geneid | 51095 |
---|---|
ensemblid | ENSG00000072756.18 |
hgncid | 17341 |
symbol | TRNT1 |
name | tRNA nucleotidyl transferase 1 |
refseq_nuc | NM_182916.3 |
refseq_prot | NP_886552.3 |
ensembl_nuc | ENST00000251607.11 |
ensembl_prot | ENSP00000251607.6 |
mane_status | MANE Select |
chr | chr3 |
start | 3126940 |
end | 3149023 |
strand | + |
ver | v1.2 |
region | chr3:3126940-3149023 |
region5000 | chr3:3121940-3154023 |
regionname0 | TRNT1_chr3_3126940_3149023 |
regionname5000 | TRNT1_chr3_3121940_3154023 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 434 | 366 | 62 | 73 | 175 | 12 | 43 | 135 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002 | 1/0 | 434 | 31 | 28 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0003 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0004 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0005 | 0/0 | 434 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0006 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0007 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1305 | 304 | 45 | 52 | 163 | 9 | 34 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0002 | 0/0 | 1305 | 54 | 10 | 21 | 11 | 3 | 9 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0003 | 1/0 | 1305 | 25 | 23 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0004 | 0/0 | 1305 | 6 | 6 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0005 | 0/0 | 1305 | 4 | 3 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0006 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0007 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0008 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0009 | 0/0 | 1305 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0010 | 0/0 | 1305 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0011 | 0/0 | 1305 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0012 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0013 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
c0014 | 0/0 | 1305 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 967 | 165 | 10 | 18 | 116 | 2 | 19 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0002 | 0/1 | 967 | 81 | 14 | 24 | 28 | 6 | 8 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0003 | 0/0 | 948 | 52 | 9 | 21 | 10 | 3 | 9 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0004 | 1/0 | 948 | 22 | 20 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0005 | 0/0 | 968 | 18 | 3 | 7 | 2 | 0 | 6 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0006 | 0/0 | 963 | 12 | 3 | 0 | 8 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0007 | 0/0 | 971 | 7 | 4 | 1 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0008 | 0/0 | 948 | 5 | 5 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0009 | 0/0 | 971 | 5 | 5 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0010 | 0/0 | 968 | 5 | 4 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0011 | 0/0 | 967 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0012 | 0/0 | 967 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0013 | 0/0 | 967 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0014 | 0/0 | 948 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0015 | 0/0 | 948 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0016 | 0/0 | 952 | 2 | 1 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0017 | 0/0 | 963 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0018 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0019 | 0/0 | 952 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0020 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0021 | 0/0 | 967 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0022 | 0/0 | 967 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0023 | 0/0 | 948 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0024 | 0/0 | 967 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0025 | 0/0 | 967 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
t0026 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 35 | 0 | 1 | 28 | 1 | 5 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0002 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0003 | 0/0 | 12 | 0 | 4 | 8 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0004 | 0/0 | 12 | 11 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0005 | 0/1 | 11 | 2 | 3 | 4 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0006 | 0/0 | 9 | 2 | 2 | 0 | 2 | 3 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0007 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0009 | 0/0 | 9 | 1 | 7 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0010 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0011 | 0/0 | 7 | 1 | 5 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0012 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0014 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0015 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0017 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0026 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1305 | 304 | 45 | 52 | 163 | 9 | 34 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0002 | 0/0 | 1305 | 54 | 10 | 21 | 11 | 3 | 9 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0004 | 0/0 | 1305 | 6 | 6 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0010 | 0/0 | 1305 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0012 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0003 | 1/0 | 1305 | 25 | 23 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0005 | 0/0 | 1305 | 4 | 3 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0006 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0008 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0003c0009 | 0/0 | 1305 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0004c0011 | 0/0 | 1305 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0005c0014 | 0/0 | 1305 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0006c0013 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0007c0007 | 0/0 | 1305 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2271 | 163 | 10 | 18 | 115 | 2 | 18 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0002 | 0/1 | 2271 | 80 | 14 | 24 | 27 | 6 | 8 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0003 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0005 | 0/0 | 2272 | 18 | 3 | 7 | 2 | 0 | 6 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0006 | 0/0 | 2267 | 12 | 3 | 0 | 8 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0007 | 0/0 | 2275 | 7 | 4 | 1 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0009 | 0/0 | 2275 | 5 | 5 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0011 | 0/0 | 2271 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0012 | 0/0 | 2271 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0013 | 0/0 | 2271 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0017 | 0/0 | 2267 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0018 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0021 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0022 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0024 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0001t0025 | 0/0 | 2271 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0002t0003 | 0/0 | 2252 | 50 | 7 | 21 | 10 | 3 | 9 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0002t0014 | 0/0 | 2252 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0002t0019 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0002t0020 | 0/0 | 2252 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0004t0008 | 0/0 | 2252 | 5 | 5 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0004t0016 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0010t0001 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0001c0012t0003 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0003t0004 | 1/0 | 2252 | 21 | 19 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0003t0015 | 0/0 | 2252 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0003t0023 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0005t0010 | 0/0 | 2272 | 4 | 3 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0006t0010 | 0/0 | 2272 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0002c0008t0004 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0003c0009t0002 | 0/0 | 2271 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0004c0011t0001 | 0/0 | 2271 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0005c0014t0016 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0006c0013t0026 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
a0007c0007t0014 | 0/0 | 2252 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | copy fasta | chr3 | 3121940 | 3154023 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 35 | 0 | 1 | 28 | 1 | 5 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0003 | 0/0 | 12 | 0 | 4 | 8 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0005 | 0/1 | 11 | 2 | 3 | 4 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0009 | 0/0 | 9 | 1 | 7 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0014 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0011 | 0/0 | 7 | 1 | 5 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0006g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0006g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0009g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0009g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0011g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0012g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0012g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0013g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0013g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0017g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0017g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0018g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0022g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0024g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0001t0025g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0006 | 0/0 | 9 | 2 | 2 | 0 | 2 | 3 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0012 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0017 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0014g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0019g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0002t0020g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0004t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0004t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0004t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0004t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0004t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0004t0016g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0001c0012t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0004 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0015g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0003t0023g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0005t0010g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0005t0010g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0006t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0002c0008t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0003c0009t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0004c0011t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0005c0014t0016g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0006c0013t0026g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
a0007c0007t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0006 | EUR | GBR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0027 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0006 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0053 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0149 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00642 | hp2 | a0005 | c0014 | t0016 | g0138 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0074 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0203 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01106 | hp2 | a0001 | c0001 | t0017 | g0148 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0150 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01167 | hp2 | a0001 | c0002 | t0003 | g0006 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0054 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01169 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0162 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01175 | hp2 | a0001 | c0001 | t0017 | g0147 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01243 | hp1 | a0002 | c0003 | t0004 | g0004 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01243 | hp2 | a0002 | c0005 | t0010 | g0146 | AMR | PUR | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0012 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0012 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0006 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0071 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0179 | EUR | IBS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01516 | hp2 | a0001 | c0002 | t0003 | g0068 | EUR | IBS | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01884 | hp2 | a0001 | c0004 | t0008 | g0047 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01891 | hp1 | a0001 | c0004 | t0008 | g0048 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01891 | hp2 | a0001 | c0001 | t0013 | g0161 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0072 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01978 | hp1 | a0001 | c0002 | t0003 | g0012 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0028 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02027 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02055 | hp2 | a0002 | c0003 | t0004 | g0038 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02135 | hp2 | a0001 | c0001 | t0021 | g0010 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0011 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0028 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02155 | hp2 | a0001 | c0002 | t0020 | g0016 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | CDX | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02257 | hp1 | a0002 | c0003 | t0004 | g0024 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02257 | hp2 | a0001 | c0004 | t0008 | g0051 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02258 | hp1 | a0006 | c0013 | t0026 | g0124 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02258 | hp2 | a0002 | c0008 | t0004 | g0004 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02280 | hp2 | a0001 | c0012 | t0003 | g0139 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0067 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PEL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02572 | hp1 | a0001 | c0002 | t0003 | g0064 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0129 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02615 | hp1 | a0002 | c0003 | t0004 | g0143 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02622 | hp1 | a0001 | c0004 | t0016 | g0137 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02622 | hp2 | a0002 | c0003 | t0004 | g0141 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02647 | hp1 | a0002 | c0003 | t0004 | g0021 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0197 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02683 | hp2 | a0001 | c0001 | t0007 | g0204 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02723 | hp1 | a0002 | c0003 | t0004 | g0021 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0131 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02735 | hp2 | a0001 | c0002 | t0003 | g0017 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0017 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0041 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02886 | hp1 | a0002 | c0003 | t0004 | g0024 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02895 | hp1 | a0001 | c0002 | t0003 | g0077 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02895 | hp2 | a0002 | c0003 | t0004 | g0004 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02896 | hp1 | a0001 | c0001 | t0013 | g0026 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02896 | hp2 | a0002 | c0003 | t0004 | g0021 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02897 | hp1 | a0001 | c0001 | t0013 | g0187 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02922 | hp1 | a0002 | c0003 | t0004 | g0145 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02965 | hp2 | a0002 | c0003 | t0015 | g0004 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02970 | hp1 | a0002 | c0003 | t0004 | g0038 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02976 | hp1 | a0002 | c0003 | t0004 | g0004 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02976 | hp2 | a0002 | c0003 | t0015 | g0004 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03041 | hp2 | a0007 | c0007 | t0014 | g0133 | AFR | GWD | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0058 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0190 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03130 | hp1 | a0002 | c0005 | t0010 | g0022 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03130 | hp2 | a0001 | c0004 | t0008 | g0050 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03139 | hp1 | a0001 | c0002 | t0003 | g0135 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03195 | hp2 | a0001 | c0001 | t0025 | g0188 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03209 | hp1 | a0001 | c0002 | t0014 | g0036 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0076 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03453 | hp1 | a0002 | c0003 | t0023 | g0004 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03453 | hp2 | a0002 | c0005 | t0010 | g0022 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03486 | hp2 | a0002 | c0003 | t0004 | g0142 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0154 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0155 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0006 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0152 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03516 | hp2 | a0002 | c0003 | t0015 | g0004 | AFR | ESN | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0062 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03579 | hp2 | a0001 | c0004 | t0008 | g0049 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0069 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03927 | hp1 | a0004 | c0011 | t0001 | g0113 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0006 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0151 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0006 | SAS | BEB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0017 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0070 | SAS | STU | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18522 | hp2 | a0002 | c0006 | t0010 | g0022 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18612 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18906 | hp1 | a0002 | c0003 | t0004 | g0004 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18940 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18944 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18952 | hp2 | a0001 | c0010 | t0001 | g0111 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18967 | hp2 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18969 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18978 | hp2 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18986 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18990 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18995 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19010 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19030 | hp2 | a0002 | c0003 | t0004 | g0004 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19054 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19056 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19060 | hp1 | a0001 | c0001 | t0012 | g0025 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19060 | hp2 | a0001 | c0001 | t0022 | g0121 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19066 | hp2 | a0003 | c0009 | t0002 | g0130 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19070 | hp1 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19076 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19077 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19084 | hp1 | a0001 | c0001 | t0012 | g0169 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19085 | hp2 | a0001 | c0001 | t0024 | g0007 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA19240 | hp2 | a0002 | c0005 | t0010 | g0022 | AFR | YRI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ASW | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ASW | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0177 | EUR | TSI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0005 | EUR | TSI | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | GIH | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02109 | hp2 | a0001 | c0002 | t0014 | g0036 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG02559 | hp2 | a0002 | c0003 | t0004 | g0004 | AFR | ACB | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03471 | hp1 | a0002 | c0003 | t0004 | g0021 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG03471 | hp2 | a0002 | c0003 | t0004 | g0024 | AFR | MSL | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20300 | hp1 | a0002 | c0003 | t0004 | g0004 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | USA | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA21309 | hp1 | a0001 | c0002 | t0019 | g0065 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0005 | REF | REF | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
homoSapiens_grch38 | hp1 | a0002 | c0003 | t0004 | g0144 | REF | REF | TRNT1_chr3_3121940_3154023 | TRNT1 | chr3 | 3121940 | 3154023 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:3129108
|
C | T | 5 | a0001a0003a0004others(2): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
missense_variant | MODERATE | c.68C>T | p.Pro23Leu | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/8 | 146/2252 | 68/1305 | 23/434 | chr3 | 3129108 | ||
chr3:3137442
|
A | G | 1 | a0006 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.331A>G | p.Ile111Val | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/8 | 409/2252 | 331/1305 | 111/434 | chr3 | 3137442 | ||
chr3:3137452
|
G | A | 1 | a0003 | 1 | NA19066.hp2 | missense_variant&splice_region_variant | MODERATE | c.341G>A | p.Arg114Lys | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/8 | 419/2252 | 341/1305 | 114/434 | chr3 | 3137452 | ||
chr3:3147495
|
A | G | 1 | a0005 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.848A>G | p.Lys283Arg | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 926/2252 | 848/1305 | 283/434 | chr3 | 3147495 | ||
chr3:3147509
|
T | A | 1 | a0007 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.862T>A | p.Phe288Ile | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 940/2252 | 862/1305 | 288/434 | chr3 | 3147509 | ||
chr3:3147953
|
C | G | 1 | a0004 | 1 | HG03927.hp1 | stop_gained | HIGH | c.1104C>G | p.Tyr368* | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 1182/2252 | 1104/1305 | 368/434 | chr3 | 3147953 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:3129173
|
C | T | 2 | a0001c0004a0005c0014 | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
synonymous_variant | LOW | c.133C>T | p.Leu45Leu | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/8 | 211/2252 | 133/1305 | 45/434 | chr3 | 3129173 | ||
chr3:3140611
|
G | T | 3 | a0001c0004a0001c0012a0005c0014 | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
synonymous_variant | LOW | c.444G>T | p.Ala148Ala | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/8 | 522/2252 | 444/1305 | 148/434 | chr3 | 3140611 | ||
chr3:3144615
|
T | C | 1 | a0002c0006 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.513T>C | p.Asn171Asn | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/8 | 591/2252 | 513/1305 | 171/434 | chr3 | 3144615 | ||
chr3:3146601
|
T | C | 1 | a0001c0010 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.780T>C | p.Asp260Asp | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/8 | 858/2252 | 780/1305 | 260/434 | chr3 | 3146601 | ||
chr3:3147592
|
C | T | 1 | a0002c0008 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.945C>T | p.Ile315Ile | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 1023/2252 | 945/1305 | 315/434 | chr3 | 3147592 | ||
chr3:3147595
|
A | G | 7 | a0001c0001a0001c0010a0002c0005others(4): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
synonymous_variant | LOW | c.948A>G | p.Ala316Ala | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/8 | 1026/2252 | 948/1305 | 316/434 | chr3 | 3147595 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:3126942
|
C | A | 3 | a0001c0004t0008a0001c0004t0016a0005c0014t0016 | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-76C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/8 | 2099 | chr3 | 3126942 | |||||
chr3:3148206
|
C | T | 1 | a0006c0013t0026 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 52 | chr3 | 3148206 | |||||
chr3:3148275
|
A | C | 1 | a0001c0001t0025 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*121A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 121 | chr3 | 3148275 | |||||
chr3:3148365
|
T | C | 1 | a0001c0001t0018 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 211 | chr3 | 3148365 | |||||
chr3:3148403
|
C | G | 1 | a0001c0001t0012 | 4 | NA18944.hp1 NA18967.hp2 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*249C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 249 | chr3 | 3148403 | |||||
chr3:3148463
|
C | T | 1 | a0001c0001t0024 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 309 | chr3 | 3148463 | |||||
chr3:3148556
|
T | C | 7 | a0001c0001t0003a0001c0002t0003a0001c0002t0019others(4): Show | 56 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*402T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 402 | chr3 | 3148556 | |||||
chr3:3148564
|
G | C | 1 | a0001c0001t0011 | 4 | NA18612.hp2 NA18969.hp2 NA18990.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*410G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 410 | chr3 | 3148564 | |||||
chr3:3148594
|
C | T | 2 | a0001c0001t0018a0001c0004t0008 | 6 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*440C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 440 | chr3 | 3148594 | |||||
chr3:3148622
|
A | G | 1 | a0002c0003t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 468 | chr3 | 3148622 | |||||
chr3:3148639
|
T | C | 1 | a0001c0001t0013 | 3 | HG01891.hp2 HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*485T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 485 | chr3 | 3148639 | |||||
chr3:3148642
|
G | A | 1 | a0001c0001t0017 | 2 | HG01106.hp2 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*488G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 488 | chr3 | 3148642 | |||||
chr3:3148767
|
G | A | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*613G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 613 | chr3 | 3148767 | |||||
chr3:3148793
|
A | G | 1 | a0001c0002t0020 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 639 | chr3 | 3148793 | |||||
chr3:3148804
|
T | TATTA | 7 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(4): Show | 101 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*662dupATTA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 663 | INFO_REALIGN_3_PRIME | chr3 | 3148804 | ||||
chr3:3148815
|
T | TA | 3 | a0001c0001t0005a0002c0005t0010a0002c0006t0010 | 23 | HG00738.hp2 HG01071.hp2 HG01081.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*662dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 663 | INFO_REALIGN_3_PRIME | chr3 | 3148815 | ||||
chr3:3148817
|
T | C | 1 | a0001c0001t0021 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 663 | chr3 | 3148817 | |||||
chr3:3148874
|
A | G | 1 | a0001c0001t0022 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 720 | chr3 | 3148874 | |||||
chr3:3148898
|
C | T | 1 | a0002c0003t0015 | 3 | HG02965.hp2 HG02976.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*744C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 744 | chr3 | 3148898 | |||||
chr3:3148952
|
C | CTATT | 1 | a0001c0001t0009 | 5 | HG02818.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*802dupTATT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 803 | INFO_REALIGN_3_PRIME | chr3 | 3148952 | ||||
chr3:3148962
|
A | ATATTCTC others(12): Show |
4 | a0001c0001t0005a0001c0001t0007a0002c0005t0010others(1): Show | 30 | HG00738.hp2 HG01071.hp1 HG01071.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*821_*822insAAGATT others(13): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 822 | INFO_REALIGN_3_PRIME | chr3 | 3148962 | ||||
chr3:3148962
|
A | ATATTCTC others(8): Show |
9 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(6): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*810_*824dupATTCTC others(9): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 825 | INFO_REALIGN_3_PRIME | chr3 | 3148962 | ||||
chr3:3148970
|
T | TAAAG | 3 | a0001c0002t0019a0001c0004t0016a0005c0014t0016 | 3 | HG00642.hp2 HG02622.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*818_*821dupAAGA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 822 | INFO_REALIGN_3_PRIME | chr3 | 3148970 | ||||
chr3:3148970
|
T | TAAAGATT others(12): Show |
7 | a0001c0001t0001a0001c0001t0011a0001c0001t0021others(4): Show | 172 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*824_*825insATTCTC others(13): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 8/8 | 825 | INFO_REALIGN_3_PRIME | chr3 | 3148970 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:3127088
|
C | A | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+98C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127088 | ||||||
chr3:3127166
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-28+176C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127166 | ||||||
chr3:3127207
|
C | T | 1 | a0001c0001t0006g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-28+217C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127207 | ||||||
chr3:3127210
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-28+220C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127210 | ||||||
chr3:3127238
|
G | T | 1 | a0001c0001t0001g0209 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-28+248G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127238 | ||||||
chr3:3127273
|
A | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+283A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127273 | ||||||
chr3:3127287
|
G | C | 4 | a0001c0002t0003g0016a0001c0002t0003g0052a0001c0002t0003g0053others(1): Show | 6 | HG00438.hp1 HG02155.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+297G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127287 | ||||||
chr3:3127354
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+364G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127354 | ||||||
chr3:3127357
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+367G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127357 | ||||||
chr3:3127360
|
A | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+370A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127360 | ||||||
chr3:3127369
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+379G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127369 | ||||||
chr3:3127370
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+380T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127370 | ||||||
chr3:3127377
|
G | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+387G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127377 | ||||||
chr3:3127381
|
C | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+391C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127381 | ||||||
chr3:3127384
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+394G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127384 | ||||||
chr3:3127386
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+396G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127386 | ||||||
chr3:3127387
|
G | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+397G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127387 | ||||||
chr3:3127389
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+399C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127389 | ||||||
chr3:3127391
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+401G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127391 | ||||||
chr3:3127394
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+404G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127394 | ||||||
chr3:3127395
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+405G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127395 | ||||||
chr3:3127396
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+406G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127396 | ||||||
chr3:3127399
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+409G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127399 | ||||||
chr3:3127400
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+410C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127400 | ||||||
chr3:3127493
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-28+503G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127493 | ||||||
chr3:3127506
|
A | T | 77 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0189others(74): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-28+516A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127506 | ||||||
chr3:3127508
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+518G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127508 | ||||||
chr3:3127534
|
A | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+544A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127534 | ||||||
chr3:3127589
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+599G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127589 | ||||||
chr3:3127590
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+600A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127590 | ||||||
chr3:3127602
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+612G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127602 | ||||||
chr3:3127605
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+615G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127605 | ||||||
chr3:3127606
|
G | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+616G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127606 | ||||||
chr3:3127619
|
A | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+629A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127619 | ||||||
chr3:3127620
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+630T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127620 | ||||||
chr3:3127622
|
C | A | 2 | a0001c0002t0003g0017a0001c0002t0003g0054 | 5 | HG01168.hp2 HG01169.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+632C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127622 | ||||||
chr3:3127633
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+643A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127633 | ||||||
chr3:3127634
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+644C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127634 | ||||||
chr3:3127635
|
A | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+645A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127635 | ||||||
chr3:3127650
|
T | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+660T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127650 | ||||||
chr3:3127651
|
C | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+661C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127651 | ||||||
chr3:3127677
|
GGTGGGGA others(26): Show |
G | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+688_-28+720del others(33): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127677 | ||||||
chr3:3127690
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-28+700G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127690 | ||||||
chr3:3127713
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+723A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127713 | ||||||
chr3:3127714
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+724C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127714 | ||||||
chr3:3127719
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+729T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127719 | ||||||
chr3:3127720
|
T | G | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0006g0027others(5): Show | 9 | HG00280.hp1 HG01106.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+730T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127720 | ||||||
chr3:3127733
|
A | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+743A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127733 | ||||||
chr3:3127734
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+744C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127734 | ||||||
chr3:3127738
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+748G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127738 | ||||||
chr3:3127739
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-28+749T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127739 | ||||||
chr3:3127739
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+749T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127739 | ||||||
chr3:3127753
|
A | ACCCAGCA others(15): Show |
1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+766_-28+767ins others(22): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3127753 | |||||
chr3:3127776
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-28+786C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127776 | ||||||
chr3:3127782
|
C | A | 31 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0002t0003g0006others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-28+792C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127782 | ||||||
chr3:3127811
|
A | C | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+821A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127811 | ||||||
chr3:3127812
|
C | T | 1 | a0001c0001t0002g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-28+822C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127812 | ||||||
chr3:3127923
|
A | C | 1 | a0001c0001t0002g0207 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-28+933A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127923 | ||||||
chr3:3127953
|
G | T | 2 | a0002c0005t0010g0022a0002c0006t0010g0022 | 4 | HG03130.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+963G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3127953 | ||||||
chr3:3128049
|
T | C | 5 | a0001c0001t0005g0151a0001c0001t0005g0152a0001c0001t0005g0153others(2): Show | 5 | HG03491.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-965T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128049 | ||||||
chr3:3128056
|
A | G | 1 | a0001c0001t0005g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-27-958A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128056 | ||||||
chr3:3128235
|
C | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-27-779C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128235 | ||||||
chr3:3128255
|
C | T | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27-759C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128255 | ||||||
chr3:3128368
|
G | A | 6 | a0001c0001t0001g0079a0001c0004t0008g0047a0001c0004t0008g0048others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-646G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128368 | ||||||
chr3:3128394
|
C | G | 31 | a0001c0001t0005g0136a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-27-620C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128394 | ||||||
chr3:3128410
|
A | G | 1 | a0001c0001t0002g0037 | 2 | HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-27-604A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128410 | ||||||
chr3:3128481
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-27-533C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128481 | ||||||
chr3:3128500
|
G | A | 1 | a0001c0001t0002g0156 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-27-514G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128500 | ||||||
chr3:3128547
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-27-467T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128547 | ||||||
chr3:3128598
|
C | CA | 36 | a0001c0001t0002g0026a0001c0001t0002g0043a0001c0001t0002g0191others(33): Show | 61 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-27-393dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | |||||
chr3:3128598
|
C | CAA | 49 | a0001c0001t0001g0189a0001c0001t0002g0005a0001c0001t0002g0014others(46): Show | 76 | HG00408.hp2 HG00621.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-27-394_-27-393dup others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | |||||
chr3:3128598
|
C | CAAA | 20 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0125others(17): Show | 22 | HG00544.hp2 HG01106.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-27-395_-27-393dup others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | |||||
chr3:3128598
|
C | CAAAA | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(52): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-27-396_-27-393dup others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | |||||
chr3:3128598
|
C | CAAAAA | 20 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0029others(17): Show | 30 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.-27-397_-27-393dup others(5): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | |||||
chr3:3128598
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0005g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-27-404_-27-393del others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | |||||
chr3:3128598
|
CAAAAAAA others(6): Show |
C | 12 | a0001c0001t0002g0009a0001c0001t0002g0044a0001c0001t0002g0045others(9): Show | 23 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.-27-405_-27-393del others(13): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128598 | |||||
chr3:3128613
|
A | AAAG | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-399_-27-398ins others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128613 | |||||
chr3:3128725
|
G | C | 77 | a0001c0001t0001g0189a0001c0001t0002g0005a0001c0001t0002g0009others(74): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-27-289G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128725 | ||||||
chr3:3128776
|
A | AGTT | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-27-237_-27-235dup others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 3128776 | |||||
chr3:3128783
|
G | A | 1 | a0002c0003t0004g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-27-231G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128783 | ||||||
chr3:3128845
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-27-169A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 1/7 | chr3 | 3128845 | ||||||
chr3:3129226
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.148+38A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129226 | ||||||
chr3:3129282
|
T | C | 31 | a0001c0001t0005g0136a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.148+94T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129282 | ||||||
chr3:3129321
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0191 | 3 | HG02559.hp1 HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.148+133G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129321 | ||||||
chr3:3129338
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 172 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.148+150C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129338 | ||||||
chr3:3129339
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.148+151A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129339 | ||||||
chr3:3129361
|
G | C | 1 | a0001c0001t0002g0166 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.148+173G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129361 | ||||||
chr3:3129425
|
G | C | 1 | a0001c0004t0008g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.148+237G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129425 | ||||||
chr3:3129441
|
G | A | 77 | a0001c0001t0001g0189a0001c0001t0002g0005a0001c0001t0002g0009others(74): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.148+253G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129441 | ||||||
chr3:3129587
|
A | C | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+399A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129587 | ||||||
chr3:3129587
|
A | G | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.148+399A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129587 | ||||||
chr3:3129602
|
TAAAAG | T | 3 | a0001c0001t0009g0041a0001c0001t0009g0042a0001c0001t0009g0190 | 5 | HG02818.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+416_148+420del others(5): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3129602 | |||||
chr3:3129705
|
T | C | 3 | a0001c0001t0006g0027a0001c0001t0006g0056a0001c0001t0006g0057 | 4 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+517T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129705 | ||||||
chr3:3129742
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.148+554C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129742 | ||||||
chr3:3129754
|
G | C | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.148+566G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129754 | ||||||
chr3:3129776
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.148+588C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129776 | ||||||
chr3:3129816
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.148+628T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129816 | ||||||
chr3:3129818
|
C | A | 76 | a0001c0001t0001g0157a0001c0001t0002g0005a0001c0001t0002g0009others(73): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.148+630C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129818 | ||||||
chr3:3129848
|
C | G | 1 | a0006c0013t0026g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.148+660C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129848 | ||||||
chr3:3129895
|
C | T | 1 | a0006c0013t0026g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.148+707C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129895 | ||||||
chr3:3129975
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG00558.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.148+787G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3129975 | ||||||
chr3:3130002
|
G | A | 1 | a0001c0002t0003g0063 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.148+814G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130002 | ||||||
chr3:3130029
|
G | GCCTGACT | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.148+843_148+844ins others(7): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3130029 | |||||
chr3:3130203
|
A | G | 1 | a0001c0001t0022g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.148+1015A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130203 | ||||||
chr3:3130213
|
T | C | 34 | a0001c0001t0002g0168a0001c0001t0003g0210a0001c0001t0005g0136others(31): Show | 56 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.148+1025T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130213 | ||||||
chr3:3130213
|
T | G | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+1025T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130213 | ||||||
chr3:3130289
|
T | C | 1 | a0002c0003t0004g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.148+1101T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130289 | ||||||
chr3:3130332
|
A | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(62): Show | 154 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.148+1144A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130332 | ||||||
chr3:3130439
|
C | T | 1 | a0006c0013t0026g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.148+1251C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130439 | ||||||
chr3:3130502
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.148+1314G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130502 | ||||||
chr3:3130513
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.148+1325A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130513 | ||||||
chr3:3130620
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.148+1432T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130620 | ||||||
chr3:3130711
|
C | T | 3 | a0001c0001t0006g0027a0001c0001t0006g0056a0001c0001t0006g0057 | 4 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+1523C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130711 | ||||||
chr3:3130752
|
T | G | 3 | a0001c0004t0016g0137a0001c0012t0003g0139a0005c0014t0016g0138 | 3 | HG00642.hp2 HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.148+1564T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130752 | ||||||
chr3:3130759
|
G | A | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0017g0147others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.148+1571G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130759 | ||||||
chr3:3130899
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148+1711C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130899 | ||||||
chr3:3130901
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(70): Show | 166 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.148+1713G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130901 | ||||||
chr3:3130915
|
C | G | 4 | a0001c0001t0006g0027a0001c0001t0006g0056a0001c0001t0006g0057others(1): Show | 5 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+1727C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130915 | ||||||
chr3:3130952
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.148+1764T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3130952 | ||||||
chr3:3131009
|
G | GA | 3 | a0001c0001t0002g0212a0001c0001t0012g0025a0001c0001t0012g0169 | 5 | NA18943.hp2 NA18944.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+1822dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3131009 | |||||
chr3:3131065
|
A | G | 1 | a0001c0002t0003g0075 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.148+1877A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131065 | ||||||
chr3:3131077
|
T | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+1889T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131077 | ||||||
chr3:3131077
|
TA | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0118a0001c0001t0001g0119others(9): Show | 12 | HG00738.hp1 HG00741.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.148+1904delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3131077 | |||||
chr3:3131176
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.148+1988C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131176 | ||||||
chr3:3131236
|
C | T | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+2048C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131236 | ||||||
chr3:3131272
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.148+2084T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131272 | ||||||
chr3:3131296
|
A | G | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+2108A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131296 | ||||||
chr3:3131313
|
G | C | 1 | a0001c0002t0003g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.148+2125G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131313 | ||||||
chr3:3131332
|
A | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(76): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.148+2144A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131332 | ||||||
chr3:3131398
|
T | A | 1 | a0001c0001t0025g0188 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.148+2210T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131398 | ||||||
chr3:3131413
|
A | G | 3 | a0001c0001t0007g0040a0001c0001t0007g0158a0001c0001t0007g0163 | 4 | HG02109.hp1 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+2225A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131413 | ||||||
chr3:3131414
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.148+2226T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131414 | ||||||
chr3:3131428
|
T | C | 2 | a0001c0001t0002g0160a0001c0001t0002g0192 | 2 | HG02135.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.148+2240T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131428 | ||||||
chr3:3131463
|
AAACTGGC others(2196): Show |
A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.148+2276_149-3594d others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131463 | ||||||
chr3:3131505
|
C | T | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+2317C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131505 | ||||||
chr3:3131544
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.148+2356A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131544 | ||||||
chr3:3131554
|
G | A | 1 | a0001c0001t0005g0154 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.148+2366G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131554 | ||||||
chr3:3131669
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.148+2481G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131669 | ||||||
chr3:3131839
|
AAAAC | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0017g0147others(1): Show | 4 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+2658_148+2661d others(6): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3131839 | |||||
chr3:3131841
|
A | G | 1 | a0001c0001t0002g0192 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.148+2653A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131841 | ||||||
chr3:3131892
|
A | G | 1 | a0001c0001t0018g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.148+2704A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131892 | ||||||
chr3:3131965
|
A | G | 80 | a0001c0001t0001g0157a0001c0001t0002g0005a0001c0001t0002g0009others(77): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.148+2777A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3131965 | ||||||
chr3:3132007
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.148+2819G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132007 | ||||||
chr3:3132122
|
G | A | 5 | a0001c0001t0005g0129a0001c0001t0005g0151a0001c0001t0005g0152others(2): Show | 5 | HG02602.hp1 HG03491.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+2934G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132122 | ||||||
chr3:3132168
|
C | T | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.148+2980C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132168 | ||||||
chr3:3132222
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.148+3034G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132222 | ||||||
chr3:3132233
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.148+3045G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132233 | ||||||
chr3:3132252
|
A | G | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.148+3064A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132252 | ||||||
chr3:3132345
|
T | C | 1 | a0001c0002t0019g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.148+3157T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132345 | ||||||
chr3:3132425
|
C | T | 1 | a0001c0001t0002g0046 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.148+3237C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132425 | ||||||
chr3:3132426
|
G | A | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+3238G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132426 | ||||||
chr3:3132519
|
CTG | C | 76 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0014others(73): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.148+3332_148+3333d others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132519 | ||||||
chr3:3132546
|
G | A | 31 | a0001c0001t0005g0136a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.148+3358G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132546 | ||||||
chr3:3132589
|
A | G | 2 | a0001c0002t0003g0017a0001c0002t0003g0054 | 5 | HG01168.hp2 HG01169.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+3401A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132589 | ||||||
chr3:3132590
|
C | A | 2 | a0001c0002t0003g0017a0001c0002t0003g0054 | 5 | HG01168.hp2 HG01169.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.148+3402C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132590 | ||||||
chr3:3132614
|
A | G | 1 | a0001c0001t0001g0030 | 2 | NA18970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.148+3426A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132614 | ||||||
chr3:3132623
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.148+3435G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132623 | ||||||
chr3:3132625
|
A | G | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3437A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132625 | ||||||
chr3:3132632
|
T | C | 8 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0032others(5): Show | 21 | HG00741.hp1 HG01069.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.148+3444T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132632 | ||||||
chr3:3132682
|
TA | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.148+3507delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132682 | |||||
chr3:3132687
|
AAAAAAAA others(3): Show |
A | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3507_148+3516d others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132687 | |||||
chr3:3132697
|
T | A | 8 | a0001c0001t0001g0084a0001c0002t0003g0018a0001c0002t0003g0028others(5): Show | 12 | HG00597.hp2 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.148+3509T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132697 | ||||||
chr3:3132704
|
A | T | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3516A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132704 | ||||||
chr3:3132714
|
A | C | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.148+3526A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132714 | ||||||
chr3:3132731
|
G | GA | 50 | a0001c0001t0002g0171a0001c0001t0002g0172a0001c0001t0002g0198others(47): Show | 88 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.148+3556dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132731 | |||||
chr3:3132737
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0134 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.148+3557_148+3566d others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132737 | |||||
chr3:3132740
|
A | C | 1 | a0001c0001t0018g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.148+3552A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132740 | ||||||
chr3:3132741
|
A | C | 2 | a0001c0001t0006g0056a0001c0001t0006g0057 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.148+3553A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132741 | ||||||
chr3:3132743
|
AAC | A | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.148+3559_148+3560d others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132743 | |||||
chr3:3132745
|
C | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.148+3557C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132745 | ||||||
chr3:3132746
|
A | AAC | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0103others(3): Show | 6 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.148+3558_148+3559i others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132746 | ||||||
chr3:3132746
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.148+3558A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132746 | ||||||
chr3:3132747
|
C | A | 7 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0103others(4): Show | 7 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.148+3559C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132747 | ||||||
chr3:3132747
|
C | CA | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 169 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.148+3569dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3132747 | |||||
chr3:3132749
|
A | C | 1 | a0002c0003t0004g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.148+3561A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132749 | ||||||
chr3:3132758
|
C | A | 39 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(36): Show | 61 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.148+3570C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132758 | ||||||
chr3:3132805
|
G | C | 1 | a0001c0001t0025g0188 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.148+3617G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132805 | ||||||
chr3:3132837
|
T | C | 1 | a0001c0001t0001g0032 | 2 | HG00741.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.148+3649T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3132837 | ||||||
chr3:3133043
|
C | G | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.148+3855C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133043 | ||||||
chr3:3133081
|
C | G | 1 | a0001c0001t0001g0116 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.148+3893C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133081 | ||||||
chr3:3133137
|
G | A | 1 | a0002c0003t0004g0024 | 3 | HG02257.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.148+3949G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133137 | ||||||
chr3:3133163
|
T | G | 1 | a0001c0002t0003g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.148+3975T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133163 | ||||||
chr3:3133232
|
G | T | 2 | a0001c0001t0017g0147a0001c0001t0017g0148 | 2 | HG01106.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.149-4028G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133232 | ||||||
chr3:3133271
|
G | C | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3989G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133271 | ||||||
chr3:3133279
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.149-3981T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133279 | ||||||
chr3:3133349
|
T | A | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3911T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133349 | ||||||
chr3:3133377
|
A | C | 1 | a0001c0001t0025g0188 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.149-3883A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133377 | ||||||
chr3:3133417
|
G | T | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3843G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133417 | ||||||
chr3:3133422
|
A | G | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-3838A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133422 | ||||||
chr3:3133490
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.149-3770G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133490 | ||||||
chr3:3133523
|
A | C | 1 | a0005c0014t0016g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.149-3737A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133523 | ||||||
chr3:3133555
|
C | CA | 8 | a0001c0001t0001g0085a0001c0004t0008g0047a0001c0004t0008g0048others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-3692dupA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3133555 | |||||
chr3:3133569
|
T | A | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3691T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133569 | ||||||
chr3:3133576
|
C | T | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-3684C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133576 | ||||||
chr3:3133588
|
C | G | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3672C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133588 | ||||||
chr3:3133665
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.149-3595G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133665 | ||||||
chr3:3133669
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3591A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133669 | ||||||
chr3:3133670
|
GT | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3589delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133670 | ||||||
chr3:3133673
|
C | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3587C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133673 | ||||||
chr3:3133677
|
G | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3583G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133677 | ||||||
chr3:3133678
|
G | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3582G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133678 | ||||||
chr3:3133682
|
T | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3578T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133682 | ||||||
chr3:3133685
|
T | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3575T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133685 | ||||||
chr3:3133688
|
ACAG | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3571_149-3569d others(5): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133688 | ||||||
chr3:3133693
|
G | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3567G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133693 | ||||||
chr3:3133695
|
G | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3565G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133695 | ||||||
chr3:3133699
|
T | TG | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3561_149-3560i others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133699 | ||||||
chr3:3133702
|
CGCTCAGT others(444): Show |
C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3557_149-3107d others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133702 | ||||||
chr3:3133708
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-3552G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133708 | ||||||
chr3:3133720
|
G | A | 1 | a0001c0004t0008g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.149-3540G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133720 | ||||||
chr3:3133786
|
G | C | 3 | a0001c0001t0002g0171a0001c0001t0002g0173a0001c0001t0002g0186 | 3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.149-3474G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133786 | ||||||
chr3:3133917
|
C | T | 3 | a0001c0002t0003g0016a0001c0002t0003g0053a0001c0002t0020g0016 | 5 | HG00438.hp1 HG02155.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.149-3343C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133917 | ||||||
chr3:3133922
|
A | G | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3338A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3133922 | ||||||
chr3:3134063
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.149-3197G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134063 | ||||||
chr3:3134090
|
T | G | 2 | a0001c0002t0014g0036a0007c0007t0014g0133 | 3 | HG02109.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.149-3170T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134090 | ||||||
chr3:3134131
|
A | T | 3 | a0001c0001t0002g0171a0001c0001t0002g0173a0001c0001t0002g0186 | 3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.149-3129A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134131 | ||||||
chr3:3134157
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3103A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134157 | ||||||
chr3:3134163
|
T | TG | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3097_149-3096i others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134163 | ||||||
chr3:3134166
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3094A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134166 | ||||||
chr3:3134167
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3093A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134167 | ||||||
chr3:3134169
|
G | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3091G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134169 | ||||||
chr3:3134171
|
A | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3089A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134171 | ||||||
chr3:3134174
|
T | TG | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3086_149-3085i others(3): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134174 | ||||||
chr3:3134176
|
G | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3084G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134176 | ||||||
chr3:3134177
|
C | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3083C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134177 | ||||||
chr3:3134180
|
A | ATGTC | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3080_149-3079i others(6): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134180 | ||||||
chr3:3134181
|
G | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3079G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134181 | ||||||
chr3:3134187
|
T | G | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-3073T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134187 | ||||||
chr3:3134190
|
A | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3070A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134190 | ||||||
chr3:3134192
|
T | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3068T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134192 | ||||||
chr3:3134192
|
T | C | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-3068T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134192 | ||||||
chr3:3134193
|
GT | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3065delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3134193 | |||||
chr3:3134197
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3063A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134197 | ||||||
chr3:3134200
|
GCC | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3059_149-3058d others(4): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134200 | ||||||
chr3:3134204
|
C | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3056C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134204 | ||||||
chr3:3134206
|
C | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3054C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134206 | ||||||
chr3:3134208
|
GT | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3049delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3134208 | |||||
chr3:3134211
|
T | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3049T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134211 | ||||||
chr3:3134214
|
GT | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3045delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134214 | ||||||
chr3:3134216
|
A | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3044A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134216 | ||||||
chr3:3134218
|
G | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3042G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134218 | ||||||
chr3:3134219
|
A | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3041A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134219 | ||||||
chr3:3134225
|
GATATCAG others(3): Show |
G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3034_149-3025d others(12): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134225 | ||||||
chr3:3134238
|
G | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3022G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134238 | ||||||
chr3:3134241
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3019A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134241 | ||||||
chr3:3134242
|
T | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3018T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134242 | ||||||
chr3:3134248
|
AATCTTGA others(27): Show |
A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-3011_149-2978d others(36): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134248 | ||||||
chr3:3134286
|
T | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2974T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134286 | ||||||
chr3:3134287
|
GT | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2972delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134287 | ||||||
chr3:3134292
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2968A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134292 | ||||||
chr3:3134294
|
T | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2966T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134294 | ||||||
chr3:3134295
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2965A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134295 | ||||||
chr3:3134297
|
G | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2963G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134297 | ||||||
chr3:3134298
|
C | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2962C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134298 | ||||||
chr3:3134306
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2954A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134306 | ||||||
chr3:3134308
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2952A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134308 | ||||||
chr3:3134309
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2951A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134309 | ||||||
chr3:3134315
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2945A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134315 | ||||||
chr3:3134318
|
ACTGCTCT others(1118): Show |
A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-2941_149-1817d others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134318 | ||||||
chr3:3134343
|
G | A | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2917G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134343 | ||||||
chr3:3134353
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.149-2907G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134353 | ||||||
chr3:3134402
|
G | T | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2858G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134402 | ||||||
chr3:3134617
|
C | T | 79 | a0001c0001t0001g0157a0001c0001t0002g0005a0001c0001t0002g0009others(76): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.149-2643C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134617 | ||||||
chr3:3134694
|
A | G | 1 | a0001c0002t0003g0067 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.149-2566A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134694 | ||||||
chr3:3134729
|
T | C | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2531T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134729 | ||||||
chr3:3134825
|
A | G | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.149-2435A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134825 | ||||||
chr3:3134864
|
T | A | 2 | a0001c0001t0003g0210a0001c0012t0003g0139 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.149-2396T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134864 | ||||||
chr3:3134943
|
G | T | 1 | a0001c0001t0002g0205 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.149-2317G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134943 | ||||||
chr3:3134962
|
T | A | 8 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-2298T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3134962 | ||||||
chr3:3135037
|
AAGAG | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0084 | 4 | HG02055.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-2219_149-2216d others(6): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3135037 | |||||
chr3:3135253
|
G | A | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-2007G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135253 | ||||||
chr3:3135415
|
C | G | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.149-1845C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135415 | ||||||
chr3:3135431
|
C | T | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-1829C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135431 | ||||||
chr3:3135435
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.149-1825T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135435 | ||||||
chr3:3135445
|
G | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1815G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135445 | ||||||
chr3:3135451
|
G | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1809G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135451 | ||||||
chr3:3135454
|
G | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1806G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135454 | ||||||
chr3:3135456
|
A | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1804A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135456 | ||||||
chr3:3135457
|
T | TCTGTCG | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1803_149-1802i others(8): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135457 | ||||||
chr3:3135458
|
T | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1802T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135458 | ||||||
chr3:3135460
|
A | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1800A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135460 | ||||||
chr3:3135464
|
G | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1796G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135464 | ||||||
chr3:3135465
|
A | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1795A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135465 | ||||||
chr3:3135468
|
T | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1792T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135468 | ||||||
chr3:3135469
|
GA | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1790delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135469 | ||||||
chr3:3135473
|
T | C | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1787T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135473 | ||||||
chr3:3135474
|
G | A | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.149-1786G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135474 | ||||||
chr3:3135480
|
A | G | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-1780A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135480 | ||||||
chr3:3135493
|
C | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.149-1767C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135493 | ||||||
chr3:3135536
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-1724G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135536 | ||||||
chr3:3135778
|
C | T | 1 | a0001c0001t0005g0185 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.149-1482C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135778 | ||||||
chr3:3135790
|
T | C | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-1470T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135790 | ||||||
chr3:3135872
|
G | C | 1 | a0001c0001t0007g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.149-1388G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135872 | ||||||
chr3:3135899
|
C | T | 2 | a0001c0001t0002g0184a0001c0001t0002g0194 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.149-1361C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135899 | ||||||
chr3:3135967
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0207 | 2 | HG01993.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.149-1293A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135967 | ||||||
chr3:3135991
|
C | T | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-1269C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3135991 | ||||||
chr3:3136018
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149-1242G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136018 | ||||||
chr3:3136151
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(69): Show | 165 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.149-1109C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136151 | ||||||
chr3:3136207
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.149-1053T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136207 | ||||||
chr3:3136238
|
A | T | 8 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.149-1022A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136238 | ||||||
chr3:3136248
|
A | T | 9 | a0001c0001t0003g0210a0001c0004t0008g0047a0001c0004t0008g0048others(6): Show | 9 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.149-1012A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136248 | ||||||
chr3:3136289
|
T | G | 30 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0016others(27): Show | 52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.149-971T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136289 | ||||||
chr3:3136293
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.149-967T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136293 | ||||||
chr3:3136304
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.149-956C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136304 | ||||||
chr3:3136363
|
A | G | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0017g0147others(1): Show | 4 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.149-897A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136363 | ||||||
chr3:3136421
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.149-839A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136421 | ||||||
chr3:3136424
|
G | A | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.149-836G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136424 | ||||||
chr3:3136426
|
A | T | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-834A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136426 | ||||||
chr3:3136506
|
T | A | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-754T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136506 | ||||||
chr3:3136638
|
G | A | 114 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0014others(111): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.149-622G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136638 | ||||||
chr3:3136644
|
CTTTCTTT others(3): Show |
C | 1 | a0002c0003t0004g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.149-602_149-593del others(10): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3136644 | |||||
chr3:3136658
|
CT | C | 41 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0034others(38): Show | 67 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.149-588delT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 3136658 | |||||
chr3:3136874
|
C | G | 2 | a0001c0001t0002g0201a0001c0001t0002g0202 | 2 | HG00323.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.149-386C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136874 | ||||||
chr3:3136942
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.149-318C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3136942 | ||||||
chr3:3137080
|
C | T | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.149-180C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137080 | ||||||
chr3:3137089
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149-171A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137089 | ||||||
chr3:3137239
|
T | C | 1 | a0001c0001t0006g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.149-21T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137239 | ||||||
chr3:3137241
|
T | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0126 | 2 | NA18973.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.149-19T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 2/7 | chr3 | 3137241 | ||||||
chr3:3137547
|
A | G | 2 | a0001c0001t0009g0042a0001c0001t0009g0190 | 3 | HG03098.hp2 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.342+94A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137547 | ||||||
chr3:3137578
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.342+125A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137578 | ||||||
chr3:3137629
|
C | T | 1 | a0001c0002t0003g0072 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.342+176C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137629 | ||||||
chr3:3137682
|
T | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0127 | 2 | HG03017.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.342+229T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137682 | ||||||
chr3:3137684
|
A | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+231A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137684 | ||||||
chr3:3137685
|
C | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+232C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137685 | ||||||
chr3:3137687
|
A | T | 8 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+234A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137687 | ||||||
chr3:3137698
|
A | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+245A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137698 | ||||||
chr3:3137699
|
A | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+246A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137699 | ||||||
chr3:3137700
|
G | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+247G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137700 | ||||||
chr3:3137701
|
A | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+248A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137701 | ||||||
chr3:3137703
|
G | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+250G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137703 | ||||||
chr3:3137705
|
G | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+252G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137705 | ||||||
chr3:3137708
|
A | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+255A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137708 | ||||||
chr3:3137709
|
C | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+256C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137709 | ||||||
chr3:3137710
|
G | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+257G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137710 | ||||||
chr3:3137712
|
A | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+259A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137712 | ||||||
chr3:3137715
|
G | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+262G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137715 | ||||||
chr3:3137716
|
A | G | 31 | a0001c0001t0005g0136a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.342+263A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137716 | ||||||
chr3:3137716
|
A | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+263A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137716 | ||||||
chr3:3137717
|
C | T | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+264C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137717 | ||||||
chr3:3137720
|
T | TGAGACGG others(269): Show |
1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+267_342+268ins others(276): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137720 | ||||||
chr3:3137723
|
A | G | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+270A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137723 | ||||||
chr3:3137724
|
T | G | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+271T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137724 | ||||||
chr3:3137725
|
A | C | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+272A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137725 | ||||||
chr3:3137726
|
A | C | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.342+273A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137726 | ||||||
chr3:3137901
|
C | T | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.342+448C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3137901 | ||||||
chr3:3138231
|
G | T | 1 | a0001c0001t0002g0200 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.342+778G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138231 | ||||||
chr3:3138235
|
G | C | 1 | a0006c0013t0026g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.342+782G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138235 | ||||||
chr3:3138257
|
C | T | 1 | a0001c0001t0002g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.342+804C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138257 | ||||||
chr3:3138373
|
G | T | 76 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0014others(73): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.342+920G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138373 | ||||||
chr3:3138489
|
C | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 177 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.342+1036C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138489 | ||||||
chr3:3138607
|
C | T | 1 | a0001c0001t0005g0154 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.342+1154C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138607 | ||||||
chr3:3138679
|
C | G | 3 | a0001c0001t0002g0171a0001c0001t0002g0173a0001c0001t0002g0186 | 3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.342+1226C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138679 | ||||||
chr3:3138768
|
G | A | 7 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(4): Show | 7 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+1315G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138768 | ||||||
chr3:3138991
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.343-1519G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3138991 | ||||||
chr3:3139022
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(80): Show | 178 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.343-1488T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139022 | ||||||
chr3:3139079
|
A | G | 1 | a0001c0001t0006g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.343-1431A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139079 | ||||||
chr3:3139178
|
A | C | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.343-1332A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139178 | ||||||
chr3:3139252
|
G | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(202): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.343-1258G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139252 | ||||||
chr3:3139556
|
G | T | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.343-954G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139556 | ||||||
chr3:3139593
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.343-917T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139593 | ||||||
chr3:3139613
|
A | G | 82 | a0001c0001t0001g0157a0001c0001t0001g0189a0001c0001t0002g0005others(79): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.343-897A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139613 | ||||||
chr3:3139629
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.343-881T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139629 | ||||||
chr3:3139647
|
G | A | 1 | a0006c0013t0026g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.343-863G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139647 | ||||||
chr3:3139656
|
A | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.343-854A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139656 | ||||||
chr3:3139658
|
A | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.343-852A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139658 | ||||||
chr3:3139671
|
G | C | 8 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-839G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139671 | ||||||
chr3:3139687
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.343-823G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139687 | ||||||
chr3:3139716
|
T | C | 39 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(36): Show | 61 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.343-794T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139716 | ||||||
chr3:3139735
|
C | A | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.343-775C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3139735 | ||||||
chr3:3140072
|
G | A | 1 | a0001c0001t0001g0033 | 2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.343-438G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140072 | ||||||
chr3:3140091
|
T | C | 1 | a0002c0003t0004g0038 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.343-419T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140091 | ||||||
chr3:3140107
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.343-403C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140107 | ||||||
chr3:3140119
|
A | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.343-391A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140119 | ||||||
chr3:3140295
|
T | TA | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.343-215_343-214ins others(1): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140295 | ||||||
chr3:3140296
|
T | A | 2 | a0001c0001t0001g0108a0002c0003t0004g0038 | 3 | HG02055.hp2 HG02970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.343-214T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140296 | ||||||
chr3:3140303
|
A | T | 32 | a0001c0001t0001g0059a0001c0001t0002g0179a0001c0002t0003g0006others(29): Show | 54 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.343-207A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140303 | ||||||
chr3:3140304
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.343-206A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140304 | ||||||
chr3:3140364
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0159 | 2 | HG00099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.343-146A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140364 | ||||||
chr3:3140392
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.343-118A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 3/7 | chr3 | 3140392 | ||||||
chr3:3140741
|
A | G | 2 | a0001c0002t0014g0036a0007c0007t0014g0133 | 3 | HG02109.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.481+93A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3140741 | ||||||
chr3:3140801
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.481+153A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3140801 | ||||||
chr3:3140805
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0087 | 5 | HG02080.hp2 NA18998.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+157G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3140805 | ||||||
chr3:3140816
|
G | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.481+168G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3140816 | ||||||
chr3:3141040
|
C | G | 3 | a0001c0001t0002g0171a0001c0001t0002g0173a0001c0001t0002g0186 | 3 | NA18973.hp1 NA18993.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.481+392C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141040 | ||||||
chr3:3141111
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481+463T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141111 | ||||||
chr3:3141180
|
C | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.481+532C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141180 | ||||||
chr3:3141216
|
C | G | 2 | a0001c0001t0002g0184a0001c0001t0002g0194 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.481+568C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141216 | ||||||
chr3:3141310
|
CAT | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0017g0147others(1): Show | 4 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+663_481+664del others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141310 | ||||||
chr3:3141337
|
A | T | 1 | a0001c0001t0002g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.481+689A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141337 | ||||||
chr3:3141451
|
T | G | 1 | a0001c0002t0003g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.481+803T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141451 | ||||||
chr3:3141453
|
T | C | 8 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+805T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141453 | ||||||
chr3:3141542
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+894A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141542 | ||||||
chr3:3141573
|
T | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0083others(7): Show | 24 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.481+925T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141573 | ||||||
chr3:3141717
|
C | G | 1 | a0006c0013t0026g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.481+1069C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141717 | ||||||
chr3:3141736
|
T | C | 1 | a0005c0014t0016g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.481+1088T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141736 | ||||||
chr3:3141887
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.481+1239A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141887 | ||||||
chr3:3141992
|
G | A | 1 | a0001c0001t0025g0188 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.481+1344G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3141992 | ||||||
chr3:3142100
|
A | C | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.481+1452A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142100 | ||||||
chr3:3142170
|
T | C | 8 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(5): Show | 8 | HG00642.hp2 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+1522T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142170 | ||||||
chr3:3142258
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.481+1610T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142258 | ||||||
chr3:3142382
|
A | C | 1 | a0005c0014t0016g0138 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.481+1734A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142382 | ||||||
chr3:3142476
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.481+1828C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142476 | ||||||
chr3:3142623
|
C | G | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.482-1961C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142623 | ||||||
chr3:3142677
|
C | T | 3 | a0001c0002t0003g0012a0001c0002t0003g0069a0001c0002t0003g0072 | 8 | HG00642.hp1 HG01168.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-1907C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142677 | ||||||
chr3:3142758
|
C | T | 31 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.482-1826C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142758 | ||||||
chr3:3142894
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.482-1690C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142894 | ||||||
chr3:3142969
|
G | C | 81 | a0001c0001t0001g0189a0001c0001t0002g0005a0001c0001t0002g0009others(78): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.482-1615G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142969 | ||||||
chr3:3142971
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.482-1613A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3142971 | ||||||
chr3:3143028
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.482-1556G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143028 | ||||||
chr3:3143229
|
C | T | 32 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(29): Show | 54 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.482-1355C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143229 | ||||||
chr3:3143241
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.482-1343A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143241 | ||||||
chr3:3143301
|
A | G | 32 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(29): Show | 54 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.482-1283A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143301 | ||||||
chr3:3143308
|
G | A | 1 | a0002c0003t0004g0038 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.482-1276G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143308 | ||||||
chr3:3143353
|
A | C | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0017g0147others(2): Show | 5 | HG01106.hp2 HG01175.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1231A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143353 | ||||||
chr3:3143379
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.482-1205A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143379 | ||||||
chr3:3143509
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.482-1075A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143509 | ||||||
chr3:3143520
|
C | T | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.482-1064C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143520 | ||||||
chr3:3143572
|
C | T | 80 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0014others(77): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.482-1012C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143572 | ||||||
chr3:3143592
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.482-992T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143592 | ||||||
chr3:3143702
|
AC | A | 84 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0014others(81): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.482-879delC | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 3143702 | |||||
chr3:3143723
|
C | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0102others(4): Show | 14 | HG00673.hp1 HG03927.hp2 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.482-861C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143723 | ||||||
chr3:3143829
|
A | C | 82 | a0001c0001t0001g0157a0001c0001t0002g0005a0001c0001t0002g0009others(79): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.482-755A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143829 | ||||||
chr3:3143906
|
A | G | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-678A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3143906 | ||||||
chr3:3144002
|
T | A | 1 | a0001c0001t0018g0058 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.482-582T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144002 | ||||||
chr3:3144043
|
A | T | 1 | a0001c0001t0002g0178 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.482-541A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144043 | ||||||
chr3:3144050
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.482-534T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144050 | ||||||
chr3:3144292
|
G | A | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.482-292G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144292 | ||||||
chr3:3144381
|
T | C | 1 | a0001c0001t0006g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.482-203T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144381 | ||||||
chr3:3144555
|
ATT | A | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-25_482-24delTT | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 3144555 | |||||
chr3:3144560
|
T | A | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-24T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 4/7 | chr3 | 3144560 | ||||||
chr3:3144888
|
T | C | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.608+178T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3144888 | ||||||
chr3:3144895
|
T | A | 1 | a0001c0001t0002g0175 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.608+185T>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3144895 | ||||||
chr3:3145035
|
T | G | 30 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0016others(27): Show | 52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.608+325T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145035 | ||||||
chr3:3145085
|
T | C | 30 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0016others(27): Show | 52 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.608+375T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145085 | ||||||
chr3:3145088
|
G | C | 81 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0014others(78): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.608+378G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145088 | ||||||
chr3:3145105
|
G | C | 3 | a0001c0001t0006g0027a0001c0001t0006g0056a0001c0001t0006g0057 | 4 | HG00280.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.608+395G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145105 | ||||||
chr3:3145128
|
G | A | 1 | a0006c0013t0026g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.608+418G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145128 | ||||||
chr3:3145169
|
C | G | 1 | a0001c0001t0017g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.608+459C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145169 | ||||||
chr3:3145210
|
C | T | 31 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.608+500C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145210 | ||||||
chr3:3145226
|
C | T | 5 | a0001c0004t0008g0047a0001c0004t0008g0048a0001c0004t0008g0049others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.608+516C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145226 | ||||||
chr3:3145255
|
C | T | 1 | a0001c0002t0014g0036 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.608+545C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145255 | ||||||
chr3:3145270
|
C | T | 1 | a0001c0001t0012g0169 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.608+560C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145270 | ||||||
chr3:3145271
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.608+561G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145271 | ||||||
chr3:3145299
|
T | TC | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.608+589_608+590ins others(1): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145299 | ||||||
chr3:3145319
|
T | C | 90 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0157others(87): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.608+609T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145319 | ||||||
chr3:3145322
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.608+612T>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145322 | ||||||
chr3:3145345
|
T | C | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.608+635T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145345 | ||||||
chr3:3145360
|
A | G | 40 | a0001c0001t0001g0035a0001c0001t0003g0210a0001c0002t0003g0006others(37): Show | 63 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.608+650A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145360 | ||||||
chr3:3145375
|
C | T | 2 | a0001c0001t0002g0045a0001c0001t0007g0204 | 3 | HG01192.hp2 HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.608+665C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145375 | ||||||
chr3:3145386
|
C | T | 1 | a0001c0002t0003g0071 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.608+676C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145386 | ||||||
chr3:3145392
|
A | C | 3 | a0001c0002t0003g0018a0001c0002t0003g0028a0001c0002t0003g0067 | 7 | HG00733.hp1 HG00735.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.608+682A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145392 | ||||||
chr3:3145426
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0087others(3): Show | 17 | HG00408.hp1 HG02080.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.608+716C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145426 | ||||||
chr3:3145427
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.608+717C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145427 | ||||||
chr3:3145465
|
C | T | 1 | a0004c0011t0001g0113 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.608+755C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145465 | ||||||
chr3:3145479
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.608+769G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145479 | ||||||
chr3:3145481
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.608+771C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145481 | ||||||
chr3:3145490
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.608+780G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145490 | ||||||
chr3:3145502
|
CA | C | 43 | a0001c0001t0001g0035a0001c0001t0001g0081a0001c0001t0001g0100others(40): Show | 71 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.608+813delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 3145502 | |||||
chr3:3145502
|
CAA | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.608+812_608+813del others(2): Show |
TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 3145502 | |||||
chr3:3145557
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.608+847G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145557 | ||||||
chr3:3145732
|
C | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.609-698C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145732 | ||||||
chr3:3145893
|
G | A | 1 | a0001c0002t0014g0036 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.609-537G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145893 | ||||||
chr3:3145943
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.609-487C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145943 | ||||||
chr3:3145959
|
G | A | 31 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.609-471G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145959 | ||||||
chr3:3145986
|
TA | T | 31 | a0001c0001t0003g0210a0001c0002t0003g0006a0001c0002t0003g0012others(28): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.609-442delA | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 3145986 | |||||
chr3:3145996
|
A | G | 1 | a0001c0012t0003g0139 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.609-434A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3145996 | ||||||
chr3:3146196
|
T | C | 1 | a0001c0001t0002g0039 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.609-234T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146196 | ||||||
chr3:3146266
|
G | A | 3 | a0001c0001t0002g0193a0001c0001t0002g0196a0001c0001t0002g0208 | 3 | NA18964.hp2 NA19012.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.609-164G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146266 | ||||||
chr3:3146295
|
C | T | 1 | a0001c0001t0002g0044 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.609-135C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146295 | ||||||
chr3:3146332
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(81): Show | 179 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.609-98A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 5/7 | chr3 | 3146332 | ||||||
chr3:3146678
|
A | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.802+55A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3146678 | ||||||
chr3:3146919
|
A | T | 2 | a0001c0002t0014g0036a0007c0007t0014g0133 | 3 | HG02109.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.802+296A>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3146919 | ||||||
chr3:3147025
|
C | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0132a0001c0001t0006g0211 | 8 | HG00609.hp2 HG02165.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+402C>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147025 | ||||||
chr3:3147050
|
T | C | 1 | a0001c0001t0002g0180 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.803-400T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147050 | ||||||
chr3:3147065
|
G | C | 2 | a0001c0004t0016g0137a0005c0014t0016g0138 | 2 | HG00642.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.803-385G>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147065 | ||||||
chr3:3147078
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.803-372C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147078 | ||||||
chr3:3147217
|
A | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.803-233A>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147217 | ||||||
chr3:3147230
|
C | G | 81 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0014others(78): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.803-220C>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147230 | ||||||
chr3:3147284
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.803-166A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147284 | ||||||
chr3:3147375
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.803-75T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147375 | ||||||
chr3:3147376
|
G | A | 38 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0016others(35): Show | 60 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.803-74G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147376 | ||||||
chr3:3147392
|
A | G | 1 | a0001c0002t0014g0036 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.803-58A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147392 | ||||||
chr3:3147413
|
C | A | 1 | a0001c0001t0025g0188 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.803-37C>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 6/7 | chr3 | 3147413 | ||||||
chr3:3147714
|
A | G | 83 | a0001c0001t0001g0157a0001c0001t0002g0005a0001c0001t0002g0009others(80): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1056+11A>G | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147714 | ||||||
chr3:3147734
|
T | C | 1 | a0002c0003t0004g0141 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1056+31T>C | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147734 | ||||||
chr3:3147748
|
G | A | 14 | a0001c0001t0002g0014a0001c0001t0002g0026a0001c0001t0002g0039others(11): Show | 21 | HG00423.hp2 HG01106.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.1056+45G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147748 | ||||||
chr3:3147789
|
G | T | 2 | a0002c0003t0004g0021a0002c0003t0004g0145 | 5 | HG02647.hp1 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056+86G>T | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147789 | ||||||
chr3:3147828
|
G | A | 2 | a0001c0004t0008g0049a0001c0004t0008g0050 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1057-78G>A | TRNT1 | ENSG00000072756.18 | transcript | ENST00000251607.11 | protein_coding | 7/7 | chr3 | 3147828 |