361 | ||||||
chr9:21809362
|
G | A | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34-6071G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809362 | ||||||
chr9:21809393
|
A | C | 2 | a0001c0001t0004g0077a0001c0001t0012g0024 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.34-6040A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809393 | ||||||
chr9:21809595
|
C | G | 1 | a0001c0003t0001g0088 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.34-5838C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809595 | ||||||
chr9:21809638
|
C | CA | 121 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(118): Show | 127 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.34-5781dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21809638 | |||||
chr9:21809653
|
G | A | 1 | a0001c0001t0003g0287 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.34-5780G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809653 | ||||||
chr9:21809803
|
G | A | 1 | a0001c0001t0002g0264 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.34-5630G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809803 | ||||||
chr9:21809838
|
G | A | 1 | a0002c0002t0002g0150 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.34-5595G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809838 | ||||||
chr9:21809858
|
C | T | 12 | a0001c0001t0003g0280a0001c0001t0003g0292a0001c0001t0003g0301others(9): Show | 12 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.34-5575C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809858 | ||||||
chr9:21809993
|
A | C | 27 | a0001c0001t0009g0113a0002c0002t0003g0101a0002c0002t0003g0341others(24): Show | 29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.34-5440A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809993 | ||||||
chr9:21810231
|
A | G | 2 | a0001c0001t0004g0077a0001c0001t0012g0024 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.34-5202A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810231 | ||||||
chr9:21810272
|
G | A | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.34-5161G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810272 | ||||||
chr9:21810307
|
C | T | 19 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(16): Show | 21 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.34-5126C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810307 | ||||||
chr9:21810308
|
A | G | 1 | a0001c0001t0015g0279 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.34-5125A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810308 | ||||||
chr9:21810412
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.34-5021A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810412 | ||||||
chr9:21810431
|
A | AAGAG | 124 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(121): Show | 130 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.34-5000_34-4997dup others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21810431 | |||||
chr9:21810532
|
T | G | 124 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(121): Show | 130 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.34-4901T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810532 | ||||||
chr9:21810703
|
T | C | 1 | a0002c0002t0003g0334 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.34-4730T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810703 | ||||||
chr9:21810861
|
G | C | 33 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0053others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.34-4572G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810861 | ||||||
chr9:21811023
|
CA | C | 10 | a0002c0002t0004g0002a0002c0002t0004g0003a0002c0002t0004g0022others(7): Show | 12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.34-4406delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21811023 | |||||
chr9:21811028
|
T | C | 119 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(116): Show | 125 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.34-4405T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811028 | ||||||
chr9:21811139
|
C | G | 1 | a0002c0002t0002g0134 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.34-4294C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811139 | ||||||
chr9:21811155
|
A | G | 110 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(107): Show | 112 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.34-4278A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811155 | ||||||
chr9:21811250
|
A | G | 15 | a0001c0003t0001g0017a0001c0003t0001g0023a0001c0003t0001g0028others(12): Show | 15 | HG01496.hp2 HG02523.hp2 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.34-4183A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811250 | ||||||
chr9:21811274
|
T | C | 2 | a0002c0002t0004g0089a0002c0002t0004g0164 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.34-4159T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811274 | ||||||
chr9:21811442
|
A | G | 119 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(116): Show | 125 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.34-3991A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811442 | ||||||
chr9:21811450
|
A | AT | 9 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(6): Show | 10 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.34-3973dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21811450 | |||||
chr9:21811451
|
T | A | 3 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197 | 3 | HG01123.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.34-3982T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811451 | ||||||
chr9:21811534
|
C | G | 120 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(117): Show | 126 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.34-3899C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811534 | ||||||
chr9:21811566
|
G | A | 30 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092others(27): Show | 32 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.34-3867G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811566 | ||||||
chr9:21811785
|
G | A | 3 | a0002c0002t0033g0208a0002c0002t0034g0165a0002c0002t0037g0114 | 3 | HG03041.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.34-3648G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811785 | ||||||
chr9:21811921
|
T | C | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34-3512T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811921 | ||||||
chr9:21812025
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.34-3408T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812025 | ||||||
chr9:21812317
|
G | A | 103 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(100): Show | 108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.34-3116G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812317 | ||||||
chr9:21812350
|
T | A | 103 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(100): Show | 108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.34-3083T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812350 | ||||||
chr9:21812553
|
C | T | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34-2880C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812553 | ||||||
chr9:21812721
|
C | T | 9 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(6): Show | 10 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.34-2712C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812721 | ||||||
chr9:21812770
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.34-2663T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812770 | ||||||
chr9:21812935
|
C | T | 1 | a0001c0003t0001g0063 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.34-2498C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812935 | ||||||
chr9:21813224
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.34-2209G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813224 | ||||||
chr9:21813242
|
T | C | 139 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(136): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.34-2191T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813242 | ||||||
chr9:21813304
|
A | C | 140 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(137): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.34-2129A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813304 | ||||||
chr9:21813313
|
G | T | 2 | a0001c0001t0005g0026a0001c0001t0031g0141 | 2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.34-2120G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813313 | ||||||
chr9:21813375
|
C | T | 2 | a0001c0001t0005g0026a0001c0001t0031g0141 | 2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.34-2058C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813375 | ||||||
chr9:21813496
|
C | T | 138 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(135): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.34-1937C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813496 | ||||||
chr9:21813519
|
C | T | 139 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(136): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.34-1914C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813519 | ||||||
chr9:21813570
|
C | G | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.34-1863C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813570 | ||||||
chr9:21813580
|
C | G | 1 | a0001c0001t0003g0263 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.34-1853C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813580 | ||||||
chr9:21813596
|
A | G | 29 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(26): Show | 31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-1837A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813596 | ||||||
chr9:21813719
|
C | T | 224 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(221): Show | 228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.34-1714C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813719 | ||||||
chr9:21813766
|
G | A | 12 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(9): Show | 13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.34-1667G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813766 | ||||||
chr9:21813770
|
G | C | 29 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092others(26): Show | 31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-1663G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813770 | ||||||
chr9:21813771
|
G | T | 12 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(9): Show | 13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.34-1662G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813771 | ||||||
chr9:21813773
|
T | C | 29 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092others(26): Show | 31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-1660T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813773 | ||||||
chr9:21813786
|
G | C | 1 | a0001c0001t0035g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.34-1647G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813786 | ||||||
chr9:21813949
|
A | G | 2 | a0002c0002t0002g0212a0002c0002t0002g0213 | 2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.34-1484A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813949 | ||||||
chr9:21813970
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0326 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.34-1463A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813970 | ||||||
chr9:21814169
|
CT | C | 4 | a0002c0002t0005g0209a0002c0002t0013g0240a0002c0002t0013g0249others(1): Show | 4 | NA18957.hp2 NA18963.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-1262delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21814169 | |||||
chr9:21814207
|
T | G | 1 | a0001c0001t0003g0327 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.34-1226T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814207 | ||||||
chr9:21814419
|
C | T | 1 | a0002c0002t0001g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.34-1014C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814419 | ||||||
chr9:21814516
|
T | C | 1 | a0001c0001t0003g0288 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.34-917T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814516 | ||||||
chr9:21814621
|
C | G | 1 | a0001c0001t0006g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.34-812C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814621 | ||||||
chr9:21814760
|
A | G | 2 | a0001c0001t0004g0077a0001c0001t0012g0024 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.34-673A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814760 | ||||||
chr9:21814979
|
C | A | 1 | a0001c0001t0009g0113 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34-454C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814979 | ||||||
chr9:21815148
|
C | G | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-285C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21815148 | ||||||
chr9:21815167
|
G | T | 74 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(71): Show | 77 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.34-266G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21815167 | ||||||
chr9:21815288
|
T | G | 4 | a0002c0002t0002g0064a0002c0002t0002g0184a0002c0002t0048g0030others(1): Show | 4 | NA18950.hp2 NA18974.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-145T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21815288 | ||||||
chr9:21815551
|
T | C | 1 | a0002c0002t0012g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.120+32T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815551 | ||||||
chr9:21815590
|
T | TAA | 98 | a0001c0001t0001g0188a0001c0001t0001g0253a0001c0001t0001g0266others(95): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.120+84_120+85dupAA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 21815590 | |||||
chr9:21815590
|
T | TAAA | 270 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(267): Show | 275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.120+83_120+85dupAA others(1): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 21815590 | |||||
chr9:21815749
|
A | G | 2 | a0002c0004t0001g0177a0002c0004t0001g0178 | 2 | HG01081.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.120+230A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815749 | ||||||
chr9:21815798
|
C | T | 91 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(88): Show | 95 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.120+279C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815798 | ||||||
chr9:21815857
|
A | G | 1 | a0001c0001t0003g0263 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.120+338A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815857 | ||||||
chr9:21815978
|
G | A | 1 | a0001c0001t0009g0113 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.120+459G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815978 | ||||||
chr9:21816083
|
A | G | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+564A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816083 | ||||||
chr9:21816154
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.121-560A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816154 | ||||||
chr9:21816215
|
C | G | 97 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(94): Show | 101 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.121-499C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816215 | ||||||
chr9:21816364
|
T | G | 1 | a0002c0002t0002g0335 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.121-350T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816364 | ||||||
chr9:21816470
|
A | G | 1 | a0001c0001t0001g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.121-244A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816470 | ||||||
chr9:21816529
|
A | G | 149 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(146): Show | 153 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.121-185A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816529 | ||||||
chr9:21816574
|
G | A | 233 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(230): Show | 240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.121-140G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816574 | ||||||
chr9:21816638
|
T | C | 108 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(105): Show | 109 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.121-76T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816638 | ||||||
chr9:21816647
|
A | G | 233 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(230): Show | 240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.121-67A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816647 | ||||||
chr9:21816800
|
T | C | 1 | a0002c0002t0049g0091 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.179+28T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21816800 | ||||||
chr9:21817088
|
A | T | 1 | a0001c0001t0009g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.179+316A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817088 | ||||||
chr9:21817283
|
A | C | 8 | a0001c0001t0002g0008a0001c0001t0002g0282a0001c0001t0006g0281others(5): Show | 8 | HG00408.hp2 HG02083.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+511A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817283 | ||||||
chr9:21817286
|
G | T | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.179+514G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817286 | ||||||
chr9:21817326
|
G | A | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.179+554G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817326 | ||||||
chr9:21817327
|
C | T | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.179+555C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817327 | ||||||
chr9:21817476
|
A | G | 2 | a0002c0002t0002g0150a0002c0002t0002g0261 | 2 | HG01069.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.180-559A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817476 | ||||||
chr9:21817525
|
G | C | 18 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(15): Show | 20 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.180-510G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817525 | ||||||
chr9:21817755
|
A | G | 249 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(246): Show | 256 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.180-280A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817755 | ||||||
chr9:21817778
|
T | C | 368 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(365): Show | 376 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(373): Show |
intron_variant | MODIFIER | c.180-257T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817778 | ||||||
chr9:21818012
|
C | T | 27 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(24): Show | 29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.180-23C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21818012 | ||||||
chr9:21818311
|
C | T | 232 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(229): Show | 239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.347+109C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818311 | ||||||
chr9:21818317
|
C | CT | 41 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0043others(38): Show | 41 | HG00597.hp1 HG00642.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.347+142dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | |||||
chr9:21818317
|
CT | C | 150 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0140others(147): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.347+142delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | |||||
chr9:21818317
|
CTT | C | 18 | a0002c0002t0003g0334a0002c0002t0004g0002a0002c0002t0004g0003others(15): Show | 20 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.347+141_347+142del others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | |||||
chr9:21818317
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+131_347+142del others(12): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | |||||
chr9:21818514
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.347+312G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818514 | ||||||
chr9:21818570
|
C | T | 1 | a0002c0002t0045g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.347+368C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818570 | ||||||
chr9:21818609
|
G | A | 1 | a0002c0002t0002g0215 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.347+407G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818609 | ||||||
chr9:21818618
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0144a0001c0001t0014g0106others(1): Show | 4 | HG00738.hp2 HG01515.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.347+416C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818618 | ||||||
chr9:21818622
|
G | C | 1 | a0001c0001t0003g0265 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.347+420G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818622 | ||||||
chr9:21818675
|
A | G | 107 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(104): Show | 108 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.347+473A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818675 | ||||||
chr9:21818729
|
T | C | 5 | a0002c0002t0004g0035a0002c0002t0004g0061a0002c0002t0004g0127others(2): Show | 5 | HG01192.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+527T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818729 | ||||||
chr9:21819027
|
T | G | 1 | a0001c0001t0051g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.347+825T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819027 | ||||||
chr9:21819044
|
A | G | 2 | a0001c0001t0005g0337a0002c0002t0002g0215 | 2 | NA18987.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.347+842A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819044 | ||||||
chr9:21819053
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.347+851G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819053 | ||||||
chr9:21819062
|
T | A | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347+860T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819062 | ||||||
chr9:21819094
|
T | C | 57 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(54): Show | 57 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.347+892T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819094 | ||||||
chr9:21819117
|
G | T | 1 | a0001c0001t0030g0010 | 2 | NA18953.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.347+915G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819117 | ||||||
chr9:21819137
|
C | CT | 221 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(218): Show | 228 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.347+949dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21819137 | |||||
chr9:21819140
|
T | TC | 3 | a0001c0001t0003g0302a0001c0001t0003g0305a0001c0001t0003g0306 | 3 | HG02145.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.347+938_347+939ins others(1): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819140 | ||||||
chr9:21819141
|
T | C | 1 | a0001c0001t0001g0342 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.347+939T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819141 | ||||||
chr9:21819152
|
A | T | 4 | a0001c0001t0003g0259a0001c0001t0003g0265a0001c0001t0003g0272others(1): Show | 4 | HG00544.hp2 NA18966.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.347+950A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819152 | ||||||
chr9:21819183
|
C | G | 27 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(24): Show | 29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.347+981C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819183 | ||||||
chr9:21819191
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.347+989G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819191 | ||||||
chr9:21819263
|
T | C | 1 | a0001c0001t0008g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.347+1061T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819263 | ||||||
chr9:21819543
|
A | T | 1 | a0002c0002t0002g0335 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.347+1341A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819543 | ||||||
chr9:21819723
|
T | G | 38 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(35): Show | 39 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.347+1521T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819723 | ||||||
chr9:21819900
|
A | G | 1 | a0002c0002t0002g0215 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.347+1698A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819900 | ||||||
chr9:21820081
|
A | G | 7 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0023g0065others(4): Show | 7 | HG01123.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+1879A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820081 | ||||||
chr9:21820092
|
T | C | 2 | a0002c0002t0004g0089a0002c0002t0004g0164 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.347+1890T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820092 | ||||||
chr9:21820170
|
G | T | 1 | a0001c0001t0003g0292 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.347+1968G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820170 | ||||||
chr9:21820182
|
A | G | 1 | a0002c0002t0002g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.347+1980A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820182 | ||||||
chr9:21820289
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.347+2087G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820289 | ||||||
chr9:21820371
|
T | G | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+2169T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820371 | ||||||
chr9:21820382
|
C | G | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+2180C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820382 | ||||||
chr9:21820419
|
T | C | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+2217T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820419 | ||||||
chr9:21820500
|
A | G | 1 | a0002c0002t0002g0285 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.347+2298A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820500 | ||||||
chr9:21820503
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.347+2301T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820503 | ||||||
chr9:21820717
|
C | G | 1 | a0001c0001t0008g0262 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.347+2515C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820717 | ||||||
chr9:21820728
|
T | G | 1 | a0001c0001t0051g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.347+2526T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820728 | ||||||
chr9:21820816
|
A | C | 4 | a0002c0002t0002g0037a0002c0002t0002g0133a0002c0002t0002g0155others(1): Show | 4 | HG01255.hp2 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.347+2614A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820816 | ||||||
chr9:21820875
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+2673C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820875 | ||||||
chr9:21821027
|
T | G | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+2825T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821027 | ||||||
chr9:21821032
|
C | T | 11 | a0001c0001t0003g0280a0001c0001t0003g0292a0001c0001t0003g0301others(8): Show | 11 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.347+2830C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821032 | ||||||
chr9:21821278
|
T | A | 1 | a0001c0001t0001g0309 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+3076T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821278 | ||||||
chr9:21821282
|
A | G | 141 | a0001c0001t0001g0042a0001c0001t0001g0070a0001c0001t0001g0117others(138): Show | 145 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.347+3080A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821282 | ||||||
chr9:21821372
|
A | G | 2 | a0001c0001t0004g0077a0001c0001t0012g0024 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+3170A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821372 | ||||||
chr9:21821388
|
A | G | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+3186A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821388 | ||||||
chr9:21821509
|
C | T | 27 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(24): Show | 29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.347+3307C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821509 | ||||||
chr9:21821515
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+3313G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821515 | ||||||
chr9:21821549
|
G | A | 1 | a0001c0001t0009g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.347+3347G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821549 | ||||||
chr9:21821591
|
T | A | 2 | a0001c0001t0004g0077a0001c0001t0012g0024 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+3389T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821591 | ||||||
chr9:21821593
|
G | T | 2 | a0001c0001t0004g0077a0001c0001t0012g0024 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+3391G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821593 | ||||||
chr9:21821595
|
T | C | 1 | a0002c0002t0007g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.347+3393T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821595 | ||||||
chr9:21821649
|
T | C | 2 | a0002c0002t0004g0089a0002c0002t0004g0164 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.347+3447T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821649 | ||||||
chr9:21821669
|
TTTATTGA others(4): Show |
T | 1 | a0001c0001t0001g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347+3468_347+3478d others(13): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821669 | ||||||
chr9:21821670
|
T | C | 117 | a0001c0001t0001g0025a0001c0001t0001g0095a0001c0001t0001g0120others(114): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.347+3468T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821670 | ||||||
chr9:21821678
|
T | C | 3 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0038g0090 | 3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.347+3476T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821678 | ||||||
chr9:21821719
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.347+3517C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821719 | ||||||
chr9:21821728
|
G | T | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+3526G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821728 | ||||||
chr9:21821765
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0044g0344 | 2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.347+3563T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821765 | ||||||
chr9:21821786
|
A | G | 1 | a0002c0002t0002g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.347+3584A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821786 | ||||||
chr9:21821952
|
A | G | 4 | a0001c0001t0005g0096a0001c0001t0005g0122a0001c0001t0019g0033others(1): Show | 4 | HG02015.hp1 NA18947.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+3750A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821952 | ||||||
chr9:21822003
|
A | G | 4 | a0001c0001t0010g0350a0001c0001t0010g0351a0001c0001t0010g0356others(1): Show | 4 | NA18948.hp1 NA18990.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+3801A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822003 | ||||||
chr9:21822079
|
A | G | 1 | a0001c0001t0014g0161 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.347+3877A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822079 | ||||||
chr9:21822108
|
G | T | 1 | a0001c0003t0001g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.347+3906G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822108 | ||||||
chr9:21822193
|
G | C | 1 | a0001c0001t0002g0289 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.347+3991G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822193 | ||||||
chr9:21822210
|
C | A | 1 | a0001c0001t0002g0289 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.347+4008C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822210 | ||||||
chr9:21822223
|
G | A | 1 | a0002c0002t0001g0241 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.347+4021G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822223 | ||||||
chr9:21822227
|
G | A | 2 | a0002c0002t0004g0111a0002c0002t0004g0130 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.347+4025G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822227 | ||||||
chr9:21822299
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.347+4097A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822299 | ||||||
chr9:21822418
|
A | G | 32 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(29): Show | 33 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.347+4216A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822418 | ||||||
chr9:21822484
|
G | A | 249 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(246): Show | 257 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.347+4282G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822484 | ||||||
chr9:21822536
|
T | A | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+4334T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822536 | ||||||
chr9:21822616
|
G | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0140 | 2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.347+4414G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822616 | ||||||
chr9:21822647
|
C | T | 1 | a0002c0002t0026g0246 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.347+4445C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822647 | ||||||
chr9:21822753
|
G | T | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+4551G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822753 | ||||||
chr9:21822779
|
A | T | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+4577A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822779 | ||||||
chr9:21822793
|
G | C | 1 | a0001c0001t0001g0342 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.347+4591G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822793 | ||||||
chr9:21823089
|
C | T | 26 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(23): Show | 28 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.347+4887C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823089 | ||||||
chr9:21823150
|
T | C | 1 | a0001c0001t0001g0342 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.347+4948T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823150 | ||||||
chr9:21823224
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+5022C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823224 | ||||||
chr9:21823460
|
T | C | 1 | a0001c0001t0005g0139 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.347+5258T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823460 | ||||||
chr9:21823669
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.347+5467A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823669 | ||||||
chr9:21823715
|
T | C | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+5513T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823715 | ||||||
chr9:21823742
|
G | A | 1 | a0001c0001t0006g0297 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.347+5540G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823742 | ||||||
chr9:21823745
|
AC | A | 3 | a0002c0002t0016g0319a0002c0002t0016g0320a0002c0002t0016g0321 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.347+5544delC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823745 | ||||||
chr9:21823756
|
A | T | 1 | a0001c0001t0003g0263 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.347+5554A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823756 | ||||||
chr9:21823803
|
G | A | 2 | a0002c0002t0012g0085a0002c0002t0012g0189 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.347+5601G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823803 | ||||||
chr9:21823865
|
A | T | 11 | a0002c0002t0002g0050a0002c0002t0002g0102a0002c0002t0002g0134others(8): Show | 11 | HG00642.hp1 HG01109.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.347+5663A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823865 | ||||||
chr9:21823866
|
A | G | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+5664A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823866 | ||||||
chr9:21823951
|
G | T | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+5749G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823951 | ||||||
chr9:21823953
|
T | C | 134 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0001g0157others(131): Show | 138 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.347+5751T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823953 | ||||||
chr9:21823975
|
T | C | 1 | a0001c0003t0001g0088 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.347+5773T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823975 | ||||||
chr9:21824050
|
G | A | 12 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(9): Show | 13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.347+5848G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824050 | ||||||
chr9:21824103
|
T | G | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.347+5901T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824103 | ||||||
chr9:21824519
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.347+6317G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824519 | ||||||
chr9:21824534
|
C | T | 2 | a0002c0002t0012g0085a0002c0002t0012g0189 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.347+6332C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824534 | ||||||
chr9:21824608
|
A | T | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+6406A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824608 | ||||||
chr9:21824611
|
A | G | 1 | a0002c0002t0001g0226 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.347+6409A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824611 | ||||||
chr9:21824707
|
T | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0070a0001c0001t0001g0105others(3): Show | 6 | HG01099.hp2 HG01168.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.347+6505T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824707 | ||||||
chr9:21824755
|
A | C | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+6553A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824755 | ||||||
chr9:21824874
|
C | G | 1 | a0002c0002t0002g0198 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.347+6672C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824874 | ||||||
chr9:21824876
|
C | T | 1 | a0002c0002t0002g0198 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.347+6674C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824876 | ||||||
chr9:21824883
|
C | T | 130 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0001g0157others(127): Show | 134 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.347+6681C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824883 | ||||||
chr9:21824895
|
C | T | 3 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0038g0090 | 3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.347+6693C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824895 | ||||||
chr9:21824906
|
C | T | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+6704C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824906 | ||||||
chr9:21824924
|
T | C | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+6722T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824924 | ||||||
chr9:21824993
|
G | A | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.347+6791G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824993 | ||||||
chr9:21825041
|
A | G | 1 | a0001c0001t0003g0271 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.347+6839A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825041 | ||||||
chr9:21825042
|
C | T | 1 | a0001c0001t0001g0355 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.347+6840C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825042 | ||||||
chr9:21825068
|
C | A | 1 | a0003c0005t0002g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.347+6866C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825068 | ||||||
chr9:21825076
|
T | C | 253 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(250): Show | 261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.347+6874T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825076 | ||||||
chr9:21825101
|
C | T | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+6899C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825101 | ||||||
chr9:21825146
|
C | T | 1 | a0002c0002t0034g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347+6944C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825146 | ||||||
chr9:21825361
|
C | A | 2 | a0002c0002t0012g0085a0002c0002t0012g0189 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.347+7159C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825361 | ||||||
chr9:21825468
|
A | G | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+7266A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825468 | ||||||
chr9:21825471
|
C | A | 5 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0003g0216others(2): Show | 5 | HG00140.hp2 HG02004.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+7269C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825471 | ||||||
chr9:21825485
|
A | T | 1 | a0001c0007t0003g0318 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.347+7283A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825485 | ||||||
chr9:21825517
|
A | G | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+7315A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825517 | ||||||
chr9:21825575
|
C | T | 4 | a0002c0002t0002g0190a0002c0002t0002g0206a0002c0002t0002g0221others(1): Show | 4 | NA18612.hp2 NA18949.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+7373C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825575 | ||||||
chr9:21825718
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0326 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.347+7516A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825718 | ||||||
chr9:21825859
|
T | C | 26 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(23): Show | 28 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.347+7657T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825859 | ||||||
chr9:21825887
|
G | C | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+7685G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825887 | ||||||
chr9:21825947
|
G | GA | 112 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(109): Show | 116 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.347+7747dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21825947 | |||||
chr9:21825997
|
A | G | 115 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(112): Show | 119 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.347+7795A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825997 | ||||||
chr9:21826068
|
C | G | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+7866C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826068 | ||||||
chr9:21826188
|
C | CT | 6 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.347+8001dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826188 | |||||
chr9:21826188
|
CT | C | 191 | a0001c0001t0001g0188a0001c0001t0001g0253a0001c0001t0001g0266others(188): Show | 197 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.347+8001delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826188 | |||||
chr9:21826188
|
CTT | C | 8 | a0001c0001t0003g0278a0001c0001t0003g0288a0001c0001t0023g0065others(5): Show | 8 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.347+8000_347+8001d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826188 | |||||
chr9:21826219
|
T | G | 1 | a0001c0001t0014g0366 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.347+8017T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826219 | ||||||
chr9:21826227
|
C | A | 2 | a0002c0002t0003g0222a0002c0002t0003g0334 | 2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.347+8025C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826227 | ||||||
chr9:21826287
|
T | G | 1 | a0002c0002t0002g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.347+8085T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826287 | ||||||
chr9:21826388
|
T | C | 95 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(92): Show | 99 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.347+8186T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826388 | ||||||
chr9:21826464
|
C | T | 92 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(89): Show | 96 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.347+8262C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826464 | ||||||
chr9:21826514
|
A | T | 1 | a0002c0002t0016g0320 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.347+8312A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826514 | ||||||
chr9:21826517
|
A | G | 104 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0001g0157others(101): Show | 106 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.347+8315A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826517 | ||||||
chr9:21826518
|
T | A | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+8316T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826518 | ||||||
chr9:21826539
|
G | A | 230 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(227): Show | 238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.347+8337G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826539 | ||||||
chr9:21826600
|
G | A | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+8398G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826600 | ||||||
chr9:21826609
|
T | TTTA | 40 | a0001c0001t0001g0043a0001c0001t0001g0058a0001c0001t0001g0059others(37): Show | 41 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.347+8446_347+8448d others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | |||||
chr9:21826609
|
T | TTTATTA | 7 | a0001c0001t0001g0367a0001c0001t0010g0350a0001c0001t0010g0351others(4): Show | 7 | HG03041.hp1 NA18946.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.347+8443_347+8448d others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | |||||
chr9:21826609
|
T | TTTATTAT others(2): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0123a0001c0001t0001g0355others(4): Show | 7 | HG01243.hp1 HG02630.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+8440_347+8448d others(11): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | |||||
chr9:21826609
|
TTTA | T | 81 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(78): Show | 81 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.347+8446_347+8448d others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | |||||
chr9:21826609
|
TTTATTA | T | 8 | a0002c0002t0001g0224a0002c0002t0002g0212a0002c0002t0002g0213others(5): Show | 8 | HG00438.hp2 HG00609.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.347+8443_347+8448d others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | |||||
chr9:21826609
|
TTTATTAT others(2): Show |
T | 102 | a0002c0002t0001g0157a0002c0002t0001g0192a0002c0002t0001g0226others(99): Show | 106 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.347+8440_347+8448d others(11): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | |||||
chr9:21826609
|
TTTATTAT others(11): Show |
T | 15 | a0001c0001t0009g0113a0002c0002t0002g0198a0002c0002t0002g0229others(12): Show | 15 | HG00544.hp1 HG00673.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+8431_347+8448d others(20): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | |||||
chr9:21826621
|
A | ATTATTG | 17 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(14): Show | 18 | HG01109.hp1 HG01123.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.347+8424_347+8425i others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826621 | |||||
chr9:21826621
|
A | T | 3 | a0002c0002t0013g0240a0002c0002t0013g0249a0002c0002t0013g0283 | 3 | NA18957.hp2 NA19056.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.347+8419A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826621 | ||||||
chr9:21826624
|
A | ATTG | 73 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(70): Show | 76 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.347+8424_347+8425i others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826624 | |||||
chr9:21826627
|
A | G | 1 | a0001c0001t0003g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.347+8425A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826627 | ||||||
chr9:21826630
|
A | G | 1 | a0001c0001t0001g0312 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.347+8428A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826630 | ||||||
chr9:21826632
|
T | G | 1 | a0002c0002t0011g0223 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.347+8430T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826632 | ||||||
chr9:21826690
|
A | C | 1 | a0001c0001t0023g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.347+8488A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826690 | ||||||
chr9:21826841
|
G | A | 93 | a0002c0002t0001g0157a0002c0002t0001g0192a0002c0002t0001g0224others(90): Show | 95 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.347+8639G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826841 | ||||||
chr9:21826845
|
G | T | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+8643G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826845 | ||||||
chr9:21826854
|
G | A | 1 | a0002c0002t0002g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.347+8652G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826854 | ||||||
chr9:21826941
|
G | T | 104 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0001g0157others(101): Show | 106 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.347+8739G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826941 | ||||||
chr9:21827044
|
T | A | 1 | a0001c0001t0009g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.347+8842T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827044 | ||||||
chr9:21827070
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+8868C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827070 | ||||||
chr9:21827169
|
G | A | 1 | a0002c0002t0003g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.347+8967G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827169 | ||||||
chr9:21827193
|
G | A | 26 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(23): Show | 28 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.347+8991G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827193 | ||||||
chr9:21827284
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.347+9082C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827284 | ||||||
chr9:21827287
|
C | G | 2 | a0001c0001t0004g0077a0001c0001t0012g0024 | 2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+9085C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827287 | ||||||
chr9:21827407
|
A | G | 104 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0001g0157others(101): Show | 106 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.347+9205A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827407 | ||||||
chr9:21827485
|
A | C | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+9283A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827485 | ||||||
chr9:21827527
|
T | G | 5 | a0001c0001t0003g0292a0001c0001t0003g0301a0001c0001t0003g0307others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+9325T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827527 | ||||||
chr9:21827913
|
A | G | 3 | a0002c0002t0033g0208a0002c0002t0034g0165a0002c0002t0037g0114 | 3 | HG03041.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.347+9711A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827913 | ||||||
chr9:21827993
|
G | A | 249 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(246): Show | 257 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.347+9791G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827993 | ||||||
chr9:21828111
|
A | C | 104 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0001g0157others(101): Show | 106 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.348-9797A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828111 | ||||||
chr9:21828243
|
T | C | 253 | a0001c0001t0001g0070a0001c0001t0001g0095a0001c0001t0001g0117others(250): Show | 261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.348-9665T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828243 | ||||||
chr9:21828248
|
G | A | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-9660G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828248 | ||||||
chr9:21828255
|
G | A | 1 | a0002c0002t0033g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348-9653G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828255 | ||||||
chr9:21828315
|
A | C | 1 | a0001c0001t0019g0033 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.348-9593A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828315 | ||||||
chr9:21828360
|
G | A | 1 | a0002c0002t0037g0114 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.348-9548G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828360 | ||||||
chr9:21828502
|
C | T | 1 | a0001c0001t0036g0354 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.348-9406C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828502 | ||||||
chr9:21828543
|
T | C | 4 | a0001c0001t0010g0350a0001c0001t0010g0351a0001c0001t0010g0356others(1): Show | 4 | NA18948.hp1 NA18990.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-9365T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828543 | ||||||
chr9:21828618
|
T | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0339others(3): Show | 6 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-9290T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828618 | ||||||
chr9:21828663
|
G | C | 1 | a0001c0001t0001g0309 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.348-9245G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828663 | ||||||
chr9:21828959
|
A | G | 1 | a0002c0002t0002g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.348-8949A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828959 | ||||||
chr9:21829059
|
C | T | 1 | a0002c0002t0002g0316 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.348-8849C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829059 | ||||||
chr9:21829065
|
T | A | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-8843T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829065 | ||||||
chr9:21829111
|
A | G | 1 | a0001c0003t0001g0063 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.348-8797A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829111 | ||||||
chr9:21829114
|
G | C | 3 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092 | 3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-8794G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829114 | ||||||
chr9:21829118
|
C | T | 31 | a0001c0001t0004g0077a0001c0001t0012g0024a0002c0002t0003g0101others(28): Show | 33 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.348-8790C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829118 | ||||||
chr9:21829129
|
T | A | 1 | a0002c0002t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348-8779T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829129 | ||||||
chr9:21829159
|
A | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-8749A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829159 | ||||||
chr9:21829273
|
G | A | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-8635G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829273 | ||||||
chr9:21829358
|
G | A | 1 | a0002c0002t0001g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.348-8550G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829358 | ||||||
chr9:21829417
|
GT | G | 222 | a0001c0001t0001g0059a0001c0001t0001g0253a0001c0001t0001g0266others(219): Show | 230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.348-8479delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21829417 | |||||
chr9:21829426
|
T | TG | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-8482_348-8481i others(3): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829426 | ||||||
chr9:21829508
|
T | C | 29 | a0002c0002t0003g0101a0002c0002t0003g0341a0002c0002t0004g0002others(26): Show | 31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.348-8400T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829508 | ||||||
chr9:21829553
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.348-8355G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829553 | ||||||
chr9:21829605
|
T | A | 87 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(84): Show | 91 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.348-8303T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829605 | ||||||
chr9:21829629
|
G | GA | 33 | a0001c0001t0005g0096a0001c0001t0009g0075a0001c0001t0009g0113others(30): Show | 35 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.348-8266dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21829629 | |||||
chr9:21829720
|
G | T | 1 | a0002c0002t0002g0193 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.348-8188G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829720 | ||||||
chr9:21829820
|
T | G | 1 | a0002c0002t0016g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.348-8088T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829820 | ||||||
chr9:21829974
|
A | G | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-7934A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829974 | ||||||
chr9:21830132
|
C | G | 1 | a0002c0002t0004g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.348-7776C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830132 | ||||||
chr9:21830158
|
A | G | 88 | a0001c0001t0001g0253a0001c0001t0001g0266a0001c0001t0001g0294others(85): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.348-7750A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830158 | ||||||
chr9:21830163
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.348-7745G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830163 | ||||||
chr9:21830268
|
A | G | 4 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0024g0092others(1): Show | 4 | HG02622.hp2 HG02630.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-7640A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830268 | ||||||
chr9:21830438
|
C | T | 2 | a0002c0002t0004g0089a0002c0002t0004g0164 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.348-7470C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830438 | ||||||
chr9:21830444
|
C | A | 1 | a0001c0003t0001g0338 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.348-7464C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830444 | ||||||
chr9:21830467
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0041g0084 | 2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.348-7441A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830467 | ||||||
chr9:21830480
|
G | A | 12 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(9): Show | 13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.348-7428G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830480 | ||||||
chr9:21830542
|
T | G | 4 | a0002c0002t0004g0061a0002c0002t0004g0127a0002c0002t0004g0181others(1): Show | 4 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-7366T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830542 | ||||||
chr9:21830554
|
A | G | 4 | a0001c0001t0023g0065a0001c0001t0023g0132a0001c0010t0009g0197others(1): Show | 4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-7354A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830554 | ||||||
chr9:21830569
|
G | A | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-7339G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830569 | ||||||
chr9:21830627
|
T | G | 1 | a0001c0001t0003g0119 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.348-7281T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830627 | ||||||
chr9:21830659
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.348-7249C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830659 | ||||||
chr9:21830661
|
C | G | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-7247C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830661 | ||||||
chr9:21830751
|
A | G | 1 | a0002c0002t0011g0223 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.348-7157A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830751 | ||||||
chr9:21830894
|
C | T | 1 | a0001c0001t0012g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348-7014C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830894 | ||||||
chr9:21830945
|
T | C | 3 | a0001c0001t0017g0118a0001c0001t0017g0136a0001c0001t0017g0169 | 3 | NA18969.hp1 NA19006.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.348-6963T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830945 | ||||||
chr9:21830954
|
A | AATGAGAT | 13 | a0001c0001t0001g0300a0001c0001t0001g0322a0001c0001t0001g0323others(10): Show | 14 | HG00323.hp1 HG01109.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.348-6953_348-6947d others(9): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21830954 | |||||
chr9:21831031
|
T | G | 3 | a0001c0001t0001g0057a0001c0001t0003g0051a0001c0001t0011g0052 | 3 | HG00323.hp2 HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.348-6877T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831031 | ||||||
chr9:21831044
|
A | G | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.348-6864A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831044 | ||||||
chr9:21831071
|
C | T | 3 | a0001c0001t0003g0011a0001c0007t0003g0317a0001c0007t0003g0318 | 4 | HG01433.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-6837C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831071 | ||||||
chr9:21831344
|
TG | T | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-6563delG | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831344 | ||||||
chr9:21831380
|
G | A | 1 | a0001c0001t0009g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348-6528G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831380 | ||||||
chr9:21831457
|
G | A | 19 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(16): Show | 19 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.348-6451G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831457 | ||||||
chr9:21831495
|
AT | A | 147 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(144): Show | 151 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.348-6401delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21831495 | |||||
chr9:21831630
|
A | G | 119 | a0001c0001t0001g0203a0001c0001t0001g0266a0001c0001t0001g0294others(116): Show | 125 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.348-6278A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831630 | ||||||
chr9:21831636
|
T | C | 3 | a0001c0001t0010g0350a0001c0001t0010g0356a0001c0001t0036g0354 | 3 | NA18990.hp2 NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.348-6272T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831636 | ||||||
chr9:21831783
|
T | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.348-6125T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831783 | ||||||
chr9:21831785
|
A | AT | 23 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(20): Show | 23 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.348-6109dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21831785 | |||||
chr9:21831785
|
AT | A | 96 | a0001c0001t0001g0362a0001c0001t0002g0264a0001c0001t0014g0106others(93): Show | 98 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.348-6109delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21831785 | |||||
chr9:21831786
|
T | C | 3 | a0002c0002t0016g0319a0002c0002t0016g0320a0002c0002t0016g0321 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.348-6122T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831786 | ||||||
chr9:21831980
|
A | G | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-5928A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831980 | ||||||
chr9:21832227
|
T | A | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-5681T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832227 | ||||||
chr9:21832358
|
T | C | 2 | a0001c0001t0029g0352a0001c0001t0029g0369 | 2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.348-5550T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832358 | ||||||
chr9:21832541
|
G | A | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-5367G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832541 | ||||||
chr9:21832551
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.348-5357T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832551 | ||||||
chr9:21832635
|
G | T | 1 | a0002c0002t0004g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.348-5273G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832635 | ||||||
chr9:21832738
|
C | T | 4 | a0001c0001t0009g0075a0002c0002t0004g0089a0002c0002t0004g0164others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-5170C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832738 | ||||||
chr9:21832743
|
A | G | 111 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(108): Show | 117 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.348-5165A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832743 | ||||||
chr9:21832786
|
T | C | 1 | a0002c0002t0002g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.348-5122T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832786 | ||||||
chr9:21832925
|
A | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4983A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832925 | ||||||
chr9:21833047
|
T | C | 110 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(107): Show | 116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.348-4861T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833047 | ||||||
chr9:21833085
|
C | T | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4823C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833085 | ||||||
chr9:21833339
|
T | C | 253 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0095others(250): Show | 261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.348-4569T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833339 | ||||||
chr9:21833421
|
G | T | 5 | a0001c0010t0009g0197a0002c0002t0012g0085a0002c0002t0012g0189others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-4487G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833421 | ||||||
chr9:21833474
|
A | G | 1 | a0001c0007t0003g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348-4434A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833474 | ||||||
chr9:21833619
|
C | T | 1 | a0001c0001t0009g0113 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.348-4289C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833619 | ||||||
chr9:21833639
|
G | A | 1 | a0002c0002t0033g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348-4269G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833639 | ||||||
chr9:21833660
|
A | G | 112 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(109): Show | 118 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.348-4248A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833660 | ||||||
chr9:21833685
|
T | C | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348-4223T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833685 | ||||||
chr9:21833710
|
G | A | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4198G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833710 | ||||||
chr9:21833763
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.348-4145T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833763 | ||||||
chr9:21833785
|
T | C | 2 | a0001c0001t0012g0024a0001c0001t0032g0251 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.348-4123T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833785 | ||||||
chr9:21833814
|
G | A | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.348-4094G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833814 | ||||||
chr9:21833843
|
T | C | 2 | a0001c0001t0009g0075a0002c0002t0052g0036 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.348-4065T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833843 | ||||||
chr9:21833869
|
C | T | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4039C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833869 | ||||||
chr9:21833884
|
A | G | 5 | a0001c0010t0009g0197a0002c0002t0012g0085a0002c0002t0012g0189others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-4024A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833884 | ||||||
chr9:21833921
|
T | C | 1 | a0001c0001t0005g0122 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.348-3987T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833921 | ||||||
chr9:21833994
|
A | G | 2 | a0002c0002t0012g0085a0002c0002t0012g0189 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.348-3914A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833994 | ||||||
chr9:21834017
|
A | G | 5 | a0001c0010t0009g0197a0002c0002t0012g0085a0002c0002t0012g0189others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-3891A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834017 | ||||||
chr9:21834031
|
T | C | 1 | a0002c0002t0004g0162 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348-3877T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834031 | ||||||
chr9:21834211
|
T | C | 99 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0362others(96): Show | 101 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.348-3697T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834211 | ||||||
chr9:21834317
|
A | T | 3 | a0001c0001t0008g0262a0001c0001t0008g0298a0001c0001t0008g0299 | 3 | HG02257.hp2 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.348-3591A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834317 | ||||||
chr9:21834382
|
A | G | 2 | a0002c0002t0003g0244a0002c0002t0003g0245 | 2 | NA18986.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.348-3526A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834382 | ||||||
chr9:21834544
|
C | G | 3 | a0001c0001t0018g0172a0001c0001t0018g0173a0001c0001t0018g0180 | 3 | HG00140.hp1 HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.348-3364C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834544 | ||||||
chr9:21834601
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0042g0205 | 3 | HG01515.hp1 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.348-3307C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834601 | ||||||
chr9:21834630
|
A | C | 2 | a0001c0001t0023g0065a0001c0001t0023g0132 | 2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.348-3278A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834630 | ||||||
chr9:21834642
|
T | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-3266T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834642 | ||||||
chr9:21834813
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0342 | 2 | NA18998.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.348-3095A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834813 | ||||||
chr9:21834823
|
A | C | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-3085A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834823 | ||||||
chr9:21834938
|
G | A | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348-2970G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834938 | ||||||
chr9:21834948
|
A | C | 5 | a0001c0010t0009g0197a0002c0002t0012g0085a0002c0002t0012g0189others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-2960A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834948 | ||||||
chr9:21834969
|
C | T | 5 | a0001c0010t0009g0197a0002c0002t0012g0085a0002c0002t0012g0189others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-2939C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834969 | ||||||
chr9:21835057
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.348-2851A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835057 | ||||||
chr9:21835115
|
T | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-2793T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835115 | ||||||
chr9:21835119
|
G | C | 4 | a0001c0001t0009g0113a0001c0001t0023g0065a0001c0001t0023g0132others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-2789G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835119 | ||||||
chr9:21835144
|
C | T | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-2764C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835144 | ||||||
chr9:21835225
|
C | T | 1 | a0002c0002t0016g0319 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.348-2683C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835225 | ||||||
chr9:21835242
|
A | C | 2 | a0001c0001t0009g0113a0001c0001t0024g0092 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-2666A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835242 | ||||||
chr9:21835330
|
C | G | 1 | a0002c0002t0002g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.348-2578C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835330 | ||||||
chr9:21835454
|
A | AGAAATAT others(31): Show |
1 | a0001c0003t0001g0087 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.348-2442_348-2405d others(40): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21835454 | |||||
chr9:21835558
|
C | G | 5 | a0001c0010t0009g0197a0002c0002t0012g0085a0002c0002t0012g0189others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-2350C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835558 | ||||||
chr9:21835640
|
T | C | 2 | a0001c0001t0009g0113a0001c0001t0024g0092 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-2268T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835640 | ||||||
chr9:21835784
|
G | T | 1 | a0001c0001t0005g0032 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.348-2124G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835784 | ||||||
chr9:21835859
|
C | G | 3 | a0001c0001t0008g0262a0001c0001t0008g0298a0001c0001t0008g0299 | 3 | HG02257.hp2 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.348-2049C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835859 | ||||||
chr9:21835969
|
C | T | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.348-1939C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835969 | ||||||
chr9:21836062
|
C | T | 4 | a0001c0001t0009g0075a0002c0002t0004g0089a0002c0002t0004g0164others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-1846C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836062 | ||||||
chr9:21836254
|
G | C | 2 | a0002c0002t0004g0089a0002c0002t0004g0164 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.348-1654G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836254 | ||||||
chr9:21836294
|
C | T | 5 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.348-1614C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836294 | ||||||
chr9:21836469
|
A | C | 1 | a0001c0001t0003g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.348-1439A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836469 | ||||||
chr9:21836521
|
T | C | 1 | a0002c0002t0045g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348-1387T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836521 | ||||||
chr9:21836586
|
A | G | 3 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0038g0090 | 3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.348-1322A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836586 | ||||||
chr9:21836802
|
G | A | 2 | a0002c0002t0012g0085a0002c0002t0012g0189 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.348-1106G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836802 | ||||||
chr9:21837005
|
C | A | 1 | a0001c0001t0003g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.348-903C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837005 | ||||||
chr9:21837145
|
GT | G | 109 | a0001c0001t0001g0362a0001c0001t0002g0109a0001c0001t0002g0264others(106): Show | 111 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.348-759delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21837145 | |||||
chr9:21837206
|
A | G | 4 | a0001c0001t0009g0075a0002c0002t0004g0089a0002c0002t0004g0164others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-702A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837206 | ||||||
chr9:21837427
|
C | T | 3 | a0002c0002t0016g0319a0002c0002t0016g0320a0002c0002t0016g0321 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.348-481C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837427 | ||||||
chr9:21837557
|
G | A | 1 | a0002c0002t0004g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.348-351G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837557 | ||||||
chr9:21837579
|
T | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-329T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837579 | ||||||
chr9:21837663
|
C | T | 1 | a0001c0001t0014g0366 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.348-245C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837663 | ||||||
chr9:21837700
|
C | T | 8 | a0001c0001t0003g0292a0001c0001t0003g0301a0001c0001t0003g0302others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.348-208C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837700 | ||||||
chr9:21837845
|
C | T | 4 | a0001c0001t0009g0075a0002c0002t0004g0089a0002c0002t0004g0164others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-63C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837845 | ||||||
chr9:21838146
|
A | G | 110 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0362others(107): Show | 112 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.450+136A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838146 | ||||||
chr9:21838180
|
C | A | 8 | a0001c0001t0001g0294a0001c0001t0001g0300a0001c0001t0001g0322others(5): Show | 8 | HG00323.hp1 HG01109.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+170C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838180 | ||||||
chr9:21838226
|
A | G | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.450+216A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838226 | ||||||
chr9:21838342
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.450+332C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838342 | ||||||
chr9:21838378
|
T | G | 1 | a0001c0001t0011g0171 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.450+368T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838378 | ||||||
chr9:21838468
|
G | A | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+458G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838468 | ||||||
chr9:21838675
|
A | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0068others(1): Show | 4 | NA18941.hp2 NA18948.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+665A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838675 | ||||||
chr9:21838820
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.450+810A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838820 | ||||||
chr9:21838837
|
G | A | 2 | a0001c0001t0003g0235a0001c0001t0003g0288 | 2 | NA19003.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.450+827G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838837 | ||||||
chr9:21839019
|
A | C | 1 | a0002c0002t0007g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+1009A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839019 | ||||||
chr9:21839173
|
G | GTT | 11 | a0001c0001t0001g0311a0001c0001t0003g0217a0001c0001t0003g0269others(8): Show | 11 | HG01975.hp2 HG02015.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+1177_450+1178d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21839173 | |||||
chr9:21839173
|
G | GTTT | 105 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(102): Show | 111 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.450+1176_450+1178d others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21839173 | |||||
chr9:21839173
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.450+1163G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839173 | ||||||
chr9:21839188
|
T | A | 2 | a0001c0001t0009g0113a0001c0001t0024g0092 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+1178T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839188 | ||||||
chr9:21839188
|
TA | T | 5 | a0001c0001t0014g0161a0002c0002t0002g0150a0002c0002t0003g0244others(2): Show | 5 | HG01069.hp2 HG01081.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+1184delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21839188 | |||||
chr9:21839189
|
A | T | 237 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0027others(234): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.450+1179A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839189 | ||||||
chr9:21839190
|
A | T | 4 | a0001c0001t0002g0256a0001c0001t0047g0268a0002c0002t0002g0243others(1): Show | 4 | HG00673.hp2 HG01169.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1180A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839190 | ||||||
chr9:21839255
|
G | A | 2 | a0001c0001t0009g0113a0001c0001t0024g0092 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+1245G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839255 | ||||||
chr9:21839376
|
G | A | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.450+1366G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839376 | ||||||
chr9:21839410
|
G | A | 2 | a0002c0002t0002g0199a0002c0002t0002g0214 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.450+1400G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839410 | ||||||
chr9:21839533
|
T | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0339others(5): Show | 8 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+1523T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839533 | ||||||
chr9:21839541
|
A | T | 2 | a0002c0002t0001g0329a0002c0002t0001g0332 | 2 | NA18983.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.450+1531A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839541 | ||||||
chr9:21839770
|
A | T | 1 | a0001c0003t0001g0338 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.450+1760A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839770 | ||||||
chr9:21839796
|
T | G | 4 | a0001c0001t0008g0262a0001c0001t0008g0298a0001c0001t0008g0299others(1): Show | 4 | HG02257.hp2 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1786T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839796 | ||||||
chr9:21840064
|
A | G | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.450+2054A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840064 | ||||||
chr9:21840148
|
C | A | 1 | a0001c0001t0020g0286 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450+2138C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840148 | ||||||
chr9:21840194
|
C | G | 108 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(105): Show | 114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+2184C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840194 | ||||||
chr9:21840221
|
C | CA | 20 | a0001c0001t0001g0079a0001c0001t0001g0362a0001c0001t0003g0066others(17): Show | 20 | HG00544.hp1 HG00621.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.450+2225dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21840221 | |||||
chr9:21840221
|
C | CAA | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.450+2224_450+2225d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21840221 | |||||
chr9:21840276
|
C | T | 4 | a0001c0001t0009g0075a0002c0002t0004g0089a0002c0002t0004g0164others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+2266C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840276 | ||||||
chr9:21840277
|
G | A | 1 | a0002c0002t0045g0074 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.450+2267G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840277 | ||||||
chr9:21840299
|
A | G | 111 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0362others(108): Show | 113 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.450+2289A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840299 | ||||||
chr9:21840388
|
C | T | 106 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(103): Show | 112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.450+2378C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840388 | ||||||
chr9:21840495
|
A | G | 1 | a0001c0001t0012g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.450+2485A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840495 | ||||||
chr9:21840532
|
G | C | 4 | a0001c0001t0009g0075a0002c0002t0004g0089a0002c0002t0004g0164others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+2522G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840532 | ||||||
chr9:21840761
|
A | G | 108 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(105): Show | 114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+2751A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840761 | ||||||
chr9:21840778
|
G | A | 109 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0362others(106): Show | 111 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.450+2768G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840778 | ||||||
chr9:21840835
|
G | T | 62 | a0001c0001t0001g0266a0001c0001t0001g0311a0001c0001t0001g0312others(59): Show | 65 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.450+2825G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840835 | ||||||
chr9:21840843
|
C | T | 108 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(105): Show | 114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+2833C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840843 | ||||||
chr9:21840966
|
C | T | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+2956C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840966 | ||||||
chr9:21841033
|
C | T | 1 | a0001c0001t0009g0113 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.450+3023C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841033 | ||||||
chr9:21841072
|
A | G | 2 | a0001c0001t0023g0065a0001c0001t0023g0132 | 2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.450+3062A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841072 | ||||||
chr9:21841119
|
C | T | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+3109C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841119 | ||||||
chr9:21841219
|
A | G | 20 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.450+3209A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841219 | ||||||
chr9:21841370
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.450+3360G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841370 | ||||||
chr9:21841484
|
C | T | 1 | a0002c0002t0001g0192 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.450+3474C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841484 | ||||||
chr9:21841659
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | NA18966.hp2 NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.450+3649C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841659 | ||||||
chr9:21841909
|
A | G | 6 | a0001c0001t0009g0113a0001c0010t0009g0197a0002c0002t0012g0085others(3): Show | 6 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+3899A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841909 | ||||||
chr9:21841956
|
C | T | 4 | a0001c0001t0001g0294a0001c0001t0001g0323a0001c0001t0001g0325others(1): Show | 4 | HG00323.hp1 HG01346.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+3946C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841956 | ||||||
chr9:21842033
|
A | G | 2 | a0001c0001t0009g0113a0001c0001t0024g0092 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+4023A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842033 | ||||||
chr9:21842101
|
A | C | 1 | a0002c0004t0001g0177 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.450+4091A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842101 | ||||||
chr9:21842155
|
G | A | 40 | a0001c0001t0001g0294a0001c0001t0001g0300a0001c0001t0001g0322others(37): Show | 43 | HG00323.hp1 HG01109.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.450+4145G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842155 | ||||||
chr9:21842178
|
C | T | 3 | a0001c0001t0001g0326a0001c0001t0023g0065a0001c0001t0023g0132 | 3 | HG02055.hp2 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.450+4168C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842178 | ||||||
chr9:21842217
|
C | G | 1 | a0001c0001t0003g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.450+4207C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842217 | ||||||
chr9:21842226
|
G | A | 106 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(103): Show | 112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.450+4216G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842226 | ||||||
chr9:21842269
|
A | G | 1 | a0001c0001t0003g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.450+4259A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842269 | ||||||
chr9:21842301
|
G | C | 105 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(102): Show | 111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.450+4291G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842301 | ||||||
chr9:21842380
|
A | G | 2 | a0001c0001t0009g0113a0001c0001t0024g0092 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+4370A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842380 | ||||||
chr9:21842506
|
A | T | 1 | a0001c0001t0035g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.450+4496A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842506 | ||||||
chr9:21842631
|
C | T | 7 | a0001c0001t0020g0286a0001c0001t0032g0251a0001c0010t0009g0197others(4): Show | 7 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+4621C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842631 | ||||||
chr9:21842677
|
G | T | 2 | a0001c0001t0001g0347a0001c0001t0001g0349 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.450+4667G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842677 | ||||||
chr9:21842734
|
A | G | 248 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0095others(245): Show | 256 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.450+4724A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842734 | ||||||
chr9:21842853
|
G | A | 5 | a0001c0010t0009g0197a0002c0002t0012g0085a0002c0002t0012g0189others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+4843G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842853 | ||||||
chr9:21843395
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.450+5385A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843395 | ||||||
chr9:21843400
|
C | G | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+5390C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843400 | ||||||
chr9:21843424
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.450+5414A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843424 | ||||||
chr9:21843425
|
T | C | 1 | a0002c0002t0003g0222 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.450+5415T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843425 | ||||||
chr9:21843465
|
G | C | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.450+5455G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843465 | ||||||
chr9:21843533
|
A | T | 1 | a0001c0001t0002g0264 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.450+5523A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843533 | ||||||
chr9:21843573
|
T | A | 1 | a0001c0001t0001g0333 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.450+5563T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843573 | ||||||
chr9:21843630
|
A | G | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+5620A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843630 | ||||||
chr9:21843737
|
A | G | 40 | a0001c0001t0001g0294a0001c0001t0001g0300a0001c0001t0001g0322others(37): Show | 43 | HG00323.hp1 HG01109.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.450+5727A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843737 | ||||||
chr9:21843827
|
C | A | 95 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(92): Show | 99 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.450+5817C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843827 | ||||||
chr9:21843843
|
A | G | 114 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0362others(111): Show | 116 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.450+5833A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843843 | ||||||
chr9:21844300
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.450+6290C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844300 | ||||||
chr9:21844449
|
T | C | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.450+6439T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844449 | ||||||
chr9:21844602
|
C | T | 1 | a0002c0002t0002g0166 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.450+6592C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844602 | ||||||
chr9:21844614
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.450+6604A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844614 | ||||||
chr9:21844644
|
A | G | 116 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0362others(113): Show | 118 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.450+6634A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844644 | ||||||
chr9:21844686
|
A | G | 2 | a0002c0002t0004g0089a0002c0002t0004g0164 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.450+6676A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844686 | ||||||
chr9:21844762
|
C | T | 1 | a0001c0001t0003g0307 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.450+6752C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844762 | ||||||
chr9:21844773
|
A | G | 117 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0100others(114): Show | 119 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.450+6763A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844773 | ||||||
chr9:21844801
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0126a0001c0001t0001g0142others(1): Show | 4 | HG03098.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+6791A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844801 | ||||||
chr9:21844826
|
T | A | 1 | a0001c0001t0003g0119 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.450+6816T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844826 | ||||||
chr9:21844827
|
C | G | 1 | a0001c0001t0001g0253 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.450+6817C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844827 | ||||||
chr9:21844827
|
C | T | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.450+6817C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844827 | ||||||
chr9:21844831
|
A | T | 2 | a0001c0001t0020g0308a0001c0001t0024g0293 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.450+6821A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844831 | ||||||
chr9:21844847
|
C | T | 6 | a0001c0010t0009g0197a0002c0002t0001g0224a0002c0002t0022g0156others(3): Show | 6 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+6837C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844847 | ||||||
chr9:21844952
|
A | G | 19 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(16): Show | 19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+6942A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844952 | ||||||
chr9:21844955
|
C | T | 3 | a0001c0001t0009g0113a0001c0001t0023g0065a0001c0001t0023g0132 | 3 | HG02055.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.450+6945C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844955 | ||||||
chr9:21845018
|
G | A | 1 | a0002c0002t0002g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.450+7008G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845018 | ||||||
chr9:21845030
|
C | CA | 211 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0027others(208): Show | 219 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.450+7035dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21845030 | |||||
chr9:21845030
|
C | CAA | 13 | a0001c0001t0003g0235a0001c0001t0003g0276a0001c0001t0043g0257others(10): Show | 13 | HG01123.hp2 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+7034_450+7035d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21845030 | |||||
chr9:21845053
|
A | G | 19 | a0001c0001t0001g0095a0001c0001t0001g0170a0001c0001t0001g0179others(16): Show | 19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+7043A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845053 | ||||||
chr9:21845056
|
A | G | 1 | a0001c0003t0001g0017 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.450+7046A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845056 | ||||||
chr9:21845188
|
C | G | 1 | a0002c0002t0004g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.450+7178C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845188 | ||||||
chr9:21845229
|
G | A | 1 | a0002c0002t0002g0049 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.450+7219G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845229 | ||||||
chr9:21845265
|
C | T | 19 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0002g0194others(16): Show | 19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+7255C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845265 | ||||||
chr9:21845309
|
A | G | 64 | a0001c0001t0001g0266a0001c0001t0002g0194a0001c0001t0003g0001others(61): Show | 67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.450+7299A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845309 | ||||||
chr9:21845342
|
A | G | 3 | a0001c0001t0009g0113a0001c0001t0023g0065a0001c0001t0023g0132 | 3 | HG02055.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.450+7332A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845342 | ||||||
chr9:21845346
|
A | G | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.450+7336A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845346 | ||||||
chr9:21845578
|
G | T | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+7568G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845578 | ||||||
chr9:21845659
|
C | T | 1 | a0002c0002t0004g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.450+7649C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845659 | ||||||
chr9:21845739
|
G | C | 227 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0095others(224): Show | 233 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.450+7729G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845739 | ||||||
chr9:21845752
|
T | TA | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.450+7753dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21845752 | |||||
chr9:21845981
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.450+7971C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845981 | ||||||
chr9:21846095
|
A | G | 1 | a0001c0001t0003g0217 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.450+8085A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846095 | ||||||
chr9:21846167
|
A | T | 30 | a0001c0001t0001g0040a0001c0001t0001g0170a0001c0001t0001g0309others(27): Show | 30 | HG01168.hp1 HG01169.hp1 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.450+8157A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846167 | ||||||
chr9:21846169
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0342 | 2 | NA18998.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.450+8159A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846169 | ||||||
chr9:21846188
|
G | A | 2 | a0001c0001t0009g0075a0002c0002t0052g0036 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.450+8178G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846188 | ||||||
chr9:21846286
|
A | G | 107 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0002g0008others(104): Show | 109 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.450+8276A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846286 | ||||||
chr9:21846328
|
C | T | 102 | a0001c0001t0002g0008a0001c0001t0002g0109a0001c0001t0002g0256others(99): Show | 104 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.451-8303C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846328 | ||||||
chr9:21846352
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.451-8279G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846352 | ||||||
chr9:21846417
|
GA | G | 125 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0179others(122): Show | 131 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.451-8202delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21846417 | |||||
chr9:21846433
|
C | T | 1 | a0001c0001t0011g0052 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.451-8198C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846433 | ||||||
chr9:21846468
|
T | A | 1 | a0002c0002t0004g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.451-8163T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846468 | ||||||
chr9:21846480
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.451-8151A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846480 | ||||||
chr9:21846493
|
C | T | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-8138C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846493 | ||||||
chr9:21846728
|
A | G | 235 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0001g0266others(232): Show | 243 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(240): Show |
intron_variant | MODIFIER | c.451-7903A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846728 | ||||||
chr9:21846820
|
T | C | 1 | a0001c0001t0001g0362 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.451-7811T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846820 | ||||||
chr9:21846848
|
A | G | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-7783A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846848 | ||||||
chr9:21846854
|
G | T | 1 | a0001c0001t0003g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.451-7777G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846854 | ||||||
chr9:21846870
|
G | A | 1 | a0002c0002t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451-7761G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846870 | ||||||
chr9:21847131
|
G | A | 3 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0038g0090 | 3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.451-7500G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847131 | ||||||
chr9:21847221
|
C | T | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-7410C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847221 | ||||||
chr9:21847226
|
T | C | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-7405T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847226 | ||||||
chr9:21847236
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.451-7395C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847236 | ||||||
chr9:21847273
|
A | G | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-7358A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847273 | ||||||
chr9:21847411
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.451-7220G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847411 | ||||||
chr9:21847573
|
T | G | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451-7058T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847573 | ||||||
chr9:21847581
|
A | G | 2 | a0001c0001t0002g0109a0001c0001t0014g0161 | 2 | HG01081.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.451-7050A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847581 | ||||||
chr9:21847584
|
T | C | 2 | a0001c0010t0009g0197a0005c0009t0009g0013 | 2 | HG01123.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.451-7047T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847584 | ||||||
chr9:21847629
|
A | G | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451-7002A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847629 | ||||||
chr9:21848250
|
C | A | 5 | a0001c0001t0010g0098a0001c0001t0010g0350a0001c0001t0010g0351others(2): Show | 5 | NA18612.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-6381C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848250 | ||||||
chr9:21848255
|
G | T | 30 | a0001c0001t0001g0040a0001c0001t0001g0170a0001c0001t0001g0309others(27): Show | 30 | HG01168.hp1 HG01169.hp1 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.451-6376G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848255 | ||||||
chr9:21848285
|
T | C | 3 | a0001c0001t0009g0113a0001c0001t0023g0065a0001c0001t0023g0132 | 3 | HG02055.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-6346T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848285 | ||||||
chr9:21848352
|
G | A | 1 | a0001c0001t0012g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451-6279G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848352 | ||||||
chr9:21848380
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.451-6251G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848380 | ||||||
chr9:21848424
|
T | TGATTTGG others(14): Show |
103 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0002g0008others(100): Show | 105 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.451-6202_451-6182d others(23): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21848424 | |||||
chr9:21848532
|
G | A | 64 | a0001c0001t0001g0266a0001c0001t0002g0194a0001c0001t0003g0001others(61): Show | 67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.451-6099G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848532 | ||||||
chr9:21848745
|
C | A | 93 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0002g0008others(90): Show | 95 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.451-5886C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848745 | ||||||
chr9:21848800
|
C | T | 1 | a0002c0002t0004g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.451-5831C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848800 | ||||||
chr9:21848801
|
G | A | 3 | a0001c0010t0009g0197a0002c0002t0040g0044a0005c0009t0009g0013 | 3 | HG01123.hp1 HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.451-5830G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848801 | ||||||
chr9:21849058
|
G | T | 1 | a0001c0001t0008g0299 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.451-5573G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849058 | ||||||
chr9:21849067
|
A | T | 105 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0002g0008others(102): Show | 107 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.451-5564A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849067 | ||||||
chr9:21849094
|
C | CAG | 238 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0095others(235): Show | 246 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.451-5535_451-5534d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21849094 | |||||
chr9:21849179
|
G | C | 237 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0095others(234): Show | 245 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.451-5452G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849179 | ||||||
chr9:21849429
|
A | G | 1 | a0002c0002t0002g0215 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.451-5202A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849429 | ||||||
chr9:21849484
|
C | T | 1 | a0002c0002t0003g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.451-5147C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849484 | ||||||
chr9:21849564
|
T | C | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-5067T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849564 | ||||||
chr9:21849759
|
A | T | 1 | a0002c0002t0002g0316 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.451-4872A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849759 | ||||||
chr9:21849842
|
A | G | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-4789A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849842 | ||||||
chr9:21849843
|
T | A | 3 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0001g0365 | 3 | NA18980.hp1 NA19011.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.451-4788T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849843 | ||||||
chr9:21849989
|
T | C | 1 | a0001c0001t0006g0315 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.451-4642T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849989 | ||||||
chr9:21850045
|
C | G | 104 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0002g0008others(101): Show | 106 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.451-4586C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850045 | ||||||
chr9:21850055
|
T | C | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-4576T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850055 | ||||||
chr9:21850148
|
C | T | 3 | a0001c0001t0003g0274a0001c0001t0003g0276a0001c0001t0003g0277 | 3 | NA18985.hp2 NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.451-4483C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850148 | ||||||
chr9:21850526
|
C | T | 1 | a0002c0002t0040g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.451-4105C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850526 | ||||||
chr9:21850597
|
T | C | 5 | a0002c0002t0002g0229a0002c0002t0002g0243a0002c0002t0002g0335others(2): Show | 5 | HG00673.hp2 HG04228.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-4034T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850597 | ||||||
chr9:21850625
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0146others(1): Show | 4 | HG01099.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-4006G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850625 | ||||||
chr9:21850835
|
G | T | 1 | a0001c0001t0002g0175 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.451-3796G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850835 | ||||||
chr9:21851120
|
C | T | 1 | a0001c0003t0001g0182 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.451-3511C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851120 | ||||||
chr9:21851158
|
C | T | 103 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(100): Show | 105 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.451-3473C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851158 | ||||||
chr9:21851166
|
G | A | 1 | a0001c0001t0005g0337 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.451-3465G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851166 | ||||||
chr9:21851245
|
T | C | 2 | a0001c0001t0009g0075a0002c0002t0052g0036 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.451-3386T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851245 | ||||||
chr9:21851247
|
G | A | 1 | a0001c0001t0003g0361 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.451-3384G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851247 | ||||||
chr9:21851277
|
G | C | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-3354G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851277 | ||||||
chr9:21851311
|
CTG | C | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-3318_451-3317d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21851311 | |||||
chr9:21851434
|
A | C | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-3197A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851434 | ||||||
chr9:21851486
|
G | T | 6 | a0001c0001t0012g0201a0001c0010t0009g0197a0002c0002t0012g0085others(3): Show | 6 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-3145G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851486 | ||||||
chr9:21851506
|
C | G | 101 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(98): Show | 103 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.451-3125C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851506 | ||||||
chr9:21851538
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451-3093C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851538 | ||||||
chr9:21851599
|
G | T | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-3032G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851599 | ||||||
chr9:21851684
|
G | A | 10 | a0001c0001t0003g0280a0001c0001t0003g0292a0001c0001t0003g0301others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-2947G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851684 | ||||||
chr9:21851688
|
G | T | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-2943G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851688 | ||||||
chr9:21851693
|
G | A | 2 | a0001c0001t0003g0119a0001c0001t0003g0327 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.451-2938G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851693 | ||||||
chr9:21851771
|
C | A | 1 | a0001c0001t0035g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.451-2860C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851771 | ||||||
chr9:21851778
|
G | A | 93 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(90): Show | 95 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.451-2853G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851778 | ||||||
chr9:21851832
|
G | A | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-2799G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851832 | ||||||
chr9:21851839
|
C | A | 108 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(105): Show | 114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.451-2792C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851839 | ||||||
chr9:21852074
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.451-2557C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852074 | ||||||
chr9:21852182
|
G | T | 110 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(107): Show | 116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.451-2449G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852182 | ||||||
chr9:21852192
|
T | C | 110 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(107): Show | 116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.451-2439T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852192 | ||||||
chr9:21852314
|
C | T | 2 | a0001c0010t0009g0197a0005c0009t0009g0013 | 2 | HG01123.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.451-2317C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852314 | ||||||
chr9:21852359
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451-2272G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852359 | ||||||
chr9:21852419
|
A | G | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-2212A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852419 | ||||||
chr9:21852427
|
T | C | 1 | a0001c0001t0012g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451-2204T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852427 | ||||||
chr9:21852483
|
G | A | 1 | a0001c0001t0015g0279 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.451-2148G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852483 | ||||||
chr9:21852509
|
C | CA | 79 | a0001c0001t0001g0053a0001c0001t0001g0266a0001c0001t0002g0194others(76): Show | 82 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.451-2105dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852509 | |||||
chr9:21852509
|
C | CAA | 53 | a0001c0001t0001g0294a0001c0001t0001g0300a0001c0001t0001g0322others(50): Show | 56 | HG00323.hp1 HG01074.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.451-2106_451-2105d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852509 | |||||
chr9:21852509
|
CA | C | 89 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0027others(86): Show | 91 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.451-2105delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852509 | |||||
chr9:21852596
|
G | A | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-2035G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852596 | ||||||
chr9:21852629
|
A | T | 3 | a0001c0001t0012g0201a0002c0002t0012g0085a0002c0002t0012g0189 | 3 | HG02109.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.451-2002A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852629 | ||||||
chr9:21852660
|
TTATATAC others(1): Show |
T | 17 | a0001c0001t0002g0264a0002c0002t0001g0227a0002c0002t0001g0241others(14): Show | 17 | HG02074.hp2 NA18940.hp1 NA18941.hp1 others(14): Show |
intron_variant | MODIFIER | c.451-1969_451-1962d others(10): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852660 | |||||
chr9:21852672
|
C | G | 1 | a0001c0001t0032g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-1959C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852672 | ||||||
chr9:21852698
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0003g0216a0001c0001t0003g0267others(1): Show | 4 | HG00140.hp2 HG02004.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-1933T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852698 | ||||||
chr9:21852707
|
G | GA | 13 | a0001c0001t0001g0070a0001c0001t0001g0117a0001c0001t0001g0140others(10): Show | 13 | HG01099.hp2 HG01168.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-1910dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852707 | |||||
chr9:21852707
|
G | GAA | 18 | a0001c0001t0001g0095a0001c0001t0001g0179a0001c0001t0005g0016others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-1911_451-1910d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852707 | |||||
chr9:21852707
|
GA | G | 8 | a0001c0001t0004g0303a0001c0010t0009g0197a0002c0002t0002g0187others(5): Show | 8 | HG00621.hp1 HG01123.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-1910delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852707 | |||||
chr9:21852853
|
C | A | 102 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(99): Show | 104 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.451-1778C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852853 | ||||||
chr9:21852882
|
T | C | 3 | a0002c0002t0016g0319a0002c0002t0016g0320a0002c0002t0016g0321 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.451-1749T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852882 | ||||||
chr9:21853034
|
T | A | 1 | a0002c0002t0003g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.451-1597T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853034 | ||||||
chr9:21853105
|
C | G | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-1526C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853105 | ||||||
chr9:21853222
|
T | C | 238 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(235): Show | 246 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.451-1409T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853222 | ||||||
chr9:21853265
|
G | A | 8 | a0002c0002t0004g0035a0002c0002t0004g0061a0002c0002t0004g0089others(5): Show | 8 | HG01192.hp2 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-1366G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853265 | ||||||
chr9:21853277
|
G | C | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-1354G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853277 | ||||||
chr9:21853340
|
A | G | 114 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(111): Show | 120 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.451-1291A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853340 | ||||||
chr9:21853410
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.451-1221T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853410 | ||||||
chr9:21853456
|
G | A | 3 | a0001c0001t0012g0201a0002c0002t0012g0085a0002c0002t0012g0189 | 3 | HG02109.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.451-1175G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853456 | ||||||
chr9:21853553
|
G | A | 1 | a0002c0002t0002g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.451-1078G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853553 | ||||||
chr9:21853630
|
G | C | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-1001G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853630 | ||||||
chr9:21853732
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.451-899A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853732 | ||||||
chr9:21853898
|
T | C | 2 | a0001c0001t0009g0113a0001c0001t0023g0132 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-733T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853898 | ||||||
chr9:21853941
|
T | C | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-690T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853941 | ||||||
chr9:21854014
|
C | T | 1 | a0001c0001t0010g0351 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.451-617C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854014 | ||||||
chr9:21854043
|
A | G | 1 | a0002c0002t0033g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-588A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854043 | ||||||
chr9:21854077
|
C | T | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-554C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854077 | ||||||
chr9:21854160
|
T | C | 61 | a0001c0001t0001g0266a0001c0001t0003g0001a0001c0001t0003g0071others(58): Show | 64 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.451-471T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854160 | ||||||
chr9:21854200
|
A | G | 106 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(103): Show | 108 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.451-431A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854200 | ||||||
chr9:21854216
|
C | G | 4 | a0001c0001t0004g0077a0002c0002t0004g0022a0002c0002t0004g0045others(1): Show | 4 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-415C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854216 | ||||||
chr9:21854275
|
A | G | 2 | a0001c0001t0024g0092a0001c0001t0032g0251 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.451-356A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854275 | ||||||
chr9:21854363
|
G | A | 1 | a0001c0001t0014g0366 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.451-268G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854363 | ||||||
chr9:21854510
|
G | A | 1 | a0001c0001t0001g0355 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.451-121G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854510 | ||||||
chr9:21854563
|
G | C | 1 | a0001c0001t0001g0357 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.451-68G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854563 | ||||||
chr9:21854921
|
A | G | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+51A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21854921 | ||||||
chr9:21854970
|
C | T | 1 | a0001c0001t0008g0298 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.690+100C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21854970 | ||||||
chr9:21855014
|
T | C | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+144T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855014 | ||||||
chr9:21855017
|
G | A | 3 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313 | 3 | HG01891.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.690+147G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855017 | ||||||
chr9:21855039
|
G | A | 103 | a0001c0001t0001g0266a0001c0001t0001g0294a0001c0001t0001g0300others(100): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.690+169G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855039 | ||||||
chr9:21855097
|
G | T | 231 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(228): Show | 239 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.690+227G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855097 | ||||||
chr9:21855119
|
C | G | 6 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0046others(3): Show | 6 | NA18939.hp2 NA18962.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+249C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855119 | ||||||
chr9:21855267
|
C | T | 2 | a0001c0001t0025g0358a0001c0001t0025g0363 | 2 | NA19058.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.690+397C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855267 | ||||||
chr9:21855309
|
A | G | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+439A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855309 | ||||||
chr9:21855346
|
G | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0144 | 2 | HG00738.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.690+476G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855346 | ||||||
chr9:21855347
|
G | A | 19 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(16): Show | 19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+477G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855347 | ||||||
chr9:21855373
|
A | G | 1 | a0001c0003t0001g0018 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.690+503A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855373 | ||||||
chr9:21855447
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.690+577T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855447 | ||||||
chr9:21855453
|
G | C | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+583G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855453 | ||||||
chr9:21855593
|
C | T | 16 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(13): Show | 16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+723C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855593 | ||||||
chr9:21855673
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0042g0205 | 3 | HG01515.hp1 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.690+803G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855673 | ||||||
chr9:21855688
|
G | A | 5 | a0002c0004t0001g0116a0002c0004t0001g0177a0002c0004t0001g0178others(2): Show | 5 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+818G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855688 | ||||||
chr9:21855966
|
T | C | 1 | a0002c0002t0002g0102 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.690+1096T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855966 | ||||||
chr9:21856280
|
T | G | 6 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0046others(3): Show | 6 | NA18939.hp2 NA18962.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+1410T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856280 | ||||||
chr9:21856471
|
A | C | 123 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(120): Show | 125 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.690+1601A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856471 | ||||||
chr9:21856573
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.690+1703T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856573 | ||||||
chr9:21856662
|
G | C | 107 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(104): Show | 110 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.690+1792G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856662 | ||||||
chr9:21856677
|
T | C | 4 | a0002c0002t0002g0190a0002c0002t0002g0206a0002c0002t0002g0221others(1): Show | 4 | NA18612.hp2 NA18949.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+1807T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856677 | ||||||
chr9:21856686
|
A | G | 56 | a0001c0001t0001g0266a0001c0001t0003g0001a0001c0001t0003g0051others(53): Show | 59 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.690+1816A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856686 | ||||||
chr9:21856778
|
C | T | 55 | a0001c0001t0001g0266a0001c0001t0003g0001a0001c0001t0003g0051others(52): Show | 58 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.690+1908C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856778 | ||||||
chr9:21856877
|
T | G | 1 | a0001c0001t0003g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.690+2007T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856877 | ||||||
chr9:21856891
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.690+2021C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856891 | ||||||
chr9:21857245
|
A | G | 197 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0203others(194): Show | 206 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.691-2058A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857245 | ||||||
chr9:21857303
|
G | A | 3 | a0002c0002t0001g0115a0002c0002t0001g0154a0002c0002t0038g0090 | 3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.691-2000G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857303 | ||||||
chr9:21857304
|
C | T | 106 | a0001c0001t0003g0001a0001c0001t0003g0011a0001c0001t0003g0039others(103): Show | 112 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.691-1999C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857304 | ||||||
chr9:21857370
|
T | G | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.691-1933T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857370 | ||||||
chr9:21857449
|
A | T | 6 | a0001c0003t0001g0017a0001c0003t0001g0029a0001c0003t0001g0046others(3): Show | 6 | NA18939.hp2 NA18962.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-1854A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857449 | ||||||
chr9:21857470
|
T | C | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-1833T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857470 | ||||||
chr9:21857715
|
C | T | 1 | a0002c0002t0002g0150 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.691-1588C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857715 | ||||||
chr9:21857739
|
T | G | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-1564T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857739 | ||||||
chr9:21857777
|
C | T | 1 | a0002c0002t0038g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.691-1526C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857777 | ||||||
chr9:21857856
|
A | G | 1 | a0001c0003t0001g0028 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.691-1447A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857856 | ||||||
chr9:21857941
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.691-1362G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857941 | ||||||
chr9:21858041
|
T | C | 6 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0032g0251others(3): Show | 6 | HG01123.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-1262T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858041 | ||||||
chr9:21858124
|
T | C | 4 | a0001c0001t0012g0024a0001c0001t0012g0201a0002c0002t0012g0085others(1): Show | 4 | HG02109.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1179T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858124 | ||||||
chr9:21858174
|
T | A | 1 | a0001c0003t0001g0182 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.691-1129T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858174 | ||||||
chr9:21858225
|
G | A | 7 | a0001c0001t0009g0075a0001c0001t0009g0113a0001c0001t0032g0251others(4): Show | 7 | HG01123.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-1078G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858225 | ||||||
chr9:21858251
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.691-1052C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858251 | ||||||
chr9:21858277
|
T | C | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-1026T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858277 | ||||||
chr9:21858308
|
A | G | 11 | a0001c0001t0004g0303a0001c0001t0004g0304a0002c0002t0004g0035others(8): Show | 11 | HG01192.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-995A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858308 | ||||||
chr9:21858320
|
A | G | 1 | a0001c0001t0024g0092 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.691-983A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858320 | ||||||
chr9:21858380
|
A | G | 5 | a0001c0001t0008g0083a0001c0001t0008g0262a0001c0001t0008g0298others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-923A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858380 | ||||||
chr9:21858393
|
G | C | 45 | a0001c0001t0003g0011a0001c0001t0003g0039a0001c0001t0003g0066others(42): Show | 48 | HG01192.hp2 HG01433.hp1 HG01516.hp2 others(45): Show |
intron_variant | MODIFIER | c.691-910G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858393 | ||||||
chr9:21858421
|
G | A | 2 | a0001c0006t0001g0067a0001c0006t0001g0078 | 2 | NA18999.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.691-882G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858421 | ||||||
chr9:21858451
|
A | G | 88 | a0001c0001t0001g0203a0001c0001t0002g0004a0001c0001t0002g0008others(85): Show | 91 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.691-852A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858451 | ||||||
chr9:21858493
|
C | T | 5 | a0001c0001t0010g0098a0001c0001t0010g0350a0001c0001t0010g0351others(2): Show | 5 | NA18612.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-810C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858493 | ||||||
chr9:21858650
|
A | G | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-653A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858650 | ||||||
chr9:21858716
|
C | G | 114 | a0001c0001t0001g0294a0001c0001t0001g0322a0001c0001t0003g0001others(111): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.691-587C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858716 | ||||||
chr9:21858720
|
A | G | 1 | a0001c0001t0024g0293 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-583A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858720 | ||||||
chr9:21858830
|
G | A | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-473G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858830 | ||||||
chr9:21859056
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.691-247G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21859056 | ||||||
chr9:21859195
|
G | T | 46 | a0001c0001t0003g0011a0001c0001t0003g0039a0001c0001t0003g0066others(43): Show | 49 | HG01192.hp2 HG01433.hp1 HG01516.hp2 others(46): Show |
intron_variant | MODIFIER | c.691-108G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21859195 | ||||||
chr9:21859196
|
G | A | 1 | a0001c0003t0001g0023 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.691-107G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21859196 | ||||||
chr9:21859663
|
A | T | 2 | a0002c0002t0004g0089a0002c0002t0004g0164 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.813+238A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859663 | ||||||
chr9:21859665
|
C | T | 1 | a0001c0001t0015g0270 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.813+240C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859665 | ||||||
chr9:21859790
|
A | C | 1 | a0001c0001t0010g0098 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.813+365A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859790 | ||||||
chr9:21859836
|
A | G | 2 | a0002c0002t0033g0208a0002c0002t0034g0165 | 2 | HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.813+411A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859836 | ||||||
chr9:21859845
|
GA | G | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.813+424delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 21859845 | |||||
chr9:21860064
|
C | T | 1 | a0002c0004t0001g0186 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.813+639C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860064 | ||||||
chr9:21860327
|
A | C | 5 | a0001c0001t0009g0075a0001c0001t0032g0251a0001c0010t0009g0197others(2): Show | 5 | HG01123.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+902A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860327 | ||||||
chr9:21860429
|
C | T | 5 | a0001c0001t0020g0286a0001c0001t0020g0308a0001c0001t0035g0236others(2): Show | 5 | HG02559.hp1 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+1004C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860429 | ||||||
chr9:21860732
|
AGTTT | A | 5 | a0001c0001t0020g0286a0001c0001t0020g0308a0001c0001t0035g0236others(2): Show | 5 | HG02559.hp1 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1235_814-1232d others(6): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 21860732 | |||||
chr9:21860773
|
C | T | 2 | a0002c0002t0001g0226a0002c0002t0001g0228 | 2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.814-1203C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860773 | ||||||
chr9:21860825
|
C | G | 27 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(24): Show | 27 | HG00597.hp1 HG00609.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.814-1151C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860825 | ||||||
chr9:21860981
|
C | A | 2 | a0001c0001t0024g0092a0001c0001t0024g0293 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.814-995C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860981 | ||||||
chr9:21861034
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.814-942T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861034 | ||||||
chr9:21861043
|
T | G | 1 | a0002c0002t0012g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.814-933T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861043 | ||||||
chr9:21861198
|
A | G | 2 | a0001c0001t0024g0092a0001c0001t0024g0293 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.814-778A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861198 | ||||||
chr9:21861319
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0179 | 2 | NA18966.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.814-657A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861319 | ||||||
chr9:21861412
|
T | G | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.814-564T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861412 | ||||||
chr9:21861450
|
C | G | 17 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(14): Show | 17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.814-526C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861450 | ||||||
chr9:21861470
|
T | G | 2 | a0002c0002t0033g0208a0002c0002t0034g0165 | 2 | HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.814-506T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861470 | ||||||
chr9:21861471
|
C | T | 1 | a0002c0002t0004g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.814-505C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861471 | ||||||
chr9:21861553
|
C | T | 22 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(19): Show | 22 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.814-423C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861553 | ||||||
chr9:21861558
|
A | G | 4 | a0001c0001t0009g0113a0001c0001t0023g0065a0001c0001t0023g0132others(1): Show | 4 | HG02055.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-418A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861558 | ||||||
chr9:21861613
|
T | C | 1 | a0001c0001t0006g0295 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.814-363T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861613 | ||||||
chr9:21861634
|
A | G | 1 | a0002c0004t0001g0186 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.814-342A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861634 | ||||||
chr9:21861861
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0027 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.814-115A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861861 | ||||||
chr9:21861878
|
A | G | 2 | a0001c0001t0024g0092a0001c0001t0024g0293 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.814-98A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861878 | ||||||
chr9:21861903
|
GT | G | 30 | a0001c0001t0005g0016a0001c0001t0005g0019a0001c0001t0005g0026others(27): Show | 30 | HG00597.hp1 HG00609.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.814-62delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 21861903 | |||||
chr9:21861904
|
T | G | 51 | a0001c0001t0003g0001a0001c0001t0003g0051a0001c0001t0003g0071others(48): Show | 54 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.814-72T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861904 | ||||||
chr9:21861905
|
T | G | 1 | a0001c0001t0051g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.814-71T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861905 |