geneid | 9112 |
---|---|
ensemblid | ENSG00000182979.18 |
hgncid | 7410 |
symbol | MTA1 |
name | metastasis associated 1 |
refseq_nuc | NM_004689.4 |
refseq_prot | NP_004680.2 |
ensembl_nuc | ENST00000331320.12 |
ensembl_prot | ENSP00000333633.7 |
mane_status | MANE Select |
chr | chr14 |
start | 105419827 |
end | 105470729 |
strand | + |
ver | v1.2 |
region | chr14:105419827-105470729 |
region5000 | chr14:105414827-105475729 |
regionname0 | MTA1_chr14_105419827_105470729 |
regionname5000 | MTA1_chr14_105414827_105475729 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 715 | 156 | 41 | 42 | 44 | 10 | 18 | 26 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0002 | 0/0 | 715 | 78 | 1 | 14 | 50 | 2 | 11 | 32 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003 | 1/0 | 715 | 39 | 34 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0004 | 0/0 | 550 | 14 | 3 | 4 | 3 | 0 | 4 | 2 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0005 | 0/0 | 550 | 10 | 0 | 3 | 4 | 0 | 3 | 3 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0006 | 0/0 | 715 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0007 | 0/0 | 715 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0008 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0009 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2148 | 150 | 40 | 40 | 43 | 9 | 17 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0002 | 0/0 | 2148 | 77 | 1 | 14 | 49 | 2 | 11 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0003 | 0/0 | 2149 | 14 | 3 | 4 | 3 | 0 | 4 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0004 | 0/0 | 2148 | 12 | 10 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0005 | 0/0 | 2149 | 10 | 0 | 3 | 4 | 0 | 3 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0006 | 0/0 | 2148 | 9 | 9 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0007 | 0/0 | 2148 | 9 | 8 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0008 | 1/0 | 2148 | 5 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0009 | 0/0 | 2148 | 3 | 2 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0010 | 0/0 | 2148 | 3 | 3 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0011 | 0/0 | 2148 | 2 | 0 | 0 | 1 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0012 | 0/0 | 2148 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0013 | 0/0 | 2148 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0014 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0015 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0016 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0017 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0018 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
c0019 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 724 | 293 | 77 | 67 | 100 | 11 | 36 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
t0002 | 0/0 | 724 | 6 | 5 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
t0003 | 0/0 | 724 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
t0004 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
t0005 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
t0006 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
t0007 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2148 | 150 | 40 | 40 | 43 | 9 | 17 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0011 | 0/0 | 2148 | 2 | 0 | 0 | 1 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0012 | 0/0 | 2148 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0017 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0019 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0002c0002 | 0/0 | 2148 | 77 | 1 | 14 | 49 | 2 | 11 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0002c0015 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0004 | 0/0 | 2148 | 12 | 10 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0006 | 0/0 | 2148 | 9 | 9 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0007 | 0/0 | 2148 | 9 | 8 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0008 | 1/0 | 2148 | 5 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0009 | 0/0 | 2148 | 3 | 2 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0014 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0004c0003 | 0/0 | 2149 | 14 | 3 | 4 | 3 | 0 | 4 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0005c0005 | 0/0 | 2149 | 10 | 0 | 3 | 4 | 0 | 3 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0006c0010 | 0/0 | 2148 | 3 | 3 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0007c0013 | 0/0 | 2148 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0008c0016 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0009c0018 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2871 | 142 | 35 | 39 | 42 | 8 | 17 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0001t0002 | 0/0 | 2871 | 6 | 5 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0001t0003 | 0/0 | 2871 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0001t0007 | 0/0 | 2852 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0011t0001 | 0/0 | 2871 | 2 | 0 | 0 | 1 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0012t0001 | 0/0 | 2871 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0017t0001 | 0/0 | 2871 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0001c0019t0001 | 0/0 | 2871 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0002c0002t0001 | 0/0 | 2871 | 76 | 1 | 14 | 48 | 2 | 11 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0002c0002t0004 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0002c0015t0001 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0004t0001 | 0/0 | 2871 | 12 | 10 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0006t0001 | 0/0 | 2871 | 8 | 8 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0006t0005 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0007t0001 | 0/0 | 2871 | 9 | 8 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0008t0001 | 1/0 | 2871 | 5 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0009t0001 | 0/0 | 2871 | 3 | 2 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0003c0014t0001 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0004c0003t0001 | 0/0 | 2872 | 14 | 3 | 4 | 3 | 0 | 4 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0005c0005t0001 | 0/0 | 2872 | 10 | 0 | 3 | 4 | 0 | 3 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0006c0010t0001 | 0/0 | 2871 | 3 | 3 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0007c0013t0001 | 0/0 | 2871 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0008c0016t0001 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
a0009c0018t0006 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | copy fasta | chr14 | 105414827 | 105475729 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0011t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0011t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0012t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0012t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0017t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0001c0019t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0001 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0002t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0002c0015t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0006t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0006t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0006t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0008t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0008t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0008t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0008t0001g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0008t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0009t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0009t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0009t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0003c0014t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0004c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0005c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0006c0010t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0006c0010t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0006c0010t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0007c0013t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0007c0013t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0008c0016t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
a0009c0018t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0231 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00280 | hp1 | a0001 | c0011 | t0001 | g0213 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0225 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0253 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00544 | hp1 | a0004 | c0003 | t0001 | g0186 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00597 | hp1 | a0005 | c0005 | t0001 | g0161 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00639 | hp1 | a0004 | c0003 | t0001 | g0072 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00639 | hp2 | a0001 | c0012 | t0001 | g0248 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00642 | hp2 | a0004 | c0003 | t0001 | g0115 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00735 | hp2 | a0003 | c0009 | t0001 | g0024 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01099 | hp2 | a0004 | c0003 | t0001 | g0266 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0277 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01167 | hp1 | a0003 | c0007 | t0001 | g0057 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01169 | hp1 | a0003 | c0004 | t0001 | g0004 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01192 | hp1 | a0005 | c0005 | t0001 | g0133 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01192 | hp2 | a0005 | c0005 | t0001 | g0220 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01433 | hp2 | a0004 | c0003 | t0001 | g0216 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01496 | hp1 | a0007 | c0013 | t0001 | g0031 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01891 | hp1 | a0003 | c0014 | t0001 | g0025 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01981 | hp2 | a0005 | c0005 | t0001 | g0063 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02015 | hp2 | a0001 | c0011 | t0001 | g0206 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02040 | hp2 | a0002 | c0002 | t0004 | g0147 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02055 | hp2 | a0003 | c0004 | t0001 | g0107 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02132 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02148 | hp1 | a0001 | c0019 | t0001 | g0209 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02257 | hp1 | a0003 | c0004 | t0001 | g0108 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02280 | hp1 | a0004 | c0003 | t0001 | g0035 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02280 | hp2 | a0003 | c0007 | t0001 | g0003 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02572 | hp1 | a0009 | c0018 | t0006 | g0003 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02572 | hp2 | a0003 | c0006 | t0001 | g0022 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02615 | hp1 | a0003 | c0007 | t0001 | g0052 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02615 | hp2 | a0003 | c0006 | t0001 | g0023 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02622 | hp1 | a0003 | c0007 | t0001 | g0055 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02622 | hp2 | a0003 | c0004 | t0001 | g0003 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0159 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02717 | hp1 | a0007 | c0013 | t0001 | g0032 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02717 | hp2 | a0004 | c0003 | t0001 | g0033 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02809 | hp2 | a0003 | c0006 | t0005 | g0021 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02818 | hp1 | a0003 | c0007 | t0001 | g0051 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02818 | hp2 | a0003 | c0004 | t0001 | g0042 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02895 | hp1 | a0003 | c0009 | t0001 | g0020 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02896 | hp1 | a0006 | c0010 | t0001 | g0164 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02897 | hp1 | a0006 | c0010 | t0001 | g0127 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02922 | hp1 | a0006 | c0010 | t0001 | g0166 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02922 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02965 | hp1 | a0003 | c0006 | t0001 | g0002 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02970 | hp1 | a0003 | c0004 | t0001 | g0118 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02970 | hp2 | a0003 | c0007 | t0001 | g0056 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03098 | hp1 | a0003 | c0008 | t0001 | g0014 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03130 | hp1 | a0003 | c0009 | t0001 | g0019 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03130 | hp2 | a0003 | c0004 | t0001 | g0048 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03195 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03225 | hp2 | a0003 | c0007 | t0001 | g0054 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03453 | hp1 | a0003 | c0006 | t0001 | g0027 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0252 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0263 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03516 | hp1 | a0003 | c0007 | t0001 | g0053 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0049 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03579 | hp2 | a0003 | c0007 | t0001 | g0059 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03654 | hp2 | a0004 | c0003 | t0001 | g0110 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03704 | hp2 | a0001 | c0017 | t0001 | g0044 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03831 | hp1 | a0005 | c0005 | t0001 | g0100 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03831 | hp2 | a0005 | c0005 | t0001 | g0090 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0158 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04184 | hp2 | a0004 | c0003 | t0001 | g0080 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04204 | hp1 | a0004 | c0003 | t0001 | g0104 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04204 | hp2 | a0005 | c0005 | t0001 | g0145 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04228 | hp1 | a0004 | c0003 | t0001 | g0257 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18906 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18953 | hp2 | a0004 | c0003 | t0001 | g0208 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18982 | hp1 | a0005 | c0005 | t0001 | g0188 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18989 | hp2 | a0005 | c0005 | t0001 | g0226 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18998 | hp2 | a0005 | c0005 | t0001 | g0082 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19003 | hp2 | a0008 | c0016 | t0001 | g0083 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19030 | hp1 | a0001 | c0012 | t0001 | g0037 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19043 | hp1 | a0003 | c0008 | t0001 | g0012 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19074 | hp1 | a0002 | c0015 | t0001 | g0121 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA19240 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ASW | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02109 | hp1 | a0003 | c0004 | t0001 | g0058 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02109 | hp2 | a0004 | c0003 | t0001 | g0269 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG02559 | hp2 | a0003 | c0006 | t0001 | g0028 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03471 | hp1 | a0003 | c0008 | t0001 | g0013 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
HG03471 | hp2 | a0003 | c0008 | t0001 | g0046 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA18955 | hp2 | a0004 | c0003 | t0001 | g0128 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | USA | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA20300 | hp2 | a0003 | c0004 | t0001 | g0050 | AFR | USA | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0202 | REF | REF | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
homoSapiens_grch38 | hp1 | a0003 | c0008 | t0001 | g0029 | REF | REF | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:105464069
|
G | A | 3 | a0002a0005a0008 | 89 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
missense_variant | MODERATE | c.1114G>A | p.Val372Ile | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/21 | 1323/2871 | 1114/2148 | 372/715 | chr14 | 105464069 | ||
chr14:105465102
|
C | G | 1 | a0008 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1543C>G | p.Arg515Gly | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/21 | 1752/2871 | 1543/2148 | 515/715 | chr14 | 105465102 | ||
chr14:105465151
|
G | A | 1 | a0009 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1592G>A | p.Arg531His | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/21 | 1801/2871 | 1592/2148 | 531/715 | chr14 | 105465151 | ||
chr14:105466438
|
G | GC | 2 | a0004a0005 | 24 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(21): Show |
frameshift_variant | HIGH | c.1644dupC | p.Lys549fs | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/21 | 1854/2871 | 1645/2148 | 549/715 | INFO_REALIGN_3_PRIME | chr14 | 105466438 | |
chr14:105466467
|
G | A | 1 | a0006 | 3 | HG02896.hp1 HG02897.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.1666G>A | p.Val556Met | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/21 | 1875/2871 | 1666/2148 | 556/715 | chr14 | 105466467 | ||
chr14:105469487
|
G | A | 7 | a0001a0002a0004others(4): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
missense_variant | MODERATE | c.1834G>A | p.Ala612Thr | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/21 | 2043/2871 | 1834/2148 | 612/715 | chr14 | 105469487 | ||
chr14:105470169
|
C | T | 1 | a0007 | 2 | HG01496.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.2102C>T | p.Pro701Leu | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 2311/2871 | 2102/2148 | 701/715 | chr14 | 105470169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:105445466
|
C | A | 3 | a0003c0006a0003c0009a0003c0014 | 13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
synonymous_variant | LOW | c.145C>A | p.Arg49Arg | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/21 | 354/2871 | 145/2148 | 49/715 | chr14 | 105445466 | ||
chr14:105450083
|
C | T | 18 | a0001c0001a0001c0011a0001c0012others(15): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
synonymous_variant | LOW | c.267C>T | p.Asn89Asn | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 5/21 | 476/2871 | 267/2148 | 89/715 | chr14 | 105450083 | ||
chr14:105454240
|
G | A | 1 | a0002c0015 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.480G>A | p.Leu160Leu | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/21 | 689/2871 | 480/2148 | 160/715 | chr14 | 105454240 | ||
chr14:105463249
|
C | T | 1 | a0003c0014 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1008C>T | p.Tyr336Tyr | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/21 | 1217/2871 | 1008/2148 | 336/715 | chr14 | 105463249 | ||
chr14:105464772
|
C | T | 4 | a0001c0019a0003c0007a0003c0009others(1): Show | 14 | HG00735.hp2 HG01167.hp1 HG02148.hp1 others(11): Show |
synonymous_variant | LOW | c.1443C>T | p.Ile481Ile | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/21 | 1652/2871 | 1443/2148 | 481/715 | chr14 | 105464772 | ||
chr14:105464817
|
G | A | 1 | a0001c0011 | 2 | HG00280.hp1 HG02015.hp2 |
synonymous_variant | LOW | c.1488G>A | p.Ala496Ala | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/21 | 1697/2871 | 1488/2148 | 496/715 | chr14 | 105464817 | ||
chr14:105465101
|
G | C | 1 | a0008c0016 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1542G>C | p.Ala514Ala | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/21 | 1751/2871 | 1542/2148 | 514/715 | chr14 | 105465101 | ||
chr14:105469963
|
C | T | 1 | a0001c0017 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1968C>T | p.Asp656Asp | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 20/21 | 2177/2871 | 1968/2148 | 656/715 | chr14 | 105469963 | ||
chr14:105470179
|
G | A | 1 | a0001c0012 | 2 | HG00639.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.2112G>A | p.Ala704Ala | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 2321/2871 | 2112/2148 | 704/715 | chr14 | 105470179 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:105419980
|
C | A | 1 | a0001c0001t0003 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/21 | 56 | chr14 | 105419980 | |||||
chr14:105470237
|
G | A | 1 | a0002c0002t0004 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 22 | chr14 | 105470237 | |||||
chr14:105470384
|
T | G | 1 | a0003c0006t0005 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 169 | chr14 | 105470384 | |||||
chr14:105470616
|
C | T | 1 | a0001c0001t0002 | 6 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*401C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 401 | chr14 | 105470616 | |||||
chr14:105470656
|
CCTTGTCT others(12): Show |
C | 1 | a0001c0001t0007 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*442_*460delCTTGTC others(13): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 442 | chr14 | 105470656 | |||||
chr14:105470697
|
G | T | 1 | a0009c0018t0006 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 482 | chr14 | 105470697 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:105420107
|
G | GCCCCCAC others(18): Show |
4 | a0001c0001t0001g0015a0003c0008t0001g0012a0003c0008t0001g0013others(1): Show | 4 | HG02300.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+50_28+74dupACCC others(21): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105420107 | |||||
chr14:105420182
|
G | C | 2 | a0001c0001t0001g0017a0001c0001t0007g0016 | 2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.28+119G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420182 | ||||||
chr14:105420298
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.28+235C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420298 | ||||||
chr14:105420344
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.28+281G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420344 | ||||||
chr14:105420576
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.28+513C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420576 | ||||||
chr14:105420627
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.28+564A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420627 | ||||||
chr14:105420753
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.28+690C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420753 | ||||||
chr14:105420950
|
C | T | 1 | a0002c0002t0001g0277 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.28+887C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420950 | ||||||
chr14:105421051
|
C | T | 235 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(232): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.28+988C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421051 | ||||||
chr14:105421115
|
T | TGG | 25 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(22): Show | 25 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.28+1054_28+1055dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105421115 | |||||
chr14:105421175
|
C | G | 1 | a0001c0001t0002g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.28+1112C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421175 | ||||||
chr14:105421180
|
C | G | 1 | a0003c0008t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.28+1117C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421180 | ||||||
chr14:105421310
|
C | T | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.28+1247C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421310 | ||||||
chr14:105421430
|
G | C | 1 | a0002c0002t0001g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.28+1367G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421430 | ||||||
chr14:105421597
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.28+1534C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421597 | ||||||
chr14:105421685
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.28+1622G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421685 | ||||||
chr14:105421801
|
A | G | 23 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0047others(20): Show | 23 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.28+1738A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421801 | ||||||
chr14:105421825
|
G | A | 1 | a0002c0002t0001g0061 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.28+1762G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421825 | ||||||
chr14:105421836
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.28+1773C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421836 | ||||||
chr14:105422081
|
C | T | 2 | a0001c0001t0001g0040a0001c0012t0001g0248 | 2 | HG00639.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.28+2018C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422081 | ||||||
chr14:105422096
|
C | T | 1 | a0002c0002t0001g0246 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.28+2033C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422096 | ||||||
chr14:105422120
|
C | T | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+2057C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422120 | ||||||
chr14:105422235
|
C | T | 4 | a0001c0001t0001g0047a0003c0004t0001g0048a0003c0004t0001g0049others(1): Show | 4 | HG03130.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+2172C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422235 | ||||||
chr14:105422261
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+2198C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422261 | ||||||
chr14:105422322
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+2259C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422322 | ||||||
chr14:105422439
|
C | G | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.28+2376C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422439 | ||||||
chr14:105422890
|
G | T | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+2827G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422890 | ||||||
chr14:105422903
|
T | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0047 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+2840T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422903 | ||||||
chr14:105423006
|
C | T | 17 | a0001c0017t0001g0044a0002c0002t0001g0045a0003c0004t0001g0003others(14): Show | 17 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.28+2943C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423006 | ||||||
chr14:105423049
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.28+2986T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423049 | ||||||
chr14:105423090
|
C | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(248): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.28+3027C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423090 | ||||||
chr14:105423204
|
T | G | 18 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0248others(15): Show | 18 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.28+3141T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423204 | ||||||
chr14:105423208
|
T | C | 1 | a0005c0005t0001g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.28+3145T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423208 | ||||||
chr14:105423215
|
A | AT | 20 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(17): Show | 20 | HG00621.hp1 HG00621.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.28+3174dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423215 | |||||
chr14:105423215
|
A | ATT | 13 | a0001c0001t0001g0041a0001c0001t0001g0245a0001c0012t0001g0248others(10): Show | 13 | HG00639.hp2 HG01167.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.28+3173_28+3174dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423215 | |||||
chr14:105423215
|
AT | A | 13 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0278others(10): Show | 13 | HG00323.hp2 HG01175.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.28+3174delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423215 | |||||
chr14:105423224
|
T | G | 1 | a0002c0002t0001g0064 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.28+3161T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423224 | ||||||
chr14:105423241
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+3178A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423241 | ||||||
chr14:105423333
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0244 | 3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28+3270C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423333 | ||||||
chr14:105423448
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+3385C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423448 | ||||||
chr14:105423464
|
G | T | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+3401G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423464 | ||||||
chr14:105423571
|
CA | C | 9 | a0001c0001t0001g0015a0001c0001t0001g0227a0001c0001t0001g0228others(6): Show | 10 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.28+3520delA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423571 | |||||
chr14:105423583
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.28+3520A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423583 | ||||||
chr14:105423648
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.28+3585G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423648 | ||||||
chr14:105423727
|
G | A | 1 | a0003c0004t0001g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.28+3664G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423727 | ||||||
chr14:105423736
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.28+3673C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423736 | ||||||
chr14:105423936
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.28+3873C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423936 | ||||||
chr14:105424124
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+4061C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424124 | ||||||
chr14:105424146
|
A | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+4083A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424146 | ||||||
chr14:105424217
|
C | T | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.28+4154C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424217 | ||||||
chr14:105424322
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0047 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+4259T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424322 | ||||||
chr14:105424344
|
C | T | 4 | a0001c0012t0001g0037a0003c0004t0001g0048a0003c0004t0001g0049others(1): Show | 4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+4281C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424344 | ||||||
chr14:105424370
|
A | AT | 9 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(6): Show | 9 | HG01928.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.28+4320dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105424370 | |||||
chr14:105424473
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28+4410T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424473 | ||||||
chr14:105424480
|
C | T | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+4417C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424480 | ||||||
chr14:105424565
|
G | A | 1 | a0003c0008t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+4502G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424565 | ||||||
chr14:105424702
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.28+4639G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424702 | ||||||
chr14:105424727
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+4664C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424727 | ||||||
chr14:105424793
|
G | A | 1 | a0002c0002t0001g0064 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.28+4730G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424793 | ||||||
chr14:105424902
|
C | T | 2 | a0002c0002t0001g0222a0002c0002t0001g0231 | 2 | HG00099.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.28+4839C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424902 | ||||||
chr14:105424903
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.28+4840G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424903 | ||||||
chr14:105425014
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0244 | 3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28+4951C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425014 | ||||||
chr14:105425120
|
T | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0047 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+5057T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425120 | ||||||
chr14:105425124
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0047 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+5061T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425124 | ||||||
chr14:105425154
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.28+5091G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425154 | ||||||
chr14:105425174
|
C | G | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+5111C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425174 | ||||||
chr14:105425205
|
A | G | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+5142A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425205 | ||||||
chr14:105425306
|
G | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.28+5243G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425306 | ||||||
chr14:105425784
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.28+5721C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425784 | ||||||
chr14:105425806
|
G | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0074others(7): Show | 11 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.28+5743G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425806 | ||||||
chr14:105425839
|
A | G | 1 | a0007c0013t0001g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.28+5776A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425839 | ||||||
chr14:105425849
|
G | C | 220 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(217): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.28+5786G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425849 | ||||||
chr14:105425956
|
G | A | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.28+5893G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425956 | ||||||
chr14:105426089
|
G | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.28+6026G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426089 | ||||||
chr14:105426183
|
A | C | 20 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0248others(17): Show | 20 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.28+6120A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426183 | ||||||
chr14:105426233
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.28+6170G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426233 | ||||||
chr14:105426262
|
G | A | 3 | a0001c0017t0001g0044a0002c0002t0001g0045a0002c0002t0001g0189 | 3 | HG03704.hp2 NA18951.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.28+6199G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426262 | ||||||
chr14:105426374
|
A | AC | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+6312dupC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426374 | |||||
chr14:105426375
|
C | CA | 212 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.28+6333dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426375 | |||||
chr14:105426375
|
C | CAA | 16 | a0001c0001t0001g0038a0001c0001t0001g0079a0001c0001t0001g0081others(13): Show | 16 | HG00673.hp1 HG00735.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.28+6332_28+6333dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426375 | |||||
chr14:105426505
|
C | T | 3 | a0003c0004t0001g0048a0003c0004t0001g0049a0003c0004t0001g0050 | 3 | HG03130.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+6442C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426505 | ||||||
chr14:105426569
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.28+6506C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426569 | ||||||
chr14:105426634
|
CGTCT | C | 3 | a0003c0004t0001g0048a0003c0004t0001g0049a0003c0004t0001g0050 | 3 | HG03130.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+6577_28+6580del others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426634 | |||||
chr14:105426745
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.28+6682C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426745 | ||||||
chr14:105426778
|
C | T | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.28+6715C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426778 | ||||||
chr14:105426895
|
G | T | 1 | a0002c0002t0001g0240 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.28+6832G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426895 | ||||||
chr14:105427071
|
C | T | 2 | a0003c0004t0001g0004a0003c0004t0001g0026 | 3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28+7008C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427071 | ||||||
chr14:105427074
|
A | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.28+7011A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427074 | ||||||
chr14:105427241
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.28+7178G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427241 | ||||||
chr14:105427402
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0167others(6): Show | 10 | HG00544.hp2 HG00558.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.28+7339C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427402 | ||||||
chr14:105427527
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.28+7464T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427527 | ||||||
chr14:105427532
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.28+7469C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427532 | ||||||
chr14:105427588
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG00323.hp2 HG00733.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+7525A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427588 | ||||||
chr14:105427611
|
T | G | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+7548T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427611 | ||||||
chr14:105427756
|
A | C | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+7693A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427756 | ||||||
chr14:105427924
|
A | ACGCAAG | 18 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0248others(15): Show | 18 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.28+7861_28+7862ins others(6): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427924 | ||||||
chr14:105427949
|
CAG | C | 10 | a0003c0006t0001g0002a0003c0006t0001g0022a0003c0006t0001g0023others(7): Show | 13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+7889_28+7890del others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105427949 | |||||
chr14:105428015
|
C | CA | 20 | a0001c0001t0001g0071a0001c0001t0001g0271a0001c0001t0001g0278others(17): Show | 23 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.28+7971dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | |||||
chr14:105428015
|
C | CAA | 233 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(230): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.28+7970_28+7971dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | |||||
chr14:105428015
|
C | CAAA | 11 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0088others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+7969_28+7971dup others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | |||||
chr14:105428015
|
C | CAAAA | 14 | a0001c0017t0001g0044a0002c0002t0001g0045a0003c0004t0001g0003others(11): Show | 14 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+7968_28+7971dup others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | |||||
chr14:105428015
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0008t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+7962_28+7971del others(10): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | |||||
chr14:105428173
|
CAGCCCCC others(1231): Show |
C | 1 | a0003c0008t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+8113_29-9259del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428173 | |||||
chr14:105428190
|
C | T | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+8127C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428190 | ||||||
chr14:105428401
|
C | T | 1 | a0002c0002t0001g0246 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.28+8338C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428401 | ||||||
chr14:105428410
|
C | T | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.28+8347C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428410 | ||||||
chr14:105428487
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.28+8424C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428487 | ||||||
chr14:105428519
|
C | T | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+8456C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428519 | ||||||
chr14:105428704
|
A | G | 4 | a0001c0012t0001g0037a0003c0004t0001g0048a0003c0004t0001g0049others(1): Show | 4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+8641A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428704 | ||||||
chr14:105428710
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.28+8647A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428710 | ||||||
chr14:105428717
|
CT | C | 278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.28+8666delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428717 | |||||
chr14:105428744
|
A | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.28+8681A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428744 | ||||||
chr14:105428850
|
G | A | 4 | a0001c0012t0001g0037a0003c0004t0001g0048a0003c0004t0001g0049others(1): Show | 4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+8787G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428850 | ||||||
chr14:105428873
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+8810C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428873 | ||||||
chr14:105428913
|
T | C | 1 | a0005c0005t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.28+8850T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428913 | ||||||
chr14:105428958
|
C | G | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.28+8895C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428958 | ||||||
chr14:105428994
|
G | A | 150 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(147): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.28+8931G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428994 | ||||||
chr14:105429041
|
G | A | 13 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+8978G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429041 | ||||||
chr14:105429075
|
G | A | 18 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0248others(15): Show | 18 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.28+9012G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429075 | ||||||
chr14:105429188
|
A | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0244 | 3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28+9125A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429188 | ||||||
chr14:105429204
|
T | G | 2 | a0003c0004t0001g0004a0003c0004t0001g0026 | 3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28+9141T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429204 | ||||||
chr14:105429279
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.28+9216C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429279 | ||||||
chr14:105429312
|
G | C | 5 | a0002c0002t0001g0086a0002c0002t0001g0238a0002c0015t0001g0121others(2): Show | 5 | HG00621.hp2 NA18942.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+9249G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429312 | ||||||
chr14:105429354
|
C | T | 2 | a0001c0001t0001g0268a0004c0003t0001g0269 | 2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.28+9291C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429354 | ||||||
chr14:105429372
|
G | A | 1 | a0002c0002t0001g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.29-9300G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429372 | ||||||
chr14:105429452
|
A | AT | 7 | a0001c0001t0001g0120a0001c0001t0001g0193a0001c0001t0001g0221others(4): Show | 7 | HG01981.hp2 HG02486.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-9203dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429452 | |||||
chr14:105429521
|
G | A | 8 | a0001c0001t0001g0043a0001c0001t0002g0067a0001c0001t0002g0091others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-9151G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429521 | ||||||
chr14:105429542
|
C | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0228others(5): Show | 9 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-9130C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429542 | ||||||
chr14:105429576
|
C | T | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.29-9096C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429576 | ||||||
chr14:105429663
|
C | T | 2 | a0005c0005t0001g0226a0008c0016t0001g0083 | 2 | NA18989.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.29-9009C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429663 | ||||||
chr14:105429743
|
G | A | 149 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(146): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.29-8929G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429743 | ||||||
chr14:105429752
|
C | CTTT | 21 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0047others(18): Show | 21 | HG01167.hp1 HG01993.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.29-8901_29-8899dup others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | |||||
chr14:105429752
|
C | CTTTT | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.29-8902_29-8899dup others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | |||||
chr14:105429752
|
C | CTTTTT | 42 | a0001c0001t0001g0043a0001c0001t0001g0068a0001c0001t0001g0077others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.29-8903_29-8899dup others(5): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | |||||
chr14:105429752
|
C | CTTTTTT | 13 | a0001c0001t0002g0251a0003c0004t0001g0048a0003c0004t0001g0049others(10): Show | 16 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-8904_29-8899dup others(6): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | |||||
chr14:105429820
|
G | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.29-8852G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429820 | ||||||
chr14:105430053
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.29-8619G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430053 | ||||||
chr14:105430385
|
C | G | 3 | a0002c0002t0001g0011a0002c0002t0001g0229a0002c0002t0001g0231 | 4 | HG00099.hp2 HG01243.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-8287C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430385 | ||||||
chr14:105430484
|
C | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0047a0003c0008t0001g0046 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-8188C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430484 | ||||||
chr14:105430520
|
A | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.29-8152A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430520 | ||||||
chr14:105430537
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0017t0001g0044others(2): Show | 5 | HG03041.hp2 HG03471.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-8135C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430537 | ||||||
chr14:105430564
|
T | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.29-8108T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430564 | ||||||
chr14:105430571
|
G | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.29-8101G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430571 | ||||||
chr14:105430582
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29-8090C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430582 | ||||||
chr14:105430658
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.29-8014G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430658 | ||||||
chr14:105430847
|
T | G | 1 | a0003c0004t0001g0118 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.29-7825T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430847 | ||||||
chr14:105430961
|
A | G | 1 | a0003c0014t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.29-7711A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430961 | ||||||
chr14:105430978
|
T | C | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.29-7694T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430978 | ||||||
chr14:105431261
|
C | G | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-7411C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431261 | ||||||
chr14:105431542
|
T | TA | 2 | a0003c0004t0001g0004a0003c0004t0001g0026 | 3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.29-7127dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105431542 | |||||
chr14:105431638
|
C | G | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.29-7034C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431638 | ||||||
chr14:105431647
|
G | C | 1 | a0002c0002t0001g0125 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.29-7025G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431647 | ||||||
chr14:105431686
|
C | T | 10 | a0003c0006t0001g0002a0003c0006t0001g0022a0003c0006t0001g0023others(7): Show | 13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-6986C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431686 | ||||||
chr14:105431696
|
G | A | 1 | a0003c0008t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.29-6976G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431696 | ||||||
chr14:105431718
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0037others(4): Show | 7 | HG03041.hp2 HG03130.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-6954C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431718 | ||||||
chr14:105431777
|
C | T | 2 | a0001c0001t0001g0034a0004c0003t0001g0033 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.29-6895C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431777 | ||||||
chr14:105431801
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.29-6871T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431801 | ||||||
chr14:105431853
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.29-6819T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431853 | ||||||
chr14:105431911
|
G | C | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-6761G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431911 | ||||||
chr14:105431915
|
T | C | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-6757T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431915 | ||||||
chr14:105431927
|
G | A | 1 | a0002c0002t0001g0174 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.29-6745G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431927 | ||||||
chr14:105432034
|
A | C | 19 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0001t0001g0116others(16): Show | 19 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.29-6638A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432034 | ||||||
chr14:105432036
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.29-6636C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432036 | ||||||
chr14:105432237
|
TTTTA | T | 3 | a0001c0001t0001g0214a0001c0001t0001g0221a0002c0002t0001g0229 | 3 | HG01243.hp1 NA18941.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.29-6419_29-6416del others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105432237 | |||||
chr14:105432295
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0047 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-6377C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432295 | ||||||
chr14:105432378
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-6294T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432378 | ||||||
chr14:105432383
|
G | GGT | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-6288_29-6287ins others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105432383 | |||||
chr14:105432396
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.29-6276A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432396 | ||||||
chr14:105432401
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0017t0001g0044others(2): Show | 5 | HG03041.hp2 HG03471.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-6271C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432401 | ||||||
chr14:105432605
|
A | T | 16 | a0001c0012t0001g0037a0001c0012t0001g0248a0003c0004t0001g0003others(13): Show | 16 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.29-6067A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432605 | ||||||
chr14:105432786
|
T | C | 5 | a0003c0004t0001g0058a0003c0007t0001g0052a0003c0007t0001g0053others(2): Show | 5 | HG02109.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-5886T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432786 | ||||||
chr14:105432976
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.29-5696C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432976 | ||||||
chr14:105432980
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.29-5692T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432980 | ||||||
chr14:105432998
|
C | T | 1 | a0001c0011t0001g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.29-5674C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432998 | ||||||
chr14:105433007
|
A | G | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.29-5665A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433007 | ||||||
chr14:105433238
|
A | G | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.29-5434A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433238 | ||||||
chr14:105433329
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-5343C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433329 | ||||||
chr14:105433330
|
G | A | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.29-5342G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433330 | ||||||
chr14:105433397
|
C | T | 7 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0037others(4): Show | 7 | HG00639.hp2 HG03041.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-5275C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433397 | ||||||
chr14:105433455
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-5217C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433455 | ||||||
chr14:105433472
|
A | G | 10 | a0003c0006t0001g0002a0003c0006t0001g0022a0003c0006t0001g0023others(7): Show | 13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-5200A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433472 | ||||||
chr14:105433481
|
G | C | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.29-5191G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433481 | ||||||
chr14:105433543
|
G | A | 1 | a0002c0002t0001g0230 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.29-5129G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433543 | ||||||
chr14:105433756
|
G | A | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.29-4916G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433756 | ||||||
chr14:105433765
|
T | A | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.29-4907T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433765 | ||||||
chr14:105433834
|
A | T | 22 | a0001c0001t0001g0047a0001c0012t0001g0037a0001c0012t0001g0248others(19): Show | 22 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.29-4838A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433834 | ||||||
chr14:105434209
|
C | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.29-4463C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434209 | ||||||
chr14:105434220
|
G | T | 4 | a0001c0012t0001g0037a0001c0017t0001g0044a0002c0002t0001g0045others(1): Show | 4 | HG03130.hp2 HG03704.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-4452G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434220 | ||||||
chr14:105434224
|
A | C | 1 | a0001c0001t0001g0212 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.29-4448A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434224 | ||||||
chr14:105434281
|
G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0248 | 3 | HG00639.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-4391G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434281 | ||||||
chr14:105434379
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.29-4293A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434379 | ||||||
chr14:105434478
|
G | A | 1 | a0002c0002t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.29-4194G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434478 | ||||||
chr14:105434490
|
CT | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0192a0001c0001t0001g0212others(5): Show | 8 | HG00597.hp2 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-4161delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434490 | |||||
chr14:105434490
|
CTT | C | 234 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(231): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.29-4162_29-4161del others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434490 | |||||
chr14:105434490
|
CTTT | C | 25 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0123others(22): Show | 25 | HG00323.hp2 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.29-4163_29-4161del others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434490 | |||||
chr14:105434591
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.29-4081C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434591 | ||||||
chr14:105434735
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.29-3937A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434735 | ||||||
chr14:105434742
|
C | G | 1 | a0004c0003t0001g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.29-3930C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434742 | ||||||
chr14:105434748
|
G | A | 8 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(5): Show | 8 | HG01074.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-3924G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434748 | ||||||
chr14:105434848
|
CTTACTCA others(4): Show |
C | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.29-3821_29-3811del others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434848 | |||||
chr14:105434919
|
G | A | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(1): Show | 4 | HG00544.hp2 HG02165.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-3753G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434919 | ||||||
chr14:105435031
|
A | G | 2 | a0001c0001t0001g0152a0002c0002t0001g0153 | 2 | HG00597.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.29-3641A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435031 | ||||||
chr14:105435118
|
A | C | 279 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.29-3554A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435118 | ||||||
chr14:105435289
|
TTTAAG | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0248 | 3 | HG00639.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-3379_29-3375del others(5): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105435289 | |||||
chr14:105435389
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(3): Show | 6 | HG02280.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-3283G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435389 | ||||||
chr14:105435413
|
C | A | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.29-3259C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435413 | ||||||
chr14:105435733
|
G | A | 13 | a0003c0004t0001g0003a0003c0004t0001g0042a0003c0004t0001g0058others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-2939G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435733 | ||||||
chr14:105435936
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.29-2736C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435936 | ||||||
chr14:105435969
|
G | A | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-2703G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435969 | ||||||
chr14:105436117
|
A | T | 1 | a0004c0003t0001g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.29-2555A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436117 | ||||||
chr14:105436176
|
G | A | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-2496G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436176 | ||||||
chr14:105436224
|
G | A | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.29-2448G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436224 | ||||||
chr14:105436269
|
A | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 16 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-2403A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436269 | ||||||
chr14:105436350
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.29-2322T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436350 | ||||||
chr14:105436382
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.29-2290G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436382 | ||||||
chr14:105436423
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.29-2249C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436423 | ||||||
chr14:105436576
|
G | A | 4 | a0003c0006t0001g0022a0003c0006t0001g0023a0003c0006t0001g0027others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-2096G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436576 | ||||||
chr14:105436609
|
C | T | 13 | a0003c0004t0001g0003a0003c0004t0001g0042a0003c0004t0001g0058others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-2063C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436609 | ||||||
chr14:105436725
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.29-1947C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436725 | ||||||
chr14:105436749
|
G | A | 14 | a0003c0004t0001g0003a0003c0004t0001g0042a0003c0004t0001g0058others(11): Show | 14 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-1923G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436749 | ||||||
chr14:105436799
|
C | T | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-1873C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436799 | ||||||
chr14:105436949
|
C | T | 1 | a0001c0011t0001g0206 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.29-1723C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436949 | ||||||
chr14:105437044
|
C | T | 90 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0036others(87): Show | 100 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.29-1628C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437044 | ||||||
chr14:105437232
|
CGGGCGTG others(63): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-1420_29-1351del others(70): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437232 | |||||
chr14:105437237
|
GTGTGCCT others(35): Show |
G | 243 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(240): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.29-1420_29-1379del others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437237 | |||||
chr14:105437266
|
TGTCCTCA others(21): Show |
T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-1393_29-1366del others(28): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437266 | |||||
chr14:105437279
|
A | G | 34 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0037others(31): Show | 38 | HG00639.hp2 HG00735.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.29-1393A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437279 | ||||||
chr14:105437295
|
G | A | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-1377G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437295 | ||||||
chr14:105437323
|
G | A | 12 | a0003c0004t0001g0004a0003c0004t0001g0026a0003c0006t0001g0002others(9): Show | 16 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.29-1349G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437323 | ||||||
chr14:105437354
|
G | C | 253 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.29-1318G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437354 | ||||||
chr14:105437387
|
G | A | 247 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.29-1285G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437387 | ||||||
chr14:105437442
|
C | CGGGCATG others(77): Show |
1 | a0002c0002t0001g0099 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.29-1210_29-1127dup others(84): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437442 | |||||
chr14:105437517
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.29-1155G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437517 | ||||||
chr14:105437557
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.29-1115C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437557 | ||||||
chr14:105437603
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.29-1069C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437603 | ||||||
chr14:105437732
|
C | T | 283 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(280): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.29-940C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437732 | ||||||
chr14:105437827
|
G | A | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.29-845G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437827 | ||||||
chr14:105437914
|
G | A | 6 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0092others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-758G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437914 | ||||||
chr14:105437919
|
G | T | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.29-753G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437919 | ||||||
chr14:105437930
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.29-742C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437930 | ||||||
chr14:105437994
|
G | A | 24 | a0001c0001t0001g0126a0001c0001t0001g0183a0002c0002t0001g0061others(21): Show | 24 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.29-678G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437994 | ||||||
chr14:105438336
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-336C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105438336 | ||||||
chr14:105438493
|
C | T | 241 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.29-179C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105438493 | ||||||
chr14:105438772
|
G | A | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.96+33G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438772 | ||||||
chr14:105438789
|
C | T | 258 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.96+50C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438789 | ||||||
chr14:105438815
|
A | T | 3 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG00733.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.96+76A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438815 | ||||||
chr14:105438835
|
G | A | 4 | a0002c0002t0001g0084a0002c0002t0001g0132a0002c0002t0001g0165others(1): Show | 4 | HG00673.hp1 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+96G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438835 | ||||||
chr14:105438899
|
C | T | 1 | a0002c0002t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.96+160C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438899 | ||||||
chr14:105439001
|
G | C | 1 | a0002c0015t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.96+262G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439001 | ||||||
chr14:105439155
|
C | CCCACCCC others(73): Show |
1 | a0003c0007t0001g0053 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.96+435_96+436insGT others(78): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105439155 | |||||
chr14:105439155
|
C | CCCACCCC others(73): Show |
277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.96+435_96+436insGT others(78): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105439155 | |||||
chr14:105439155
|
C | CCCACCCC others(73): Show |
1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.96+435_96+436insGT others(78): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105439155 | |||||
chr14:105439208
|
A | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0239 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.96+469A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439208 | ||||||
chr14:105439215
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.96+476C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439215 | ||||||
chr14:105439566
|
G | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.96+827G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439566 | ||||||
chr14:105439581
|
G | A | 3 | a0001c0017t0001g0044a0002c0002t0001g0045a0003c0004t0001g0048 | 3 | HG03130.hp2 HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.96+842G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439581 | ||||||
chr14:105439687
|
G | C | 1 | a0003c0006t0001g0002 | 4 | HG02922.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+948G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439687 | ||||||
chr14:105439736
|
C | T | 152 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.96+997C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439736 | ||||||
chr14:105439759
|
G | A | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+1020G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439759 | ||||||
chr14:105440010
|
C | T | 6 | a0001c0012t0001g0037a0001c0017t0001g0044a0002c0002t0001g0045others(3): Show | 6 | HG03130.hp2 HG03579.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1271C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440010 | ||||||
chr14:105440065
|
G | T | 1 | a0002c0002t0001g0103 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.96+1326G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440065 | ||||||
chr14:105440185
|
A | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0081a0001c0001t0001g0089others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+1446A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440185 | ||||||
chr14:105440243
|
C | T | 13 | a0003c0004t0001g0003a0003c0004t0001g0042a0003c0004t0001g0058others(10): Show | 13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+1504C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440243 | ||||||
chr14:105440244
|
G | A | 9 | a0003c0006t0001g0002a0003c0006t0001g0022a0003c0006t0001g0023others(6): Show | 12 | HG00735.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+1505G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440244 | ||||||
chr14:105440359
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.96+1620T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440359 | ||||||
chr14:105440454
|
C | T | 4 | a0001c0012t0001g0037a0003c0004t0001g0048a0003c0004t0001g0049others(1): Show | 4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1715C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440454 | ||||||
chr14:105440460
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.96+1721C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440460 | ||||||
chr14:105440504
|
G | A | 6 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0092others(3): Show | 6 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1765G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440504 | ||||||
chr14:105440696
|
C | T | 1 | a0001c0011t0001g0206 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.96+1957C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440696 | ||||||
chr14:105440822
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.96+2083C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440822 | ||||||
chr14:105440969
|
C | T | 1 | a0003c0008t0001g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+2230C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440969 | ||||||
chr14:105440999
|
G | A | 4 | a0002c0002t0001g0084a0002c0002t0001g0132a0002c0002t0001g0165others(1): Show | 4 | HG00673.hp1 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2260G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440999 | ||||||
chr14:105441096
|
C | T | 35 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0001t0001g0236others(32): Show | 38 | HG00639.hp2 HG00735.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.96+2357C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441096 | ||||||
chr14:105441098
|
C | T | 9 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG00733.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+2359C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441098 | ||||||
chr14:105441111
|
TG | T | 15 | a0001c0001t0001g0236a0001c0012t0001g0248a0003c0004t0001g0003others(12): Show | 15 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+2378delG | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441111 | |||||
chr14:105441126
|
T | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0012t0001g0037others(2): Show | 5 | HG00639.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+2387T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441126 | ||||||
chr14:105441232
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.96+2493G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441232 | ||||||
chr14:105441260
|
G | GC | 13 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0236others(10): Show | 13 | HG00597.hp2 HG00642.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+2528dupC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441260 | |||||
chr14:105441260
|
GC | G | 12 | a0001c0001t0001g0041a0001c0001t0001g0114a0003c0006t0001g0002others(9): Show | 15 | HG00735.hp2 HG02559.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+2528delC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441260 | |||||
chr14:105441268
|
GC | G | 6 | a0003c0004t0001g0042a0003c0004t0001g0058a0003c0007t0001g0052others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+2533delC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441268 | |||||
chr14:105441269
|
C | G | 18 | a0001c0001t0001g0040a0001c0001t0001g0114a0001c0001t0001g0173others(15): Show | 19 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+2530C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441269 | ||||||
chr14:105441305
|
C | T | 223 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(220): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.96+2566C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441305 | ||||||
chr14:105441404
|
C | T | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.96+2665C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441404 | ||||||
chr14:105441447
|
T | C | 9 | a0001c0001t0001g0096a0003c0004t0001g0003a0003c0006t0001g0027others(6): Show | 9 | HG01167.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+2708T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441447 | ||||||
chr14:105441450
|
G | A | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.96+2711G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441450 | ||||||
chr14:105441516
|
T | C | 54 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0040others(51): Show | 58 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.96+2777T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441516 | ||||||
chr14:105441519
|
A | G | 15 | a0001c0001t0001g0040a0001c0012t0001g0037a0003c0004t0001g0108others(12): Show | 18 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.96+2780A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441519 | ||||||
chr14:105441523
|
A | G | 19 | a0001c0001t0001g0040a0001c0001t0001g0239a0001c0012t0001g0037others(16): Show | 22 | HG00639.hp2 HG00735.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+2784A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441523 | ||||||
chr14:105441525
|
G | T | 13 | a0001c0012t0001g0037a0003c0006t0001g0002a0003c0006t0001g0022others(10): Show | 16 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+2786G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441525 | ||||||
chr14:105441538
|
G | T | 14 | a0001c0001t0001g0038a0001c0012t0001g0037a0003c0006t0001g0002others(11): Show | 17 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.96+2799G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441538 | ||||||
chr14:105441554
|
A | G | 6 | a0003c0004t0001g0026a0003c0004t0001g0049a0003c0004t0001g0050others(3): Show | 6 | HG02615.hp1 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+2815A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441554 | ||||||
chr14:105441561
|
G | C | 278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.96+2822G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441561 | ||||||
chr14:105441566
|
G | A | 279 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.96+2827G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441566 | ||||||
chr14:105441569
|
C | T | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.96+2830C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441569 | ||||||
chr14:105441570
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.96+2831G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441570 | ||||||
chr14:105441580
|
A | G | 5 | a0002c0002t0001g0099a0002c0002t0001g0180a0002c0002t0001g0181others(2): Show | 5 | HG02056.hp2 NA18955.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+2841A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441580 | ||||||
chr14:105441606
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.96+2867A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441606 | ||||||
chr14:105441619
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0088 | 2 | HG01106.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.96+2880T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441619 | ||||||
chr14:105441621
|
C | T | 1 | a0005c0005t0001g0063 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.96+2882C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441621 | ||||||
chr14:105441641
|
A | C | 1 | a0003c0004t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.96+2902A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441641 | ||||||
chr14:105441650
|
C | G | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+2911C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441650 | ||||||
chr14:105441650
|
C | T | 1 | a0002c0002t0001g0174 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.96+2911C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441650 | ||||||
chr14:105441654
|
C | T | 3 | a0001c0012t0001g0248a0001c0017t0001g0044a0002c0002t0001g0045 | 3 | HG00639.hp2 HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.96+2915C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441654 | ||||||
chr14:105441655
|
G | T | 1 | a0002c0002t0001g0174 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.96+2916G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441655 | ||||||
chr14:105441656
|
T | A | 3 | a0001c0001t0001g0030a0007c0013t0001g0031a0007c0013t0001g0032 | 3 | HG01496.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.96+2917T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441656 | ||||||
chr14:105441656
|
T | C | 3 | a0003c0004t0001g0048a0003c0004t0001g0049a0003c0004t0001g0050 | 3 | HG03130.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+2917T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441656 | ||||||
chr14:105441657
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0197 | 3 | HG03491.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.96+2918G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441657 | ||||||
chr14:105441662
|
C | T | 1 | a0006c0010t0001g0166 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96+2923C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441662 | ||||||
chr14:105441663
|
G | A | 2 | a0001c0001t0001g0015a0002c0002t0001g0225 | 2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.96+2924G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441663 | ||||||
chr14:105441666
|
C | T | 2 | a0001c0001t0001g0015a0002c0002t0001g0225 | 2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.96+2927C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441666 | ||||||
chr14:105441673
|
G | A | 3 | a0001c0001t0001g0015a0001c0012t0001g0037a0002c0002t0001g0225 | 3 | HG00323.hp1 HG02300.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+2934G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441673 | ||||||
chr14:105441674
|
A | G | 3 | a0001c0001t0001g0015a0001c0012t0001g0037a0002c0002t0001g0225 | 3 | HG00323.hp1 HG02300.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+2935A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441674 | ||||||
chr14:105441686
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.96+2947C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441686 | ||||||
chr14:105441699
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.96+2960C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441699 | ||||||
chr14:105441712
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.96+2973T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441712 | ||||||
chr14:105441719
|
G | A | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.96+2980G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441719 | ||||||
chr14:105441725
|
T | C | 6 | a0001c0001t0001g0151a0002c0002t0001g0196a0003c0004t0001g0004others(3): Show | 7 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+2986T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441725 | ||||||
chr14:105441726
|
G | A | 1 | a0002c0002t0001g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.96+2987G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441726 | ||||||
chr14:105441733
|
G | C | 6 | a0001c0001t0001g0087a0001c0001t0001g0228a0002c0002t0001g0011others(3): Show | 7 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+2994G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441733 | ||||||
chr14:105441742
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.96+3003C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441742 | ||||||
chr14:105441743
|
G | A | 28 | a0001c0001t0001g0041a0001c0017t0001g0044a0002c0002t0001g0045others(25): Show | 31 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+3004G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441743 | ||||||
chr14:105441748
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+3009C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441748 | ||||||
chr14:105441749
|
C | A | 275 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.96+3010C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441749 | ||||||
chr14:105441749
|
C | G | 2 | a0001c0001t0001g0245a0002c0002t0001g0196 | 2 | HG01261.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.96+3010C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441749 | ||||||
chr14:105441750
|
C | T | 2 | a0002c0002t0001g0179a0002c0002t0001g0185 | 2 | HG00438.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.96+3011C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441750 | ||||||
chr14:105441754
|
A | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0228a0002c0002t0001g0011others(3): Show | 7 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+3015A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441754 | ||||||
chr14:105441757
|
A | G | 13 | a0001c0001t0001g0087a0001c0001t0001g0150a0001c0001t0001g0228others(10): Show | 14 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+3018A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441757 | ||||||
chr14:105441763
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+3024C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441763 | ||||||
chr14:105441772
|
C | T | 1 | a0005c0005t0001g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.96+3033C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441772 | ||||||
chr14:105441781
|
G | A | 1 | a0004c0003t0001g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.96+3042G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441781 | ||||||
chr14:105441788
|
T | C | 11 | a0001c0001t0001g0041a0003c0006t0001g0002a0003c0006t0001g0022others(8): Show | 14 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+3049T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441788 | ||||||
chr14:105441814
|
A | C | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+3075A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441814 | ||||||
chr14:105441840
|
AG | A | 3 | a0001c0012t0001g0037a0003c0004t0001g0026a0003c0008t0001g0046 | 3 | HG03471.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+3104delG | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441840 | |||||
chr14:105441875
|
G | A | 21 | a0001c0012t0001g0037a0001c0012t0001g0248a0001c0017t0001g0044others(18): Show | 21 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+3136G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441875 | ||||||
chr14:105441887
|
T | A | 278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.96+3148T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441887 | ||||||
chr14:105442057
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0244 | 3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.96+3318C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442057 | ||||||
chr14:105442102
|
G | A | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97-3316G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442102 | ||||||
chr14:105442149
|
A | G | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97-3269A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442149 | ||||||
chr14:105442235
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97-3183C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442235 | ||||||
chr14:105442249
|
G | T | 2 | a0002c0002t0001g0069a0002c0002t0001g0148 | 2 | HG00738.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.97-3169G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442249 | ||||||
chr14:105442259
|
G | A | 255 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.97-3159G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442259 | ||||||
chr14:105442333
|
G | A | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97-3085G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442333 | ||||||
chr14:105442443
|
G | A | 278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.97-2975G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442443 | ||||||
chr14:105442546
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.97-2872G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442546 | ||||||
chr14:105442555
|
T | C | 272 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.97-2863T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442555 | ||||||
chr14:105442606
|
G | A | 4 | a0001c0001t0001g0199a0001c0001t0001g0214a0001c0001t0001g0221others(1): Show | 4 | NA18941.hp1 NA18942.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-2812G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442606 | ||||||
chr14:105442642
|
T | TCAGAACA others(46): Show |
24 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(21): Show | 24 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-2728_97-2676dup others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442642 | |||||
chr14:105442645
|
G | GAACAGAC others(1404): Show |
1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97-2694_97-2693ins others(1411): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442645 | |||||
chr14:105442645
|
G | GAACAGAC others(152): Show |
1 | a0001c0001t0001g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-2676_97-2675ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442645 | |||||
chr14:105442725
|
G | A | 3 | a0001c0001t0001g0040a0001c0012t0001g0037a0003c0004t0001g0026 | 3 | HG02451.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.97-2693G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442725 | ||||||
chr14:105442743
|
G | A | 9 | a0001c0001t0001g0126a0001c0001t0001g0233a0001c0001t0001g0234others(6): Show | 9 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-2675G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442743 | ||||||
chr14:105442743
|
GCAGAACA others(46): Show |
G | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-2672_97-2620del others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442743 | |||||
chr14:105442746
|
G | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0126a0001c0001t0001g0233others(8): Show | 11 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-2672G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442746 | ||||||
chr14:105442751
|
C | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0126a0001c0001t0001g0233others(8): Show | 11 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-2667C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442751 | ||||||
chr14:105442778
|
G | GCTGTGTG others(205): Show |
13 | a0001c0001t0001g0006a0001c0001t0001g0081a0001c0001t0001g0089others(10): Show | 14 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-2623_97-2622ins others(212): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442778 | |||||
chr14:105442778
|
G | GCTGTGTG others(311): Show |
1 | a0001c0001t0001g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.97-2623_97-2622ins others(318): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442778 | |||||
chr14:105442778
|
GCTGTGTG others(46): Show |
G | 1 | a0001c0001t0001g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97-2622_97-2570del others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442778 | |||||
chr14:105442782
|
T | C | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-2636T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442782 | ||||||
chr14:105442796
|
A | ACACAACA others(205): Show |
1 | a0001c0001t0001g0009 | 2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(212): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(152): Show |
130 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(127): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(311): Show |
4 | a0002c0002t0001g0061a0002c0002t0001g0175a0002c0002t0001g0241others(1): Show | 4 | HG00609.hp1 HG00621.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(318): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(152): Show |
4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0244others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(470): Show |
1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97-2588_97-2587ins others(477): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(258): Show |
20 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0068others(17): Show | 21 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(265): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(364): Show |
2 | a0001c0001t0001g0088a0001c0001t0001g0235 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(371): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(470): Show |
1 | a0001c0001t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.97-2588_97-2587ins others(477): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(311): Show |
1 | a0001c0001t0001g0111 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.97-2588_97-2587ins others(318): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | ACACAACA others(152): Show |
3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0003g0253 | 3 | HG00323.hp2 HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.97-2605_97-2604ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | |||||
chr14:105442796
|
A | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0081a0001c0001t0001g0089others(11): Show | 15 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-2622A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442796 | ||||||
chr14:105442831
|
A | ACTGTGTG others(46): Show |
1 | a0001c0001t0001g0255 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-2567_97-2566ins others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442831 | |||||
chr14:105442831
|
A | ACTGTGTG others(46): Show |
94 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0034others(91): Show | 100 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.97-2567_97-2566ins others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442831 | |||||
chr14:105442831
|
A | ACTGTGTG others(629): Show |
1 | a0004c0003t0001g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.97-2567_97-2566ins others(636): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442831 | |||||
chr14:105442831
|
A | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(180): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.97-2587A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442831 | ||||||
chr14:105443000
|
G | T | 272 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(269): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.97-2418G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443000 | ||||||
chr14:105443043
|
A | T | 274 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(271): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.97-2375A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443043 | ||||||
chr14:105443099
|
C | T | 247 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.97-2319C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443099 | ||||||
chr14:105443153
|
G | A | 2 | a0003c0004t0001g0004a0003c0004t0001g0026 | 3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.97-2265G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443153 | ||||||
chr14:105443190
|
A | G | 274 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(271): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.97-2228A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443190 | ||||||
chr14:105443313
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.97-2105C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443313 | ||||||
chr14:105443635
|
A | C | 263 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(260): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.97-1783A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443635 | ||||||
chr14:105443690
|
T | C | 2 | a0001c0012t0001g0037a0003c0004t0001g0048 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-1728T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443690 | ||||||
chr14:105443730
|
G | T | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.97-1688G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443730 | ||||||
chr14:105443816
|
T | C | 275 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.97-1602T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443816 | ||||||
chr14:105443856
|
T | C | 275 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.97-1562T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443856 | ||||||
chr14:105443901
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.97-1517C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443901 | ||||||
chr14:105443946
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0116 | 2 | NA18939.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.97-1472G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443946 | ||||||
chr14:105444112
|
G | T | 1 | a0003c0004t0001g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.97-1306G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444112 | ||||||
chr14:105444122
|
C | G | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.97-1296C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444122 | ||||||
chr14:105444231
|
C | T | 2 | a0001c0001t0001g0137a0002c0002t0001g0155 | 2 | HG01099.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.97-1187C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444231 | ||||||
chr14:105444252
|
G | A | 1 | a0003c0009t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-1166G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444252 | ||||||
chr14:105444272
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0047 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.97-1146G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444272 | ||||||
chr14:105444343
|
C | G | 2 | a0003c0009t0001g0020a0003c0009t0001g0024 | 2 | HG00735.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.97-1075C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444343 | ||||||
chr14:105444353
|
C | T | 1 | a0002c0002t0001g0064 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.97-1065C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444353 | ||||||
chr14:105444399
|
A | T | 261 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(258): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.97-1019A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444399 | ||||||
chr14:105444444
|
C | A | 2 | a0001c0012t0001g0037a0003c0004t0001g0048 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-974C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444444 | ||||||
chr14:105444461
|
G | A | 34 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0036others(31): Show | 34 | HG00733.hp1 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.97-957G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444461 | ||||||
chr14:105444514
|
C | G | 1 | a0002c0002t0004g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.97-904C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444514 | ||||||
chr14:105444675
|
C | T | 1 | a0002c0002t0001g0160 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.97-743C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444675 | ||||||
chr14:105444789
|
TTA | T | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-628_97-627delTA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444789 | ||||||
chr14:105444790
|
T | TA | 22 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(19): Show | 25 | HG00733.hp1 HG00735.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.97-611dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105444790 | |||||
chr14:105444790
|
TA | T | 22 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0071others(19): Show | 22 | HG00558.hp1 HG01168.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-611delA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105444790 | |||||
chr14:105444856
|
C | T | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-562C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444856 | ||||||
chr14:105444937
|
C | T | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-481C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444937 | ||||||
chr14:105444938
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-480G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444938 | ||||||
chr14:105444992
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0047 | 2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.97-426C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444992 | ||||||
chr14:105445101
|
C | G | 1 | a0003c0008t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-317C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445101 | ||||||
chr14:105445111
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.97-307G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445111 | ||||||
chr14:105445141
|
T | C | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.97-277T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445141 | ||||||
chr14:105445225
|
T | C | 281 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(278): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.97-193T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445225 | ||||||
chr14:105445245
|
T | C | 1 | a0002c0002t0001g0156 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.97-173T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445245 | ||||||
chr14:105445302
|
G | A | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.97-116G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445302 | ||||||
chr14:105445330
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.97-88G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445330 | ||||||
chr14:105445372
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.97-46C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445372 | ||||||
chr14:105445546
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.190+35G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445546 | ||||||
chr14:105445554
|
C | T | 12 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(9): Show | 12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.190+43C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445554 | ||||||
chr14:105445555
|
G | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190+44G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445555 | ||||||
chr14:105445573
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0219 | 2 | NA18960.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.190+62G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445573 | ||||||
chr14:105445720
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.190+209C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445720 | ||||||
chr14:105446126
|
C | T | 1 | a0002c0002t0001g0103 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.190+615C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446126 | ||||||
chr14:105446127
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.190+616G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446127 | ||||||
chr14:105446353
|
G | A | 1 | a0003c0004t0001g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.190+842G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446353 | ||||||
chr14:105446353
|
G | C | 2 | a0001c0001t0001g0006a0004c0003t0001g0080 | 3 | HG00140.hp1 HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.190+842G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446353 | ||||||
chr14:105446440
|
C | T | 2 | a0001c0001t0001g0015a0002c0002t0001g0225 | 2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.190+929C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446440 | ||||||
chr14:105446517
|
C | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0224 | 2 | NA19003.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.190+1006C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446517 | ||||||
chr14:105446525
|
C | T | 2 | a0003c0008t0001g0013a0003c0008t0001g0014 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.190+1014C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446525 | ||||||
chr14:105446774
|
C | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0001t0001g0190others(3): Show | 6 | HG03041.hp2 NA19003.hp1 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+1263C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446774 | ||||||
chr14:105446812
|
G | C | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.190+1301G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446812 | ||||||
chr14:105446818
|
C | T | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190+1307C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446818 | ||||||
chr14:105446828
|
G | T | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.190+1317G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446828 | ||||||
chr14:105446876
|
G | A | 1 | a0005c0005t0001g0133 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.190+1365G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446876 | ||||||
chr14:105447002
|
G | A | 1 | a0002c0002t0001g0157 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.190+1491G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447002 | ||||||
chr14:105447111
|
G | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190+1600G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447111 | ||||||
chr14:105447183
|
C | T | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.190+1672C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447183 | ||||||
chr14:105447276
|
G | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 8 | HG00642.hp1 HG00738.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+1765G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447276 | ||||||
chr14:105447287
|
C | T | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.190+1776C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447287 | ||||||
chr14:105447299
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.190+1788G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447299 | ||||||
chr14:105447437
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.191-1922C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447437 | ||||||
chr14:105447554
|
A | T | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1805A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447554 | ||||||
chr14:105447557
|
G | T | 1 | a0003c0008t0001g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.191-1802G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447557 | ||||||
chr14:105447604
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.191-1755G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447604 | ||||||
chr14:105447680
|
G | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1679G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447680 | ||||||
chr14:105447686
|
C | T | 1 | a0002c0002t0001g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.191-1673C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447686 | ||||||
chr14:105447822
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.191-1537C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447822 | ||||||
chr14:105447824
|
C | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1535C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447824 | ||||||
chr14:105447844
|
C | G | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1515C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447844 | ||||||
chr14:105448122
|
C | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1237C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448122 | ||||||
chr14:105448200
|
C | T | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1159C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448200 | ||||||
chr14:105448240
|
T | A | 1 | a0001c0001t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.191-1119T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448240 | ||||||
chr14:105448264
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.191-1095C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448264 | ||||||
chr14:105448276
|
C | T | 2 | a0001c0001t0001g0275a0001c0001t0003g0253 | 2 | HG00323.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191-1083C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448276 | ||||||
chr14:105448518
|
C | A | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-841C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448518 | ||||||
chr14:105448601
|
A | C | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-758A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448601 | ||||||
chr14:105448611
|
G | A | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.191-748G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448611 | ||||||
chr14:105448712
|
A | AAC | 247 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.191-645_191-644dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr14 | 105448712 | |||||
chr14:105448834
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.191-525G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448834 | ||||||
chr14:105448857
|
T | C | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.191-502T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448857 | ||||||
chr14:105448871
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.191-488C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448871 | ||||||
chr14:105448907
|
G | A | 1 | a0003c0014t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.191-452G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448907 | ||||||
chr14:105448951
|
C | T | 273 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.191-408C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448951 | ||||||
chr14:105449091
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.191-268T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105449091 | ||||||
chr14:105449185
|
C | T | 1 | a0002c0015t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.191-174C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105449185 | ||||||
chr14:105449223
|
C | T | 1 | a0004c0003t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.191-136C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105449223 | ||||||
chr14:105449531
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.241+122C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449531 | ||||||
chr14:105449572
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.241+163G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449572 | ||||||
chr14:105449720
|
C | T | 1 | a0005c0005t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.241+311C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449720 | ||||||
chr14:105449872
|
G | T | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.242-186G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449872 | ||||||
chr14:105449890
|
C | A | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-168C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449890 | ||||||
chr14:105449901
|
T | G | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-157T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449901 | ||||||
chr14:105449902
|
A | G | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-156A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449902 | ||||||
chr14:105449906
|
T | G | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-152T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449906 | ||||||
chr14:105449908
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.242-150G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449908 | ||||||
chr14:105449914
|
T | G | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-144T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449914 | ||||||
chr14:105449920
|
A | AGGGGGGG others(4): Show |
1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-137_242-136ins others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr14 | 105449920 | |||||
chr14:105449922
|
T | G | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-136T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449922 | ||||||
chr14:105449924
|
T | C | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-134T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449924 | ||||||
chr14:105449925
|
C | G | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-133C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449925 | ||||||
chr14:105449926
|
C | G | 1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-132C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449926 | ||||||
chr14:105449926
|
C | T | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.242-132C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449926 | ||||||
chr14:105449968
|
C | T | 1 | a0005c0005t0001g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.242-90C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449968 | ||||||
chr14:105449977
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0191 | 3 | NA18612.hp2 NA18947.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.242-81G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449977 | ||||||
chr14:105449977
|
G | T | 3 | a0003c0009t0001g0019a0003c0009t0001g0020a0003c0009t0001g0024 | 3 | HG00735.hp2 HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.242-81G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449977 | ||||||
chr14:105450028
|
C | T | 2 | a0001c0017t0001g0044a0002c0002t0001g0045 | 2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.242-30C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105450028 | ||||||
chr14:105450327
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.432+3G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450327 | ||||||
chr14:105450345
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.432+21G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450345 | ||||||
chr14:105450364
|
G | A | 1 | a0003c0014t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.432+40G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450364 | ||||||
chr14:105450432
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0088a0001c0001t0001g0235 | 3 | HG01175.hp2 HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.432+108C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450432 | ||||||
chr14:105450460
|
G | A | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.432+136G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450460 | ||||||
chr14:105450503
|
G | A | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+179G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450503 | ||||||
chr14:105450520
|
G | A | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+196G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450520 | ||||||
chr14:105450680
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.432+356C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450680 | ||||||
chr14:105450730
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.432+406G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450730 | ||||||
chr14:105450878
|
G | A | 1 | a0003c0009t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.432+554G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450878 | ||||||
chr14:105450888
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.432+564G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450888 | ||||||
chr14:105450907
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0271 | 2 | HG00099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.432+583G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450907 | ||||||
chr14:105450911
|
G | A | 1 | a0005c0005t0001g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.432+587G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450911 | ||||||
chr14:105450929
|
G | A | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+605G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450929 | ||||||
chr14:105450959
|
T | C | 267 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.432+635T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450959 | ||||||
chr14:105450969
|
C | T | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.432+645C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450969 | ||||||
chr14:105451096
|
G | A | 2 | a0001c0001t0001g0259a0004c0003t0001g0257 | 2 | HG01358.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.432+772G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451096 | ||||||
chr14:105451160
|
G | C | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(3): Show | 6 | HG00733.hp1 HG01243.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+836G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451160 | ||||||
chr14:105451360
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.432+1036G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451360 | ||||||
chr14:105451479
|
G | C | 60 | a0001c0001t0001g0015a0001c0001t0001g0070a0001c0001t0001g0087others(57): Show | 70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.432+1155G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451479 | ||||||
chr14:105451482
|
C | T | 8 | a0001c0001t0001g0041a0001c0012t0001g0248a0003c0004t0001g0058others(5): Show | 8 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+1158C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451482 | ||||||
chr14:105451747
|
A | T | 1 | a0003c0004t0001g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+1423A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451747 | ||||||
chr14:105451775
|
CTTTTTTT others(2): Show |
C | 17 | a0001c0001t0001g0009a0001c0001t0001g0154a0001c0001t0001g0199others(14): Show | 18 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.432+1459_432+1467d others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451775 | |||||
chr14:105451775
|
CTTTTTTT others(3): Show |
C | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(164): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.432+1459_432+1468d others(12): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451775 | |||||
chr14:105451775
|
CTTTTTTT others(4): Show |
C | 9 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0002g0091others(6): Show | 9 | HG00099.hp2 HG01257.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.432+1459_432+1469d others(13): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451775 | |||||
chr14:105451783
|
G | GT | 8 | a0001c0001t0001g0151a0001c0001t0001g0234a0001c0001t0001g0258others(5): Show | 8 | HG01175.hp1 HG01261.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+1483dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451783 | |||||
chr14:105451783
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.432+1459G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451783 | ||||||
chr14:105451783
|
GT | G | 12 | a0001c0001t0001g0062a0001c0001t0001g0097a0001c0001t0001g0233others(9): Show | 15 | HG01069.hp2 HG01358.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.432+1483delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451783 | |||||
chr14:105451786
|
T | TG | 4 | a0001c0012t0001g0248a0001c0017t0001g0044a0002c0002t0001g0045others(1): Show | 4 | HG00639.hp2 HG02818.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+1462_432+1463i others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451786 | ||||||
chr14:105451787
|
T | G | 5 | a0001c0001t0001g0047a0001c0012t0001g0037a0003c0004t0001g0004others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+1463T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451787 | ||||||
chr14:105451791
|
T | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0250a0001c0011t0001g0206 | 3 | HG00673.hp2 HG02015.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.432+1467T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451791 | ||||||
chr14:105451883
|
C | T | 233 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(230): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.432+1559C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451883 | ||||||
chr14:105452212
|
G | A | 1 | a0003c0006t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.432+1888G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452212 | ||||||
chr14:105452473
|
A | C | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.433-1720A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452473 | ||||||
chr14:105452661
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.433-1532G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452661 | ||||||
chr14:105452768
|
C | T | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.433-1425C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452768 | ||||||
chr14:105452869
|
T | G | 2 | a0001c0001t0001g0047a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.433-1324T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452869 | ||||||
chr14:105452912
|
C | G | 1 | a0002c0002t0001g0064 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.433-1281C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452912 | ||||||
chr14:105452940
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.433-1253C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452940 | ||||||
chr14:105452977
|
A | G | 7 | a0003c0004t0001g0004a0003c0006t0001g0002a0003c0006t0001g0022others(4): Show | 11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-1216A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452977 | ||||||
chr14:105453036
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0007g0016 | 2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.433-1157C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453036 | ||||||
chr14:105453088
|
C | T | 266 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(263): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.433-1105C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453088 | ||||||
chr14:105453132
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.433-1061C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453132 | ||||||
chr14:105453185
|
C | T | 16 | a0001c0001t0001g0041a0003c0004t0001g0003a0003c0004t0001g0058others(13): Show | 16 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-1008C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453185 | ||||||
chr14:105453207
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.433-986G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453207 | ||||||
chr14:105453222
|
C | T | 15 | a0003c0004t0001g0003a0003c0004t0001g0058a0003c0007t0001g0003others(12): Show | 15 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.433-971C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453222 | ||||||
chr14:105453301
|
G | A | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.433-892G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453301 | ||||||
chr14:105453321
|
A | G | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.433-872A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453321 | ||||||
chr14:105453538
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.433-655A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453538 | ||||||
chr14:105453580
|
C | T | 1 | a0002c0002t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.433-613C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453580 | ||||||
chr14:105453953
|
C | T | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.433-240C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453953 | ||||||
chr14:105454023
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.433-170T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454023 | ||||||
chr14:105454114
|
C | T | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.433-79C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454114 | ||||||
chr14:105454115
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.433-78G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454115 | ||||||
chr14:105454118
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-75C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454118 | ||||||
chr14:105454534
|
T | C | 270 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.550+224T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454534 | ||||||
chr14:105454602
|
T | C | 2 | a0001c0001t0001g0154a0004c0003t0001g0128 | 2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.550+292T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454602 | ||||||
chr14:105454629
|
C | T | 1 | a0002c0002t0001g0184 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.550+319C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454629 | ||||||
chr14:105454661
|
C | T | 2 | a0003c0009t0001g0020a0003c0009t0001g0024 | 2 | HG00735.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.550+351C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454661 | ||||||
chr14:105454670
|
G | A | 2 | a0001c0012t0001g0037a0001c0017t0001g0044 | 2 | HG03704.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.550+360G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454670 | ||||||
chr14:105454731
|
C | T | 6 | a0003c0004t0001g0003a0003c0007t0001g0003a0003c0007t0001g0051others(3): Show | 6 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+421C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454731 | ||||||
chr14:105454799
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.550+489G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454799 | ||||||
chr14:105454806
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.550+496C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454806 | ||||||
chr14:105454845
|
C | T | 1 | a0003c0006t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.550+535C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454845 | ||||||
chr14:105454862
|
T | A | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.550+552T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454862 | ||||||
chr14:105455064
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.550+754C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455064 | ||||||
chr14:105455098
|
G | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+788G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455098 | ||||||
chr14:105455117
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.550+807G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455117 | ||||||
chr14:105455157
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 4 | HG02280.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+847C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455157 | ||||||
chr14:105455262
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.550+952C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455262 | ||||||
chr14:105455312
|
G | A | 1 | a0002c0002t0004g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.550+1002G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455312 | ||||||
chr14:105455345
|
T | A | 249 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.550+1035T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455345 | ||||||
chr14:105455609
|
A | G | 255 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.550+1299A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455609 | ||||||
chr14:105455755
|
C | T | 3 | a0002c0002t0001g0176a0002c0002t0001g0177a0002c0002t0001g0178 | 3 | NA18943.hp2 NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.550+1445C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455755 | ||||||
chr14:105455894
|
C | T | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.550+1584C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455894 | ||||||
chr14:105455954
|
ACTGTGCT others(31): Show |
A | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.550+1682_550+1719d others(40): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr14 | 105455954 | |||||
chr14:105455980
|
T | TGTGGGGA others(202): Show |
1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1674_550+1675i others(211): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr14 | 105455980 | |||||
chr14:105455985
|
A | G | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1675A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455985 | ||||||
chr14:105455991
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0250 | 2 | HG00673.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.550+1681C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455991 | ||||||
chr14:105455992
|
G | A | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1682G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455992 | ||||||
chr14:105456023
|
A | G | 3 | a0003c0004t0001g0049a0003c0004t0001g0050a0003c0008t0001g0046 | 3 | HG03471.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.550+1713A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456023 | ||||||
chr14:105456039
|
G | C | 247 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(244): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.550+1729G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456039 | ||||||
chr14:105456203
|
G | A | 1 | a0002c0002t0001g0101 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.550+1893G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456203 | ||||||
chr14:105456210
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1900C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456210 | ||||||
chr14:105456436
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.551-1834G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456436 | ||||||
chr14:105456537
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.551-1733C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456537 | ||||||
chr14:105456585
|
C | T | 3 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0094 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.551-1685C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456585 | ||||||
chr14:105456726
|
C | G | 251 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(248): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.551-1544C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456726 | ||||||
chr14:105457083
|
A | G | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.551-1187A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457083 | ||||||
chr14:105457548
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.551-722C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457548 | ||||||
chr14:105457563
|
G | T | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.551-707G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457563 | ||||||
chr14:105457604
|
A | C | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.551-666A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457604 | ||||||
chr14:105457634
|
A | G | 1 | a0003c0004t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.551-636A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457634 | ||||||
chr14:105457751
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.551-519C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457751 | ||||||
chr14:105457795
|
G | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0260a0001c0001t0001g0267 | 3 | HG01261.hp2 HG02145.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.551-475G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457795 | ||||||
chr14:105457928
|
A | AAAT | 3 | a0001c0001t0001g0047a0001c0001t0001g0273a0003c0006t0001g0023 | 3 | HG00733.hp2 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.551-319_551-317dup others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr14 | 105457928 | |||||
chr14:105458156
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.551-114C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458156 | ||||||
chr14:105458201
|
G | A | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.551-69G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458201 | ||||||
chr14:105458214
|
G | A | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.551-56G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458214 | ||||||
chr14:105458225
|
C | T | 26 | a0001c0001t0001g0047a0003c0004t0001g0003a0003c0004t0001g0004others(23): Show | 30 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.551-45C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458225 | ||||||
chr14:105458266
|
G | T | 1 | a0001c0001t0001g0272 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.551-4G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458266 | ||||||
chr14:105458375
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02965.hp2 | splice_region_variant&intron_variant | LOW | c.653+3G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458375 | ||||||
chr14:105458449
|
G | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.653+77G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458449 | ||||||
chr14:105458587
|
G | A | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.653+215G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458587 | ||||||
chr14:105458828
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0068others(22): Show | 26 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.653+456C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458828 | ||||||
chr14:105458868
|
C | T | 249 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(246): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.653+496C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458868 | ||||||
chr14:105458888
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.653+516G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458888 | ||||||
chr14:105458898
|
C | G | 2 | a0005c0005t0001g0226a0008c0016t0001g0083 | 2 | NA18989.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.653+526C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458898 | ||||||
chr14:105458928
|
C | A | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.653+556C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458928 | ||||||
chr14:105458963
|
T | C | 8 | a0001c0001t0001g0006a0001c0001t0001g0081a0001c0001t0001g0089others(5): Show | 9 | HG00140.hp1 HG00642.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+591T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458963 | ||||||
chr14:105459008
|
G | T | 2 | a0001c0001t0001g0126a0002c0002t0001g0140 | 2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.653+636G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459008 | ||||||
chr14:105459019
|
CGCTGCCC others(288): Show |
C | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.653+733_654-959del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459019 | |||||
chr14:105459050
|
GGGGAGCT others(111): Show |
G | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.653+733_653+850del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459050 | |||||
chr14:105459105
|
A | G | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+733A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459105 | ||||||
chr14:105459130
|
G | C | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+758G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459130 | ||||||
chr14:105459136
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG01069.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.653+764G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459136 | ||||||
chr14:105459137
|
C | T | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+765C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459137 | ||||||
chr14:105459145
|
G | A | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+773G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459145 | ||||||
chr14:105459145
|
GTGGCCCC others(111): Show |
G | 3 | a0001c0001t0001g0193a0001c0001t0001g0227a0002c0002t0001g0230 | 3 | HG01168.hp2 HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.653+796_653+913del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459145 | |||||
chr14:105459164
|
CCCTAGGG others(406): Show |
C | 243 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(240): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.653+796_654-778del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459164 | |||||
chr14:105459164
|
CCCTAGGG others(524): Show |
C | 1 | a0005c0005t0001g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.653+796_654-660del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459164 | |||||
chr14:105459168
|
A | G | 5 | a0001c0001t0001g0047a0001c0001t0001g0274a0001c0012t0001g0037others(2): Show | 5 | HG00639.hp2 HG03471.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+796A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459168 | ||||||
chr14:105459196
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.653+824T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459196 | ||||||
chr14:105459204
|
A | G | 2 | a0001c0001t0001g0274a0001c0012t0001g0037 | 2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+832A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459204 | ||||||
chr14:105459222
|
C | T | 2 | a0001c0001t0001g0274a0001c0012t0001g0037 | 2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+850C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459222 | ||||||
chr14:105459223
|
G | C | 2 | a0001c0001t0001g0274a0001c0012t0001g0037 | 2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+851G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459223 | ||||||
chr14:105459248
|
C | G | 3 | a0001c0001t0001g0274a0001c0012t0001g0037a0001c0012t0001g0248 | 3 | HG00639.hp2 HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+876C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459248 | ||||||
chr14:105459281
|
T | C | 2 | a0001c0001t0001g0274a0001c0012t0001g0037 | 2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+909T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459281 | ||||||
chr14:105459282
|
C | G | 2 | a0001c0001t0001g0274a0001c0012t0001g0037 | 2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+910C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459282 | ||||||
chr14:105459313
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.653+941G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459313 | ||||||
chr14:105459314
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0227a0002c0002t0001g0230 | 3 | HG01168.hp2 HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.653+942T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459314 | ||||||
chr14:105459322
|
G | A | 3 | a0001c0001t0001g0274a0001c0012t0001g0037a0001c0012t0001g0248 | 3 | HG00639.hp2 HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+950G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459322 | ||||||
chr14:105459340
|
T | C | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.653+968T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459340 | ||||||
chr14:105459341
|
C | G | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.653+969C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459341 | ||||||
chr14:105459366
|
G | A | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-992G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459366 | ||||||
chr14:105459373
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654-985T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459373 | ||||||
chr14:105459400
|
G | A | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-958G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459400 | ||||||
chr14:105459425
|
G | A | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-933G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459425 | ||||||
chr14:105459431
|
G | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0227a0001c0001t0001g0274others(1): Show | 4 | HG01168.hp2 HG01975.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-927G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459431 | ||||||
chr14:105459432
|
T | C | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-926T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459432 | ||||||
chr14:105459440
|
A | G | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-918A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459440 | ||||||
chr14:105459458
|
T | C | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-900T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459458 | ||||||
chr14:105459459
|
C | A | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-899C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459459 | ||||||
chr14:105459459
|
CCCTGGGG others(465): Show |
C | 1 | a0001c0001t0001g0274 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654-874_654-403del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459459 | |||||
chr14:105459491
|
T | C | 5 | a0001c0001t0001g0193a0001c0001t0001g0227a0001c0012t0001g0037others(2): Show | 5 | HG01168.hp2 HG01975.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-867T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459491 | ||||||
chr14:105459499
|
G | A | 3 | a0001c0012t0001g0248a0003c0004t0001g0049a0003c0004t0001g0050 | 3 | HG00639.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.654-859G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459499 | ||||||
chr14:105459517
|
C | T | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-841C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459517 | ||||||
chr14:105459518
|
G | A | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-840G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459518 | ||||||
chr14:105459518
|
G | C | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-840G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459518 | ||||||
chr14:105459518
|
GCCTGGGG others(465): Show |
G | 1 | a0002c0002t0001g0230 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.654-815_654-344del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459518 | |||||
chr14:105459536
|
CTGGGGGC others(524): Show |
C | 2 | a0001c0001t0001g0193a0001c0001t0001g0227 | 2 | HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.654-815_654-285del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459536 | |||||
chr14:105459543
|
C | A | 28 | a0001c0001t0001g0047a0003c0004t0001g0003a0003c0004t0001g0004others(25): Show | 32 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.654-815C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459543 | ||||||
chr14:105459543
|
C | G | 2 | a0001c0012t0001g0037a0001c0017t0001g0044 | 2 | HG03704.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-815C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459543 | ||||||
chr14:105459550
|
T | C | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-808T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459550 | ||||||
chr14:105459558
|
A | G | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-800A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459558 | ||||||
chr14:105459576
|
C | T | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-782C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459576 | ||||||
chr14:105459577
|
A | C | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-781A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459577 | ||||||
chr14:105459577
|
A | G | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-781A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459577 | ||||||
chr14:105459602
|
G | C | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-756G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459602 | ||||||
chr14:105459609
|
C | T | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-749C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459609 | ||||||
chr14:105459617
|
G | A | 3 | a0001c0012t0001g0037a0003c0004t0001g0049a0003c0004t0001g0050 | 3 | HG03579.hp1 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.654-741G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459617 | ||||||
chr14:105459636
|
CCCTGGGG others(229): Show |
C | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.654-682_654-447del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459636 | |||||
chr14:105459661
|
GAGTCCGT others(52): Show |
G | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-664_654-606del others(59): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459661 | |||||
chr14:105459695
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.654-663G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459695 | ||||||
chr14:105459695
|
G | T | 1 | a0002c0002t0001g0103 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.654-663G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459695 | ||||||
chr14:105459713
|
CTGGGGGC others(112): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.654-644_654-526del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459713 | ||||||
chr14:105459720
|
C | G | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.654-638C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459720 | ||||||
chr14:105459726
|
G | A | 241 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.654-632G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459726 | ||||||
chr14:105459726
|
G | C | 1 | a0004c0003t0001g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.654-632G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459726 | ||||||
chr14:105459727
|
T | C | 1 | a0005c0005t0001g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.654-631T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459727 | ||||||
chr14:105459735
|
A | G | 3 | a0001c0012t0001g0037a0003c0008t0001g0046a0005c0005t0001g0145 | 3 | HG03471.hp2 HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-623A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459735 | ||||||
chr14:105459747
|
CCCTGGTC others(118): Show |
C | 1 | a0001c0001t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.654-605_654-481del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459747 | |||||
chr14:105459754
|
CCCTGGGG others(111): Show |
C | 241 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(238): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.654-546_654-429del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459754 | |||||
chr14:105459786
|
T | C | 2 | a0001c0001t0001g0075a0001c0017t0001g0044 | 2 | HG02273.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.654-572T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459786 | ||||||
chr14:105459794
|
G | A | 17 | a0001c0012t0001g0037a0003c0004t0001g0003a0003c0004t0001g0026others(14): Show | 17 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.654-564G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459794 | ||||||
chr14:105459812
|
T | C | 2 | a0001c0012t0001g0037a0005c0005t0001g0145 | 2 | HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-546T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459812 | ||||||
chr14:105459813
|
C | G | 2 | a0001c0012t0001g0037a0005c0005t0001g0145 | 2 | HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-545C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459813 | ||||||
chr14:105459813
|
CCCTGGGG others(52): Show |
C | 2 | a0001c0001t0001g0075a0001c0017t0001g0044 | 2 | HG02273.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.654-505_654-447del others(59): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459813 | |||||
chr14:105459844
|
G | A | 2 | a0001c0001t0001g0170a0005c0005t0001g0145 | 2 | HG00558.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.654-514G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459844 | ||||||
chr14:105459871
|
C | T | 3 | a0001c0001t0001g0170a0001c0012t0001g0037a0005c0005t0001g0145 | 3 | HG00558.hp1 HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-487C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459871 | ||||||
chr14:105459872
|
G | C | 3 | a0001c0001t0001g0170a0001c0012t0001g0037a0005c0005t0001g0145 | 3 | HG00558.hp1 HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-486G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459872 | ||||||
chr14:105459872
|
G | GCCTGGGG others(52): Show |
2 | a0001c0001t0001g0047a0003c0008t0001g0046 | 2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.654-447_654-446ins others(59): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459872 | |||||
chr14:105459897
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.654-461G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459897 | ||||||
chr14:105459904
|
T | C | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.654-454T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459904 | ||||||
chr14:105459971
|
A | G | 4 | a0001c0001t0001g0041a0001c0012t0001g0037a0001c0012t0001g0248others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-387A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459971 | ||||||
chr14:105460030
|
A | G | 17 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0058others(14): Show | 17 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.654-328A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460030 | ||||||
chr14:105460059
|
C | T | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-299C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460059 | ||||||
chr14:105460060
|
G | T | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-298G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460060 | ||||||
chr14:105460067
|
G | C | 277 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.654-291G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460067 | ||||||
chr14:105460177
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.654-181T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460177 | ||||||
chr14:105460197
|
C | T | 4 | a0001c0012t0001g0037a0001c0012t0001g0248a0003c0004t0001g0049others(1): Show | 4 | HG00639.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-161C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460197 | ||||||
chr14:105460264
|
C | T | 4 | a0002c0002t0001g0084a0002c0002t0001g0132a0002c0002t0001g0165others(1): Show | 4 | HG00673.hp1 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-94C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460264 | ||||||
chr14:105460272
|
G | C | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-86G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460272 | ||||||
chr14:105460482
|
G | C | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.753+25G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 9/20 | chr14 | 105460482 | ||||||
chr14:105460972
|
G | A | 1 | a0003c0007t0001g0051 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.942+19G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105460972 | ||||||
chr14:105461014
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.942+61G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461014 | ||||||
chr14:105461096
|
T | C | 44 | a0001c0001t0001g0018a0001c0001t0001g0062a0001c0001t0001g0065others(41): Show | 44 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.942+143T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461096 | ||||||
chr14:105461134
|
A | G | 21 | a0001c0001t0001g0018a0001c0001t0001g0062a0001c0001t0001g0065others(18): Show | 21 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.942+181A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461134 | ||||||
chr14:105461213
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.942+260T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461213 | ||||||
chr14:105461273
|
C | T | 22 | a0001c0001t0001g0071a0001c0001t0001g0129a0001c0001t0001g0130others(19): Show | 22 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.942+320C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461273 | ||||||
chr14:105461346
|
G | A | 1 | a0002c0002t0001g0153 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.942+393G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461346 | ||||||
chr14:105461439
|
G | GGACCCCC others(21): Show |
1 | a0008c0016t0001g0083 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.942+487_942+514dup others(28): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105461439 | |||||
chr14:105461599
|
C | T | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.942+646C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461599 | ||||||
chr14:105461684
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.942+731C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461684 | ||||||
chr14:105461710
|
A | T | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.942+757A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461710 | ||||||
chr14:105461768
|
C | T | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.942+815C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461768 | ||||||
chr14:105462110
|
A | ACGGTCTC others(33): Show |
278 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(275): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.943-1045_943-1044i others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462110 | |||||
chr14:105462110
|
A | ACGGTCTC others(35): Show |
1 | a0005c0005t0001g0226 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.943-1061_943-1060i others(44): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462110 | |||||
chr14:105462110
|
A | ACGGTCTT others(33): Show |
1 | a0001c0001t0001g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.943-1068_943-1067i others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462110 | |||||
chr14:105462110
|
A | ATGGTCTC others(33): Show |
1 | a0003c0004t0001g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.943-1074_943-1073i others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462110 | ||||||
chr14:105462110
|
A | G | 1 | a0005c0005t0001g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.943-1074A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462110 | ||||||
chr14:105462337
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.943-847G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462337 | ||||||
chr14:105462395
|
G | C | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.943-789G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462395 | ||||||
chr14:105462459
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.943-725C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462459 | ||||||
chr14:105462548
|
C | T | 29 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0036others(26): Show | 29 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.943-636C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462548 | ||||||
chr14:105462560
|
ACT | A | 8 | a0003c0004t0001g0004a0003c0006t0001g0002a0003c0006t0001g0022others(5): Show | 12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.943-621_943-620del others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462560 | |||||
chr14:105462594
|
C | T | 1 | a0003c0008t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943-590C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462594 | ||||||
chr14:105462672
|
C | T | 2 | a0002c0002t0001g0238a0005c0005t0001g0161 | 2 | HG00597.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.943-512C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462672 | ||||||
chr14:105462673
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0197 | 3 | HG03491.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.943-511G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462673 | ||||||
chr14:105462726
|
G | A | 1 | a0005c0005t0001g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.943-458G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462726 | ||||||
chr14:105462784
|
G | C | 1 | a0003c0004t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.943-400G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462784 | ||||||
chr14:105462796
|
G | A | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.943-388G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462796 | ||||||
chr14:105462856
|
G | A | 2 | a0003c0006t0001g0028a0003c0014t0001g0025 | 2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.943-328G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462856 | ||||||
chr14:105462863
|
C | CGTCTCAA others(4): Show |
8 | a0001c0001t0001g0015a0001c0001t0001g0087a0001c0001t0001g0228others(5): Show | 9 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.943-312_943-311ins others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462863 | |||||
chr14:105462998
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.943-186C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462998 | ||||||
chr14:105463050
|
C | T | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.943-134C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463050 | ||||||
chr14:105463068
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.943-116C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463068 | ||||||
chr14:105463085
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.943-99C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463085 | ||||||
chr14:105463104
|
G | GCTGCAGC others(11): Show |
1 | a0002c0015t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.943-79_943-78insTG others(16): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105463104 | |||||
chr14:105463106
|
C | T | 239 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(236): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.943-78C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463106 | ||||||
chr14:105463168
|
G | A | 17 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(14): Show | 17 | HG00323.hp2 HG01069.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.943-16G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463168 | ||||||
chr14:105463284
|
C | T | 1 | a0002c0002t0001g0189 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1017+26C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463284 | ||||||
chr14:105463292
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1017+34G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463292 | ||||||
chr14:105463320
|
C | T | 1 | a0001c0012t0001g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1017+62C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463320 | ||||||
chr14:105463408
|
C | T | 32 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0036others(29): Show | 33 | HG00099.hp2 HG01069.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1018-85C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463408 | ||||||
chr14:105463560
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1076+9G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463560 | ||||||
chr14:105463562
|
C | T | 2 | a0001c0001t0001g0278a0001c0017t0001g0044 | 2 | HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1076+11C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463562 | ||||||
chr14:105463628
|
C | CG | 3 | a0003c0006t0001g0022a0003c0009t0001g0024a0004c0003t0001g0208 | 3 | HG00735.hp2 HG02572.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1076+80dupG | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr14 | 105463628 | |||||
chr14:105463634
|
C | T | 1 | a0003c0014t0001g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1076+83C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463634 | ||||||
chr14:105463693
|
A | T | 1 | a0001c0012t0001g0037 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+142A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463693 | ||||||
chr14:105463719
|
G | A | 3 | a0001c0001t0001g0030a0007c0013t0001g0031a0007c0013t0001g0032 | 3 | HG01496.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1076+168G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463719 | ||||||
chr14:105463726
|
C | T | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1076+175C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463726 | ||||||
chr14:105463824
|
G | C | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1077-208G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463824 | ||||||
chr14:105463832
|
C | T | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1077-200C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463832 | ||||||
chr14:105463833
|
G | A | 7 | a0001c0001t0001g0210a0001c0001t0002g0067a0001c0001t0002g0091others(4): Show | 7 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-199G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463833 | ||||||
chr14:105463869
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1077-163T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463869 | ||||||
chr14:105463907
|
G | A | 1 | a0001c0019t0001g0209 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1077-125G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463907 | ||||||
chr14:105463927
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077-105C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463927 | ||||||
chr14:105464190
|
G | A | 1 | a0004c0003t0001g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1192+43G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/20 | chr14 | 105464190 | ||||||
chr14:105464269
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1192+122C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/20 | chr14 | 105464269 | ||||||
chr14:105464280
|
T | C | 1 | a0002c0002t0001g0069 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1192+133T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/20 | chr14 | 105464280 | ||||||
chr14:105464573
|
G | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0278 | 2 | HG03041.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.1344+6G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464573 | ||||||
chr14:105464573
|
G | T | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.1344+6G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464573 | ||||||
chr14:105464586
|
G | A | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1344+19G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464586 | ||||||
chr14:105464616
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1344+49C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464616 | ||||||
chr14:105464632
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1345-42G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464632 | ||||||
chr14:105464641
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1345-33G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464641 | ||||||
chr14:105464978
|
GTCC | G | 18 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0258others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1535-110_1535-108d others(5): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr14 | 105464978 | |||||
chr14:105465044
|
C | T | 1 | a0002c0002t0001g0159 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1535-50C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/20 | chr14 | 105465044 | ||||||
chr14:105465225
|
C | G | 3 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0276 | 3 | HG01261.hp2 HG01981.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1624+42C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465225 | ||||||
chr14:105465247
|
C | T | 1 | a0002c0002t0001g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1624+64C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465247 | ||||||
chr14:105465248
|
A | G | 271 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1624+65A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465248 | ||||||
chr14:105465296
|
C | T | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1624+113C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465296 | ||||||
chr14:105465572
|
A | C | 3 | a0001c0001t0002g0067a0001c0001t0002g0091a0001c0001t0002g0094 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1624+389A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465572 | ||||||
chr14:105465684
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1624+501G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465684 | ||||||
chr14:105465736
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1624+553G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465736 | ||||||
chr14:105466069
|
G | C | 1 | a0003c0004t0001g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1625-357G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466069 | ||||||
chr14:105466119
|
G | A | 173 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0015others(170): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1625-307G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466119 | ||||||
chr14:105466207
|
G | A | 131 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0030others(128): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1625-219G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466207 | ||||||
chr14:105466215
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1625-211C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466215 | ||||||
chr14:105466217
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1625-209C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466217 | ||||||
chr14:105466225
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1625-201C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466225 | ||||||
chr14:105466299
|
C | CAG | 80 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 84 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1625-127_1625-126i others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466299 | ||||||
chr14:105466589
|
CCCCCGCC others(16): Show |
C | 1 | a0002c0002t0001g0143 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1777+27_1777+49del others(23): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr14 | 105466589 | |||||
chr14:105466597
|
C | T | 1 | a0001c0017t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1777+19C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/20 | chr14 | 105466597 | ||||||
chr14:105466757
|
C | T | 27 | a0001c0001t0001g0041a0003c0004t0001g0003a0003c0004t0001g0004others(24): Show | 31 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1813+15C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466757 | ||||||
chr14:105466764
|
G | A | 3 | a0002c0002t0001g0134a0002c0002t0001g0156a0002c0002t0001g0189 | 3 | NA18951.hp1 NA18975.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1813+22G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466764 | ||||||
chr14:105466772
|
C | T | 1 | a0003c0008t0001g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1813+30C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466772 | ||||||
chr14:105466786
|
G | A | 1 | a0002c0002t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1813+44G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466786 | ||||||
chr14:105466822
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1813+80C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466822 | ||||||
chr14:105466954
|
T | C | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+212T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466954 | ||||||
chr14:105467159
|
A | G | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+417A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467159 | ||||||
chr14:105467216
|
C | T | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1813+474C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467216 | ||||||
chr14:105467525
|
C | T | 2 | a0003c0004t0001g0049a0003c0004t0001g0050 | 2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1813+783C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467525 | ||||||
chr14:105467619
|
C | T | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+877C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467619 | ||||||
chr14:105467804
|
C | G | 2 | a0001c0012t0001g0037a0001c0012t0001g0248 | 2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+1062C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467804 | ||||||
chr14:105468051
|
G | T | 20 | a0003c0004t0001g0003a0003c0004t0001g0026a0003c0004t0001g0042others(17): Show | 20 | HG00735.hp2 HG01167.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1813+1309G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468051 | ||||||
chr14:105468121
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0038others(3): Show | 6 | HG02280.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1814-1346C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468121 | ||||||
chr14:105468260
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1814-1207G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468260 | ||||||
chr14:105468265
|
C | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0237a0001c0001t0001g0279 | 3 | HG02451.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1814-1202C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468265 | ||||||
chr14:105468398
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1069T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468398 | ||||||
chr14:105468399
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1068T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468399 | ||||||
chr14:105468406
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1061G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468406 | ||||||
chr14:105468407
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1060G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468407 | ||||||
chr14:105468413
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1054T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468413 | ||||||
chr14:105468414
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1053G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468414 | ||||||
chr14:105468416
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1051G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468416 | ||||||
chr14:105468418
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1049T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468418 | ||||||
chr14:105468420
|
T | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1047T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468420 | ||||||
chr14:105468444
|
G | A | 1 | a0001c0001t0001g0007 | 2 | NA18971.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1814-1023G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468444 | ||||||
chr14:105468444
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1023G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468444 | ||||||
chr14:105468448
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1019A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468448 | ||||||
chr14:105468449
|
T | G | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1018T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468449 | ||||||
chr14:105468451
|
A | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1016A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468451 | ||||||
chr14:105468455
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1012A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468455 | ||||||
chr14:105468457
|
C | G | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1010C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468457 | ||||||
chr14:105468459
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1008G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468459 | ||||||
chr14:105468461
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1006G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468461 | ||||||
chr14:105468462
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1005C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468462 | ||||||
chr14:105468464
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1003C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468464 | ||||||
chr14:105468465
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1002C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468465 | ||||||
chr14:105468466
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1001C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468466 | ||||||
chr14:105468468
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-999C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468468 | ||||||
chr14:105468473
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-994C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468473 | ||||||
chr14:105468475
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-992C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468475 | ||||||
chr14:105468477
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-990G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468477 | ||||||
chr14:105468488
|
C | G | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-979C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468488 | ||||||
chr14:105468494
|
A | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-973A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468494 | ||||||
chr14:105468495
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-972A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468495 | ||||||
chr14:105468496
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-971A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468496 | ||||||
chr14:105468499
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-968G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468499 | ||||||
chr14:105468500
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-967G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468500 | ||||||
chr14:105468507
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-960A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468507 | ||||||
chr14:105468508
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-959A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468508 | ||||||
chr14:105468514
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-953A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468514 | ||||||
chr14:105468515
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-952C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468515 | ||||||
chr14:105468543
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-924C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468543 | ||||||
chr14:105468544
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-923C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468544 | ||||||
chr14:105468548
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-919G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468548 | ||||||
chr14:105468549
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-918G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468549 | ||||||
chr14:105468559
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-908A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468559 | ||||||
chr14:105468561
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-906T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468561 | ||||||
chr14:105468564
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-903G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468564 | ||||||
chr14:105468611
|
T | A | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1814-856T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468611 | ||||||
chr14:105468704
|
A | G | 246 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1814-763A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468704 | ||||||
chr14:105468786
|
A | G | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1814-681A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468786 | ||||||
chr14:105468859
|
G | C | 4 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0210others(1): Show | 4 | NA19003.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814-608G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468859 | ||||||
chr14:105468870
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1814-597G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468870 | ||||||
chr14:105469075
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1814-392G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469075 | ||||||
chr14:105469112
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1814-355G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469112 | ||||||
chr14:105469167
|
GGGTGGAC others(25): Show |
G | 1 | a0005c0005t0001g0220 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1814-298_1814-267d others(34): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr14 | 105469167 | |||||
chr14:105469187
|
T | C | 1 | a0004c0003t0001g0266 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1814-280T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469187 | ||||||
chr14:105469259
|
C | T | 1 | a0002c0002t0001g0178 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1814-208C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469259 | ||||||
chr14:105469287
|
C | T | 2 | a0007c0013t0001g0031a0007c0013t0001g0032 | 2 | HG01496.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1814-180C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469287 | ||||||
chr14:105469384
|
A | G | 279 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1814-83A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469384 | ||||||
chr14:105469416
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1814-51T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469416 | ||||||
chr14:105469523
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1845+25G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469523 | ||||||
chr14:105469670
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1846-171C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469670 | ||||||
chr14:105469714
|
G | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG00544.hp2 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1846-127G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469714 | ||||||
chr14:105469727
|
A | G | 280 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1846-114A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469727 | ||||||
chr14:105469763
|
A | ACCTTGGC others(8): Show |
250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(247): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1846-75_1846-74ins others(15): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr14 | 105469763 | |||||
chr14:105469817
|
C | T | 8 | a0003c0004t0001g0004a0003c0006t0001g0002a0003c0006t0001g0022others(5): Show | 12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1846-24C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469817 | ||||||
chr14:105470015
|
G | A | 1 | a0002c0002t0001g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1997+23G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 20/20 | chr14 | 105470015 | ||||||
chr14:105470036
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0001g0280a0006c0010t0001g0127others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998-29C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 20/20 | chr14 | 105470036 |