Item | Value |
---|---|
geneid | 4547 |
ensemblid | ENSG00000138823.14 |
hgncid | 7467 |
symbol | MTTP |
name | microsomal triglyceride transfer protein |
refseq_nuc | NM_001386140.1 |
refseq_prot | NP_001373069.1 |
ensembl_nuc | ENST00000265517.10 |
ensembl_prot | ENSP00000265517.5 |
mane_status | MANE Select |
chr | chr4 |
start | 99574824 |
end | 99623997 |
strand | + |
ver | v1.2 |
region | chr4:99574824-99623997 |
region5000 | chr4:99569824-99628997 |
regionname0 | MTTP_chr4_99574824_99623997 |
regionname5000 | MTTP_chr4_99569824_99628997 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 894 | 101 | 26 | 8 | 62 | 0 | 5 | 49 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002 | 1/1 | 894 | 80 | 6 | 21 | 32 | 6 | 13 | 25 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0003 | 0/0 | 894 | 66 | 12 | 5 | 48 | 0 | 1 | 42 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0004 | 0/0 | 894 | 43 | 5 | 5 | 28 | 0 | 5 | 24 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0005 | 0/0 | 894 | 21 | 18 | 1 | 0 | 0 | 2 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0006 | 0/0 | 894 | 18 | 6 | 6 | 1 | 0 | 5 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0007 | 0/0 | 894 | 9 | 4 | 5 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0008 | 0/0 | 894 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0009 | 0/0 | 894 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0010 | 0/0 | 894 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0011 | 0/0 | 894 | 3 | 0 | 1 | 1 | 0 | 1 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0012 | 0/0 | 894 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0013 | 0/0 | 894 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0014 | 0/0 | 894 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0015 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0016 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0017 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0018 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0019 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0020 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2685 | 101 | 26 | 8 | 62 | 0 | 5 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0002 | 1/1 | 2685 | 75 | 4 | 20 | 32 | 6 | 11 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0003 | 0/0 | 2685 | 66 | 12 | 5 | 48 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0004 | 0/0 | 2685 | 42 | 5 | 5 | 28 | 0 | 4 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0005 | 0/0 | 2685 | 21 | 18 | 1 | 0 | 0 | 2 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0006 | 0/0 | 2685 | 18 | 6 | 6 | 1 | 0 | 5 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0007 | 0/0 | 2685 | 9 | 4 | 5 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0008 | 0/0 | 2685 | 4 | 4 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0009 | 0/0 | 2685 | 3 | 0 | 3 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0010 | 0/0 | 2685 | 3 | 0 | 1 | 1 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0011 | 0/0 | 2685 | 3 | 3 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0012 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0013 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0014 | 0/0 | 2685 | 2 | 1 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0015 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0016 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0017 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0018 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0019 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0020 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0021 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0022 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0023 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0024 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0025 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0026 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
c0027 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1236 | 242 | 71 | 21 | 135 | 0 | 15 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0002 | 1/1 | 1236 | 77 | 3 | 21 | 32 | 6 | 13 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0003 | 0/0 | 1233 | 13 | 8 | 5 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0004 | 0/0 | 1234 | 10 | 0 | 3 | 1 | 0 | 6 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0005 | 0/0 | 1234 | 4 | 2 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0006 | 0/0 | 1237 | 3 | 0 | 3 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0007 | 0/0 | 1233 | 3 | 3 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0008 | 0/0 | 1236 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0009 | 0/0 | 1237 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0010 | 0/0 | 1236 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0011 | 0/0 | 1236 | 2 | 1 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0012 | 0/0 | 1237 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0013 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0014 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
t0015 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0002 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2685 | 101 | 26 | 8 | 62 | 0 | 5 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0002c0002 | 1/1 | 2685 | 75 | 4 | 20 | 32 | 6 | 11 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0002c0014 | 0/0 | 2685 | 2 | 1 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0002c0017 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0002c0021 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0002c0023 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0003c0003 | 0/0 | 2685 | 66 | 12 | 5 | 48 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0004c0004 | 0/0 | 2685 | 42 | 5 | 5 | 28 | 0 | 4 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0004c0026 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0005c0005 | 0/0 | 2685 | 21 | 18 | 1 | 0 | 0 | 2 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0006c0006 | 0/0 | 2685 | 18 | 6 | 6 | 1 | 0 | 5 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0007c0007 | 0/0 | 2685 | 9 | 4 | 5 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0008c0008 | 0/0 | 2685 | 4 | 4 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0009c0012 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0009c0015 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0010c0011 | 0/0 | 2685 | 3 | 3 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0011c0010 | 0/0 | 2685 | 3 | 0 | 1 | 1 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0012c0009 | 0/0 | 2685 | 3 | 0 | 3 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0013c0013 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0014c0018 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0014c0019 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0015c0027 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0016c0016 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0017c0025 | 0/0 | 2685 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0018c0024 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0019c0022 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 | |
a0020c0020 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3920 | 100 | 26 | 8 | 61 | 0 | 5 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0001c0001t0009 | 0/0 | 3921 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002c0002t0002 | 1/1 | 3920 | 73 | 3 | 20 | 31 | 6 | 11 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002c0002t0012 | 0/0 | 3921 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002c0002t0013 | 0/0 | 3920 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002c0014t0001 | 0/0 | 3920 | 2 | 1 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002c0017t0002 | 0/0 | 3920 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002c0021t0001 | 0/0 | 3920 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0002c0023t0002 | 0/0 | 3920 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0003c0003t0001 | 0/0 | 3920 | 63 | 10 | 5 | 47 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0003c0003t0009 | 0/0 | 3921 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0003c0003t0010 | 0/0 | 3920 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0004c0004t0001 | 0/0 | 3920 | 38 | 4 | 4 | 26 | 0 | 4 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0004c0004t0008 | 0/0 | 3920 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0004c0004t0011 | 0/0 | 3920 | 2 | 1 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0004c0026t0001 | 0/0 | 3920 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0005c0005t0001 | 0/0 | 3920 | 21 | 18 | 1 | 0 | 0 | 2 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0006c0006t0001 | 0/0 | 3920 | 5 | 4 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0006c0006t0004 | 0/0 | 3918 | 9 | 0 | 3 | 1 | 0 | 5 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0006c0006t0005 | 0/0 | 3918 | 4 | 2 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0007c0007t0003 | 0/0 | 3917 | 9 | 4 | 5 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0008c0008t0001 | 0/0 | 3920 | 4 | 4 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0009c0012t0007 | 0/0 | 3917 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0009c0015t0007 | 0/0 | 3917 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0010c0011t0003 | 0/0 | 3917 | 3 | 3 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0011c0010t0001 | 0/0 | 3920 | 2 | 0 | 1 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0011c0010t0015 | 0/0 | 3920 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0012c0009t0006 | 0/0 | 3921 | 3 | 0 | 3 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0013c0013t0001 | 0/0 | 3920 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0014c0018t0003 | 0/0 | 3917 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0014c0019t0014 | 0/0 | 3920 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0015c0027t0001 | 0/0 | 3920 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0016c0016t0001 | 0/0 | 3920 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0017c0025t0002 | 0/0 | 3920 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0018c0024t0002 | 0/0 | 3920 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0019c0022t0001 | 0/0 | 3920 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
a0020c0020t0004 | 0/0 | 3918 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | copy fasta | chr4 | 99569824 | 99628997 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0281 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0002t0013g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0014t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0014t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0017t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0021t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0002c0023t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0002 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0009g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0003c0003t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0008g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0004t0011g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0004c0026t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0005c0005t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0005g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0006c0006t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0007c0007t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0008c0008t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0008c0008t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0008c0008t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0008c0008t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0009c0012t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0009c0012t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0009c0015t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0010c0011t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0010c0011t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0010c0011t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0011c0010t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0011c0010t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0011c0010t0015g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0012c0009t0006g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0012c0009t0006g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0012c0009t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0013c0013t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0013c0013t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0014c0018t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0014c0019t0014g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0015c0027t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0016c0016t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0017c0025t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0018c0024t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0019c0022t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
a0020c0020t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0002 | t0002 | g0296 | EUR | FIN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0300 | EUR | FIN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0204 | EUR | FIN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0205 | EUR | FIN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00544 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00558 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | CHS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00639 | hp1 | a0012 | c0009 | t0006 | g0321 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00639 | hp2 | a0007 | c0007 | t0003 | g0312 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00642 | hp1 | a0004 | c0004 | t0001 | g0053 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0298 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00733 | hp1 | a0003 | c0003 | t0001 | g0145 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00733 | hp2 | a0007 | c0007 | t0003 | g0311 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00735 | hp1 | a0002 | c0014 | t0001 | g0092 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00735 | hp2 | a0006 | c0006 | t0001 | g0307 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00741 | hp1 | a0004 | c0004 | t0011 | g0027 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0280 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01070 | hp1 | a0003 | c0003 | t0001 | g0164 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01070 | hp2 | a0006 | c0006 | t0005 | g0009 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01071 | hp2 | a0006 | c0006 | t0005 | g0009 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01074 | hp1 | a0011 | c0010 | t0001 | g0023 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0286 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0285 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01106 | hp2 | a0004 | c0004 | t0001 | g0057 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0193 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01167 | hp1 | a0004 | c0004 | t0001 | g0052 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0301 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01192 | hp1 | a0005 | c0005 | t0001 | g0120 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0284 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01256 | hp1 | a0007 | c0007 | t0003 | g0310 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01256 | hp2 | a0006 | c0006 | t0004 | g0075 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01257 | hp2 | a0012 | c0009 | t0006 | g0322 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01258 | hp1 | a0007 | c0007 | t0003 | g0309 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0272 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0282 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01361 | hp1 | a0006 | c0006 | t0004 | g0062 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01361 | hp2 | a0012 | c0009 | t0006 | g0323 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0290 | EUR | IBS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0291 | EUR | IBS | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01884 | hp2 | a0005 | c0005 | t0001 | g0013 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01891 | hp1 | a0002 | c0002 | t0012 | g0201 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01934 | hp1 | a0004 | c0004 | t0001 | g0049 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01975 | hp1 | a0003 | c0003 | t0001 | g0146 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01978 | hp2 | a0017 | c0025 | t0002 | g0277 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0276 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0274 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02015 | hp1 | a0004 | c0004 | t0001 | g0064 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02027 | hp2 | a0004 | c0004 | t0001 | g0043 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02040 | hp2 | a0004 | c0004 | t0001 | g0056 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02055 | hp2 | a0005 | c0005 | t0001 | g0132 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02056 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02145 | hp1 | a0002 | c0021 | t0001 | g0091 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02145 | hp2 | a0013 | c0013 | t0001 | g0144 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0271 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02148 | hp2 | a0006 | c0006 | t0004 | g0045 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0275 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02257 | hp2 | a0010 | c0011 | t0003 | g0302 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02258 | hp2 | a0004 | c0004 | t0011 | g0065 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0158 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02280 | hp1 | a0008 | c0008 | t0001 | g0054 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02280 | hp2 | a0010 | c0011 | t0003 | g0261 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0195 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02300 | hp2 | a0007 | c0007 | t0003 | g0317 | AMR | PEL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02451 | hp1 | a0014 | c0019 | t0014 | g0319 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02451 | hp2 | a0005 | c0005 | t0001 | g0013 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02602 | hp1 | a0005 | c0005 | t0001 | g0122 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02615 | hp2 | a0009 | c0015 | t0007 | g0022 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02647 | hp1 | a0003 | c0003 | t0010 | g0171 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02647 | hp2 | a0005 | c0005 | t0001 | g0105 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02717 | hp1 | a0005 | c0005 | t0001 | g0083 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02717 | hp2 | a0005 | c0005 | t0001 | g0104 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0190 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02723 | hp2 | a0003 | c0003 | t0010 | g0173 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0203 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02735 | hp2 | a0006 | c0006 | t0004 | g0068 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02738 | hp2 | a0006 | c0006 | t0004 | g0024 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02809 | hp2 | a0003 | c0003 | t0001 | g0152 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02818 | hp1 | a0004 | c0004 | t0001 | g0034 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02818 | hp2 | a0005 | c0005 | t0001 | g0131 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02886 | hp1 | a0005 | c0005 | t0001 | g0134 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02895 | hp1 | a0005 | c0005 | t0001 | g0135 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02895 | hp2 | a0007 | c0007 | t0003 | g0313 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02896 | hp1 | a0006 | c0006 | t0001 | g0070 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02896 | hp2 | a0010 | c0011 | t0003 | g0260 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02897 | hp1 | a0005 | c0005 | t0001 | g0129 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02897 | hp2 | a0006 | c0006 | t0001 | g0076 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02922 | hp2 | a0007 | c0007 | t0003 | g0315 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02970 | hp1 | a0005 | c0005 | t0001 | g0136 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02970 | hp2 | a0004 | c0004 | t0001 | g0308 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02976 | hp1 | a0005 | c0005 | t0001 | g0130 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02976 | hp2 | a0013 | c0013 | t0001 | g0169 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03017 | hp1 | a0005 | c0005 | t0001 | g0124 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03017 | hp2 | a0002 | c0023 | t0002 | g0188 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0165 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03098 | hp1 | a0006 | c0006 | t0005 | g0078 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0138 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03130 | hp2 | a0006 | c0006 | t0001 | g0060 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03139 | hp2 | a0009 | c0012 | t0007 | g0318 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03195 | hp1 | a0006 | c0006 | t0005 | g0079 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0087 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03209 | hp1 | a0007 | c0007 | t0003 | g0314 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03209 | hp2 | a0005 | c0005 | t0001 | g0106 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03225 | hp1 | a0008 | c0008 | t0001 | g0048 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03225 | hp2 | a0002 | c0014 | t0001 | g0206 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03453 | hp2 | a0004 | c0004 | t0001 | g0035 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03486 | hp1 | a0003 | c0003 | t0001 | g0088 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03490 | hp2 | a0004 | c0004 | t0001 | g0073 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03491 | hp1 | a0006 | c0006 | t0004 | g0008 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0279 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03492 | hp1 | a0006 | c0006 | t0004 | g0008 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03516 | hp1 | a0004 | c0004 | t0001 | g0306 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03540 | hp2 | a0005 | c0005 | t0001 | g0137 | AFR | GWD | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03579 | hp1 | a0003 | c0003 | t0001 | g0170 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03579 | hp2 | a0019 | c0022 | t0001 | g0080 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0089 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03654 | hp2 | a0004 | c0004 | t0001 | g0046 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03688 | hp1 | a0004 | c0004 | t0001 | g0032 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03688 | hp2 | a0002 | c0017 | t0002 | g0179 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03704 | hp1 | a0006 | c0006 | t0004 | g0063 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03704 | hp2 | a0003 | c0003 | t0001 | g0265 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0297 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03834 | hp2 | a0020 | c0020 | t0004 | g0069 | SAS | BEB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0174 | SAS | BEB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0191 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04115 | hp2 | a0004 | c0026 | t0001 | g0033 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04184 | hp1 | a0004 | c0004 | t0001 | g0028 | SAS | BEB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0293 | SAS | BEB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0180 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04204 | hp2 | a0015 | c0027 | t0001 | g0074 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04228 | hp1 | a0011 | c0010 | t0001 | g0071 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0021 | SAS | STU | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0108 | EAS | CHB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18906 | hp2 | a0005 | c0005 | t0001 | g0133 | AFR | YRI | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18939 | hp1 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18940 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0126 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18941 | hp2 | a0018 | c0024 | t0002 | g0202 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18944 | hp2 | a0004 | c0004 | t0001 | g0039 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18946 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18948 | hp1 | a0004 | c0004 | t0008 | g0029 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18948 | hp2 | a0002 | c0002 | t0013 | g0207 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18949 | hp1 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0168 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18956 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18960 | hp1 | a0003 | c0003 | t0001 | g0262 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18960 | hp2 | a0004 | c0004 | t0001 | g0040 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18961 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18965 | hp1 | a0004 | c0004 | t0001 | g0058 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18965 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18967 | hp2 | a0004 | c0004 | t0001 | g0047 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18969 | hp1 | a0004 | c0004 | t0001 | g0050 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18972 | hp1 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18973 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18975 | hp1 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18975 | hp2 | a0004 | c0004 | t0001 | g0077 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18978 | hp1 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18979 | hp1 | a0004 | c0004 | t0001 | g0037 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18982 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18986 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18987 | hp1 | a0006 | c0006 | t0004 | g0036 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18987 | hp2 | a0003 | c0003 | t0001 | g0268 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18991 | hp2 | a0004 | c0004 | t0001 | g0026 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18994 | hp1 | a0001 | c0001 | t0009 | g0221 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18994 | hp2 | a0004 | c0004 | t0001 | g0044 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19001 | hp1 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19003 | hp1 | a0004 | c0004 | t0001 | g0059 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19004 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19005 | hp1 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19010 | hp2 | a0004 | c0004 | t0001 | g0031 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19011 | hp2 | a0003 | c0003 | t0001 | g0086 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19012 | hp2 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19030 | hp1 | a0008 | c0008 | t0001 | g0055 | AFR | LWK | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19043 | hp1 | a0014 | c0018 | t0003 | g0320 | AFR | LWK | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19043 | hp2 | a0007 | c0007 | t0003 | g0316 | AFR | LWK | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19054 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19056 | hp1 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19058 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19060 | hp1 | a0004 | c0004 | t0001 | g0041 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19062 | hp1 | a0004 | c0004 | t0001 | g0030 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19065 | hp1 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19066 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19068 | hp1 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19075 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19077 | hp1 | a0003 | c0003 | t0001 | g0267 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19077 | hp2 | a0004 | c0004 | t0001 | g0051 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19078 | hp2 | a0016 | c0016 | t0001 | g0266 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19080 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19080 | hp2 | a0004 | c0004 | t0001 | g0007 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19081 | hp1 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19083 | hp2 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19086 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19087 | hp1 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19088 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19089 | hp2 | a0003 | c0003 | t0009 | g0125 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19090 | hp1 | a0004 | c0004 | t0001 | g0038 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19090 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19091 | hp1 | a0004 | c0004 | t0001 | g0066 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA19091 | hp2 | a0011 | c0010 | t0015 | g0072 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ASW | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA20129 | hp2 | a0005 | c0005 | t0001 | g0123 | AFR | ASW | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0299 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02109 | hp1 | a0003 | c0003 | t0001 | g0147 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02109 | hp2 | a0008 | c0008 | t0001 | g0067 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0148 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0128 | AFR | ACB | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03471 | hp1 | a0003 | c0003 | t0001 | g0085 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG03471 | hp2 | a0005 | c0005 | t0001 | g0263 | AFR | MSL | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG06807 | hp1 | a0006 | c0006 | t0001 | g0061 | AFR | USA | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
HG06807 | hp2 | a0009 | c0012 | t0007 | g0022 | AFR | USA | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18955 | hp1 | a0004 | c0004 | t0008 | g0025 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA20300 | hp1 | a0005 | c0005 | t0001 | g0121 | AFR | USA | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | USA | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA21309 | hp1 | a0003 | c0003 | t0001 | g0166 | AFR | LWK | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0281 | REF | REF | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0283 | REF | REF | MTTP_chr4_99569824_99628997 | MTTP | chr4 | 99569824 | 99628997 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99581979 | C | G | 1 | a0015 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.136C>G | p.Arg46Gly | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 2/18 | 222/3920 | 136/2685 | 46/894 | chr4 | 99581979 | ||
chr4:99583409 | G | C | 2 | a0007a0009 | 12 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(9): Show |
missense_variant | MODERATE | c.285G>C | p.Gln95His | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/18 | 371/3920 | 285/2685 | 95/894 | chr4 | 99583409 | ||
chr4:99583418 | G | C | 3 | a0003a0013a0016 | 69 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(66): Show |
missense_variant | MODERATE | c.294G>C | p.Glu98Asp | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/18 | 380/3920 | 294/2685 | 98/894 | chr4 | 99583418 | ||
chr4:99583507 | T | C | 10 | a0004a0006a0007others(7): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
missense_variant | MODERATE | c.383T>C | p.Ile128Thr | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/18 | 469/3920 | 383/2685 | 128/894 | chr4 | 99583507 | ||
chr4:99589739 | A | G | 1 | a0020 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.490A>G | p.Thr164Ala | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/18 | 576/3920 | 490/2685 | 164/894 | chr4 | 99589739 | ||
chr4:99589746 | A | G | 3 | a0003a0016a0019 | 68 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(65): Show |
missense_variant | MODERATE | c.497A>G | p.Asn166Ser | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/18 | 583/3920 | 497/2685 | 166/894 | chr4 | 99589746 | ||
chr4:99591235 | G | A | 1 | a0011 | 3 | HG01074.hp1 HG04228.hp1 NA19091.hp2 |
missense_variant&splice_region_variant | MODERATE | c.502G>A | p.Val168Ile | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 5/18 | 588/3920 | 502/2685 | 168/894 | chr4 | 99591235 | ||
chr4:99591679 | C | T | 1 | a0017 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.647C>T | p.Ser216Phe | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/18 | 733/3920 | 647/2685 | 216/894 | chr4 | 99591679 | ||
chr4:99591762 | C | G | 3 | a0009a0010a0014 | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
missense_variant | MODERATE | c.730C>G | p.Gln244Glu | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/18 | 816/3920 | 730/2685 | 244/894 | chr4 | 99591762 | ||
chr4:99594865 | C | G | 13 | a0001a0003a0005others(10): Show | 231 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(228): Show |
missense_variant | MODERATE | c.891C>G | p.His297Gln | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/18 | 977/3920 | 891/2685 | 297/894 | chr4 | 99594865 | ||
chr4:99600571 | G | C | 1 | a0018 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.1074G>C | p.Gln358His | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/18 | 1160/3920 | 1074/2685 | 358/894 | chr4 | 99600571 | ||
chr4:99600648 | A | C | 1 | a0005 | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
missense_variant | MODERATE | c.1151A>C | p.Asp384Ala | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/18 | 1237/3920 | 1151/2685 | 384/894 | chr4 | 99600648 | ||
chr4:99600708 | A | G | 1 | a0016 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.1211A>G | p.Asn404Ser | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/18 | 1297/3920 | 1211/2685 | 404/894 | chr4 | 99600708 | ||
chr4:99611445 | G | A | 1 | a0012 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
missense_variant | MODERATE | c.1981G>A | p.Gly661Ser | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/18 | 2067/3920 | 1981/2685 | 661/894 | chr4 | 99611445 | ||
chr4:99622799 | A | G | 1 | a0008 | 4 | HG02109.hp2 HG02280.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.2636A>G | p.Lys879Arg | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 2722/3920 | 2636/2685 | 879/894 | chr4 | 99622799 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99574948 | C | G | 1 | a0005c0005 | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
synonymous_variant | LOW | c.39C>G | p.Ser13Ser | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/18 | 125/3920 | 39/2685 | 13/894 | chr4 | 99574948 | ||
chr4:99581987 | A | G | 1 | a0004c0026 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.144A>G | p.Lys48Lys | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 2/18 | 230/3920 | 144/2685 | 48/894 | chr4 | 99581987 | ||
chr4:99583493 | G | A | 1 | a0002c0017 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.369G>A | p.Thr123Thr | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/18 | 455/3920 | 369/2685 | 123/894 | chr4 | 99583493 | ||
chr4:99589702 | T | C | 17 | a0001c0001a0002c0014a0002c0021others(14): Show | 234 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
synonymous_variant | LOW | c.453T>C | p.Gly151Gly | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/18 | 539/3920 | 453/2685 | 151/894 | chr4 | 99589702 | ||
chr4:99591255 | T | C | 5 | a0003c0003a0006c0006a0016c0016others(2): Show | 87 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(84): Show |
synonymous_variant | LOW | c.522T>C | p.Cys174Cys | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 5/18 | 608/3920 | 522/2685 | 174/894 | chr4 | 99591255 | ||
chr4:99591692 | T | C | 1 | a0012c0009 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
synonymous_variant | LOW | c.660T>C | p.Tyr220Tyr | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/18 | 746/3920 | 660/2685 | 220/894 | chr4 | 99591692 | ||
chr4:99597072 | G | A | 1 | a0002c0023 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.915G>A | p.Ser305Ser | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/18 | 1001/3920 | 915/2685 | 305/894 | chr4 | 99597072 | ||
chr4:99597090 | C | A | 1 | a0005c0005 | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
synonymous_variant | LOW | c.933C>A | p.Thr311Thr | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/18 | 1019/3920 | 933/2685 | 311/894 | chr4 | 99597090 | ||
chr4:99597126 | T | C | 7 | a0007c0007a0009c0012a0009c0015others(4): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
synonymous_variant | LOW | c.969T>C | p.Ala323Ala | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/18 | 1055/3920 | 969/2685 | 323/894 | chr4 | 99597126 | ||
chr4:99597129 | G | A | 1 | a0002c0021 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.972G>A | p.Glu324Glu | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/18 | 1058/3920 | 972/2685 | 324/894 | chr4 | 99597129 | ||
chr4:99597180 | A | G | 1 | a0014c0019 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1023A>G | p.Lys341Lys | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/18 | 1109/3920 | 1023/2685 | 341/894 | chr4 | 99597180 | ||
chr4:99612966 | G | A | 1 | a0009c0012 | 2 | HG03139.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.2043G>A | p.Glu681Glu | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/18 | 2129/3920 | 2043/2685 | 681/894 | chr4 | 99612966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99574889 | A | C | 1 | a0011c0010t0015 | 1 | NA19091.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/18 | 21 | chr4 | 99574889 | |||||
chr4:99622961 | G | C | 1 | a0012c0009t0006 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*113G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 113 | chr4 | 99622961 | |||||
chr4:99623031 | C | T | 6 | a0007c0007t0003a0009c0012t0007a0009c0015t0007others(3): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*183C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 183 | chr4 | 99623031 | |||||
chr4:99623032 | G | A | 1 | a0004c0004t0008 | 2 | NA18948.hp1 NA18955.hp1 |
3_prime_UTR_variant | MODIFIER | c.*184G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 184 | chr4 | 99623032 | |||||
chr4:99623115 | A | C | 1 | a0006c0006t0005 | 4 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*267A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 267 | chr4 | 99623115 | |||||
chr4:99623127 | C | G | 1 | a0004c0004t0011 | 2 | HG00741.hp1 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*279C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 279 | chr4 | 99623127 | |||||
chr4:99623283 | G | GA | 4 | a0001c0001t0009a0002c0002t0012a0003c0003t0009others(1): Show | 6 | HG00639.hp1 HG01257.hp2 HG01361.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*454dupA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 455 | INFO_REALIGN_3_PRIME | chr4 | 99623283 | ||||
chr4:99623283 | GAA | G | 3 | a0006c0006t0004a0006c0006t0005a0020c0020t0004 | 14 | HG01070.hp2 HG01071.hp2 HG01256.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*453_*454delAA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 453 | INFO_REALIGN_3_PRIME | chr4 | 99623283 | ||||
chr4:99623283 | GAAA | G | 5 | a0007c0007t0003a0009c0012t0007a0009c0015t0007others(2): Show | 16 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*452_*454delAAA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 452 | INFO_REALIGN_3_PRIME | chr4 | 99623283 | ||||
chr4:99623354 | A | G | 6 | a0007c0007t0003a0009c0012t0007a0009c0015t0007others(3): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*506A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 506 | chr4 | 99623354 | |||||
chr4:99623436 | A | G | 2 | a0009c0012t0007a0009c0015t0007 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*588A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 588 | chr4 | 99623436 | |||||
chr4:99623644 | C | T | 1 | a0003c0003t0010 | 2 | HG02647.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*796C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 796 | chr4 | 99623644 | |||||
chr4:99623710 | C | A | 6 | a0007c0007t0003a0009c0012t0007a0009c0015t0007others(3): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*862C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 862 | chr4 | 99623710 | |||||
chr4:99623894 | C | G | 30 | a0001c0001t0001a0001c0001t0009a0002c0014t0001others(27): Show | 285 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1046C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 1046 | chr4 | 99623894 | |||||
chr4:99623966 | C | T | 1 | a0002c0002t0013 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 18/18 | 1118 | chr4 | 99623966 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99575104 | CTT | C | 61 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(58): Show | 67 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.61+136_61+137delTT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99575104 | |||||
chr4:99575107 | T | C | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.61+137T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99575107 | ||||||
chr4:99575347 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.61+377T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99575347 | ||||||
chr4:99575734 | C | G | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+764C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99575734 | ||||||
chr4:99575906 | A | C | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+936A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99575906 | ||||||
chr4:99575991 | G | A | 1 | a0011c0010t0001g0023 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.61+1021G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99575991 | ||||||
chr4:99576015 | T | G | 1 | a0006c0006t0004g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.61+1045T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576015 | ||||||
chr4:99576030 | T | C | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+1060T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576030 | ||||||
chr4:99576161 | GAGA | G | 3 | a0006c0006t0005g0009a0006c0006t0005g0078a0006c0006t0005g0079 | 4 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+1198_61+1200del others(3): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99576161 | |||||
chr4:99576288 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.61+1318A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576288 | ||||||
chr4:99576421 | C | T | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+1451C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576421 | ||||||
chr4:99576470 | C | T | 1 | a0004c0004t0001g0077 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.61+1500C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576470 | ||||||
chr4:99576472 | G | A | 1 | a0002c0002t0002g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61+1502G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576472 | ||||||
chr4:99576502 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.61+1532C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576502 | ||||||
chr4:99576597 | C | A | 82 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(79): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.61+1627C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576597 | ||||||
chr4:99576643 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.61+1673C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576643 | ||||||
chr4:99576675 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.61+1705A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99576675 | ||||||
chr4:99576694 | C | CA | 178 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0093others(175): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.61+1748dupA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99576694 | |||||
chr4:99576694 | C | CAA | 32 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0014t0001g0092others(29): Show | 33 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.61+1747_61+1748dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99576694 | |||||
chr4:99577185 | A | G | 1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61+2215A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577185 | ||||||
chr4:99577265 | G | A | 1 | a0002c0002t0013g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.61+2295G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577265 | ||||||
chr4:99577441 | G | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(245): Show | 283 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(280): Show |
intron_variant | MODIFIER | c.61+2471G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577441 | ||||||
chr4:99577488 | C | G | 1 | a0014c0018t0003g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.61+2518C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577488 | ||||||
chr4:99577605 | C | CA | 14 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(11): Show | 15 | HG01106.hp1 HG01123.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.61+2652dupA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99577605 | |||||
chr4:99577605 | C | CAA | 8 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | HG02451.hp1 HG02602.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+2651_61+2652dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99577605 | |||||
chr4:99577605 | C | CAAA | 53 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(50): Show | 59 | HG00544.hp1 HG00642.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.61+2650_61+2652dup others(3): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99577605 | |||||
chr4:99577605 | C | CAAAA | 7 | a0004c0004t0001g0034a0004c0004t0001g0035a0004c0004t0001g0037others(4): Show | 7 | HG01256.hp2 HG02818.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+2649_61+2652dup others(4): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99577605 | |||||
chr4:99577605 | CA | C | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(25): Show | 30 | HG00323.hp1 HG00323.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.61+2652delA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99577605 | |||||
chr4:99577605 | CAA | C | 69 | a0002c0014t0001g0092a0002c0014t0001g0206a0002c0021t0001g0091others(66): Show | 81 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.61+2651_61+2652del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99577605 | |||||
chr4:99577618 | AAAAAG | A | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+2652_61+2656del others(5): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99577618 | |||||
chr4:99577620 | A | G | 1 | a0012c0009t0006g0323 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.61+2650A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577620 | ||||||
chr4:99577622 | AG | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 10 | HG01192.hp2 HG01257.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+2653delG | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577622 | ||||||
chr4:99577623 | G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(128): Show | 152 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.61+2653G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577623 | ||||||
chr4:99577833 | A | G | 1 | a0002c0002t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.61+2863A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577833 | ||||||
chr4:99577881 | C | A | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+2911C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577881 | ||||||
chr4:99577976 | C | G | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+3006C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99577976 | ||||||
chr4:99578179 | A | C | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.61+3209A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578179 | ||||||
chr4:99578321 | A | G | 58 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(55): Show | 69 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.61+3351A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578321 | ||||||
chr4:99578396 | T | C | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.61+3426T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578396 | ||||||
chr4:99578513 | T | A | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-3392T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578513 | ||||||
chr4:99578530 | T | A | 3 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-3375T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578530 | ||||||
chr4:99578790 | T | C | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.62-3115T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578790 | ||||||
chr4:99578816 | G | A | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-3089G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578816 | ||||||
chr4:99578945 | A | G | 1 | a0007c0007t0003g0317 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.62-2960A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578945 | ||||||
chr4:99578973 | C | T | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-2932C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99578973 | ||||||
chr4:99579311 | G | A | 5 | a0004c0004t0001g0034a0004c0004t0001g0035a0011c0010t0001g0023others(2): Show | 5 | HG01074.hp1 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-2594G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579311 | ||||||
chr4:99579483 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.62-2422G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579483 | ||||||
chr4:99579541 | C | G | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-2364C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579541 | ||||||
chr4:99579618 | C | T | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-2287C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579618 | ||||||
chr4:99579820 | T | C | 3 | a0006c0006t0005g0009a0006c0006t0005g0078a0006c0006t0005g0079 | 4 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-2085T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579820 | ||||||
chr4:99579822 | G | A | 1 | a0002c0002t0002g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.62-2083G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579822 | ||||||
chr4:99579874 | C | T | 1 | a0011c0010t0001g0023 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.62-2031C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579874 | ||||||
chr4:99579984 | C | T | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.62-1921C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99579984 | ||||||
chr4:99580035 | C | CA | 13 | a0001c0001t0001g0098a0001c0001t0001g0208a0001c0001t0001g0213others(10): Show | 14 | HG01070.hp2 HG01071.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.62-1849dupA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580035 | |||||
chr4:99580035 | CA | C | 48 | a0001c0001t0001g0119a0001c0001t0001g0250a0001c0001t0001g0251others(45): Show | 49 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.62-1849delA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580035 | |||||
chr4:99580075 | A | G | 1 | a0005c0005t0001g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.62-1830A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580075 | ||||||
chr4:99580296 | C | G | 1 | a0006c0006t0004g0075 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.62-1609C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580296 | ||||||
chr4:99580306 | G | A | 1 | a0005c0005t0001g0130 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.62-1599G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580306 | ||||||
chr4:99580435 | C | T | 69 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(66): Show | 75 | HG00544.hp1 HG00642.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.62-1470C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580435 | ||||||
chr4:99580533 | T | C | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-1372T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580533 | ||||||
chr4:99580574 | C | CA | 65 | a0002c0002t0002g0090a0002c0002t0002g0174a0002c0002t0002g0180others(62): Show | 71 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.62-1305dupA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAA | 18 | a0001c0001t0001g0259a0002c0002t0002g0089a0002c0017t0002g0179others(15): Show | 18 | HG00741.hp1 HG01192.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.62-1306_62-1305dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAA | 10 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(7): Show | 10 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-1307_62-1305dup others(3): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-1314_62-1305dup others(10): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.62-1319_62-1305dup others(15): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.62-1322_62-1305dup others(18): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0114a0001c0001t0001g0210a0001c0001t0001g0212others(1): Show | 4 | HG02083.hp1 HG02132.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-1323_62-1305dup others(19): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(13): Show |
21 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0231others(18): Show | 25 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.62-1324_62-1305dup others(20): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(14): Show |
28 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0018others(25): Show | 39 | HG01891.hp2 HG02055.hp1 HG02071.hp2 others(36): Show |
intron_variant | MODIFIER | c.62-1325_62-1305dup others(21): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG02056.hp2 HG02523.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-1326_62-1305dup others(22): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.62-1327_62-1305dup others(23): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(18): Show |
4 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0112others(1): Show | 4 | HG01169.hp2 HG01255.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-1329_62-1305dup others(25): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(19): Show |
6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG01106.hp1 HG01123.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-1330_62-1305dup others(26): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0111 | 4 | HG02258.hp1 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-1305_62-1304ins others(28): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(22): Show |
1 | a0002c0002t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.62-1305_62-1304ins others(29): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.62-1305_62-1304ins others(30): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | CA | C | 16 | a0001c0001t0001g0012a0001c0001t0001g0116a0001c0001t0001g0117others(13): Show | 17 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-1305delA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | CAA | C | 49 | a0002c0014t0001g0092a0002c0014t0001g0206a0003c0003t0001g0002others(46): Show | 59 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.62-1306_62-1305del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | CAAA | C | 5 | a0001c0001t0001g0249a0003c0003t0001g0015a0003c0003t0001g0138others(2): Show | 6 | HG03098.hp2 HG03579.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-1307_62-1305del others(3): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580574 | CAAAAA | C | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.62-1309_62-1305del others(5): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99580574 | |||||
chr4:99580601 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.62-1304G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580601 | ||||||
chr4:99580626 | C | T | 18 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0106others(15): Show | 19 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-1279C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580626 | ||||||
chr4:99580664 | C | T | 58 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(55): Show | 69 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.62-1241C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580664 | ||||||
chr4:99580742 | A | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 87 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-1163A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580742 | ||||||
chr4:99580890 | C | T | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.62-1015C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99580890 | ||||||
chr4:99581011 | A | G | 2 | a0002c0002t0002g0199a0002c0002t0002g0200 | 2 | NA19005.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.62-894A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581011 | ||||||
chr4:99581098 | G | T | 3 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.62-807G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581098 | ||||||
chr4:99581243 | A | G | 1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.62-662A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581243 | ||||||
chr4:99581291 | C | T | 1 | a0004c0004t0001g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.62-614C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581291 | ||||||
chr4:99581350 | A | G | 64 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(61): Show | 70 | HG00544.hp1 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.62-555A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581350 | ||||||
chr4:99581590 | T | C | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0096others(1): Show | 4 | HG01106.hp1 HG01255.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-315T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581590 | ||||||
chr4:99581612 | G | T | 1 | a0002c0002t0002g0205 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.62-293G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581612 | ||||||
chr4:99581621 | C | T | 4 | a0003c0003t0001g0087a0003c0003t0001g0088a0013c0013t0001g0144others(1): Show | 4 | HG02145.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-284C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581621 | ||||||
chr4:99581621 | CA | C | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-275delA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr4 | 99581621 | |||||
chr4:99581665 | G | T | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.62-240G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 1/17 | chr4 | 99581665 | ||||||
chr4:99582463 | A | T | 1 | a0010c0011t0003g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.249+371A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 2/17 | chr4 | 99582463 | ||||||
chr4:99582604 | C | T | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.249+512C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 2/17 | chr4 | 99582604 | ||||||
chr4:99583284 | T | C | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-90T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 2/17 | chr4 | 99583284 | ||||||
chr4:99583656 | T | C | 1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.393+139T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583656 | ||||||
chr4:99583751 | G | A | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.393+234G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583751 | ||||||
chr4:99583788 | A | G | 1 | a0004c0004t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.393+271A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583788 | ||||||
chr4:99583817 | G | A | 1 | a0014c0019t0014g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.393+300G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583817 | ||||||
chr4:99583828 | G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(248): Show | 286 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(283): Show |
intron_variant | MODIFIER | c.393+311G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583828 | ||||||
chr4:99583853 | A | G | 2 | a0004c0004t0011g0027a0004c0004t0011g0065 | 2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.393+336A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583853 | ||||||
chr4:99583881 | G | T | 1 | a0001c0001t0001g0230 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.393+364G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583881 | ||||||
chr4:99583918 | G | T | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.393+401G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583918 | ||||||
chr4:99583980 | A | G | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.393+463A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99583980 | ||||||
chr4:99584169 | A | T | 81 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(78): Show | 87 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.393+652A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584169 | ||||||
chr4:99584259 | C | G | 15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(12): Show | 17 | HG01884.hp1 HG01975.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.393+742C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584259 | ||||||
chr4:99584348 | C | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(12): Show | 17 | HG01884.hp1 HG01975.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.393+831C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584348 | ||||||
chr4:99584468 | C | T | 3 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.393+951C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584468 | ||||||
chr4:99584628 | C | CACATGCC others(33): Show |
1 | a0003c0003t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.393+1112_393+1113i others(42): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99584628 | |||||
chr4:99584630 | T | A | 1 | a0003c0003t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.393+1113T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584630 | ||||||
chr4:99584637 | G | A | 5 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+1120G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584637 | ||||||
chr4:99584644 | C | A | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.393+1127C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584644 | ||||||
chr4:99584650 | C | T | 1 | a0014c0018t0003g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+1133C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584650 | ||||||
chr4:99584740 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.393+1223G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584740 | ||||||
chr4:99584962 | C | T | 1 | a0012c0009t0006g0322 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.393+1445C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99584962 | ||||||
chr4:99585033 | G | A | 1 | a0002c0002t0002g0016 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.393+1516G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99585033 | ||||||
chr4:99585111 | A | G | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.393+1594A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99585111 | ||||||
chr4:99585215 | G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 104 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.393+1698G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99585215 | ||||||
chr4:99585345 | T | A | 1 | a0006c0006t0001g0307 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.393+1828T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99585345 | ||||||
chr4:99585646 | C | T | 1 | a0002c0014t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.393+2129C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99585646 | ||||||
chr4:99585791 | G | A | 2 | a0005c0005t0001g0104a0005c0005t0001g0105 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.393+2274G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99585791 | ||||||
chr4:99586478 | C | T | 12 | a0002c0002t0002g0017a0002c0002t0002g0082a0002c0002t0002g0176others(9): Show | 13 | HG00408.hp1 HG00621.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.393+2961C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586478 | ||||||
chr4:99586504 | G | C | 54 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(51): Show | 65 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.393+2987G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586504 | ||||||
chr4:99586507 | T | C | 1 | a0003c0003t0001g0146 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.393+2990T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586507 | ||||||
chr4:99586734 | T | C | 4 | a0010c0011t0003g0260a0010c0011t0003g0261a0010c0011t0003g0302others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-2909T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586734 | ||||||
chr4:99586745 | A | G | 1 | a0004c0004t0001g0064 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.394-2898A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586745 | ||||||
chr4:99586868 | C | A | 2 | a0002c0014t0001g0092a0002c0014t0001g0206 | 2 | HG00735.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.394-2775C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586868 | ||||||
chr4:99586920 | T | A | 1 | a0004c0004t0001g0028 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.394-2723T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586920 | ||||||
chr4:99586923 | G | A | 1 | a0015c0027t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.394-2720G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99586923 | ||||||
chr4:99586989 | A | AC | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-2652dupC | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99586989 | |||||
chr4:99587152 | A | T | 3 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0300 | 3 | HG00280.hp2 HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.394-2491A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587152 | ||||||
chr4:99587360 | G | A | 1 | a0004c0004t0001g0064 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.394-2283G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587360 | ||||||
chr4:99587387 | T | C | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-2256T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587387 | ||||||
chr4:99587390 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.394-2253A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587390 | ||||||
chr4:99587399 | A | G | 18 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.394-2244A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587399 | ||||||
chr4:99587694 | C | G | 4 | a0010c0011t0003g0260a0010c0011t0003g0261a0010c0011t0003g0302others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-1949C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587694 | ||||||
chr4:99587716 | A | G | 3 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.394-1927A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587716 | ||||||
chr4:99587780 | C | G | 2 | a0004c0004t0001g0032a0004c0004t0001g0046 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.394-1863C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587780 | ||||||
chr4:99587817 | T | C | 1 | a0003c0003t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-1826T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99587817 | ||||||
chr4:99588010 | A | G | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-1633A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588010 | ||||||
chr4:99588064 | T | C | 1 | a0002c0002t0002g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-1579T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588064 | ||||||
chr4:99588143 | CTCT | C | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-1493_394-1491d others(5): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588143 | |||||
chr4:99588164 | T | G | 40 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(37): Show | 41 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.394-1479T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588164 | ||||||
chr4:99588491 | G | A | 4 | a0003c0003t0001g0085a0003c0003t0001g0138a0003c0003t0001g0148others(1): Show | 4 | HG02559.hp1 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-1152G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588491 | ||||||
chr4:99588696 | T | TAC | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-941_394-940dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588696 | |||||
chr4:99588698 | C | CACACACA others(21): Show |
1 | a0002c0002t0002g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.394-940_394-939ins others(28): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588698 | |||||
chr4:99588702 | C | T | 2 | a0010c0011t0003g0260a0010c0011t0003g0261 | 2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.394-941C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588702 | ||||||
chr4:99588702 | CAT | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 103 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.394-930_394-929del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588702 | |||||
chr4:99588704 | T | C | 58 | a0002c0002t0002g0279a0004c0004t0001g0004a0004c0004t0001g0007others(55): Show | 62 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.394-939T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588704 | ||||||
chr4:99588704 | T | TATATATA others(21): Show |
10 | a0002c0002t0002g0016a0002c0002t0002g0089a0002c0002t0002g0090others(7): Show | 11 | HG00323.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-706_394-679dup others(28): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588704 | |||||
chr4:99588706 | T | TATATATA others(123): Show |
1 | a0005c0005t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-903_394-902ins others(130): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588706 | |||||
chr4:99588708 | T | TATATATG others(49): Show |
1 | a0002c0002t0002g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.394-885_394-884ins others(56): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588708 | |||||
chr4:99588720 | T | C | 3 | a0007c0007t0003g0313a0010c0011t0003g0302a0014c0018t0003g0320 | 3 | HG02257.hp2 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.394-923T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588720 | ||||||
chr4:99588732 | CAT | C | 4 | a0002c0002t0002g0181a0002c0002t0002g0182a0002c0002t0002g0197others(1): Show | 4 | HG00621.hp1 NA18986.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-902_394-901del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588732 | |||||
chr4:99588734 | T | TATATATG others(43): Show |
2 | a0005c0005t0001g0104a0005c0005t0001g0105 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.394-903_394-902ins others(50): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588734 | |||||
chr4:99588734 | T | TATATATG others(69): Show |
1 | a0005c0005t0001g0136 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-903_394-902ins others(76): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588734 | |||||
chr4:99588734 | T | TATATATG others(95): Show |
3 | a0005c0005t0001g0106a0005c0005t0001g0120a0005c0005t0001g0121 | 3 | HG01192.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.394-903_394-902ins others(102): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588734 | |||||
chr4:99588734 | T | TATATATG others(121): Show |
11 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0122others(8): Show | 12 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-903_394-902ins others(128): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588734 | |||||
chr4:99588734 | T | TATATATG others(147): Show |
2 | a0005c0005t0001g0124a0005c0005t0001g0137 | 2 | HG03017.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.394-903_394-902ins others(154): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588734 | |||||
chr4:99588748 | T | C | 11 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(8): Show | 11 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-895T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588748 | ||||||
chr4:99588760 | CAT | C | 5 | a0001c0001t0001g0103a0005c0005t0001g0104a0005c0005t0001g0105others(2): Show | 5 | HG00735.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-874_394-873del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588760 | |||||
chr4:99588776 | T | C | 11 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(8): Show | 11 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-867T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588776 | ||||||
chr4:99588787 | A | ACATATAT others(7): Show |
1 | a0002c0002t0002g0021 | 2 | HG04228.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.394-845_394-832dup others(14): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588787 | |||||
chr4:99588788 | CAT | C | 14 | a0001c0001t0001g0103a0003c0003t0001g0143a0003c0003t0001g0168others(11): Show | 14 | HG00621.hp2 HG00639.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-846_394-845del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588788 | |||||
chr4:99588790 | T | TATATATA others(19): Show |
1 | a0004c0004t0001g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.394-844_394-819dup others(26): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588790 | |||||
chr4:99588804 | T | C | 14 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(11): Show | 14 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-839T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588804 | ||||||
chr4:99588810 | TAC | T | 8 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-827_394-826del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588810 | |||||
chr4:99588813 | A | T | 1 | a0007c0007t0003g0313 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.394-830A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588813 | ||||||
chr4:99588815 | A | ACATATAT others(423): Show |
1 | a0014c0018t0003g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-819_394-818ins others(430): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(485): Show |
1 | a0004c0004t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.394-819_394-818ins others(492): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(391): Show |
1 | a0006c0006t0001g0307 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(398): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(267): Show |
1 | a0003c0003t0001g0087 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(274): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(443): Show |
1 | a0003c0003t0001g0014 | 2 | NA18973.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.394-819_394-818ins others(450): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(451): Show |
1 | a0003c0003t0001g0107 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(458): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(447): Show |
1 | a0003c0003t0001g0108 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(454): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(341): Show |
1 | a0003c0003t0001g0168 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(348): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(289): Show |
1 | a0003c0003t0001g0154 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(296): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(315): Show |
1 | a0003c0003t0001g0155 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.394-819_394-818ins others(322): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(341): Show |
3 | a0003c0003t0001g0156a0003c0003t0001g0265a0003c0003t0009g0125 | 3 | HG03704.hp2 NA19058.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.394-819_394-818ins others(348): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(393): Show |
1 | a0003c0003t0001g0002 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.394-819_394-818ins others(400): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(419): Show |
3 | a0003c0003t0001g0141a0003c0003t0001g0148a0003c0003t0001g0267 | 3 | HG02559.hp1 NA19077.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.394-819_394-818ins others(426): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(445): Show |
4 | a0003c0003t0001g0161a0003c0003t0001g0162a0003c0003t0001g0262others(1): Show | 4 | NA18960.hp1 NA18987.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-819_394-818ins others(452): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(471): Show |
1 | a0003c0003t0001g0163 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(478): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(339): Show |
1 | a0003c0003t0001g0145 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.394-819_394-818ins others(346): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(365): Show |
2 | a0003c0003t0001g0006a0003c0003t0001g0010 | 4 | HG00558.hp1 HG02132.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-819_394-818ins others(372): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(255): Show |
1 | a0006c0006t0004g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(262): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(281): Show |
3 | a0006c0006t0004g0036a0006c0006t0004g0063a0006c0006t0004g0075 | 3 | HG01256.hp2 HG03704.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.394-819_394-818ins others(288): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(307): Show |
2 | a0006c0006t0004g0008a0020c0020t0004g0069 | 3 | HG03491.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.394-819_394-818ins others(314): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(459): Show |
2 | a0006c0006t0001g0070a0006c0006t0001g0076 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.394-819_394-818ins others(466): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ACATATAT others(341): Show |
1 | a0003c0003t0001g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.394-819_394-818ins others(348): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588815 | |||||
chr4:99588815 | A | ATATATAT others(249): Show |
1 | a0007c0007t0003g0313 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.394-828_394-827ins others(256): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588815 | ||||||
chr4:99588815 | A | T | 8 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-828A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588815 | ||||||
chr4:99588816 | CAT | C | 33 | a0001c0001t0001g0103a0001c0001t0001g0259a0003c0003t0001g0002others(30): Show | 40 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.394-818_394-817del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588816 | |||||
chr4:99588832 | T | C | 13 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(10): Show | 13 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-811T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588832 | ||||||
chr4:99588838 | TAC | T | 27 | a0003c0003t0001g0002a0003c0003t0001g0014a0003c0003t0001g0107others(24): Show | 29 | HG00621.hp2 HG00733.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.394-799_394-798del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588838 | |||||
chr4:99588840 | C | T | 11 | a0003c0003t0001g0006a0003c0003t0001g0010a0003c0003t0001g0087others(8): Show | 13 | HG00558.hp1 HG00735.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.394-803C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588840 | ||||||
chr4:99588841 | A | T | 16 | a0003c0003t0001g0006a0003c0003t0001g0010a0003c0003t0001g0087others(13): Show | 18 | HG00558.hp1 HG00639.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.394-802A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588841 | ||||||
chr4:99588842 | C | T | 27 | a0003c0003t0001g0002a0003c0003t0001g0014a0003c0003t0001g0107others(24): Show | 29 | HG00621.hp2 HG00733.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.394-801C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588842 | ||||||
chr4:99588843 | A | ACATATAT others(167): Show |
1 | a0009c0012t0007g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.394-791_394-790ins others(174): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(193): Show |
2 | a0009c0012t0007g0022a0009c0015t0007g0022 | 2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.394-791_394-790ins others(200): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(179): Show |
1 | a0014c0019t0014g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(186): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(269): Show |
1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.394-791_394-790ins others(276): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(315): Show |
1 | a0003c0003t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(322): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(417): Show |
1 | a0003c0003t0001g0140 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(424): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(393): Show |
2 | a0003c0003t0001g0002a0003c0003t0001g0269 | 5 | HG02056.hp1 NA18951.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-791_394-790ins others(400): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(391): Show |
1 | a0003c0003t0001g0010 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(398): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(409): Show |
1 | a0006c0006t0001g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(416): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(357): Show |
1 | a0006c0006t0004g0045 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.394-791_394-790ins others(364): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(383): Show |
1 | a0006c0006t0004g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(390): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(359): Show |
1 | a0006c0006t0005g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(366): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(383): Show |
1 | a0006c0006t0005g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.394-791_394-790ins others(390): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(357): Show |
1 | a0006c0006t0005g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.394-791_394-790ins others(364): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ACATATAT others(569): Show |
1 | a0003c0003t0010g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.394-791_394-790ins others(576): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588843 | |||||
chr4:99588843 | A | ATATATAT others(17): Show |
6 | a0003c0003t0001g0006a0003c0003t0001g0010a0003c0003t0001g0087others(3): Show | 8 | HG00558.hp1 HG02132.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-800_394-799ins others(24): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588843 | ||||||
chr4:99588843 | A | ATATATAT others(223): Show |
1 | a0007c0007t0003g0311 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.394-800_394-799ins others(230): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588843 | ||||||
chr4:99588843 | A | ATATATAT others(223): Show |
2 | a0007c0007t0003g0312a0007c0007t0003g0317 | 2 | HG00639.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.394-800_394-799ins others(230): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588843 | ||||||
chr4:99588843 | A | ATATATAT others(249): Show |
2 | a0007c0007t0003g0309a0007c0007t0003g0310 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.394-800_394-799ins others(256): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588843 | ||||||
chr4:99588843 | A | ATATATAT others(273): Show |
1 | a0007c0007t0003g0316 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394-800_394-799ins others(280): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588843 | ||||||
chr4:99588843 | A | ATATATAT others(15): Show |
2 | a0006c0006t0001g0307a0006c0006t0004g0036 | 2 | HG00735.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.394-800_394-799ins others(22): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588843 | ||||||
chr4:99588843 | A | T | 27 | a0003c0003t0001g0002a0003c0003t0001g0014a0003c0003t0001g0107others(24): Show | 29 | HG00621.hp2 HG00733.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.394-800A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588843 | ||||||
chr4:99588844 | CAT | C | 43 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0249others(40): Show | 45 | HG01070.hp1 HG01192.hp2 HG01891.hp2 others(42): Show |
intron_variant | MODIFIER | c.394-790_394-789del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588844 | |||||
chr4:99588846 | T | TATATATG others(383): Show |
1 | a0006c0006t0001g0060 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.394-791_394-790ins others(390): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588846 | |||||
chr4:99588860 | T | C | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-783T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588860 | ||||||
chr4:99588866 | TAC | T | 55 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(52): Show | 64 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.394-771_394-770del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588866 | |||||
chr4:99588868 | C | T | 5 | a0006c0006t0004g0008a0006c0006t0004g0063a0007c0007t0003g0309others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-775C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588868 | ||||||
chr4:99588869 | A | T | 5 | a0006c0006t0004g0008a0006c0006t0004g0063a0007c0007t0003g0309others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-774A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588869 | ||||||
chr4:99588870 | C | T | 53 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(50): Show | 62 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.394-773C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588870 | ||||||
chr4:99588871 | A | ACATATAT others(367): Show |
3 | a0003c0003t0001g0088a0003c0003t0001g0146a0003c0003t0001g0157 | 3 | HG01975.hp1 HG03486.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.394-763_394-762ins others(374): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588871 | |||||
chr4:99588871 | A | ACATATAT others(393): Show |
6 | a0003c0003t0001g0002a0003c0003t0001g0015a0003c0003t0001g0158others(3): Show | 8 | HG02083.hp2 HG02273.hp2 NA19054.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-763_394-762ins others(400): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588871 | |||||
chr4:99588871 | A | ACATATAT others(445): Show |
1 | a0003c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-763_394-762ins others(452): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588871 | |||||
chr4:99588871 | A | ACATATAT others(497): Show |
2 | a0003c0003t0001g0085a0003c0003t0001g0164 | 2 | HG01070.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.394-763_394-762ins others(504): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588871 | |||||
chr4:99588871 | A | ACATATAT others(391): Show |
1 | a0003c0003t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.394-763_394-762ins others(398): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588871 | |||||
chr4:99588871 | A | ACATATAT others(391): Show |
2 | a0003c0003t0001g0142a0003c0003t0001g0167 | 2 | NA18940.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.394-763_394-762ins others(398): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588871 | |||||
chr4:99588871 | A | ACATATAT others(677): Show |
1 | a0003c0003t0010g0171 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-763_394-762ins others(684): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588871 | |||||
chr4:99588871 | A | ATATATAT others(15): Show |
3 | a0006c0006t0004g0008a0006c0006t0004g0063a0020c0020t0004g0069 | 4 | HG03491.hp1 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-772_394-771ins others(22): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588871 | ||||||
chr4:99588871 | A | T | 55 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(52): Show | 64 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.394-772A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588871 | ||||||
chr4:99588872 | C | T | 2 | a0007c0007t0003g0309a0007c0007t0003g0310 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.394-771C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588872 | ||||||
chr4:99588872 | CAT | C | 52 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(49): Show | 52 | HG00558.hp2 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.394-762_394-761del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588872 | |||||
chr4:99588874 | T | C | 2 | a0002c0002t0002g0176a0002c0002t0002g0177 | 2 | NA18970.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.394-769T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588874 | ||||||
chr4:99588883 | G | A | 2 | a0007c0007t0003g0309a0007c0007t0003g0310 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.394-760G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588883 | ||||||
chr4:99588888 | T | C | 9 | a0007c0007t0003g0311a0007c0007t0003g0312a0007c0007t0003g0313others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-755T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588888 | ||||||
chr4:99588894 | TAC | T | 68 | a0001c0001t0001g0103a0003c0003t0001g0002a0003c0003t0001g0006others(65): Show | 81 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.394-743_394-742del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588894 | |||||
chr4:99588895 | A | T | 1 | a0006c0006t0004g0068 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.394-748A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588895 | ||||||
chr4:99588896 | C | T | 8 | a0006c0006t0004g0024a0006c0006t0004g0075a0007c0007t0003g0311others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-747C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588896 | ||||||
chr4:99588897 | A | T | 8 | a0006c0006t0004g0024a0006c0006t0004g0075a0007c0007t0003g0311others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-746A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588897 | ||||||
chr4:99588898 | C | T | 65 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(62): Show | 78 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.394-745C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588898 | ||||||
chr4:99588899 | A | ACACATAT others(425): Show |
1 | a0002c0014t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.394-742_394-741ins others(432): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(403): Show |
1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.394-735_394-734ins others(410): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(421): Show |
1 | a0003c0003t0001g0149 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.394-735_394-734ins others(428): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(315): Show |
1 | a0003c0003t0001g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.394-735_394-734ins others(322): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(367): Show |
2 | a0003c0003t0001g0086a0003c0003t0001g0151 | 2 | NA19001.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.394-735_394-734ins others(374): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(393): Show |
1 | a0003c0003t0001g0138 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394-735_394-734ins others(400): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(419): Show |
1 | a0003c0003t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.394-735_394-734ins others(426): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(471): Show |
1 | a0003c0003t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394-735_394-734ins others(478): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(497): Show |
1 | a0003c0003t0001g0084 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.394-735_394-734ins others(504): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(391): Show |
1 | a0003c0003t0001g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.394-735_394-734ins others(398): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(417): Show |
2 | a0003c0003t0001g0126a0003c0003t0001g0153 | 2 | NA18941.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.394-735_394-734ins others(424): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(265): Show |
1 | a0010c0011t0003g0260 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.394-737_394-736ins others(272): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ACATATAT others(239): Show |
1 | a0010c0011t0003g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.394-737_394-736ins others(246): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588899 | |||||
chr4:99588899 | A | ATATATAT others(223): Show |
1 | a0007c0007t0003g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.394-744_394-743ins others(230): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588899 | ||||||
chr4:99588899 | A | ATATATAT others(15): Show |
2 | a0006c0006t0004g0024a0006c0006t0004g0075 | 2 | HG01256.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.394-744_394-743ins others(22): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588899 | ||||||
chr4:99588899 | A | ATATATGT others(357): Show |
1 | a0006c0006t0004g0068 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.394-744_394-743ins others(364): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588899 | ||||||
chr4:99588899 | A | T | 68 | a0001c0001t0001g0103a0003c0003t0001g0002a0003c0003t0001g0006others(65): Show | 81 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.394-744A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588899 | ||||||
chr4:99588900 | C | T | 5 | a0007c0007t0003g0311a0007c0007t0003g0312a0007c0007t0003g0313others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-743C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588900 | ||||||
chr4:99588900 | CAT | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(105): Show | 126 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.394-734_394-733del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588900 | |||||
chr4:99588902 | T | TATATATA others(19): Show |
1 | a0004c0004t0001g0026 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.394-732_394-707dup others(26): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588902 | |||||
chr4:99588902 | T | TATATATA others(21): Show |
1 | a0018c0024t0002g0202 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.394-714_394-713ins others(28): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588902 | |||||
chr4:99588902 | T | TATATATG others(17): Show |
1 | a0004c0004t0001g0044 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.394-735_394-734ins others(24): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588902 | |||||
chr4:99588904 | T | TATGTTCA others(1): Show |
5 | a0007c0007t0003g0311a0007c0007t0003g0312a0007c0007t0003g0313others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-737_394-736ins others(8): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588904 | |||||
chr4:99588911 | G | A | 5 | a0007c0007t0003g0311a0007c0007t0003g0312a0007c0007t0003g0313others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-732G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588911 | ||||||
chr4:99588916 | T | C | 4 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0314others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-727T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588916 | ||||||
chr4:99588922 | TAC | T | 83 | a0002c0014t0001g0092a0003c0003t0001g0002a0003c0003t0001g0006others(80): Show | 96 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.394-715_394-714del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588922 | |||||
chr4:99588923 | A | ATGTT | 5 | a0007c0007t0003g0311a0007c0007t0003g0312a0007c0007t0003g0313others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-720_394-719ins others(4): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588923 | ||||||
chr4:99588923 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.394-720A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588923 | ||||||
chr4:99588924 | C | T | 4 | a0007c0007t0003g0314a0012c0009t0006g0321a0012c0009t0006g0322others(1): Show | 4 | HG00639.hp1 HG01257.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-719C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588924 | ||||||
chr4:99588925 | A | T | 4 | a0007c0007t0003g0314a0012c0009t0006g0321a0012c0009t0006g0322others(1): Show | 4 | HG00639.hp1 HG01257.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-718A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588925 | ||||||
chr4:99588926 | C | T | 84 | a0001c0001t0001g0103a0002c0014t0001g0092a0003c0003t0001g0002others(81): Show | 97 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.394-717C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588926 | ||||||
chr4:99588927 | A | ACATATAT others(567): Show |
1 | a0005c0005t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-707_394-706ins others(574): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588927 | |||||
chr4:99588927 | A | ACATATAT others(475): Show |
1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.394-707_394-706ins others(482): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588927 | |||||
chr4:99588927 | A | ACATATAT others(653): Show |
1 | a0001c0001t0001g0249 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.394-707_394-706ins others(660): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588927 | |||||
chr4:99588927 | A | ACATATAT others(421): Show |
1 | a0002c0014t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.394-707_394-706ins others(428): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588927 | |||||
chr4:99588927 | A | ACATATAT others(443): Show |
2 | a0003c0003t0001g0172a0003c0003t0001g0264 | 2 | NA18939.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.394-707_394-706ins others(450): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588927 | |||||
chr4:99588927 | A | ATATATAT others(223): Show |
1 | a0007c0007t0003g0314 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.394-716_394-715ins others(230): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588927 | ||||||
chr4:99588927 | A | ATATATAT others(3): Show |
2 | a0012c0009t0006g0321a0012c0009t0006g0323 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.394-716_394-715ins others(10): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588927 | ||||||
chr4:99588927 | A | ATATATAT others(1): Show |
5 | a0007c0007t0003g0311a0007c0007t0003g0312a0007c0007t0003g0313others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-716_394-715ins others(8): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588927 | ||||||
chr4:99588927 | A | ATATATGT others(577): Show |
1 | a0001c0001t0001g0103 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.394-716_394-715ins others(584): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588927 | ||||||
chr4:99588927 | A | T | 84 | a0002c0014t0001g0092a0003c0003t0001g0002a0003c0003t0001g0006others(81): Show | 97 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.394-716A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588927 | ||||||
chr4:99588928 | C | T | 3 | a0005c0005t0001g0106a0005c0005t0001g0121a0005c0005t0001g0123 | 3 | HG03209.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.394-715C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588928 | ||||||
chr4:99588928 | CAT | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(136): Show | 157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.394-706_394-705del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588928 | |||||
chr4:99588930 | T | C | 1 | a0018c0024t0002g0202 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.394-713T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588930 | ||||||
chr4:99588930 | T | TATATATA others(19): Show |
1 | a0002c0002t0002g0286 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.394-678_394-653dup others(26): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588930 | |||||
chr4:99588930 | T | TATATATG others(591): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0113 | 2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.394-707_394-706ins others(598): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588930 | |||||
chr4:99588944 | T | C | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-699T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588944 | ||||||
chr4:99588951 | A | G | 3 | a0001c0001t0001g0109a0012c0009t0006g0321a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01361.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.394-692A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588951 | ||||||
chr4:99588952 | C | T | 101 | a0001c0001t0001g0012a0001c0001t0001g0103a0001c0001t0001g0109others(98): Show | 114 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.394-691C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588952 | ||||||
chr4:99588953 | A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0113a0012c0009t0006g0322 | 3 | HG01257.hp2 HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.394-690A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588953 | ||||||
chr4:99588953 | A | T | 98 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0249others(95): Show | 111 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.394-690A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588953 | ||||||
chr4:99588954 | C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0113a0012c0009t0006g0322others(1): Show | 4 | HG01257.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-689C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588954 | ||||||
chr4:99588955 | A | ACATATAT others(399): Show |
1 | a0005c0005t0001g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(406): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588955 | |||||
chr4:99588955 | A | ACATATAT others(519): Show |
1 | a0001c0001t0001g0303 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(526): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588955 | |||||
chr4:99588955 | A | ACATATAT others(541): Show |
1 | a0001c0001t0001g0114 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(548): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588955 | |||||
chr4:99588955 | A | ACATATAT others(567): Show |
1 | a0001c0001t0001g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.394-666_394-665ins others(574): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588955 | |||||
chr4:99588955 | A | ACATATAT others(593): Show |
1 | a0001c0001t0001g0012 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.394-666_394-665ins others(600): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588955 | |||||
chr4:99588955 | A | ATATATAT others(3): Show |
1 | a0005c0005t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-688_394-687ins others(10): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588955 | ||||||
chr4:99588955 | A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0113a0012c0009t0006g0322others(1): Show | 4 | HG01257.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-688A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588955 | ||||||
chr4:99588956 | C | CAT | 51 | a0002c0002t0002g0017a0002c0002t0002g0019a0002c0002t0002g0020others(48): Show | 54 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.394-680_394-679dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588956 | |||||
chr4:99588956 | C | CATATATA others(23): Show |
2 | a0002c0002t0002g0183a0002c0002t0002g0280 | 2 | HG00741.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.394-679_394-678ins others(30): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588956 | |||||
chr4:99588956 | C | T | 98 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0249others(95): Show | 111 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.394-687C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588956 | ||||||
chr4:99588967 | TCATATAT others(7): Show |
T | 1 | a0012c0009t0006g0322 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.394-665_394-652del others(14): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588967 | |||||
chr4:99588970 | T | C | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-673T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588970 | ||||||
chr4:99588973 | A | T | 2 | a0003c0003t0001g0152a0003c0003t0001g0165 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.394-670A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588973 | ||||||
chr4:99588976 | TAC | T | 99 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0110others(96): Show | 112 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.394-661_394-660del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588976 | |||||
chr4:99588977 | A | ATGTT | 7 | a0001c0001t0001g0012a0001c0001t0001g0113a0001c0001t0001g0114others(4): Show | 8 | HG01884.hp1 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-666_394-665ins others(4): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588977 | ||||||
chr4:99588977 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.394-666A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588977 | ||||||
chr4:99588978 | C | T | 36 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0094others(33): Show | 36 | HG00558.hp2 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.394-665C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588978 | ||||||
chr4:99588979 | A | ATATATAT others(3): Show |
1 | a0005c0005t0001g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.394-664_394-663ins others(10): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588979 | ||||||
chr4:99588979 | A | T | 36 | a0001c0001t0001g0011a0001c0001t0001g0093a0001c0001t0001g0094others(33): Show | 36 | HG00558.hp2 HG00639.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.394-664A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588979 | ||||||
chr4:99588980 | C | T | 105 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0103others(102): Show | 119 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.394-663C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588980 | ||||||
chr4:99588981 | A | ACATATAT others(541): Show |
2 | a0005c0005t0001g0013a0005c0005t0001g0130 | 2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.394-653_394-652ins others(548): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(515): Show |
1 | a0005c0005t0001g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(522): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(541): Show |
2 | a0005c0005t0001g0129a0005c0005t0001g0135 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.394-653_394-652ins others(548): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(511): Show |
1 | a0005c0005t0001g0120 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(518): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(555): Show |
1 | a0002c0002t0002g0176 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(601): Show |
1 | a0003c0003t0001g0139 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(608): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(525): Show |
1 | a0001c0001t0001g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(532): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(553): Show |
1 | a0001c0001t0001g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(599): Show |
1 | a0001c0001t0001g0246 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(606): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(621): Show |
1 | a0001c0001t0001g0212 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(628): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(569): Show |
1 | a0001c0001t0001g0210 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(576): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(457): Show |
1 | a0004c0004t0001g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(464): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(509): Show |
1 | a0004c0004t0001g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(516): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(285): Show |
1 | a0011c0010t0001g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(292): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(455): Show |
1 | a0004c0004t0011g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(462): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(481): Show |
1 | a0004c0004t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(488): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(609): Show |
2 | a0004c0004t0001g0051a0004c0004t0001g0052 | 2 | HG01167.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.394-653_394-652ins others(616): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(505): Show |
2 | a0004c0004t0001g0041a0004c0004t0001g0053 | 2 | HG00642.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.394-653_394-652ins others(512): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(517): Show |
1 | a0008c0008t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(524): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(479): Show |
4 | a0004c0004t0001g0004a0004c0004t0001g0042a0008c0008t0001g0054others(1): Show | 7 | HG00544.hp1 HG02280.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-653_394-652ins others(486): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(505): Show |
2 | a0004c0004t0001g0037a0004c0004t0001g0039 | 2 | NA18944.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.394-653_394-652ins others(512): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(479): Show |
5 | a0004c0004t0001g0035a0004c0004t0001g0056a0004c0004t0001g0066others(2): Show | 5 | HG02040.hp2 HG03453.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-653_394-652ins others(486): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(453): Show |
2 | a0004c0004t0008g0025a0004c0004t0008g0029 | 2 | NA18948.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.394-653_394-652ins others(460): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(477): Show |
1 | a0002c0002t0002g0297 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(484): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(529): Show |
1 | a0004c0004t0001g0057 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(536): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(505): Show |
1 | a0004c0004t0011g0027 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(512): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(477): Show |
2 | a0004c0004t0001g0007a0004c0004t0001g0077 | 3 | NA18975.hp2 NA19066.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.394-653_394-652ins others(484): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(475): Show |
3 | a0004c0004t0001g0038a0004c0004t0001g0044a0004c0004t0001g0058 | 3 | NA18965.hp1 NA18994.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.394-653_394-652ins others(482): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ACATATAT others(427): Show |
1 | a0004c0004t0001g0043 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(434): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588981 | |||||
chr4:99588981 | A | ATATATAT others(553): Show |
1 | a0001c0001t0001g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(598): Show |
1 | a0001c0001t0001g0252 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(605): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(601): Show |
3 | a0001c0001t0001g0253a0013c0013t0001g0144a0013c0013t0001g0169 | 3 | HG01891.hp2 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.394-662_394-661ins others(608): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(601): Show |
2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.394-662_394-661ins others(608): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(547): Show |
1 | a0001c0001t0001g0227 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(554): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(547): Show |
1 | a0001c0001t0001g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(554): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(613): Show |
1 | a0001c0001t0001g0248 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(620): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(501): Show |
1 | a0001c0001t0001g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(508): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(527): Show |
1 | a0001c0001t0001g0119 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(534): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(553): Show |
1 | a0001c0001t0001g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(527): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0111 | 2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.394-662_394-661ins others(534): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(597): Show |
1 | a0001c0001t0001g0096 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(604): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(571): Show |
1 | a0001c0001t0001g0220 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(578): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(595): Show |
1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(602): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(571): Show |
1 | a0001c0001t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(578): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(597): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0305 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.394-662_394-661ins others(604): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(623): Show |
1 | a0001c0001t0001g0093 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(630): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(597): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0099 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.394-662_394-661ins others(604): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(619): Show |
1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(626): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(569): Show |
1 | a0004c0004t0001g0059 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.394-662_394-661ins others(576): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(555): Show |
1 | a0004c0004t0001g0031 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(427): Show |
1 | a0011c0010t0015g0072 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(434): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(529): Show |
1 | a0002c0002t0002g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(536): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(491): Show |
1 | a0004c0004t0001g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(498): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(545): Show |
1 | a0001c0001t0001g0229 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.394-662_394-661ins others(552): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | ATATATAT others(571): Show |
2 | a0001c0001t0001g0228a0001c0001t0001g0245 | 2 | HG00558.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.394-662_394-661ins others(578): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588981 | A | T | 99 | a0001c0001t0001g0011a0001c0001t0001g0103a0001c0001t0001g0110others(96): Show | 112 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.394-662A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588981 | ||||||
chr4:99588982 | C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0109a0001c0001t0001g0113others(4): Show | 8 | HG01884.hp1 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-661C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588982 | ||||||
chr4:99588982 | CAT | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.394-652_394-651del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588982 | |||||
chr4:99588984 | T | TATATATG others(503): Show |
1 | a0002c0002t0002g0177 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.394-653_394-652ins others(510): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588984 | |||||
chr4:99588984 | T | TATATATG others(557): Show |
1 | a0011c0010t0001g0023 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(564): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588984 | |||||
chr4:99588984 | T | TATATATG others(43): Show |
1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.394-653_394-652ins others(50): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588984 | |||||
chr4:99588984 | T | TATGTTCA others(27): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0113a0001c0001t0001g0114others(2): Show | 6 | HG01884.hp1 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-657_394-656ins others(34): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99588984 | |||||
chr4:99588998 | T | C | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-645T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588998 | ||||||
chr4:99588999 | A | G | 1 | a0002c0021t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.394-644A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99588999 | ||||||
chr4:99589001 | A | T | 2 | a0003c0003t0001g0152a0003c0003t0001g0165 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.394-642A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589001 | ||||||
chr4:99589003 | A | ATGTTCAT others(23): Show |
6 | a0005c0005t0001g0013a0005c0005t0001g0120a0005c0005t0001g0129others(3): Show | 6 | HG01192.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-639_394-638ins others(30): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589003 | |||||
chr4:99589005 | A | ATG | 6 | a0001c0001t0001g0012a0001c0001t0001g0109a0001c0001t0001g0113others(3): Show | 7 | HG01884.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-638_394-637ins others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589005 | ||||||
chr4:99589005 | A | ATGTTCAT others(21): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG01975.hp2 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.394-638_394-637ins others(28): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589005 | ||||||
chr4:99589005 | A | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0118others(9): Show | 12 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.394-638A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589005 | ||||||
chr4:99589006 | C | T | 178 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0093others(175): Show | 196 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.394-637C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589006 | ||||||
chr4:99589007 | A | ATATATAT others(661): Show |
1 | a0001c0001t0001g0118 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.394-636_394-635ins others(668): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589007 | ||||||
chr4:99589007 | A | ATATATAT others(557): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0110 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.394-636_394-635ins others(564): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589007 | ||||||
chr4:99589007 | A | T | 178 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0093others(175): Show | 196 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.394-636A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589007 | ||||||
chr4:99589008 | C | T | 11 | a0002c0021t0001g0091a0005c0005t0001g0013a0005c0005t0001g0106others(8): Show | 11 | HG01192.hp1 HG01257.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-635C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589008 | ||||||
chr4:99589009 | A | ACATATAT others(513): Show |
1 | a0005c0005t0001g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.394-611_394-610ins others(520): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(537): Show |
1 | a0005c0005t0001g0105 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.394-611_394-610ins others(544): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(529): Show |
1 | a0005c0005t0001g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.394-611_394-610ins others(536): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(527): Show |
1 | a0005c0005t0001g0122 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.394-611_394-610ins others(534): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(373): Show |
1 | a0005c0005t0001g0123 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.394-611_394-610ins others(380): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(397): Show |
1 | a0005c0005t0001g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.394-611_394-610ins others(404): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(533): Show |
1 | a0005c0005t0001g0263 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.394-611_394-610ins others(540): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(557): Show |
5 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0132others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-611_394-610ins others(564): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ACATATAT others(531): Show |
1 | a0005c0005t0001g0136 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-611_394-610ins others(538): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589009 | |||||
chr4:99589009 | A | ATATATAT others(5): Show |
1 | a0002c0014t0001g0206 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.394-634_394-633ins others(12): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589009 | ||||||
chr4:99589009 | A | ATATATGT others(389): Show |
1 | a0002c0021t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.394-634_394-633ins others(396): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589009 | ||||||
chr4:99589009 | A | T | 1 | a0012c0009t0006g0322 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.394-634A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589009 | ||||||
chr4:99589010 | C | T | 188 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0093others(185): Show | 207 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(204): Show |
intron_variant | MODIFIER | c.394-633C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589010 | ||||||
chr4:99589021 | T | A | 1 | a0014c0019t0014g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-622T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589021 | ||||||
chr4:99589024 | T | C | 8 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(5): Show | 8 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-619T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589024 | ||||||
chr4:99589024 | T | TATATATA others(5): Show |
2 | a0002c0014t0001g0206a0002c0021t0001g0091 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.394-612_394-611ins others(12): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589024 | |||||
chr4:99589024 | T | TGTATATT others(581): Show |
1 | a0002c0002t0002g0192 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.394-619_394-618ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589024 | ||||||
chr4:99589024 | T | TGTATATT others(479): Show |
1 | a0004c0004t0001g0030 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.394-619_394-618ins others(486): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589024 | ||||||
chr4:99589024 | T | TGTATATT others(401): Show |
1 | a0004c0004t0001g0040 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.394-619_394-618ins others(408): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589024 | ||||||
chr4:99589027 | A | T | 2 | a0003c0003t0001g0152a0003c0003t0001g0165 | 2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.394-616A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589027 | ||||||
chr4:99589029 | A | ATG | 8 | a0005c0005t0001g0013a0005c0005t0001g0106a0005c0005t0001g0120others(5): Show | 8 | HG01192.hp1 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-613_394-612ins others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589029 | |||||
chr4:99589030 | T | TATTC | 3 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.394-612_394-611ins others(4): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589030 | |||||
chr4:99589030 | TAC | T | 62 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(59): Show | 66 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.394-607_394-606del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589030 | |||||
chr4:99589031 | A | ATATGTTC others(11): Show |
12 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.394-612_394-611ins others(18): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589031 | ||||||
chr4:99589031 | A | ATT | 10 | a0002c0002t0002g0017a0002c0002t0002g0082a0002c0002t0002g0175others(7): Show | 10 | HG00408.hp1 HG01169.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-612_394-611ins others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589031 | ||||||
chr4:99589031 | A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(11): Show | 16 | HG01884.hp1 HG01975.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-612A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589031 | ||||||
chr4:99589031 | A | T | 10 | a0001c0001t0001g0211a0005c0005t0001g0013a0005c0005t0001g0106others(7): Show | 10 | HG01192.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-612A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589031 | ||||||
chr4:99589032 | C | CTCATATA others(531): Show |
1 | a0002c0002t0002g0272 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.394-611_394-610ins others(538): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589032 | ||||||
chr4:99589032 | C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(186): Show | 217 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.394-611C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589032 | ||||||
chr4:99589033 | A | ATATATAT others(557): Show |
1 | a0002c0002t0002g0175 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.394-610_394-609ins others(564): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | ATATATAT others(555): Show |
1 | a0002c0002t0002g0017 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.394-610_394-609ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | ATATATAT others(555): Show |
1 | a0002c0002t0002g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.394-610_394-609ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | ATATATAT others(555): Show |
2 | a0002c0002t0002g0182a0002c0002t0002g0293 | 2 | HG04184.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.394-610_394-609ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | ATATATAT others(555): Show |
1 | a0002c0002t0002g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.394-610_394-609ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | ATATATAT others(579): Show |
1 | a0002c0002t0002g0198 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.394-610_394-609ins others(586): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | ATATATAT others(553): Show |
1 | a0002c0002t0002g0301 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.394-610_394-609ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | G | 2 | a0002c0014t0001g0206a0002c0021t0001g0091 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.394-610A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589033 | A | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(178): Show | 209 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.394-610A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589033 | ||||||
chr4:99589034 | C | T | 94 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 99 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.394-609C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589034 | ||||||
chr4:99589035 | A | ACATATAT others(661): Show |
1 | a0002c0002t0002g0019 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.394-586_394-585ins others(668): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(627): Show |
1 | a0001c0001t0009g0221 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.394-586_394-585ins others(634): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(651): Show |
1 | a0001c0001t0001g0231 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.394-586_394-585ins others(658): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(661): Show |
1 | a0002c0002t0002g0286 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(668): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(607): Show |
1 | a0002c0002t0002g0284 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(614): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(605): Show |
1 | a0002c0002t0002g0271 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(612): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(599): Show |
1 | a0001c0001t0001g0232 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(606): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(627): Show |
1 | a0001c0001t0001g0222 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(634): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(625): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0213a0001c0001t0001g0215others(4): Show | 10 | HG00408.hp2 NA18961.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-573_394-572ins others(632): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(651): Show |
1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(658): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(583): Show |
1 | a0002c0002t0002g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(590): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(635): Show |
1 | a0002c0002t0002g0205 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(642): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(505): Show |
1 | a0004c0004t0001g0034 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(512): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(531): Show |
1 | a0004c0004t0001g0026 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(538): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(685): Show |
1 | a0002c0002t0002g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(692): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(633): Show |
1 | a0002c0002t0002g0281 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(640): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(607): Show |
1 | a0002c0002t0002g0128 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(614): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(633): Show |
1 | a0002c0002t0002g0282 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(640): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(633): Show |
1 | a0002c0002t0002g0274 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(640): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(607): Show |
2 | a0002c0002t0002g0089a0002c0002t0002g0187 | 2 | HG02523.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.394-573_394-572ins others(614): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(555): Show |
1 | a0002c0023t0002g0188 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(581): Show |
1 | a0002c0002t0002g0285 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(555): Show |
1 | a0002c0002t0002g0016 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.394-573_394-572ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(609): Show |
1 | a0018c0024t0002g0202 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(616): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(579): Show |
2 | a0002c0002t0002g0090a0002c0002t0002g0189 | 2 | HG02071.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.394-573_394-572ins others(586): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(553): Show |
1 | a0002c0002t0002g0184 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(581): Show |
1 | a0002c0002t0002g0280 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(605): Show |
1 | a0002c0002t0002g0185 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(612): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ACATATAT others(579): Show |
2 | a0002c0002t0002g0183a0002c0002t0002g0186 | 2 | NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.394-573_394-572ins others(586): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589035 | |||||
chr4:99589035 | A | ATATATAT others(581): Show |
1 | a0002c0002t0002g0276 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(561): Show |
1 | a0001c0001t0001g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(568): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(625): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0223 | 2 | NA18944.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.394-608_394-607ins others(632): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(653): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0235 | 2 | HG00609.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.394-608_394-607ins others(660): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(599): Show |
2 | a0001c0001t0001g0236a0001c0001t0001g0304 | 2 | NA19012.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.394-608_394-607ins others(606): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(601): Show |
1 | a0001c0001t0001g0247 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(608): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(625): Show |
1 | a0001c0001t0001g0225 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(632): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(599): Show |
1 | a0001c0001t0001g0237 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(606): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(599): Show |
11 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0098others(8): Show | 22 | HG00544.hp2 HG02040.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.394-608_394-607ins others(606): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(625): Show |
3 | a0001c0001t0001g0101a0001c0001t0001g0226a0001c0001t0001g0239 | 3 | NA18951.hp1 NA18973.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.394-608_394-607ins others(632): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(677): Show |
1 | a0001c0001t0001g0238 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(684): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(573): Show |
1 | a0001c0001t0001g0242 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(580): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(599): Show |
1 | a0001c0001t0001g0018 | 2 | NA18997.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.394-608_394-607ins others(606): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(601): Show |
1 | a0001c0001t0001g0243 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(608): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(569): Show |
1 | a0001c0001t0001g0208 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(576): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(479): Show |
1 | a0002c0002t0002g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(486): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(507): Show |
1 | a0015c0027t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(514): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(583): Show |
1 | a0002c0002t0012g0201 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(590): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(583): Show |
1 | a0002c0002t0002g0180 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(590): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(531): Show |
1 | a0008c0008t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(538): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(607): Show |
1 | a0002c0002t0002g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(614): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(531): Show |
1 | a0002c0002t0002g0287 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(538): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(557): Show |
1 | a0004c0004t0001g0028 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(564): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(453): Show |
1 | a0004c0004t0001g0064 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(460): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(609): Show |
1 | a0002c0002t0002g0199 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(616): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(555): Show |
1 | a0002c0002t0002g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(635): Show |
1 | a0002c0002t0002g0288 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(642): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(659): Show |
2 | a0002c0002t0002g0194a0002c0002t0002g0289 | 2 | HG01071.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.394-608_394-607ins others(666): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(581): Show |
1 | a0002c0002t0002g0195 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(607): Show |
3 | a0002c0002t0002g0181a0002c0002t0002g0200a0002c0002t0002g0203 | 3 | HG02735.hp1 NA18990.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.394-608_394-607ins others(614): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(607): Show |
1 | a0002c0002t0013g0207 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(614): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(581): Show |
1 | a0002c0002t0002g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(505): Show |
1 | a0002c0002t0002g0273 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(512): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(609): Show |
2 | a0002c0002t0002g0290a0002c0002t0002g0291 | 2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.394-608_394-607ins others(616): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(583): Show |
1 | a0002c0002t0002g0197 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(590): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(581): Show |
3 | a0002c0002t0002g0178a0002c0002t0002g0191a0002c0002t0002g0292 | 3 | HG04115.hp1 NA18956.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.394-608_394-607ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(555): Show |
1 | a0002c0002t0002g0270 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(503): Show |
1 | a0002c0002t0002g0294 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(510): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(553): Show |
1 | a0002c0017t0002g0179 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(553): Show |
1 | a0002c0002t0002g0196 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(553): Show |
1 | a0017c0025t0002g0277 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(555): Show |
1 | a0002c0002t0002g0300 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(562): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(607): Show |
1 | a0002c0002t0002g0295 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(614): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(529): Show |
1 | a0002c0002t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(536): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(529): Show |
1 | a0004c0004t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(536): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(503): Show |
1 | a0004c0004t0001g0050 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(510): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(579): Show |
1 | a0002c0002t0002g0020 | 2 | HG01934.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.394-608_394-607ins others(586): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(553): Show |
1 | a0002c0002t0002g0296 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(560): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATAT others(15): Show |
1 | a0002c0014t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.394-608_394-607ins others(22): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | ATATATGT others(567): Show |
1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.394-608_394-607ins others(574): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589035 | A | T | 68 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(65): Show | 72 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.394-608A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589035 | ||||||
chr4:99589036 | C | CATATATA others(609): Show |
1 | a0002c0002t0002g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.394-573_394-572ins others(616): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589036 | |||||
chr4:99589036 | C | T | 133 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(130): Show | 149 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.394-607C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589036 | ||||||
chr4:99589036 | C | TATATATA others(17): Show |
10 | a0002c0002t0002g0017a0002c0002t0002g0082a0002c0002t0002g0182others(7): Show | 10 | HG00408.hp1 HG00642.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-608_394-607ins others(24): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589036 | ||||||
chr4:99589053 | A | T | 1 | a0003c0003t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.394-590A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589053 | ||||||
chr4:99589057 | A | G | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(35): Show | 41 | HG01192.hp1 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.394-586A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589057 | ||||||
chr4:99589060 | C | CATATATA others(627): Show |
1 | a0001c0001t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.394-573_394-572ins others(634): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589060 | |||||
chr4:99589062 | T | TATATATA others(581): Show |
1 | a0002c0002t0002g0021 | 2 | HG04228.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.394-573_394-572ins others(588): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589062 | |||||
chr4:99589066 | T | TATATATG others(15): Show |
4 | a0010c0011t0003g0260a0010c0011t0003g0261a0010c0011t0003g0302others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-571_394-570ins others(22): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589066 | |||||
chr4:99589073 | A | AT | 11 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(8): Show | 11 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.394-560dupT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr4 | 99589073 | |||||
chr4:99589074 | T | TA | 2 | a0002c0002t0002g0021a0004c0004t0001g0043 | 3 | HG02027.hp2 HG04228.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.394-569_394-568ins others(1): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589074 | ||||||
chr4:99589075 | T | A | 120 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(117): Show | 134 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.394-568T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589075 | ||||||
chr4:99589181 | C | A | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-462C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589181 | ||||||
chr4:99589198 | A | G | 9 | a0006c0006t0004g0008a0006c0006t0004g0024a0006c0006t0004g0036others(6): Show | 10 | HG01256.hp2 HG01361.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-445A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589198 | ||||||
chr4:99589334 | G | T | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-309G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589334 | ||||||
chr4:99589385 | C | T | 1 | a0006c0006t0001g0307 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.394-258C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589385 | ||||||
chr4:99589393 | G | A | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-250G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589393 | ||||||
chr4:99589439 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-204C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589439 | ||||||
chr4:99589611 | T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(61): Show | 79 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.394-32T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589611 | ||||||
chr4:99589636 | C | T | 1 | a0014c0019t0014g0319 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.394-7C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 3/17 | chr4 | 99589636 | ||||||
chr4:99589858 | G | A | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.501+108G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99589858 | ||||||
chr4:99590097 | C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 231 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.501+347C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590097 | ||||||
chr4:99590104 | C | CT | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.501+363dupT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 99590104 | |||||
chr4:99590256 | C | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.501+506C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590256 | ||||||
chr4:99590257 | G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 103 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.501+507G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590257 | ||||||
chr4:99590381 | C | T | 1 | a0003c0003t0001g0084 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.501+631C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590381 | ||||||
chr4:99590466 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.501+716C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590466 | ||||||
chr4:99590468 | C | G | 1 | a0001c0001t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.501+718C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590468 | ||||||
chr4:99590471 | T | G | 1 | a0001c0001t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.501+721T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590471 | ||||||
chr4:99590473 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.501+723C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590473 | ||||||
chr4:99590716 | A | G | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.502-519A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590716 | ||||||
chr4:99590792 | C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 103 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.502-443C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590792 | ||||||
chr4:99590836 | T | TAC | 5 | a0002c0002t0002g0187a0002c0002t0002g0280a0002c0002t0002g0285others(2): Show | 5 | HG00741.hp2 HG01099.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-372_502-371dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 99590836 | |||||
chr4:99590836 | TAC | T | 45 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(42): Show | 49 | HG00544.hp1 HG00642.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.502-372_502-371del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 99590836 | |||||
chr4:99590836 | TACAC | T | 84 | a0002c0002t0002g0271a0003c0003t0001g0002a0003c0003t0001g0006others(81): Show | 97 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.502-374_502-371del others(4): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 99590836 | |||||
chr4:99590836 | TACACAC | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(92): Show | 112 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.502-376_502-371del others(6): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr4 | 99590836 | |||||
chr4:99590857 | ACAC | A | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-377_502-375del others(3): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590857 | ||||||
chr4:99590863 | A | C | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-372A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590863 | ||||||
chr4:99590864 | C | A | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-371C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590864 | ||||||
chr4:99590955 | C | A | 1 | a0003c0003t0001g0168 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.502-280C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590955 | ||||||
chr4:99590981 | C | T | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-254C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99590981 | ||||||
chr4:99591193 | C | T | 2 | a0002c0002t0002g0204a0002c0002t0012g0201 | 2 | HG00323.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.502-42C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 4/17 | chr4 | 99591193 | ||||||
chr4:99591495 | A | T | 1 | a0005c0005t0001g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.618+144A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 5/17 | chr4 | 99591495 | ||||||
chr4:99591870 | TTGTG | T | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.758+95_758+98delTG others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 99591870 | |||||
chr4:99591991 | A | T | 2 | a0004c0004t0001g0306a0004c0004t0001g0308 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.758+201A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99591991 | ||||||
chr4:99592140 | G | GAA | 11 | a0003c0003t0001g0006a0003c0003t0001g0010a0003c0003t0001g0014others(8): Show | 15 | HG00558.hp1 HG02132.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.758+354_758+355dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 99592140 | |||||
chr4:99592186 | A | T | 4 | a0002c0002t0002g0204a0002c0002t0002g0205a0002c0002t0012g0201others(1): Show | 4 | HG00323.hp1 HG00323.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.758+396A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592186 | ||||||
chr4:99592252 | A | C | 5 | a0001c0001t0001g0220a0001c0001t0001g0227a0001c0001t0001g0228others(2): Show | 5 | HG00558.hp2 HG02056.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.758+462A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592252 | ||||||
chr4:99592389 | G | A | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.758+599G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592389 | ||||||
chr4:99592423 | G | C | 114 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(111): Show | 128 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(125): Show |
intron_variant | MODIFIER | c.758+633G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592423 | ||||||
chr4:99592468 | CA | C | 12 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0129others(9): Show | 13 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.758+684delA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 99592468 | |||||
chr4:99592530 | AT | A | 18 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0106others(15): Show | 19 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.758+747delT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 99592530 | |||||
chr4:99592537 | T | A | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.758+747T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592537 | ||||||
chr4:99592542 | T | C | 1 | a0006c0006t0001g0307 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.758+752T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592542 | ||||||
chr4:99592594 | TAC | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 103 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.758+808_758+809del others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 99592594 | |||||
chr4:99592610 | C | A | 1 | a0002c0002t0002g0282 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.758+820C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592610 | ||||||
chr4:99592874 | T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 87 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.758+1084T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592874 | ||||||
chr4:99592895 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.758+1105C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99592895 | ||||||
chr4:99593107 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.758+1317G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99593107 | ||||||
chr4:99593207 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.758+1417C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99593207 | ||||||
chr4:99593392 | T | TA | 7 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01106.hp1 HG01123.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.759-1333dupA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr4 | 99593392 | |||||
chr4:99593428 | G | A | 18 | a0002c0002t0002g0288a0007c0007t0003g0309a0007c0007t0003g0310others(15): Show | 18 | HG00639.hp2 HG00733.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.759-1305G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99593428 | ||||||
chr4:99593565 | T | C | 1 | a0004c0004t0001g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.759-1168T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99593565 | ||||||
chr4:99593677 | C | G | 1 | a0004c0004t0001g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.759-1056C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99593677 | ||||||
chr4:99594016 | G | A | 2 | a0002c0014t0001g0092a0002c0014t0001g0206 | 2 | HG00735.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.759-717G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99594016 | ||||||
chr4:99594089 | C | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(247): Show | 285 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(282): Show |
intron_variant | MODIFIER | c.759-644C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99594089 | ||||||
chr4:99594129 | C | T | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.759-604C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99594129 | ||||||
chr4:99594409 | T | C | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.759-324T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99594409 | ||||||
chr4:99594543 | A | C | 2 | a0004c0004t0001g0032a0004c0004t0001g0046 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.759-190A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99594543 | ||||||
chr4:99594617 | A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 103 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.759-116A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 6/17 | chr4 | 99594617 | ||||||
chr4:99594893 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.909+10G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99594893 | ||||||
chr4:99595171 | G | A | 1 | a0002c0002t0002g0189 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.909+288G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99595171 | ||||||
chr4:99595223 | T | A | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.909+340T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99595223 | ||||||
chr4:99595384 | C | T | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.909+501C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99595384 | ||||||
chr4:99595501 | C | A | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.909+618C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99595501 | ||||||
chr4:99595755 | G | GT | 74 | a0001c0001t0001g0209a0003c0003t0001g0002a0003c0003t0001g0006others(71): Show | 87 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.909+882dupT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr4 | 99595755 | |||||
chr4:99595848 | A | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.909+965A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99595848 | ||||||
chr4:99595987 | T | A | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.910-1080T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99595987 | ||||||
chr4:99596089 | C | T | 2 | a0004c0004t0001g0004a0004c0004t0001g0042 | 5 | HG00544.hp1 NA18946.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-978C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99596089 | ||||||
chr4:99596167 | C | T | 54 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(51): Show | 65 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.910-900C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99596167 | ||||||
chr4:99596453 | G | A | 18 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0106others(15): Show | 19 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.910-614G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99596453 | ||||||
chr4:99596538 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.910-529G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99596538 | ||||||
chr4:99596757 | G | A | 1 | a0002c0002t0002g0276 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.910-310G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 7/17 | chr4 | 99596757 | ||||||
chr4:99597276 | T | C | 2 | a0005c0005t0001g0104a0005c0005t0001g0105 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1067+52T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99597276 | ||||||
chr4:99597326 | A | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1067+102A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99597326 | ||||||
chr4:99597557 | T | G | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1067+333T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99597557 | ||||||
chr4:99597574 | T | C | 1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1067+350T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99597574 | ||||||
chr4:99597589 | A | T | 17 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1067+365A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99597589 | ||||||
chr4:99598227 | A | G | 1 | a0014c0019t0014g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1067+1003A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99598227 | ||||||
chr4:99598240 | C | G | 12 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0129others(9): Show | 13 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.1067+1016C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99598240 | ||||||
chr4:99598653 | C | CT | 22 | a0002c0002t0002g0182a0002c0002t0002g0193a0002c0002t0002g0271others(19): Show | 23 | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1067+1457dupT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99598653 | |||||
chr4:99598653 | C | CTT | 73 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(70): Show | 86 | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.1067+1456_1067+145 others(6): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99598653 | |||||
chr4:99598653 | C | CTTT | 12 | a0003c0003t0001g0085a0003c0003t0001g0138a0003c0003t0001g0139others(9): Show | 12 | HG00621.hp2 HG00735.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1067+1455_1067+145 others(7): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99598653 | |||||
chr4:99598653 | C | CTTTTTT | 6 | a0007c0007t0003g0310a0007c0007t0003g0312a0007c0007t0003g0313others(3): Show | 6 | HG00639.hp2 HG01256.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067+1452_1067+145 others(10): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99598653 | |||||
chr4:99598653 | CTTTTT | C | 14 | a0001c0001t0001g0098a0001c0001t0001g0111a0001c0001t0001g0113others(11): Show | 14 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1067+1453_1067+145 others(9): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99598653 | |||||
chr4:99598653 | CTTTTTT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(73): Show | 93 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1067+1452_1067+145 others(10): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99598653 | |||||
chr4:99598653 | CTTTTTTT others(3): Show |
C | 1 | a0005c0005t0001g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1067+1448_1067+145 others(14): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99598653 | |||||
chr4:99598694 | G | A | 8 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067+1470G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99598694 | ||||||
chr4:99598771 | A | G | 74 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(71): Show | 87 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1067+1547A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99598771 | ||||||
chr4:99598791 | A | G | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1067+1567A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99598791 | ||||||
chr4:99599120 | G | C | 1 | a0004c0004t0001g0051 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1068-1445G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599120 | ||||||
chr4:99599255 | T | A | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1068-1310T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599255 | ||||||
chr4:99599348 | A | G | 1 | a0002c0002t0002g0291 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1068-1217A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599348 | ||||||
chr4:99599361 | C | G | 13 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(10): Show | 14 | HG01256.hp2 HG01361.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1068-1204C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599361 | ||||||
chr4:99599364 | G | A | 17 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1068-1201G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599364 | ||||||
chr4:99599427 | A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 103 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1068-1138A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599427 | ||||||
chr4:99599453 | A | G | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1068-1112A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599453 | ||||||
chr4:99599485 | G | A | 4 | a0010c0011t0003g0260a0010c0011t0003g0261a0010c0011t0003g0302others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068-1080G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599485 | ||||||
chr4:99599606 | G | A | 4 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0096others(1): Show | 4 | HG01106.hp1 HG01255.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068-959G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99599606 | ||||||
chr4:99600111 | T | C | 1 | a0004c0026t0001g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1068-454T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99600111 | ||||||
chr4:99600301 | G | A | 4 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(1): Show | 4 | HG02451.hp1 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068-264G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99600301 | ||||||
chr4:99600447 | TA | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1068-108delA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr4 | 99600447 | |||||
chr4:99600480 | C | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1068-85C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99600480 | ||||||
chr4:99600481 | C | T | 3 | a0002c0002t0002g0128a0002c0002t0002g0190a0002c0002t0002g0290 | 3 | HG01515.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1068-84C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 8/17 | chr4 | 99600481 | ||||||
chr4:99601246 | T | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0113a0001c0001t0001g0114others(5): Show | 9 | HG01884.hp1 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1237-361T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | chr4 | 99601246 | ||||||
chr4:99601283 | T | TTTTACTC others(11): Show |
3 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0300 | 3 | HG00280.hp2 HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1237-307_1237-306i others(20): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 99601283 | |||||
chr4:99601301 | T | A | 3 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0300 | 3 | HG00280.hp2 HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1237-306T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | chr4 | 99601301 | ||||||
chr4:99601321 | C | CT | 32 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(29): Show | 34 | HG00735.hp1 HG01884.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.1237-267dupT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 99601321 | |||||
chr4:99601321 | CT | C | 76 | a0001c0001t0001g0249a0003c0003t0001g0002a0003c0003t0001g0006others(73): Show | 88 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1237-267delT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 99601321 | |||||
chr4:99601321 | CTTTTTTT others(3): Show |
C | 3 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0300 | 3 | HG00280.hp2 HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1237-276_1237-267d others(12): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 99601321 | |||||
chr4:99601382 | T | G | 5 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(2): Show | 5 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-225T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | chr4 | 99601382 | ||||||
chr4:99601385 | GAATTCCC others(79): Show |
G | 3 | a0002c0002t0002g0298a0002c0002t0002g0299a0002c0002t0002g0300 | 3 | HG00280.hp2 HG00642.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1237-219_1237-134d others(88): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr4 | 99601385 | |||||
chr4:99601435 | C | T | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1237-172C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | chr4 | 99601435 | ||||||
chr4:99601522 | G | A | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1237-85G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 9/17 | chr4 | 99601522 | ||||||
chr4:99601791 | T | C | 2 | a0004c0004t0001g0031a0004c0004t0001g0059 | 2 | NA19003.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1344+77T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99601791 | ||||||
chr4:99601810 | TTACTC | T | 4 | a0002c0002t0002g0019a0002c0002t0002g0274a0002c0002t0002g0281others(1): Show | 5 | HG01346.hp2 HG01981.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+99_1344+103de others(6): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99601810 | |||||
chr4:99601813 | C | T | 3 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1344+99C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99601813 | ||||||
chr4:99601975 | C | T | 1 | a0002c0002t0002g0287 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1344+261C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99601975 | ||||||
chr4:99602209 | T | C | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1344+495T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602209 | ||||||
chr4:99602245 | C | T | 17 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1344+531C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602245 | ||||||
chr4:99602286 | A | G | 2 | a0005c0005t0001g0104a0005c0005t0001g0105 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1344+572A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602286 | ||||||
chr4:99602362 | A | G | 3 | a0002c0002t0002g0182a0002c0002t0002g0197a0002c0002t0002g0198 | 3 | HG00621.hp1 NA18986.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1344+648A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602362 | ||||||
chr4:99602646 | G | A | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1344+932G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602646 | ||||||
chr4:99602723 | C | T | 1 | a0002c0002t0002g0288 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1344+1009C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602723 | ||||||
chr4:99602741 | G | T | 57 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(54): Show | 68 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.1344+1027G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602741 | ||||||
chr4:99602991 | G | A | 17 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1344+1277G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602991 | ||||||
chr4:99602992 | C | A | 17 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1344+1278C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99602992 | ||||||
chr4:99603007 | G | C | 1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1344+1293G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99603007 | ||||||
chr4:99603040 | A | T | 4 | a0010c0011t0003g0260a0010c0011t0003g0261a0010c0011t0003g0302others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+1326A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99603040 | ||||||
chr4:99603115 | T | C | 1 | a0012c0009t0006g0322 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1344+1401T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99603115 | ||||||
chr4:99603139 | A | G | 1 | a0012c0009t0006g0323 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1344+1425A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99603139 | ||||||
chr4:99603522 | C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 234 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.1344+1808C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99603522 | ||||||
chr4:99603524 | T | C | 1 | a0003c0003t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1344+1810T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99603524 | ||||||
chr4:99603581 | A | G | 1 | a0015c0027t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1344+1867A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99603581 | ||||||
chr4:99604023 | T | C | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1344+2309T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99604023 | ||||||
chr4:99604358 | T | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 106 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1345-2390T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99604358 | ||||||
chr4:99604489 | G | A | 3 | a0005c0005t0001g0106a0005c0005t0001g0121a0005c0005t0001g0123 | 3 | HG03209.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1345-2259G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99604489 | ||||||
chr4:99604615 | TTTTACTT others(18): Show |
T | 1 | a0002c0002t0002g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1345-2130_1345-210 others(29): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99604615 | |||||
chr4:99604777 | T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(143): Show | 174 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.1345-1971T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99604777 | ||||||
chr4:99604954 | T | A | 1 | a0003c0003t0001g0158 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1345-1794T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99604954 | ||||||
chr4:99604981 | C | T | 3 | a0006c0006t0005g0009a0006c0006t0005g0078a0006c0006t0005g0079 | 4 | HG01070.hp2 HG01071.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-1767C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99604981 | ||||||
chr4:99605019 | T | C | 1 | a0014c0018t0003g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1345-1729T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605019 | ||||||
chr4:99605290 | T | C | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-1458T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605290 | ||||||
chr4:99605430 | C | G | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-1318C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605430 | ||||||
chr4:99605457 | T | C | 1 | a0004c0004t0001g0052 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1345-1291T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605457 | ||||||
chr4:99605520 | A | C | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-1228A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605520 | ||||||
chr4:99605788 | A | G | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1345-960A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605788 | ||||||
chr4:99605869 | A | ATGTG | 53 | a0002c0002t0002g0204a0002c0002t0002g0205a0002c0002t0012g0201others(50): Show | 57 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1345-863_1345-860d others(6): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTG | 8 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1345-865_1345-860d others(8): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(1): Show |
12 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.1345-867_1345-860d others(10): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(3): Show |
16 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0109others(13): Show | 18 | HG01884.hp1 HG01975.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.1345-869_1345-860d others(12): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(5): Show |
86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 102 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1345-871_1345-860d others(14): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(7): Show |
4 | a0001c0001t0001g0103a0005c0005t0001g0104a0005c0005t0001g0105others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-873_1345-860d others(16): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(9): Show |
15 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(12): Show | 16 | HG01070.hp2 HG01071.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1345-875_1345-860d others(18): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(11): Show |
3 | a0006c0006t0001g0307a0006c0006t0004g0008a0006c0006t0004g0063 | 4 | HG00735.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-877_1345-860d others(20): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(13): Show |
4 | a0003c0003t0001g0085a0003c0003t0001g0138a0003c0003t0001g0159others(1): Show | 4 | HG03098.hp2 HG03471.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-860_1345-859i others(22): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(15): Show |
6 | a0003c0003t0001g0084a0003c0003t0001g0143a0003c0003t0001g0148others(3): Show | 6 | HG00621.hp2 HG02083.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-860_1345-859i others(24): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(17): Show |
42 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(39): Show | 53 | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1345-860_1345-859i others(26): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605869 | A | ATGTGTGT others(19): Show |
4 | a0003c0003t0001g0139a0003c0003t0001g0150a0003c0003t0001g0151others(1): Show | 4 | NA18949.hp1 NA18987.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-860_1345-859i others(28): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr4 | 99605869 | |||||
chr4:99605911 | G | T | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1345-837G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605911 | ||||||
chr4:99605917 | T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 106 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1345-831T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99605917 | ||||||
chr4:99606015 | A | G | 1 | a0004c0004t0001g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1345-733A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606015 | ||||||
chr4:99606107 | G | T | 2 | a0002c0002t0002g0019a0002c0002t0002g0274 | 3 | HG01981.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1345-641G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606107 | ||||||
chr4:99606385 | C | T | 4 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(1): Show | 4 | HG02451.hp1 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-363C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606385 | ||||||
chr4:99606439 | A | C | 1 | a0003c0003t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1345-309A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606439 | ||||||
chr4:99606557 | T | A | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1345-191T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606557 | ||||||
chr4:99606558 | A | T | 1 | a0002c0002t0002g0289 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1345-190A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606558 | ||||||
chr4:99606632 | A | G | 1 | a0014c0018t0003g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1345-116A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606632 | ||||||
chr4:99606671 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1345-77C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 10/17 | chr4 | 99606671 | ||||||
chr4:99606967 | T | A | 1 | a0002c0002t0002g0300 | 1 | HG00280.hp2 | splice_region_variant&intron_variant | LOW | c.1557+7T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99606967 | ||||||
chr4:99606997 | G | GAA | 11 | a0004c0004t0001g0037a0004c0004t0001g0039a0007c0007t0003g0309others(8): Show | 11 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1557+47_1557+48dup others(2): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 99606997 | |||||
chr4:99607143 | CCTATAT | C | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1557+191_1557+196d others(8): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 99607143 | |||||
chr4:99607224 | C | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1557+264C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99607224 | ||||||
chr4:99607513 | C | T | 1 | a0002c0002t0002g0205 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1557+553C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99607513 | ||||||
chr4:99607794 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1557+834C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99607794 | ||||||
chr4:99607928 | C | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1558-838C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99607928 | ||||||
chr4:99607973 | T | TA | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 87 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1558-785dupA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr4 | 99607973 | |||||
chr4:99608119 | A | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 234 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.1558-647A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608119 | ||||||
chr4:99608185 | G | A | 8 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1558-581G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608185 | ||||||
chr4:99608279 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1558-487T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608279 | ||||||
chr4:99608350 | C | T | 1 | a0002c0002t0002g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1558-416C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608350 | ||||||
chr4:99608400 | G | A | 1 | a0004c0004t0001g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1558-366G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608400 | ||||||
chr4:99608431 | C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 7 | HG01975.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1558-335C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608431 | ||||||
chr4:99608557 | C | T | 56 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(53): Show | 67 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1558-209C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608557 | ||||||
chr4:99608620 | C | T | 5 | a0004c0004t0001g0034a0004c0004t0001g0035a0011c0010t0001g0023others(2): Show | 5 | HG01074.hp1 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1558-146C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 11/17 | chr4 | 99608620 | ||||||
chr4:99608986 | C | T | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1769+9C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99608986 | ||||||
chr4:99608991 | C | T | 8 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1769+14C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99608991 | ||||||
chr4:99609096 | A | G | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1769+119A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609096 | ||||||
chr4:99609390 | A | G | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1769+413A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609390 | ||||||
chr4:99609429 | G | A | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1769+452G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609429 | ||||||
chr4:99609566 | G | A | 1 | a0006c0006t0001g0307 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1769+589G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609566 | ||||||
chr4:99609605 | T | C | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1769+628T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609605 | ||||||
chr4:99609699 | G | A | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1769+722G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609699 | ||||||
chr4:99609906 | A | G | 47 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(44): Show | 51 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1769+929A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609906 | ||||||
chr4:99609922 | C | G | 20 | a0005c0005t0001g0013a0005c0005t0001g0083a0005c0005t0001g0104others(17): Show | 21 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1769+945C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609922 | ||||||
chr4:99609959 | C | T | 1 | a0003c0003t0001g0267 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1769+982C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609959 | ||||||
chr4:99609984 | A | C | 2 | a0004c0004t0011g0027a0004c0004t0011g0065 | 2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1769+1007A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99609984 | ||||||
chr4:99610006 | A | G | 13 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(10): Show | 14 | HG01256.hp2 HG01361.hp1 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.1769+1029A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99610006 | ||||||
chr4:99610152 | T | C | 1 | a0003c0003t0001g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1770-991T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99610152 | ||||||
chr4:99610435 | C | T | 1 | a0004c0004t0001g0064 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1770-708C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99610435 | ||||||
chr4:99610633 | T | C | 1 | a0010c0011t0003g0260 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1770-510T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99610633 | ||||||
chr4:99610840 | C | A | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-303C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99610840 | ||||||
chr4:99610918 | T | G | 1 | a0005c0005t0001g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1770-225T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99610918 | ||||||
chr4:99610929 | T | G | 2 | a0004c0004t0008g0025a0004c0004t0008g0029 | 2 | NA18948.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1770-214T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99610929 | ||||||
chr4:99611020 | G | A | 1 | a0003c0003t0001g0149 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1770-123G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99611020 | ||||||
chr4:99611065 | AT | A | 21 | a0006c0006t0004g0068a0007c0007t0003g0309a0007c0007t0003g0310others(18): Show | 21 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1770-68delT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr4 | 99611065 | |||||
chr4:99611096 | A | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 87 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1770-47A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 12/17 | chr4 | 99611096 | ||||||
chr4:99611276 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1867+36C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 13/17 | chr4 | 99611276 | ||||||
chr4:99611480 | T | C | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1989+27T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99611480 | ||||||
chr4:99611645 | T | A | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1989+192T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99611645 | ||||||
chr4:99612158 | T | G | 1 | a0003c0003t0001g0268 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1989+705T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612158 | ||||||
chr4:99612339 | T | C | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1990-574T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612339 | ||||||
chr4:99612366 | CT | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(70): Show | 88 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.1990-531delT | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr4 | 99612366 | |||||
chr4:99612401 | G | C | 1 | a0003c0003t0001g0084 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1990-512G>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612401 | ||||||
chr4:99612502 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1990-411C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612502 | ||||||
chr4:99612565 | C | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 234 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.1990-348C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612565 | ||||||
chr4:99612756 | C | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1990-157C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612756 | ||||||
chr4:99612795 | T | G | 1 | a0002c0002t0002g0292 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1990-118T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612795 | ||||||
chr4:99612884 | G | A | 67 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(64): Show | 72 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.1990-29G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 14/17 | chr4 | 99612884 | ||||||
chr4:99613193 | C | T | 1 | a0002c0002t0002g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2217+53C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613193 | ||||||
chr4:99613224 | C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0245 | 3 | HG00558.hp2 HG02071.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2217+84C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613224 | ||||||
chr4:99613325 | A | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2217+185A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613325 | ||||||
chr4:99613397 | T | G | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2217+257T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613397 | ||||||
chr4:99613500 | G | A | 1 | a0002c0002t0002g0294 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2217+360G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613500 | ||||||
chr4:99613653 | C | T | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2217+513C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613653 | ||||||
chr4:99613746 | T | G | 1 | a0006c0006t0001g0307 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2217+606T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613746 | ||||||
chr4:99613802 | A | G | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2217+662A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613802 | ||||||
chr4:99613858 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2217+718A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99613858 | ||||||
chr4:99614072 | A | G | 1 | a0006c0006t0001g0307 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2217+932A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99614072 | ||||||
chr4:99614173 | C | T | 28 | a0001c0001t0001g0012a0001c0001t0001g0113a0001c0001t0001g0114others(25): Show | 29 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.2217+1033C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99614173 | ||||||
chr4:99614436 | A | T | 1 | a0002c0002t0002g0174 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2217+1296A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99614436 | ||||||
chr4:99614765 | G | A | 1 | a0014c0018t0003g0320 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2217+1625G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99614765 | ||||||
chr4:99614788 | T | G | 4 | a0008c0008t0001g0048a0008c0008t0001g0054a0008c0008t0001g0055others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2217+1648T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99614788 | ||||||
chr4:99614946 | G | T | 47 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(44): Show | 51 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.2217+1806G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99614946 | ||||||
chr4:99615127 | C | T | 1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2217+1987C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615127 | ||||||
chr4:99615206 | C | T | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2217+2066C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615206 | ||||||
chr4:99615295 | G | A | 1 | a0004c0004t0001g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2217+2155G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615295 | ||||||
chr4:99615390 | T | A | 4 | a0004c0004t0001g0034a0011c0010t0001g0023a0011c0010t0001g0071others(1): Show | 4 | HG01074.hp1 HG02818.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.2217+2250T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615390 | ||||||
chr4:99615395 | T | C | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.2217+2255T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615395 | ||||||
chr4:99615526 | T | C | 17 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(14): Show | 19 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2217+2386T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615526 | ||||||
chr4:99615540 | C | T | 9 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(6): Show | 9 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.2217+2400C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615540 | ||||||
chr4:99615675 | G | A | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2217+2535G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615675 | ||||||
chr4:99615691 | G | A | 8 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2217+2551G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615691 | ||||||
chr4:99615912 | A | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 234 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.2217+2772A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615912 | ||||||
chr4:99615998 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2217+2858T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99615998 | ||||||
chr4:99616078 | T | C | 16 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(13): Show | 18 | HG01070.hp2 HG01071.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.2218-2896T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99616078 | ||||||
chr4:99616131 | C | T | 3 | a0005c0005t0001g0106a0005c0005t0001g0121a0005c0005t0001g0123 | 3 | HG03209.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2218-2843C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99616131 | ||||||
chr4:99616775 | T | A | 1 | a0002c0002t0002g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2218-2199T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99616775 | ||||||
chr4:99616779 | C | T | 1 | a0002c0002t0002g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2218-2195C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99616779 | ||||||
chr4:99617023 | A | G | 8 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2218-1951A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617023 | ||||||
chr4:99617064 | T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 231 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.2218-1910T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617064 | ||||||
chr4:99617266 | A | G | 20 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(17): Show | 20 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.2218-1708A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617266 | ||||||
chr4:99617289 | G | A | 56 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(53): Show | 67 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.2218-1685G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617289 | ||||||
chr4:99617297 | C | G | 21 | a0001c0001t0001g0216a0005c0005t0001g0013a0005c0005t0001g0083others(18): Show | 22 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2218-1677C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617297 | ||||||
chr4:99617357 | A | G | 2 | a0007c0007t0003g0309a0007c0007t0003g0310 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2218-1617A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617357 | ||||||
chr4:99617604 | G | A | 1 | a0002c0002t0002g0271 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2218-1370G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617604 | ||||||
chr4:99617674 | A | G | 3 | a0012c0009t0006g0321a0012c0009t0006g0322a0012c0009t0006g0323 | 3 | HG00639.hp1 HG01257.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2218-1300A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617674 | ||||||
chr4:99617682 | G | T | 1 | a0002c0002t0002g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2218-1292G>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617682 | ||||||
chr4:99617786 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2218-1188C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617786 | ||||||
chr4:99617922 | A | ATTGC | 81 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(78): Show | 92 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2218-1050_2218-104 others(8): Show |
MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr4 | 99617922 | |||||
chr4:99617979 | C | T | 56 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(53): Show | 67 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.2218-995C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99617979 | ||||||
chr4:99618046 | AC | A | 78 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(75): Show | 89 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.2218-927delC | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99618046 | ||||||
chr4:99618131 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2218-843C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99618131 | ||||||
chr4:99618140 | G | A | 81 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(78): Show | 92 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.2218-834G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99618140 | ||||||
chr4:99618304 | C | T | 1 | a0002c0002t0002g0191 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2218-670C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99618304 | ||||||
chr4:99618739 | T | C | 102 | a0001c0001t0001g0216a0003c0003t0001g0002a0003c0003t0001g0006others(99): Show | 114 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.2218-235T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99618739 | ||||||
chr4:99618806 | G | A | 2 | a0005c0005t0001g0104a0005c0005t0001g0105 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2218-168G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99618806 | ||||||
chr4:99618942 | T | G | 21 | a0001c0001t0001g0216a0005c0005t0001g0013a0005c0005t0001g0083others(18): Show | 22 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2218-32T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 15/17 | chr4 | 99618942 | ||||||
chr4:99619336 | A | G | 5 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2342+238A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99619336 | ||||||
chr4:99619441 | G | A | 1 | a0002c0002t0002g0200 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2342+343G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99619441 | ||||||
chr4:99619651 | C | A | 1 | a0019c0022t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2342+553C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99619651 | ||||||
chr4:99619754 | C | G | 2 | a0003c0003t0001g0139a0003c0003t0001g0141 | 2 | NA18949.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.2342+656C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99619754 | ||||||
chr4:99619855 | A | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 234 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.2342+757A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99619855 | ||||||
chr4:99620048 | A | T | 17 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(14): Show | 19 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2342+950A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620048 | ||||||
chr4:99620125 | T | C | 21 | a0001c0001t0001g0216a0005c0005t0001g0013a0005c0005t0001g0083others(18): Show | 22 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2343-936T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620125 | ||||||
chr4:99620202 | G | A | 1 | a0002c0021t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2343-859G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620202 | ||||||
chr4:99620254 | G | A | 45 | a0003c0003t0001g0002a0003c0003t0001g0006a0003c0003t0001g0010others(42): Show | 56 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2343-807G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620254 | ||||||
chr4:99620256 | G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 103 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.2343-805G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620256 | ||||||
chr4:99620369 | A | C | 3 | a0003c0003t0001g0152a0003c0003t0001g0164a0003c0003t0001g0165 | 3 | HG01070.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2343-692A>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620369 | ||||||
chr4:99620479 | A | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 87 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.2343-582A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620479 | ||||||
chr4:99620818 | T | A | 2 | a0004c0004t0001g0035a0004c0004t0001g0308 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2343-243T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620818 | ||||||
chr4:99620872 | A | G | 4 | a0006c0006t0001g0060a0006c0006t0001g0061a0006c0006t0001g0070others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2343-189A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99620872 | ||||||
chr4:99621010 | A | T | 17 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.2343-51A>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 16/17 | chr4 | 99621010 | ||||||
chr4:99621325 | A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 231 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.2513+94A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621325 | ||||||
chr4:99621415 | CA | C | 21 | a0001c0001t0001g0216a0005c0005t0001g0013a0005c0005t0001g0083others(18): Show | 22 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2513+193delA | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr4 | 99621415 | |||||
chr4:99621421 | A | G | 21 | a0001c0001t0001g0216a0005c0005t0001g0013a0005c0005t0001g0083others(18): Show | 22 | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2513+190A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621421 | ||||||
chr4:99621466 | T | C | 8 | a0009c0012t0007g0022a0009c0012t0007g0318a0009c0015t0007g0022others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2513+235T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621466 | ||||||
chr4:99621655 | C | A | 1 | a0004c0004t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2513+424C>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621655 | ||||||
chr4:99621656 | G | A | 3 | a0006c0006t0004g0045a0006c0006t0004g0062a0006c0006t0004g0075 | 3 | HG01256.hp2 HG01361.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2513+425G>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621656 | ||||||
chr4:99621764 | A | G | 17 | a0007c0007t0003g0309a0007c0007t0003g0310a0007c0007t0003g0311others(14): Show | 17 | HG00639.hp2 HG00733.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.2513+533A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621764 | ||||||
chr4:99621840 | T | C | 12 | a0002c0002t0002g0019a0002c0002t0002g0274a0002c0002t0002g0275others(9): Show | 13 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2513+609T>C | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621840 | ||||||
chr4:99621944 | T | A | 1 | a0003c0003t0001g0167 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2513+713T>A | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99621944 | ||||||
chr4:99622068 | C | T | 5 | a0001c0001t0001g0220a0001c0001t0001g0227a0001c0001t0001g0228others(2): Show | 5 | HG00558.hp2 HG02056.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.2514-609C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99622068 | ||||||
chr4:99622147 | T | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(69): Show | 87 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.2514-530T>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99622147 | ||||||
chr4:99622227 | C | T | 2 | a0004c0004t0001g0032a0004c0004t0001g0046 | 2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2514-450C>T | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99622227 | ||||||
chr4:99622268 | C | G | 7 | a0004c0004t0001g0007a0004c0004t0001g0038a0004c0004t0001g0044others(4): Show | 8 | HG01934.hp1 NA18965.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.2514-409C>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99622268 | ||||||
chr4:99622385 | A | G | 1 | a0010c0011t0003g0302 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2514-292A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99622385 | ||||||
chr4:99622588 | A | G | 47 | a0004c0004t0001g0004a0004c0004t0001g0007a0004c0004t0001g0026others(44): Show | 51 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.2514-89A>G | MTTP | ENSG00000138823.14 | transcript | ENST00000265517.10 | protein_coding | 17/17 | chr4 | 99622588 |